Tantalum- and ruthenium-based diffusion barriers/adhesion .../67531/metadc... · Zhao, Xiaopeng, Tantalum- and ruthenium-based diffusion barriers/adhesion promoters for copper/silicon
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APPROVED: Jeffry A. Kelber, Major Professor William E. Acree, Jr., Committee Member Mohammad Omary, Committee Member Angela Wilson, Committee Member Ruthanne D. Thomas, Chair of the Department of
Chemistry Sandra L. Terrell, Dean of the Robert B. Toulouse
School of Graduate Studies
TANTALUM- AND RUTHENIUM-BASED DIFFUSION BARRIERS/ADHESION
PROMOTERS FOR COPPER/SILICON DIOXIDE AND
COPPER/LOW κ INTEGRATION
Xiaopeng Zhao, B.E., M.E.
Dissertation Prepared for the Degree of
DOCTOR OF PHILOSOPHY
UNIVERSITY OF NORTH TEXAS
December 2004
Zhao, Xiaopeng, Tantalum- and ruthenium-based diffusion barriers/adhesion promoters
for copper/silicon dioxide and copper/low κ integration. Doctor of Philosophy (Analytical
Chemistry), December 2004, 84 pp., 2 tables, 32 illustrations, 105 references.
The TaSiO6 films, ~8Å thick, were formed by sputter deposition of Ta onto ultrathin SiO2
substrates at 300 K, followed by annealing to 600 K in 2 torr O2. X-ray photoelectron
spectroscopy (XPS) measurements of the films yielded a Si(2p) binding energy at 102.1 eV and
Ta(4f7/2) binding energy at 26.2 eV, indicative of Ta silicate formation. O(1s) spectra indicate
that the film is substantially hydroxylated. Annealing the film to > 900 K in UHV resulted in
silicate decomposition to SiO2 and Ta2O5. The Ta silicate film is stable in air at 300K. XPS data
show that sputter-deposited Cu (300 K) displays conformal growth on Ta silicate surface
(TaSiO6) but 3-D growth on the annealed and decomposed silicate surface. Initial Cu/silicate
interaction involves Cu charge donation to Ta surface sites, with Cu(I) formation and Ta
reduction. The results are similar to those previously reported for air-exposed TaSiN, and
indicate that Si-modified Ta barriers should maintain Cu wettability under oxidizing conditions
for Cu interconnect applications.
XPS has been used to study the reaction of tert-butylimino tris(diethylamino) tantalum
(TBTDET) with atomic hydrogen on SiO2 and organosilicate glass (OSG) substrates. The results
on both substrates indicate that at 300K, TBTDET partially dissociates, forming Ta-O bonds
with some precursor still attached. Subsequent bombardment with atomic hydrogen at 500K
results in stoichiometric TaN formation, with a Ta(4f7/2) feature at binding energy 23.2 eV and
N(1s) at 396.6 eV, leading to a TaN phase bonded to the substrate by Ta-O interactions.
Subsequent depositions of the precursor on the reacted layer on SiO2 and OSG, followed by
atomic hydrogen bombardment, result in increased TaN formation. These results indicate that
TBTDET and atomic hydrogen may form the basis for a low temperature atomic layer deposition
(ALD) process for the formation of ultraconformal TaNx or Ru/TaNx barriers.
The interactions of sputter-deposited ruthenium with OSG at 300 K have been studied by
XPS for Ru coverages from ~ 0.1 monolayer to several monolayers, using in-situ sample transfer
between the deposition and analysis chambers. The results indicate Stranski-Krastanov (SK)
type growth, with the completion of the first layer of Ru at an average thickness corresponding to
1 monolayer average coverage. Ru(0) is the only electronic state present. XPS core level spectra
indicate weak chemical interactions between Ru and the substrate. A less pronounced tendency
towards SK growth was observed for Ru deposition on parylene. Deposition of Ru on OSG
followed by electroless deposition of Cu resulted in the formation of a shiny copper film that
failed the Scotch® tape test. Results indicate failure mainly at the Ru/OSG interface.
ii
ACKNOWLEDGMENTS
The author wishes to express his gratitude to Prof. Jeffry A. Kelber for his
guidance and careful instruction. Special thanks are extended to Dr. William E. Acree,
Jr., Dr. Mohammad Omary, Dr. Angela Wilson and Dr. Robert M. Wallace, for their
informative discussions. Financial supports provided by the Semiconductor Research
Corporation (SRC) through the Center for Advanced Interconnect Science and
Technology (CAIST), SRC through a Novellus/SRC customized research program, and
from the Robert Welch Foundation (grant no. B-1356), are gratefully acknowledged.
Finally, the author would like to express sincere appreciation to his wife, Liqin Zhang for
her constant encouragement and support.
iii
TABLE OF CONTENTS
Page
ACKNOWLEDGMENTS ............................................................................................... ii LIST OF TABLES........................................................................................................... vi LIST OF ILLUSTRATIONS........................................................................................... vii LIST OF ABBREVIATIONS.......................................................................................... x CHAPTER
1. INTRODUCTION ........................................................................................... 1
1.1. RC Delay................................................................................................. 3
1.2. Copper Metallization for Interconnection Technology .......................... 4
1.3. Diffusion Barriers ................................................................................... 6
1.4. Thin Film Deposition ............................................................................. 8
1.4.1. Physical Vapor Deposition (PVD)-DC Magnetron Sputtering.. 8
1.4.2. Chemical Vapor Deposition (CVD) .......................................... 9
1.5. Low-κ Dielectric..................................................................................... 11
1.6. Nucleation Modes Characterized by XPS............................................... 14
1.7. Experimental Aspects. ........................................................................... 15
1.7.1. Apparatus ................................................................................... 15
1.7.2. X-Ray Photoelectron Spectroscopy (XPS) ................................ 16
1.8. Chapter References ................................................................................. 22
iv
2. COPPER INTERACTION WITH A TANTALUM SILICATE SURFACE:
IMPLICATIONS FOR INTERCONNECT TECHNOLOGY ........................ 26
2.1. Introduction............................................................................................. 26
2.2. Experimental Details............................................................................... 28
2.3. Results..................................................................................................... 30
2.3.1. Ta Silicate Formation................................................................. 30
2.3.2. Thermal Decomposition............................................................. 34
2.3.3. Air-Exposure of Ta Silicate Film .............................................. 35
2.3.4. Cu/Film Interactions .................................................................. 35
2.4. Discussion ............................................................................................... 42
2.5. Conclusions............................................................................................. 43
2.6. Chapter References ................................................................................. 44
3. CHEMICAL VAPOR DEPOSITION OF TANTALUM NITRIDE WITH
TERTT-BUTYLIMINO TRIS(DIETHYLAMINO) TANTALUM AND
ATOMIC HYDROGEN .................................................................................. 47
3.1. Introduction............................................................................................. 47
3.2. Experimental Details............................................................................... 49
3.3. Results..................................................................................................... 50
3.3.1. TaN Formation on SiO2 ............................................................ 50
3.3.2. TaN Formation on OSG............................................................. 56
3.4. Discussion ............................................................................................... 62
v
3.5. Conclusions............................................................................................. 64
3.6. Chapter References ................................................................................. 65
4. RETHENIUM SPUTTER DEPOSITION ON ORGANOSILICATE GLASS
AND ON PARYLENE: AN XPS STUDY OF INTERFACIAL
CHEMISTRY, NUCLEATION AND GROWTH ........................................ 68
4.1. Introduction............................................................................................. 68
4.2. Experimental Detail ................................................................................ 69
4.3. Results..................................................................................................... 69
4.4. Discussion ............................................................................................... 74
4.5. Conclusions............................................................................................. 75
4.6. Chapter References ................................................................................. 76
BIBLIOGRAPHY............................................................................................................ 78
vi
LIST OF TABLES
Table Page 1.1. Properties of possible interconnect metals.............................................................. 5 1.2. Requirements for low dielectric constant intralayer-dielectric materials ...............13
vii
LIST OF ILLUSTRATIONS
Figure Page 1.1. Comparison of intrinsic gate delay and interconnect (RC) delay as a function of
feature size. ............................................................................................................. 4
1.2. Schematic diagram of a basic Cu interconnect structure. ....................................... 6
1.3. The DC magnetron sputtering process .................................................................. 9
1.4. Deposition profiles of (a) PVD and (b) CVD .......................................................10
1.5. Principle of MOCVD process................................................................................11
1.6. OSG schematic bonding structure .........................................................................13
1.7. Intensity vs. time plots of (a) Frank−Van der Merwe (layer-by-layer);
(b) Stranski−Krastanov growth (monolayer then islanding) and (c) Volmer−Weber
(islanding) ..............................................................................................................15
1.8. Combined XPS and DC magnetron PVD/CVD apparatus ...................................16
1.9. The XPS emission process for a model atom ........................................................17
1.10. Schematic drawing of a X-ray photoelectron spectrometer .................................19
1.11. Angle resolved XPS .............................................................................................21
1.12. Schematic of the Auger process of a model atom .................................................21
2.1. Formation of SiO2 and Ta silicate. (a) Si(2p); (b) O(1s) and (c) Ta(4f) Spectra ...32
2.2. XPS intensity ratio as a function of annealing temperature....................................34
2.3. XPS spectra of Ta silicate at room temperature and after annealing at 900 K for 30
min in UHV. (a) Si(2p) Spectra and (b) Ta(4f) Spectra. ........................................36
viii
2.4. XPS spectra of Ta silicate before and after air exposure. (a) Si(2p) spectra; (b)
O(1s) spectra and (c) Ta(4f) spectra .......................................................................37
2.5. X-ray excited Cu(L3VV) Auger spectral evolution as a function of Cu deposition on
the unannealed silicate film. ...................................................................................39
2.6. Cu(2p)/Si(99) XPS intensity ratio vs. deposition time (a) before and (b) after
annealing the silicate film at 1000K .......................................................................40
2.7. Ta(4f) XPS spectra at Cu deposition for 1min and 5.5 min....................................41
3.1. Tert-butylimino tris(diethylamino) tantalum (TBTDET) structure. .......................48
3.2. XPS spectral changes upon reaction with TBTDET precursor. (Bottom traces) SiO2
sample before precursor exposure; (bottom middle traces) precursor adsorption at
120 K; (top middle traces) after annealing to 300K; (top traces) after H/H2
exposure. (a) Si(2p); (b) O(1s); (c) Ta(4f); (d) N(1s) and (e) C(1s). ......................52
3.3. XPS spectra change after annealing without and with subsequent H2/H flux
exposure on SiO2 sample. (a) Ta(4f) and (b) N(1s) ................................................54
3.4. XPS spectra change with cycles of TBTDET dose and H2/H flux exposure on SiO2
sample. (a) Ta(4f) and (b) N(1s). ............................................................................55
3.5. Ta(4f) XPS spectra after TBTDET dose and H2/H flux exposure on SiO2. (a)
Normal incidence and (b) Grazing incidence .........................................................56
3.6. XPS spectral changes upon reaction with TBTDET precursor. (Bottom traces) OSG
sample before precursor exposure; (middle traces) precursor adsorption at 120 K
followed by annealing to 300K; (top traces) after H/H2 exposure. (a) Si(2p); (b)
O(1s); (c) Ta(4f); (d) N(1s) and (e) C(1s)................................................................59
ix
3.7. XPS charge shift during various process stages of TaN formation, stage 1: OSG
sample as received; 2: cool down to 120K; 3: TBTDET dose at 120K; 4: anneal to
300K; 5: hydrogen flux exposure for 90 min; 6: hydrogen flux exposure for 270
min ..........................................................................................................................60
3.8. XPS spectra change with cycles of TBTDET dose and H2/H flux exposure on OSG
sample. (a) Ta(4f) and (b) N(1s). ............................................................................61
3.9. Ta(4f) XPS spectra after TBTDET dose and H2/H flux exposure. (a) on SiO2 and
(b) on OSG..............................................................................................................63
4.1. Core level XPS spectra for the OSG film before (bottom) and after (top) annealing
at 500 K for 30 min. in UHV ..................................................................................70
4.2. Ru(3d)/C(1s) region, showing the partial overlap of the Ru(3d) and C(1s) core
level features. Spectrum corresponds to about 30 min Ru deposition
(approximately 3 monolayers). Ru(3d3/2) component indicated by dashed line was
determined from the intensity and binding energy of the Ru(3d5/2) component ....71
4.3. The evolution of the Ru(3d5/2)/C(1s) intensity ratio as function of Ru deposition vs
time at 300 K. (Left) Deposition of Ru on OSG. The film thickness at 10 min
corresponds to 1 monolayer. (Right) Deposition of Ru on Parylene.....................72
4.4. XPS C(1s)/Ru(3d) spectra (left), and O(1s) spectra (right) .....................................73
x
LIST OF ABBREVIATIONS
ALD Atomic layer deposition
AP Auger parameter
ARXPS Angle resolved X-ray photoelectron spectroscopy
CAE Constant analyzer energy
CHA Concentric hemispherical analyzer
CVD Chemical vapor deposition
FAT Fixed analyzer transmission
FM Mode Frank - Van der Merve mode
FWHM Full width at half maximum
HSA Hemispherical sector analyzer
IC Integrated circuit
ILD Intralayer dielectric
IMFP Inelastic mean free path
MOCVD Metal-organic chemical vapor deposition
OSG Organosilicate glass
PVD Physical vapor deposition
RC Delay Resistance – capacitance delay
SEM Scanning electron microscopy
SK Mode Stranski - Krastanov mode
xi
TBTDET Tert-butylimino tris(diethylamino) tantalum
UHV Ultra-high vacuum
ULSI Ultra-large scale integrated
VW Mode Volmer - Weber mode
XPS X-ray photoelectron spectroscopy
1
CHAPTER 1
INTRODUCTION
With the shrinkage of integrated circuit geometry, the resistance-capacitance (RC) delay
in interconnects starts to become one of the major problems as the width of interconnect lines
becomes < 1 µm [1, 2]. Strategies to reduce the delay include incorporating metals with lower
resistivity and higher electromigration resistance, such as copper, and providing isolation with
low dielectric constant materials [3]. Copper (Cu) is an attractive substitute for aluminum (Al)
because it offers a lower resistivity (1.67 µΩ⋅cm versus 2.66 µΩ⋅cm for Al) and better
electromigration resistance. Cu integration is challenged, however, by its rapid diffusion into
silicon (Si) through silicon dioxide (SiO2) and poor adhesion to SiO2 [4]. The diffusion of Cu
into Si results in adverse effects, including the increase of junction leakage currents and a
degradation of oxide quality if it is present in device regions [5, 6]. Consequently, diffusion
barriers and adhesion promoters that do not alloy with Cu, adhere well to both Cu and dielectrics,
and exhibit electrical stability in high temperature are required for Cu integration [4, 7].
Diffusion barriers such as tantalum (Ta), tungsten (W), ruthenium (Ru) and corresponding
nitrides or carbides have been proposed as barriers [8-14]. The ability of Cu to wet, or grow
conformally, on most surfaces during deposition is extremely sensitive to oxygen (O)
contamination at the Cu/substrate interface. A partial monolayer of oxygen at the Cu/barrier
interface will significantly degrade wettability and step coverage, and allow facile agglomeration
at temperatures at or above 300K [8-10]. This sensitivity to low-level oxygen contamination
poses a significant threat to processing reliability, since Cu deposition is typically not done under
UHV conditions [4]. An air-stable diffusion barrier is desirable for Cu deposition.
2
At the same time, the signal processing times and signal cross talk between adjacent lines
in ultra-large scale integrated (ULSI) circuits can be improved by replacing SiO2 with materials
having low dielectric constants than that of SiO2 (κ ~ 4). The surface chemical state and
structure of low-κ dielectric materials are different from SiO2. The potential for relatively poor
adhesion between low k dielectric materials and barrier layers is one of the main issues involved
in the integration of Cu and low k materials into a standard microfabrication process [15].
The studies presented in this dissertation focus on the interactions of diffusion
barriers/adhesion promoters with Cu, SiO2 and low-κ dielectric materials. X-ray photoelectron
spectroscopy (XPS) was used for surface analysis. Thin film deposition technologies used in
these studies include DC magnetron sputtering and metal-organic chemical vapor deposition
(MOCVD). These studies include:
(1) Cu interaction with a Ta silicate surface: implications for interconnect technology.
(2) Chemical vapor deposition of TaN with tert-butylimino tris(diethylamino) tantalum
(TBTDET) and atomic hydrogen.
(3) Ruthenium sputter deposition on organosilicate glass and on parylene: an XPS study
of interfacial chemistry, nucleation and growth.
This dissertation consists of four chapters. The first chapter provides background
information on the fundamental interconnect integration, namely, role of RC delay, necessity of
Cu and low-κ dielectric materials, diffusion barriers, thin film deposition methods, nucleation
modes, as well as experimental methodologies. Chapter 2 presents the studies on Cu interaction
with a Ta silicate surface and its implications for interconnect technology. Chapter 3 includes
studies of chemical vapor deposition of tantalum nitride (TaN) with Tert-butylimino
3
tris(diethylamino) tantalum and atomic hydrogen. Chapter 4 contains the study of ruthenium
sputter deposition on organosilicate glass and on parylene.
1.1. RC Delay
With the shrinking of transistor size in integrated circuits (IC) to improve chip
performance, speed and device density have increased. The effective measure of device
performance or total circuit delay is a combination of two components – the switching time of an
individual transistor, known as intrinsic gate delay, and the signal propagation time between
transistors, known as interconnect (RC) delay [16-18]:
RC =2ρκε0(4L2/P2+L2/T2), (1-1)
where R is metal wire resistance, C is intralayer dielectric (ILD) capacitance, ρ is metal
resistivity, κ and ε0 are dielectric constant of the intralayer dielectric and vacuum respectively, L,
T are the length and thickness of the conductor respectively, P is the distance between two
conducting lines.
For feature size below 1 µm, the intrinsic gate delay decreases continuously with
decreasing size of the transistors and the RC delay becomes the dominant factor (Fig.1.1) [1, 2].
New materials are being utilized by industry to reduce the RC delay by either lowering the
interconnect wire resistivity, or by reducing the dielectric constant of the ILD. A significant
improvement has been achieved by replacing the Al interconnects with Cu, which has ~30%
lower resistivity than that of Al [2]. Since no other metal can offer lower resistance without other
disadvantages (e.g., low electromigration resistance), Cu will remain the choice for interconnect.
Therefore, further advances can be achieved by reducing the dielectric constant of the ILD, i.e.,
by replacing SiO2 with a low-κ material.
4
Fig. 1.1 Comparison of intrinsic gate delay and interconnect (RC) delay as a function of feature
size.
1.2. Copper Metallization for Interconnect Technology
Al has been widely used in the past due to its relatively low resistivity, good corrosion
resistance in air and the formation of stable Al/SiO2 interfaces [4, 19]. Despite these favorable
characteristics, poor resistance to electromigration and hillock formation of Al leads to lower
lifetime and shorts between levels. In addition, the need to lower interconnect delay (Fig. 1.1)
has lead to the examination of other metals as replacements to Al [2, 4, 20].
A comparison of Al to some other lower-resistivity metals that are potential replacements
is listed in Table 1.1. Applications of silver (Ag) and gold (Au) to replace Al have been
suggested in the last three decades. Although Au has very low corrosion in the air, it is far more
costly and has a higher resistivity and lower electromigration resistance than Cu [4, 20, 21]. The
0
0.5
1
1.5
2
2.5
3
0 0.5 1 1.5 2 2.5 3 3.5
Interconnect Delay (RC)Intrinsic Gate Delay
Feature Size (µm)
Del
ay T
ime(
*10– 9
sec )
5
advantage of Ag is its low resistivity, about 5% lower than that of Cu. However, it is more costly
than Cu, has a poor electromigration resistance, and diffuses into SiO2 at a much faster rate than
Cu, especially under electrical bias [4, 20, 21]. Cu is the best choice to replace Al due to its low
resistivity, high melting point and high electromigration resistance [4, 20, 21]. Because Cu is
more conductive than Al and smaller interconnect lines can provide the same current-carrying
capability, Cu makes it possible to reduce the number of levels of metal and reduce the
capacitance. However, several processing and reliability issues need to be addressed before Cu
technology can be fully integrated with device manufacteruring. Cu will react with Si very
strongly to form Cu silicide at temperatures as low as 200C, and the reaction is detrimental to
the electrical performance of Si [22, 23]. Cu can also move easily through the oxide to the Si/O
interface, under conditions of combined elevated temperature and electric field (“bias/thermal
stress- BTS”) [5, 24]. For the low κ replacement of SiO2, the potential interaction between Cu
and low κ materials is a serious reliability issue [25, 26]. Therefore, diffusion barriers that can
block the Cu transport and adhesion promoters that can improve Cu adhesion are required for Cu
integration into device manufacturing.
Table 1.1 Properties of possible interconnect metals.
Properties
Cu Ag Au Al
Resistivity (µΩ.cm)
1.67 1.59 2.35 2.66
Electromigration Resistance
Very High
Low High Low
Corrosion in Air
High High Very Low
Low
6
1.3. Diffusion Barriers
A diffusion barrier/adhesion promoter (Fig. 1.2) is very important for Cu–based
metallization due to the high diffusivity of Cu into SiO2 and low k dielectric materials [4]. A
successful diffusion barrier must form strong chemical bonds to the dielectric substrate and to
Cu. The chemical bonding at these interfaces should be the result of self-limiting reactions,
otherwise reactions will continue to occur with time and the properties of substrates, barriers and
metals may be compromised. Thus the ultimate objective is to find an adhesion promoter that
will also perform as a diffusion barrier.
Fig. 1.2 Schematic diagram of a basic Cu interconnect structure. “ILD” is the intralayer
dielectric: currently SiO2 or a lower k dielectric material.
The refractory metals, and their binary and ternary compounds, such as Ta, W, Ru,
molybdenum (Mo), vanadium (V), TaN and tantalum silicon nitride (TaSiN), have been widely
ILD
Substrate
ILD
Cu
Diffusion Barrier /Adhesion Promoter
ILD
Substrate
ILD
Cu
Diffusion Barrier /Adhesion Promoter
7
investigated as diffusion barriers [8-12, 26]. These refractory metals are not miscible with Cu at
low temperature [4, 27, 28]. In addition, they have high melting points for thermal stability
during processing [4, 27, 28].
Titanium (Ti) and titanium nitride (TiN) are widely used in Al-based interconnect
systems [27, 29]. Unfortunately, they cannot provide enough Cu barrier performance since Cu
and Ti form a bulk alloy, and a Cu grain boundary diffusion proceeds readily in TiN [30, 31].
For Cu-based interconnect systems, Ta-based diffusion barriers possess an inherent advantage
over Ti-based barriers because Ta is thermodynamically stable with respect to Cu. Cu and Ta are
almost completely immiscible up to their melting point and do not react [32]. In addition, the
Ta/Si interface is stable up to ~920K [33]. TaN has been widely recognized as an attractive
diffusion barrier due to its thermal stability and high conductivity [12-14]. Ta nitride is highly
stable with respect to Cu due to the absence of Cu-Ta and Cu-N compounds [27]. Furthermore,
the TaNx/Si interface is more stable than Ta/Si interface because higher activation energy is
needed to dissociate Ta-N bond before silicide formation [27]. It has been shown that
stoichiometric TaN fails through Cu diffusion along grain boundaries, but at a higher
temperature than Ta [34, 35]. TaSixNy has been investigated as a diffusion barrier for Cu since
being amorphous over a broad temperature range lacks grain boundaries that can act as diffusion
pathways [10, 27, 36]. Addition of a third element into a Ta nitride matrix disrupts the crystal
lattice and leads to the formation of a stable amorphous ternary phase TaSixNy with significantly
higher recrystallization temperature than TaN.
Ru-based materials are of growing interest as diffusion barriers for Cu due to ruthenium’s
high melting point (2310°C) and immiscibility with Cu [11, 37]. It shows negligible solid
solubility with Cu even at 900°C [32, 38]. Strong adhesion between Cu/Ru is confirmed by
8
scribe and tape-peel tests [11, 39]. Ruthenium is relatively noble, allowing for facile
electrodeposition of Cu films [11, 37].
1.4. Thin Film Deposition Methods
In these studies, tantalum, copper and ruthenium depositions were performed by direct
current (DC) magnetron sputtering deposition. Tantalum nitride was deposited by metal-organic
chemical vapor deposition (MOCVD) using tert-butylimino tris(diethylamino) tantalum
(TBTDET) as precursor.
1.4.1. Physical Vapor Deposition (PVD) - DC Magnetron Sputtering
The process of DC magnetron sputtering process is shown in Fig. 1.3. The electrons that
are ejected from the cathode are accelerated away from the cathode. A magnetic field is imposed
in such a way that the electrons can be made to circulate on a closed path near the target surface.
This high flux of electrons creates a high density argon (Ar) plasma from which Ar ions can be
extracted to sputter the target material. The cathode (negative) potential attracts Ar ions from
near the edge of the plasma region and they are accelerated across the cathode fall region to
impinge on the cathode target, resulting in atoms of target materials ejected from the surface.
Once sputtered, the target atoms travel until they reach the substrate. The principal advantage of
this magnetron sputtering configuration is that a dense plasma can be formed near the cathode at
low pressures so that ions can be accelerated from the plasma to the cathode without loss of
energy due to physical and charge-exchange collisions. This allows a high sputtering rate with a
low potential on the target, lower pressures and less gas incorporation into the sputtered film.
9
This DC sputtering cannot be used to sputter dielectric target materials, since charge buildup on
the cathode surface will prevent bombardment of the surface.
Fig. 1.3 The DC magnetron sputtering process.
1.4.2. Chemical Vapor Deposition (CVD)
PVD is not expected to be applied beyond 45 nm technology nodes due to the poor (non-
conformal) step coverage caused by the shadowing effect in the small feature size, high aspect
ratio via geometries (Fig. 1.4a) [40]. Accordingly, CVD is of interest since it can provide more
uniform (conformal) step coverage over high aspect ratio structures (Fig. 1.4b) [27, 40]. In CVD,
the constituents of a vapor phase react at a hot surface (typically higher than 300˚C) to deposit a
solid film. CVD process is schematically illustrated in Fig. 1.5. Reactants are first transferred
Target (Cathode) Negative High Voltage
“E” Field
“B” Field
Substrate (Anode)
Growing film
ee
e
e
e
e
e
Target Atoms
e Electrons
Ar Ar Atoms
Ar+ Ar ions
Plasma region
Ar
Ar
Ar
Ar
Ar
Ar
ArAr
Ar+Ar+
Ar+
Ar+
Target (Cathode) Negative High Voltage
“E” Field
“B” Field
Substrate (Anode)
Growing film
ee
e
e
e
e
e
Target Atoms
e Electrons
Ar Ar Atoms
Ar+ Ar ions
Plasma region
Ar
Ar
Ar
Ar
Ar
Ar
ArAr
Ar+Ar+
Ar+
Ar+
10
from the reactor inlet to the deposition zone. Gas phase reactions can occur, resulting in the
deposition of low molecular weight clusters and usually poor adhesion, low density and high-
defect film. If significant gas-phase reactions are avoided, film precursors and reactants are
absorbed on the growth surface and surface reactions (heterogeneous) occur on the heated
surface, following by surface migration of film formers and nucleation on the growth sites. By-
products of the surface reaction are then transported away from the deposition zone toward the
reactor exit. The sample surface chemistry, temperature and thermodynamics determine the
compound deposited. The most favorable end product on the substrate is a clean,
stoichiometricly-correct film. MOCVD is a CVD method, in which the precursor is a metal-
organic species. MOCVD can provide thickness control within one atomic monolayer [27, 40]. It
has become a cost-effective manufacturing process for a variety of compound semiconductor
devices [4, 27, 40].
Fig. 1.4 Deposition profiles of (a) PVD and (b) CVD.
(a) PVD, Non-conformal (b) CVD, Conformal
11
Fig. 1.5 Principle of CVD process.
1.5. Low-κ Dielectric
Since Cu has replaced Al and become the common metallization material, one of the
main challenges to further decrease RC delay today is to replace SiO2 (κ ~ 4) with lower κ
dielectrics [15]. Power consumption is another major concern for interconnects besides signal
delay. The increasing frequencies and densities lead to a dramatic increase in power
consumption. The dynamic power dissipation can be decreased by a lower wire capacitance,
resulting from the low κ dielectrics [15, 41]. The low k dielectrics can also be used to reduce
cross-talk noise between metal wires [4, 15, 41].
The dielectric constant (κ), or relative permittivity (εr) is represented in equation:
ε = εr ε0 = κε0 = (1+χe)ε0, (1-2)
Substrate
Carrier Gas Flow
+Gas phase reactions
Transport to surface
Surface reactionSurface diffusion
=Desorption of by-product
+Redesorption of film precursor
Substrate
Carrier Gas Flow
+Gas phase reactions
Transport to surface
Surface reactionSurface diffusion
=Desorption of by-product
+Redesorption of film precursor
12
where ε0 is the permitivity of vacuum, and χe is the electric susceptibility, describing the
tendency of a material to permit an applied electric field to induce dipoles in the material. The
microelectronics community has adopted κ in contrast to the scientific community using εr.
Thermal stability is another important requirement for low k dielectrics. Low k materials
must be able to withstand the temperature up to 670-720 K for several hours during Cu
metallization and the following annealing step to ensure void free copper deposits [4]. New low
k materials should also have a lot additional properties (Table 1-2) related to performance and
reliability for use as an intralayer dielectric material [42, 43].
A low κ value relative to that of SiO2 (κ ~ 4) can be achieved by either compositional
changes (e.g. less polarizable chemical bonds), or reduction of density through change of
network structure (e.g. via addition of bulky terminal groups) or introduction of porosity [15].
Organosilicate glass (OSG, κ = 2.8-3.3) is one of the leading low-k materials for use as an
intralayer dielectric [44]. The OSG schematic bonding structure is shown in Fig. 1.6. In OSG,
CH3 terminal groups that cannot network are introduced in the silicate glasses to decrease
dielectric constant. Replacement of O with organic groups also lowers the ionic contributions to
κ. Typical densities of OSG are between 1.2 and 1.4 g/cm3, much lower than that of SiO2 (2.1-
2.3 g/cm3) [15]. The κ value of OSG (κ = 2.8-3.3) depends on the number of CH3 groups
because they lower both polarity and density of the material by steric hindrance [44]. The surface
chemical state and structure of OSG are different from SiO2. Potential relatively poor adhesion
between low k dielectric materials and barrier layers is one of the main issues when low k
materials are integrated into a standard microfabrication process [15].
13
Table 1.2 Requirements for low dielectric constant intralayer-dielectric materials.
Low κ dielectrics properties Value
Dielectric Constant < 3
Thermal Stability >400°C
Adhesion (to metal, self-adhesion) Pass tape test after thermal cycles to 450°C
Breakdown Strength >2 MV.cm-1
Moisture Adsorption <1%
Etch Rate >3nm/s
Chemical Strong acid/base resistance, no solvent
adsoption
Gap Fill No voids at 0.35 µm, aspect ratio = 2
Fig. 1.6 OSG schematic bonding structure.
Si O Si
OO
Si CH3
O
Si
CH3
OSi
OH3C
O
Si
O
O
CH3H
H
Si O Si
OO
Si CH3
O
Si
CH3
OSi
OH3C
O
Si
O
O
CH3H
H
14
1.6. Nucleation Modes Characterized by XPS
The thermodynamics of the growth mode of film on the substrate can be expressed by the
surface energy criteria [45], as a balance between the free energies of the film, substrate and
interface (γF, γS and γFS, respectively) :
∆γ = γF + γFS - γS. (1-3)
∆γ < 0 will favor the covering over the substrate by spreading of the condensate film (i.e. the
film “wets” the substrate), leading to the layer-by-layer growth (Frank - van der Merve, or FM)
Mode. If the lattice spacing of the film and substrate are different, there will be an increase of
strain and the value of ∆γ with film thickness under epitaxial growth conditions. To release the
strain, the growth mode transforms from layer-by-layer growth to islanding after the formation of
the first (usually) 1-3 monolayers. This is known as Stranski - Krastanov, or SK mode. ∆γ ≥ 0
will favor the non-wetting or 3D islanding growth (Volmer - Weber, or VW) mode.
XPS can be used to characterize the growth mode of an overlayer on a substrate [46-48].
The change in metal film and substrate XPS intensities with deposition time, the so-called
“uptake” curve, is used to analyze the growth modes. Typical uptake curves for the three growth
modes are shown in Fig. 1.7. The FM growth mode (Fig. 1.7a) typically has a plot with several
breakpoints, with each breakpoint indicating the completion of a monolayer. The SK growth
mode (Figure 1.7b) is characterized by one or two breaks, followed by level off at higher
coverage. There are no further breaks when islanding occurs with the increase of metal
deposition. For VW growth (Fig. 1.7c), the uptake curve increases linearly with no changes or
breaks in slope.
15
Fig. 1.7 Intensity vs. time plots of (a) Frank−Van der Merwe (layer-by-layer);
(b) Stranski−Krastanov (monolayer then islanding) and (c) Volmer−Weber (islanding) growth.
1.7. Experimental Aspects
1.7.1. Apparatus
The combined XPS/PVD/CVD system used in this study is shown schematically in figure
1.8. The UHV main chamber (with a base pressure of 7 x 10-10 torr after bake out) is equipped
with a hemispherical analyzer (VG AX100), an unmonochromatized Mg/Al x-ray source (PHI)
for XPS and Ar+ sputter-cleaning capabilities (PHI). PVD/CVD chamber (with a base pressure of
1 x 10-8 torr after bake out) is isolated from the analysis chamber and sputtering target/sample
distance is adjusted so that an appropriate deposition rates can be achieved.
Substrate(S)Substrate(S)
Metal(M)
Substrate(S)
M/S
XPS
Inte
nsity
Deposition Time
(a) (b) (c)
1st layer
2nd layer
3rd layer
1st layer
Metal(M)
Substrate(S)Substrate(S)
Metal(M)
Substrate(S)
M/S
XPS
Inte
nsity
Deposition Time
(a) (b) (c)
1st layer
2nd layer
3rd layer
1st layer
Metal(M)
16
Fig. 1.8 Combined XPS and DC magnetron PVD/CVD apparatus.
1.7.2. X-Ray Photoelectron Spectroscopy (XPS)
XPS is performed by analyzing the energy distribution of photoelectrons emitted from a
solid surface as a result of X-ray excitation. The process of XPS emission is shown
schematically in Fig. 1.9. Photons with sufficient energy strike the surface and are absorbed,
resulting in ionization and emission of core (inner shell) electrons. The kinetic energy (KE) of
the electron is dependent on the photon energy of the X-ray employed and not an intrinsic
material property. The binding energy of the electron (EB) is a parameter identifying the electron
specifically in terms of its parent element and atomic energy level. The binding energy of the
electron is given by [49]:
EB = hv - KE- ϕs, (1-4)
XPS
RGA
CVD Precursor Introduction System
PVD Tower (Magnetron Sputter Deposition)
Sample Introductionand Manipulation
e -Beam
TPDCapability
XPS
RGA
PVD Tower
Sample Introduction
e -Beam
TPDCapability
Hydrogen Cracker
TurboPump
Main Chamber (7*10-10)
PVD Tower #2 (backside)
CVD Precursor Introduction System
PVD/CVD Chamber (1*10-8)
XPS
RGA
CVD Precursor Introduction System
PVD Tower (Magnetron Sputter Deposition)
Sample Introductionand Manipulation
e -Beam
TPDCapability
XPS
RGA
PVD Tower
Sample Introduction
e -Beam
TPDCapability
Hydrogen Cracker
TurboPump
Main Chamber (7*10-10 torr
PVD Tower #2 (backside)
CVD Precursor Introduction System
torr
17
where hv is the energy of the incident X-rays and ϕs is the spectrometer work function (a
constant for a given analyzer). As all these three parameters are known or measurable [49], the
binding energy can be determined using Eq. (1-4).
Fig. 1.9 The XPS emission process for a model atom.
X-ray photoelectron spectroscopy requires an X-ray source, electron energy analyzer,
electron detector and a recorder. The choice of anode materials for the X-ray source must obey
two rules [50]. First, the source must have high enough photon energy and intensity for sufficient
core electrons to be photoejected from all elements. Second, the source must possess narrow X-
ray line width that will not broaden the resultant spectrum excessively. Al Kα (1486.6eV), Mg Kα
(1253.6eV) or monochromatic Al Kα (1486.7eV) X-ray sources [49] are usually used due to their
relatively narrow linewidths and high photon energies. Bombarding an Al or Mg anode material
with high-energy electrons generates X-rays. The electrons are emitted from a thermal source,
Al Ka or Mg Ka
hv
Photoelectron
KE
EB = hv - KE-ϕs
18
usually in the form of an electrically heated tungsten filament. An electron energy analyzer
measures the kinetic energy distribution of the emitted photoelectrons. A concentric
hemispherical analyzer (CHA) (Fig. 1.10), otherwise known as hemispherical sector analyzer
(HSA) is currently the most popular analyzer. There is a gap between a pair of concentric
hemispherical electrodes for the electrons to pass. The lens between the sample and analyzer
retards the photoelectrons to produce sufficiently high resolution, and focuses photoelectrons
emitted from the substrate onto the entrance slit to the analyzer. A potential difference is applied
across the two hemispheres with the outer voltage being more negative than the inner one. The
kinetic energy of the electrons that reach the detector is given by [50]:
E=ke∆V, (1-5)
where e is the charge on the electron, ∆V is the potential difference between the hemispheres and
k is the spectrometer constant and equal to R1R2/(R22-R1
2) (R1 and R2 are the radii of the inner
and outer hemispheres, respectively). Fixed analyzer transmission (FAT), sometimes known as
constant analyzer energy (CAE) is a popular operation mode for CHA [50]. In the FAT mode,
absolute resolution (∆E) is constant and electrons are accelerated or retarded to a user-defined
energy that the electrons possess as they pass through the analyzer (Pass Energy Ep). Only
electrons with energy E= Ep +∆E can pass through the spectrometer. The energy resolution
(±∆E) is fixed across the entire spectrum by retarding the electrons to a constant kinetic energy.
Channel electron multipliers (channeltrons) are used to count the electrons arriving at the
detector [50]. They consist of a glass tube with a collector at one end and an anode at the other.
The internal surface of the detector is coated with a material that will emit many secondary
electrons when hit by an electron with an energy more than the threshold kinetic energy. When a
large potential difference is applied across the channeltron, each electron arriving at the detector
19
will typically result in ~108 electrons reaching the anode. Channeltrons can detect up to 3*106
counts/s [50]. A computer based recorder plots the number of detected electrons versus the
binding energy in the resulting spectrum.
Fig. 1.10 Schematic drawing of an X-ray photoelectron spectrometer.
For every element, there will be a characteristic binding energy associated with each core
atomic orbital, resulting in a characteristic set of peaks in the photoelectron spectrum [49, 50].
The exact binding energy of an electron depends on the level from which photoemission is
occurring, the formal oxidation state of the atom, and the local chemical and physical
environment. Changes in any of these give rise to a small shift in the peak positions (chemical
shift) in the spectrum. A higher binding energy of the core-level photoelectron is generally
Sample
Multi-channel Detector
X-ray s
ourc
e
Lens
Outer hemisphere
Inner hemisphere
R1
R2-V1
-V2
Sample
Multi-channel Detector
X-ray s
ourc
e
Lens
Outer hemisphere
Inner hemisphere
R1
R2-V1
-V2
20
observed for an atom of a higher positive oxidation state due to the extra coulombic interaction
between the photo-emitted electron and the ion core [50]. Variations in the binding energies
arising from differences in the chemical potential and polarizability of compounds can be used to
identify the chemical state of the materials. XPS can also be used to identify and determine the
concentration of the elements in the surface since each element has a unique set of binding
energies [50].
XPS also provides a non-destructive analysis for compositional information as a function
of depth. Angle resolved XPS (ARXPS) is shown in Fig. 1.11. The escape depth within the solid
sample is proportional to λcosθ [50], where λ is the inelastic mean free path (IMFP) and θ is the
angle between the sample surface normal and analyzer axis. As θ increases, the effective
electron escape depth decreases and the analyzed region becomes more surface localized, leading
to an increase of the surface sensitivity. There are two advantages for ARXPS. First, it can be
applied to films that are too thin to be analyzed by conventional depth profiling techniques or
polymers that are irretrievably damaged by such methods. Second, unlike sputtering, it is a non-
destructive technique that can provide chemical state information. By comparing relative
intensities at different θ, a species can be determined to be enriched or depleted in the surface
region.
X-ray sources also excite Auger electrons. The Auger process for the KLL transition is
shown schematically in Fig. 1.12. After the K level is ionized by the creation of a hole in the
level K, the atom relaxes by filling the hole via a transition from higher level (with energy EL1).
As a result of the transition, the energy difference (EK-EL1) becomes available as excess kinetic
energy. A fraction of this energy is given to another electron either in the same level or in a
more shallow level (e.g. L23), whereupon the second electron is ejected. The kinetic energy (KE)
21
Fig. 1.11 Angle resolved XPS.
of Auger electron is approximated by [49]:
KE = (EK – EL1) – EL3. (1-6)
The Auger electron KE is independent of the exciting radiation and characteristic of the element
in the sample. Chemical bonding information can be obtained from Auger peak energy positions
and lineshapes in some cases, although the greater complexity of the Auger peaks often
complicates the extraction of chemical information.
Fig. 1.12 Schematic of the Auger process of a model atom.
Analyzer
e-
AnalyzerMean free path
Escape depth
Mean free path
e-
θ
hν hν
Surface normalAnalyzer
e-e-
AnalyzerMean free path
Escape depth
Mean free path
e-e-
θ
hν hν
Surface normal
L1
L*2,3
M, etc.
K
Auger Emission
hv
L1
L*2,3
L1
L*2,3
M, etc.
K
Auger Emission
hv
22
1.8. Chapter References
[1] Jeng, S.-P., Havemann, R. H. and Chang, M.-C., Mat. Res. Soc. Symp. Proc. 337 (1994)
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[21] Murarka, S. P., Gutmann, R. J., Kaloyeros, A. E. and Lanford, W. A., Thin Solid Films
236 (1993) 257.
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Fraser, D. B., Proc. VMIC (1994) 414.
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Technol. B 18 (1999) 221.
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Appl. Phys. 71 (1992) 5433.
24
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(2003) 690.
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Eng. 60 (2002) 107.
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Loffler, E. and Muhler, M., J. Catalysis 202 (2001) 296.
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[44] Cheng, Y. L., Wang, Y. L., Wu, Y. L., Liu, C. P., Liu, C. W., Lan, J. K., O'Neil, M. L.,
Ay, C. and Feng, M. S., Thin Solid Films 447-448 (2004) 681.
[45] Zhang, L., Persaud, R. and Madey, T. E., Phys. Rev. B 56 (1997) 549.
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5321.
[47] Argile, S. and Rhead, G. E., Surf. Sci. Repts. 10 (1989) 277.
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[49] Moulder, J. F., Sticle, W. F., Sobol, P. E. and Bomben, K. D., Handbook of X-ray
Photoelectron Spectroscopy, Physical Electronics, Inc., Eden Prairie, Minnesota, 1995.
25
[50] Seah, M. P., In Auger and X-ray Photoelectron Spectroscopy, D. Briggs and M. P. Seah
(New York, 1990), Vol. 1, 245.
26
CHAPTER 2
COPPER INTERACTION WITH A TANTALUM SILICATE SURFACE: IMPLICATIONS
FOR INTERCONNECT TECHNOLOGY [1]*
2.1. Introduction
A critical issue in copper (Cu) interconnect technology is the wetting and adhesion of Cu
to the barrier substrate. Cu will wet — grow conformally — on many barrier surfaces (e.g.,
tantalum (Ta) and tungsten (W)) under ultra-high vacuum (UHV) conditions [2-4]. Cu
wettability, however, is very sensitive to oxygen contamination; even a partial monolayer of
oxygen at the Cu/barrier interface will significantly degrade wettability and step coverage, and
allow facile agglomeration at temperatures at or above 300 K [2-4]. The sensitivity of Cu
wetting to low-level contamination is of practical importance for reliable processing since Cu
deposition is typically not done under UHV conditions [5]. Tantalum silicon nitride (TaSiN) is
an exception to such behavior. Recent X-ray photoelectron spectroscopy (XPS) studies [2] have
demonstrated that sputter-deposition Cu will wet air-exposed TaSiN at 300K. This is in
agreement with scanning electron microscopy (SEM) studies [6] reporting superior Cu thermal
stability on TaSiN relative to Ta and tantalum nitride (TaN) for deposition under non-UHV
conditions. XPS data of air-exposed TaSiN revealed a silicon (Si) (2p) binding energy of 102 eV
[2], consistent with metal silicate formation [7].
* Reproduced with permission from [Zhao, X., Magtoto, N. P., Leavy, M. and Kelber, J. A., Thin
Solid Films 415 (2002) 308]. Copyright [2004] Thin Solid Films.
27
Silicate thin films are of increasing interest as high dielectric materials for gate oxide [8,
9] and system-on-a-chip [10] applications. Although high dielectric materials in bulk form are
suitable for interconnect applications due to capacitance-induced coupling between interconnects
and resulting delays in signal propagation [11], the formation of an extremely thin silicate
interface between Cu and the barrier substrate may not prove a hindrance. Evidence of this is the
finding that TaSiN [12] is a potential diffusion barrier with good electrical properties.
In this study, we report the formation of Ta silicate and the Cu wetting behavior on this
silicate film. The growth mode of a film on the substrate is governed by the surface free energies
of the film (γF), substrate (γS) and film-substrate interface (γFS) according to Eq. (1-3) [13].
Wetting will occur for ∆γ<0. Since most surface free energies of metals (γF) are positive and
larger than those of oxides (γS), γFS must be very large and negative for wetting to occur [13].
The data reported here demonstrate that Ta silicate films were formed by sputter
deposition of Ta onto ultrathin silicon dioxide (SiO2) substrates at 300 K, followed by annealing
in oxygen (O) (600 K, 2 torr). The XPS data of the films were characterized by an Si(2p)
binding energy at 102.1 eV and Ta(4f7/2) binding energy at 26.2 eV, in agreement with findings
for other silicate materials [2, 7]. Annealing Ta silicate films to > 900 K in UHV results in
silicate decomposition to SiO2 and tantalum oxide (Ta2O5). Sputter deposition of Cu onto the
unannealed Ta silicate substrate at 300 K results in the initial formation of Cu(I) and a linear
increase in Cu signal vs. deposition time (uptake curve) until an average Cu thickness of ~1 Å is
achieved. At this point, the formation of Cu(0) is observed, coincident with a change in the slope
of the uptake curve. These findings are similar to those previously reported for air-exposed
TaSiN [2].
28
2.2. Experiment Details
Experiments were carried out in a UHV main chamber equipped with a hemispherical
analyzer (VG AX100), an unmonochromatized Mg/Al x-ray source (PHI) for XPS, argon (Ar)
sputter capabilities (PHI), and a base pressure of 7 x 10-10 torr. All XPS data reported here were
acquired at 25 eV constant pass energy. XPS data analysis was carried out using commercially
available software (ESCA Tools) that utilizes Gaussian-Lorentzian functions and Shirely
background subtraction to synthesize peak components [14]. XPS spectra were acquired with the
sample aligned normal to the analyzer lens axis (normal emission) and at 60° with respect to the
normal emission (grazing emission). Atomic concentrations were calculated with atomic
sensitivity factors specific for the hemispherical analyzer (VG100 AX) and were obtained
directly from the manufacturer (VG Microtech). Relative atomic concentrations were derived
from the XPS intensities according to [15]:
NA/NB = (IASB)/(IBSA), (2.1)
where N, S and I are, respectively, the atomic concentrations, atomic sensitivity factors and XPS
signal intensities.
The film thickness dA was determined by the XPS intensity ratio of the film to substrate
(IA/IB) [16] according to:
IA/IB =( IA∞/IB
∞)[(1-e-dA/(λAcosθ) )/e-dA/(λBcosθ)
], (2.2)
where λA and λB are the photoelectron inelastic mean free path (IMFP) in the overlayer and
substrate, respectively, dA is the thickness of the overlayer, and θ is the angle between
photoelectron analyzer and sample surface normal. IA∞ and IB
∞ are XPS intensities of infinitely
29
thick overlayer and substrate, respectively. IA∞ and IB
∞ are usually unavailable, therefore
sensitivity factors of the overlayer and substrate are normally used, which are proportional to IA∞
and IB∞. Calculated [17, 18] IMFP value for Si(2p) electrons in SiO2 is 31.3 Å. For Cu
overlayers, the Cu(2p3/2) intensity was monitored (λA= 19.8 Å). The calculated SiO2 and silicate
thickness is thinner than the actual thickness due to the enhanced Si(2p) photoelectron emission
of substrate along the Si(100) single crystal [16]. Previous study [19] has shown that the actual
SiO2 and silicate thickness is larger than those calculated by ~43%. Therefore, the actual SiO2
and silicate thickness obtained from multiplying the calculated thickness (Eq (2.2)) by 1.4, is
reported in this study.
The UHV main chamber was attached to a dual magnetron (Maxteck) sputtering chamber
(base pressure 1 x 10-8 torr) capable of sputter depositing either Ta or Cu. Sputter deposition
was carried out using a commercial water-cooled magnetron source (MiniMak) and Argon
plasma with a partial pressure of 15 mtorr of Argon. Argon of 99.999% purity, tantalum target
of 99.999% purity and cooper targets of 99.999% purity were used for sputter deposition. The
deposition rate could be controlled by adjusting the plasma power, with a constant power of 50W
for Ta and 25W for Cu. Ta deposition rates of 0.2 Å/sec and Cu deposition rates of 0.2 Å/min
were achieved, allowing a study of the film/substrate interface. All Ta and Cu depositions
reported in this paper were done at room temperature (~300K). Sample temperature in either
chamber could be varied between 100 K and 1300 K by a combination of liquid nitrogen cooling
and resistive heating of the sample holders. A chromel-alumel thermocouple between the sample
and Ti holder was used to monitor the temperature. Sample transport between chambers was
accomplished under UHV conditions.
30
A 1cm2 silicon sample cut from an n-doped Si (100) wafer was first cleaned successively
in dilute HF solution, acetone and deionized water to remove surface oxide, and then was
inserted to the UHV chamber. Adventitious carbon and oxygen were removed by heating the
sample to 1100 K in UHV. Sample cleanliness was verified by XPS.
2.3. Results
2.3.1. Ta Silicate Formation
Ta silicate films were formed by a two-step process. First, a 6 Å (Eq. (2.2)) thick SiO2
film was grown by direct oxidation of a Si(100) substrate (1.7 x 109 L O2 at 2 torr, 600 K).
Second, 6 Å (Eq. (2.2)) of Ta were deposited on the SiO2 film at 300 K, and annealed at 600 K in
1.7 x 109 L O2 at 2 torr. The evolution of Si(2p) spectra during SiO2 formation and subsequent
reaction with Ta is displayed in fig. 2.1a. Corresponding O(1s) spectra are displayed in Fig.
2.1b.
The formation of an SiO2 film is marked by a feature at 103.1 eV in the Si(2p) spectrum
(Fig. 2.1a), in good agreement with accepted binding energy values for SiO2 [15]. Analysis of
the relative intensity of the Si103/Si99 relative intensity yields an average SiO2 film thickness of 6
Å (Eq. (2.2)). The corresponding O(1s) spectrum (Fig. 2.1b) has a full width at half-maximum
(FWHM) of 2.5 eV, significantly broader than the FWHM of 2.1 eV observed under these
conditions for non-hydroxylated stoichiometric SiO2 films. Assigning one component (FWHM
= 2.1 eV) to the reported value of 532 eV for O in SiO2 [17], the O(1s) peak (Fig. 2.1b) is well fit
by the addition of a second component (FWHM = 2.1 eV) at 533 eV, corresponding to Si-OH
[20], indicating that the ultrathin SiO2 film has observable hydroxyl content.
31
Deposition of Ta followed by annealing in oxidizing conditions results in changes to
both Si(2p) and O(1s) spectra. A new feature at 102.1 eV is observed in the Si(2p) spectrum
(Fig. 2.1a). A corresponding spectrum, acquired at grazing emission (Fig. 2.1a) shows an
enhanced intensity for this feature, indicating that the new feature is associated with the surface
region of the film. The FWHM of the O(1s) spectrum (Fig. 2.1b) increases from 2.5 eV to 2.7
eV, and the peak maximum shifts from 532.2 eV to 531.1 eV. A Si(2p) feature at ~102.1 eV has
been reported for aluminum silicate formation [7], and for stoichiometric zirconium silicate
(ZrSiO4)[21]. A comparison of O(1s) spectra for ZrSiO4 and SiO2 reveals a trend similar to that
shown in Fig. 2.1b; a broader peak for the silicate than for SiO2 (2.3 eV vs 2.0 eV), and a lower
silicate binding energy (531.1 eV vs 532.2 eV for SiO2) [21]. The similarity of Si(2p) spectra
shown in Fig. 2.1a indicates that Ta reaction with the SiO2 film results in silicate formation. The
large FWHM for the O(1s) spectrum (Fig. 2.1b) indicates two oxygen environments, and the
peak is well fit by two components (FWHM = 2.1 eV) at 530.6 eV and 531.9 eV. Previous
studies of silicate films [22] indicate that the component at 530.6 eV can be assigned to oxygens
bridging between Ta and Si sites. The component at 531.9 eV is consistent with SiO2 [2, 20],
and with metal hydroxide Ta-OH [2, 15]. An assignment to SiO2, however, is inconsistent with
the fact that there is negligible Si(2p) intensity at 103 eV after reaction with Ta (Fig. 2.1a), and
that the Si103/O531.9 intensity ratio corresponds to a Si/O atomic ratio of 1:10. The O(1s)
component at 531.9 eV (Fig. 2.1b) is therefore assigned to hydroxylated Ta. A comparison of
O(1s) spectra acquired at normal and grazing emission indicates that the hydroxyl and bridging
oxygen components is constant through the thin film (O531.9/O530.6 ~2/3). This may be due to the
extremely thin nature of the film (6Å) or may indicate that the film is uniformly hydroxylated.
32
The Ta(4f) spectra acquired after Ta deposition and annealing are shown in Fig. 2.1c. The
spectra include both the Ta(4f7/2) and the Ta(4f5/2) photoelectron lines, which are present in a 4:3
Fig. 2.1 Formation of SiO2 and Ta silicate. (a) Si(2p); (b) O(1s) and (c) Ta(4f) Spectra.
108 104 100 96 92
SiOx(102.1 eV)
SiO2 (103.1 eV)
XPS
Inte
nsity
SiO2 at normal emission
silicate at normalemission
silicate at grazingemission
538 536 534 532 530 528 526
530.6 eV532 eV
533 eV
silicate at normalemission
silicate at grazing emission
26.2 eV
34 32 30 28 26 24 22 20 18 16
Silicate at normalemission
Silicate at grazingemission
Binding Energy (eV)
(a)
(b)
(c)
Si(99.1 eV)
SiO2 at normal emission
33
intensity ratio, with a 1.9 eV separation [15]. The binding energies reported in this paper refer to
the Ta(4f7/2) photoelectron line. Ta spectra acquired at normal emission and grazing emission
(Fig. 2.1c) are well fit by a doublet with an individual component FWHM of 2.3 eV and a
Ta(4f7/2) binding energy of 26.2 eV. Similar results were reported [2] for air-exposed TaSiN and
attributed to a homogeneous tantalum silicate (TaxSiyOz) mixture.
The Si(2p) at 102.1 eV, Ta(4f) at 26.2 eV and O(1s) at 530.6 eV are consistent
with the formation of a Ta silicate film [2, 7, 21, 22]. The O531.9/O530.6 intensity ratios for normal
emission and grazing emission (Fig. 2.1b) are both 2/3, indicating a film with uniform hydroxyl
composition. A Ta/Si102 /O elemental ratio of 1:1:6 was obtained by Eq. (2.1) for the grown film,
suggesting either a Ta-deficient silicate or a Ta oxide component, or possibly a hydroxylated
silicate. The latter possibility is consistent with the O(1s) spectrum (Fig. 2.1b). The estimated
thickness of the silicate film was ~8Å (Eq. (2.2)). This estimation is an upper bound to the
thickness, since the electron inelastic mean free path (IMFP) in Ta silicate may be less than in
SiO2, due to heavy atom scattering [15, 16].
For Ta reaction with an ultrathin SiO2 substrate, a Si(2p) feature at ~ 102.1 eV might
arguably be assigned to a Si-suboxide, due to Ta removal of the oxide overlayer, revealing the
Si/SiO2 interface region. In order to explore this possibility, similar experiments were carried
out on ultrathin SiO2 films, but with annealing to 600 K in the absence of O2. Negligible growth
in Si(2p) intensity at ~102.1 eV and Ta(4f) intensity at ~26.2 eV were observed. Subsequent
anneals in 2 torr O2, however, immediately resulted in a significant increase of Si(2p) intensity
at 102.1 eV and Ta(4f) intensity at 26.2 eV, indicating that these features are formed only under
oxidizing conditions. The features of Si(2p) at 102.1 eV and Ta(4f) at 26.2 eV are therefore
assigned to a Ta silicate film.
34
2.3.2. Thermal Decomposition
The silicate film was annealed in UHV in 100 K increments starting from 300 K.
Following each anneal period (30min), the sample was cooled to room temperature and XPS
spectra were acquired. Annealing of the silicate film up to 900 K results in a significant increase
of the Si103/Si99 XPS intensity ratio, and a decrease of the Si102.1/Si99 intensity ratio (Fig. 2.2).
Si(2p) spectra of the sample acquired at 300K and after annealing to 900K are shown in Fig.
2.3a. The Si(2p) spectrum shifts from 102.1 eV to 103 eV, indicating the formation of SiO2 [15].
Additionally, the Ta(4f7/2) spectra at 300K and annealing to 900K(Fig. 2.3b) were observed to
shift from 26.2 eV to 26.7 eV. The feature of Si(2p) at 103 eV is assigned to Si in SiO2 [15] and
Ta(4f) at 26.7 eV is assigned to Ta in Ta2O5 [15]. These changes are consistent with silicate
decomposition to form SiO2 and Ta2O5, in accord with the published phase diagram for this
system [23, 24].
Fig. 2.2 XPS intensity ratio as a function of annealing temperature.
Temperature (K)
XPS
Int e
n si ty
Ra t
i o
0
0.05
0.1
0.15
0.2
0.25
0.3
0.35
0.4
0 200 400 600 800 1000 1200
Si102.1/Si99
Si103/Si99
35
2.3.3. Air-Exposure of Ta Silicate Film
A Ta silicate sample formed as described above was exposed to air for 2 hours, then
transferred to the UHV main chamber for XPS analysis. Si(2p) spectra of the sample before and
after air-exposure are shown in Fig. 2.4a. No shift for Si(2p) spectra is observed upon air
exposure. Similarly, air-exposure induces no shift for O(1s)(Fig. 2.4b) and Ta(4f)(Fig. 2.4c)
spectra. However, the intensities of Si(2p)(Fig. 2.4a), O(1s)(Fig. 2.4b) and Ta(4f) (Fig. 2.4c)
decrease after air-exposure. C(1s) intensity (not shown) at 284.5 eV increases after air-
exposition. The component at 284.5 eV is assigned to adventitious C [15]. This is in accord with
the decrease of the Si(2p), O(1s) and Ta(4f) intensities of the Ta silicate film. This result
suggests that the silicate surface is stable in the air and can act as a “robust” diffusion barrier
since Cu deposition is typically not done under UHV conditions [4].
2.3.4. Cu/Film Interactions
Cu was sputter deposited onto an unannealed Ta silicate film in sequential depositions at
300K. After each deposition, the sample was transferred from the deposition chamber back to the
main chamber for XPS analysis. The Cu(L3VV) Auger line shape (X-ray excited) as a function
of deposition time, displayed in Fig. 2.5, provides a “fingerprint” of the oxidation state of the
deposited Cu on the silicate film [2, 25]. The feature at 914.9 eV Auger kinetic energy is
assigned to Cu(I), whereas the feature at 917.6 eV is assigned to Cu(0) [26, 27]. The oxidation
state of the Cu evolves with deposition time from Cu(I) to Cu(0). Cu depositions at short (1– 4.5
minutes) deposition times (Fig. 2.5) yield a Cu(L3VV) Auger feature at 914.9 eV, indicative of
formation of Cu(I). At longer deposition times (Fig. 2.5), a new component at 917.6 eV was
36
Fig. 2.3 XPS spectra of Ta silicate at room temperature and after annealing at 900 K for 30 min
in UHV. (a) Si(2p) Spectra and (b) Ta(4f) Spectra.
108 104 100 96 92
Si(99.1 eV)Si(102.1eV)
Si(103eV)
XPS
I nt e
n si ty
Roomtemperature
Annealed at900K for
30 min
34 32 30 28 26 24 22 20 18
26.2 eV26.7 eV
Annealed at900K for
30 min
Roomtemperature
Binding Energy (eV)
(a)
(b)
37
Fig. 2.4 XPS spectra of Ta silicate before and after air exposure. (a) Si(2p) spectra; (b) O(1s)
spectra and (c) Ta(4f) spectra.
108 104 100 96 92
XPS
Int e
nsity
Before air exposure
After air exposure
536 534 532 530 528 526
Before air exposure
After air exposure
34 32 30 28 26 24 22 20 18
Before air exposure
After air exposure
Binding Energy (eV)
(c)
(b)
(a) Si(2p)
O(1s)
Ta(4f)
38
observed, indicative of formation of Cu(0). The Cu Auger parameter (AP) was calculated
according to the following [28, 29]:
AP = KE(CuL3VV)+ EB (Cu2p), (2.3)
KE(CuL3VV) = hν– EB(CuL3VV), (2.4)
where KE and EB are kinetic energy and binding energy, respectively. The calculated Auger
parameter associated with the Cu(I) spectral feature is 1848.2 eV(Fig. 2.5). An Auger parameter
value of 1848.2 eV is in the range of Auger parameters reported for other Cu(I) compounds [15].
The Auger parameter associated with Cu(0) (Fig. 2.5) is 1850.5 eV, lower than that reported for
bulk Cu that is 1851.3 eV. Similar results were reported for Cu growth on oxidized TaSiN [2],
Cu0.6Al0.4 growth on SiO2 [30] and Cu growth on Al2O3 [31], and were attributed to the
ineffective screening of the holes in the Auger final state for small Cu particles [2, 15, 30, 31].
The growth mode of the sputter deposited Cu on the substrate can be characterized by
plotting the increase in the Cu(2p3/2) intensity (relative to Si(2p)) ratio as a function of deposition
time [32]. Fig. 2.6a and 2.6b includes the growth mode of sputter deposited Cu on the
unannealed and decomposed (Annealed to 1000K) Ta silicate film respectively. For unannealed
Ta silicate film, the Cu(2p3/2)/Si(2p) intensity ratio increases linearly with deposition time, but
exhibits a change in slope at 4.5 min deposition time (Fig. 2.6a). This change in slope coincides
with termination of Cu(I) formation and the initiation of Cu(0) growth (Fig. 2.5). Such behavior
indicates conformal growth of a Cu(I) ad-layer, followed by formation of a Cu(0) layer [33]. For
Cu depositions on the annealed and decomposed Ta silicate film, the linearity without
change in slope observed in Fig. 2.6b indicates that copper deposition occurs with the formation
of 3-D islands consistent with the behavior of Cu on SiO2 [2]. The X-ray excited Auger data for
39
Cu on the annealed, decomposed film (not shown) show little Cu(I) formation, indicating
negligible Cu/surface charge transfer.
Fig. 2.5 X-ray excited Cu(L3VV) Auger spectral evolution as a function of Cu deposition on the
unannealed silicate film.
905 910 915 920 925
Cu(
L 3VV
) XPS
Inte
nsity
Kinetic Energy (eV)
Cu(I) Cu(0)
8.59.5
5.5
1.04.5
11.5
Dep
ositi
on T
ime
(min
)
40
Fig. 2.6 Cu(2p)/Si(99) XPS intensity ratio vs. deposition time (a) before and (b) after annealing
the silicate film at 1000K.
The data in Figures 2.5 and 2.6a demonstrate that initially deposited copper reacts with
the Ta silicate film to form Cu(I) at 300K. At higher coverage, Cu(0) formation is observed.
Figs. 2.5 and 2.6a indicate that formation of Cu(0) coincides with the change in slope in the
uptake curve. This indicates SK (conformal) growth. Cu “wets” the silicate surface. The
deposited Cu grows conformally as Cu(I) to a maximum average thickness of ~1Å (Eq. (2.2)).
This corresponds to a surface coverage of ~0.5 monolayers, assuming a Cu+ ion diameter of
1.92Å [34]. Similar effects have been observed for Cu (0.5 ML) on polycrystalline aluminum
oxide surface [35], Cu (~0.35ML) on hydroxylated α–Al2O3(0001) [30] and Cu (~0.4 ML) on
air-exposed TaSiN samples [2]. In these systems, the deposited Cu exhibits conformal growth
[33], with the initial formation of a Cu(I) ad-layer, followed by growth of Cu(0) over the Cu(I)
Cu(
2p3/
2)/S
i(2p)
XPS
Inte
nsity
Rat
ioCu(I)
1st layer
0.0
0.5
1.0
1.5
2.0
2.5
0 2 4 6 8 10 12 14
(a) Before Silicate Decomposition
Cu(0) 2nd layer
(b) After Silicate Decomposition
Cu Deposition Time (min)
Cu(0)
41
interface. It is not known whether maximum Cu(I) coverage is limited by Cu(I)-Cu(I) repulsive
interactions, or by the surface concentration of appropriate active sites.
The Ta(4f7/2) XPS spectra are shown in Fig. 2.7, acquired after Cu depositions for 1 min
and 5.5 min respectively. The Ta(4f7/2) spectrum shifts from 27.2 eV to 26.7 eV with Cu
depositions from 1 min to 5.5 min, indicating that Ta is reduced as the deposited Cu metal is
oxidized to Cu(I). No changes were obtained for corresponding Si(2p) and O(1s) spectra (not
shown).
Fig. 2.7 Ta(4f) XPS spectra at Cu deposition for 1min and 5.5 min.
34 32 30 28 26 24 22 20 18
Cu depositionfor 5.5 min
Cu depositionfor 1 min
27.2 eV 26.7 eV
XPS
Inte
nsity
Binding Energy (eV)
42
2.4. Discussion
The XPS data (Fig. 2.1) indicate the formation of an 8Å thick film of uniform
composition with the stoichiometry TaSiO6. The Si(2p) intensity at 102.1 eV indicates that the Si
atoms are bonded to oxygen atoms bridging between the Si and metal, as expected for a silicate
structure [7, 21]. The O(1s) spectrum, however, indicates at least two oxygen chemical
environments within the film, at 531.9 eV and at 530.6 eV, with an intensity ratio of ~2:3. A
binding energy of 531.9 eV could be assigned to SiO2, but this contradicts the Si(2p) data which
indicates a main component at binding energy of 102.1 eV and a negligible component at
binding energy at 103.1 eV. A possible assignment of O(1s) spectrum is to assign the 531.9 eV
feature to OH groups located (presumably) on the Ta sites. Other evidence suggesting that this is
a hydroxalated structure derives from the fact that the film is stable to air exposure (Figs. 2.4a,
2.4b and 2.4c), with the only change (other than adventitious carbon) resulting from a slight
increase in the relative O(1s) intensity near 532 eV (Fig. 2.4b). On this basis, a structure such as
displayed below is tentatively proposed:
The above structure is consistent with two oxygen environments, and with the formation of a
formal Ta(V) species. Such a formal structure, however, would yield a stoichiometry of TaSiO5
and an O531.9/O530.6 intensity ratio of only 1:4 instead of the observed 2:3. In a film only 8 Å
thick, however, considerable non-stoichiometry may be expected due to the high proportion of
interfacial sites between the film and the Si substrate. In addition, the choice of Ta as a
O OH
Si Ta
O
43
hydroxylation site is reasonable but purely conjectural. It is not known, for example, whether OH
bonded to Si would yield an O(1s) binding energy distinguishable from OH/Ta under existing
experimental conditions. Obviously, a complete determination of film structure requires
additional measurements (e.g., FTIR).
The x-ray excited Cu(L3VV) Auger spectra (Fig. 2.5) and uptake curve (Fig. 2.6a)
demonstrate that copper reacts with Ta silicate film in the first layer and forms Cu(I) at 300K to a
maximum coverage of 0.5 ML. At higher coverage, Cu(0) is formed. The behavior of Cu on the
Ta silicate film can be compared with Cu on the decomposed Ta silicate film, a mixture of SiO2
and Ta2O5 (Fig. 6b). Copper interacts only weakly with the SiO2 and Ta2O5 surface, forming
Cu(0) even at low coverage [2]. The copper uptake curve (Fig. 2.6b) for the decomposed film
does not display the change in slope that is characteristic of layer-by-layer growth [2, 33]. In
contrast to Cu on the decomposed film, Cu on the unannealed Ta silicate film displays initial
conformal growth with formation of Cu(I). This demonstrates significant charge exchange
between the initial Cu atoms and the Ta silicate surface. This could be the result of the more
ionic Ta cation and more covalent ionic Si formation on the Ta silicate surface [21, 34]. There is
a strong interaction between initially deposited Cu and Ta silicate surface. Cu “wets” the surface
because of the significant charge exchange between Cu and Ta silicate film.
2.5. Conclusions
A 6Å SiO2 film is formed by exposing clean Si(100) to 1.7 x 109 L O2 at 1000K. An 8Å
Ta silicate film is formed after Ta deposition and oxidation in 2 torr oxygen at 600K. The Si(2p)
component at binding energy of 102.1 eV ,Ta(4f7/2) component at binding energy of 26.2 eV and
44
O(1s) at binding energy of 530.6 eV demonstrate a Ta silicate environment. The Ta silicate film
is stable up to 900K in UHV and stable at room temperature in the air. These data indicate Ta
silicate film can act as a “robust” diffusion barrier since Cu deposition is typically done under
non-UHV environment. Ta silicate film decomposed to form SiO2 and Ta2O5 ~900K.
Copper was sputter deposited onto silicate film before and after annealing the silicate
sample ~1000K. Copper grows conformally on the unannealed Ta silicate surface and is
characterized by a feature in the Cu(L3VV) Auger line shape at 914.9 eV indicative of Cu(I).
Further deposition of copper results in the Cu(L3VV) Auger line shape at 917.6 eV indicative of
Cu(0). These data indicate that the initially deposited copper reacts with the Ta silicate surface
and forms Cu(I) for the first ad-layer. Subsequent copper deposition results in Cu(0) formation.
2.6. Chapter References
[1] Zhao, X., Magtoto, N. P., Leavy, M. and Kelber, J. A., Thin Solid Films 415 (2002) 308. [2] Shepherd, K. and Kelber, J., Appl. Surf. Sci. 151 (1999) 287.
[3] Chen, L., Magtoto, N. P., Ekstrom, B. and Kelber, J. A., Thin Solid Films 376 (2000)
115.
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[5] Murarka, S. P., Mater. Sci. Eng. R 19 (1997) 87.
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Interconnect Technology Conference (IEEE), New York, USA (2000) 125.
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Baumvol, I. J. R. and Parsons, G. N., Appl. Phys. Lett. 75 (1999) 4001.
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[9] Wilk, G. D. and Wallace, R. M., Appl. Phys. Lett. 76 (2000) 112.
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Urdahl, R. S., Appl. Phys. Lett. 73 (1998) 1517.
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47
CHAPTER 3
CHEMICAL VAPOR DEPOSITION OF TANTALUM NITRIDE WITH TERTT-
BUTYLIMINO TRIS(DIETHYLAMINO) TANTALUM AND ATOMIC HYDROGEN
3.1. Introduction
Due to the high melting point, chemical and thermal stability, and excellent conductivity,
refractory metal nitrides are widely recognized as diffusion barriers in metal-semiconductor
interconnects. Among these metal nitrides, Tantalum nitride (TaN) is one of the most extensively
studied materials for silicon (Si) device fabrication [1, 2]. TaN films are usually deposited using
physical vapor deposition (PVD), such as reactive sputtering [1, 3-7]. PVD, however, is not
expected to be applied beyond 45 nm technology nodes due to the poor step coverage caused by
the shadowing effect in the small feature size, high aspect ratio contact and via holes [8].
Accordingly, chemical vapor deposition (CVD) and atomic layer deposition (ALD) processes are
being developed for deposition of transition metal nitride thin films with high-quality step
coverage.
Only a few results have been reported on TaN CVD films since there are only a few
tantalum (Ta) source gases that have a high vapor pressure convenient for CVD processing. Ta
halides such as tantalum chloride (TaCl5) [2] and TaF5 [9, 10] have been used as Ta sources, but
these can result in the incorporation of chlorine (Cl) and fluorine (F) impurities in the growing
films [11]. In order to avoid problems associated with the presence of halides, attention has
shifted to halide-free precursors, including tert-butylimino tris(dimethylamino) tantalum
(TBTDET) (Fig. 3.1) [12-14]. TBTDET is liquid at the room temperature and has a high vapor
48
pressure (0.1 torr at 363 K). Ta nitride films with good step coverage and electrical properties
have been deposited on Si and SiO2 by TBTDET CVD at ~720K – 920K [12, 13, 15]. This
temperature range is relatively high for most low-κ materials. Carbon-containing low κ materials
are often thermally unstable above ~670K [16]. Ta nitride was formed on SiO2 by TBTDET and
hydrogen radicals at low temperature of ~530K [14], but there are few reports about TaN CVD
deposition on low κ materials at low temperature. Additionally, previous studies [17] of PVD Ta
on silicon(Si):oxygen(O):carbon(C) low-k substrates indicate that sputter deposition results in a
relatively diffuse (~ 50 Å) interfacial layer containing tantalum carbide (TaC). PVD Cu will not
wet this TaC interfacial layer at 300 K, thus imposing a lower limit on the thickness of reliable
PVD Ta barriers for PVD Cu seed.
Fig. 3.1 Tert-butylimino tris(diethylamino) tantalum (TBTDET) structure.
In this study, XPS has been used to characterize the reaction of TBTDET with atomic
hydrogen on silicon dioxide (SiO2) and organosilicate glass (OSG) substrates. TBTDET partially
N
Ta
tBu
Et2NNEt2
NEt2
N
Ta
tBu
Et2NNEt2
NEt2
49
reacts with O atoms in both SiO2 and OSG substrates by 300 K to form strong Ta-O interfacial
bonds. Subsequent bombardment with atomic hydrogen at 500K results in formation of a
stoichiometric TaN phase on top of the Ta-O interfacial phase (“interphase”). Subsequent
depositions of the precursor on the reacted layer on SiO2 and OSG, followed by atomic hydrogen
bombardment, result in increased TaN formation. The data summarized here indicate that
TBTDET is a potential precursor for an atomic hydrogen driven ALD/CVD process.
3.2. Experiment Details
Experiments were carried out in a combined UHV analysis/dual magnetron sputter
deposition system, which has been described previously in chapter 2. For the charging shift of
apparent photoelectron energies on insulating samples, XPS spectra were calibrated by
referencing the peak from adventitious carbon at 284.5 eV [18]. Relative film composition was
derived from XPS intensities according to Eq. (2.1). The film thickness d was determined by the
attenuation of the Si(2p) substrate signal (photoelectron inelastic mean free path (IMFP) for
Si(2p) electrons (λ) = 31.3 Ǻ), according to Eq. (2.2).
Ta precursor exposures were carried out in the PVD/CVD chamber (with a base pressure
of 1 x 10-8 torr after bake out), followed by sample transfer to and XPS analysis in the ultra high
vacuum (UHV) chamber. TBTDET (Schumacher) was used as Ta precursor. The liquid
precursor was contained in a bubbler heated to 343K. TBTDET was condensed onto a clean SiO2
or OSG sample at 120K, annealed to 300K, and then exposed to hydrogen (H/H2) flux. Atomic H
was generated within the UHV chamber by passing H2 through a TC-50 thermal gas cracker
(Oxford Applied Research), which consisted of a heated tungsten tube and external cooling
50
system. In this study, atomic hydrogen was generated at a constant power of 55 W and caused a
slight rise in the sample temperature to 500K. Hydrogen pressure was 2*10–7 torr during H2/H
bombardment. According to manufacturer specifications, such operating conditions should result
in ~50% dissociation of H2. That significant H2 dissociation occurred was demonstrated by the
fact that results obtained using the thermal gas cracker differed sharply from those observed for
exposure to pure H2 at 500K, which had no significant effect.
The 1cm2 samples consisted of either a 4000Å SiO2 on Si substrate, or commercially
prepared OSG film grown on Si. Adventitious carbon was removed by heating the sample to
1000 K for SiO2 and 500K for OSG in the UHV chamber. Sample cleanliness was verified by
XPS.
3.3. Results
3.3.1. TaN Formation on SiO2
TBTDET precursor was condensed on SiO2 at 120 K in the PVD/CVD chamber. After
the dose, the sample was transferred to the UHV chamber for XPS analysis at 120K. The sample
was then annealed to 300K in UHV, followed by exposure to an H/H2 flux for 90 mins
(involving an incidental temperature increase to 500K). XPS analyses were obtained after each
treatment. The Si(2p) spectrum (Fig. 3.2a) of a clean SiO2 substrate is well fit by a single
component with a FWHM of 2.1eV at binding energy of 103.2eV. The corresponding oxygen
(O) (1s) spectrum (Fig. 3.2b) is similarly well fit with a single component (FWHM of 2.1 eV) at
binding energy of 532.1 eV [19]. After exposure to TBTDET precursor at 120 K, the absence of
51
Si(2p) and O(1s) intensity from the substrate (Fig. 3.2a and 3.2b) indicates that precursor dosing
at 120 K results in a thick multilayer. The adsorbed multilayer on SiO2 exhibits significant
carbon (C) (1s) intensity at ~285 eV (Fig. 3.2e), N(1s) intensity at ~398eV (Fig. 2d) and
negligible Ta(4f) intensity (Fig. 3.2c). The XPS spectra acquired after annealing to 300K are
shown in Fig. 3.2. The Ta(4f) spectra (Fig. 3.2c) include both the Ta(4f7/2) and the Ta(4f5/2)
photoelectron lines, which are present in a 4:3 intensity ratio, with a 1.9 eV separation [18]. The
binding energies reported in this paper refer to the Ta(4f7/2) photoelectron line. By 300K,
considerable precursor interaction with SiO2 substrate has occurred and resulted in Ta-O bond
formation, characterized by Ta(4f7/2) peaks at 24.7 eV and 25.8 eV for Ta suboxides [4, 20, 21],
and the corresponding O(1s) peak at 529.8 eV [18]. The existence of the nitrogen (N) (1s) 398
eV feature (Fig. 3.2d) and C(1s) 285 eV peak (Fig. 3.2e) at 300K indicates that some precursor
species still remained in the film. The total average film thickness determined by Eq. (2.2), was
101Ǻ. Interaction with atomic hydrogen resulted in the formation of a new Ta(4f7/2) feature at
23.2 eV binding energy (top of Fig. 3.2c), which indicates the formation of Ta nitride [4]. The
formation of Ta nitride is corroborated by the emergence of a new N(1s) feature at 396.6 eV (top
of Fig. 3.2d) [4]. The Ta(4p3/2) feature overlaps this portion of the N(1s) spectrum, with a broad
Ta(4p3/2) peak at binding energy of 403-404 eV [1, 22]. According to the intensities of the Ta(4f)
and N(1s) features at 23.2 eV and 396.6 eV, Ta:N atomic ratio, determined by Eq. (2.1), is 1:1,
indicating a stoichiometric phase: TaN. The atomic hydrogen flux induced more Ta/oxide
reactions as evidenced by enhanced Ta(4f7/2) and O(1s) intensities at 24.7 eV and 529.8 eV,
respectively (sub-oxide) and the appearance of new Ta(4f7/2) feature at 26.5 eV (Ta2O5) [18].
The formation of a new Si(2p) feature at 102.1 eV indicates that SiO2 is partially reduced as the
deposited Ta is oxidized. The atomic hydrogen flux induced the shifting of C(1s) feature to
52
Fig. 3.2 XPS spectral changes upon reaction with TBTDET precursor. (Bottom traces) SiO2
sample before precursor exposure; (bottom middle traces) precursor adsorption at 120 K; (top
middle traces) after annealing to 300K; (top traces) after H/H2 exposure. (a) Si(2p); (b) O(1s); (c)
Ta(4f); (d) N(1s) and (e) C(1s).
SiO2
300K annealing
H2/H exposure
(a)
XPS
Inte
nsity
(Arb
itrar
y U
nits
)
Binding Energy (eV)
SiO2SiOx
(b)
Ta-OSiO2
SiO2
H2/H exposure
SiO2
H2/H exposure TaN
Ta2O5(c) TaOx
108 104 100 96 536 528 524532 3236 28 24 20
Si(2p) O(1s) Ta(4f)
16
TBTDET dose
300K annealing
300K annealing
TBTDET dose
TBTDET dose
TaN
SiO2
300K annealing
H2/H exposure
XPS
Inte
nsity
(Arb
itrar
y U
nits
)
Binding Energy (eV)
(d)Ta(4p3/2)
Precursor
SiO2
300K annealing
H2/H exposure
(e)
XPS
Inte
nsity
(Arb
itrar
y U
nits
)
Binding Energy (eV)
Adventitious C
Reaction of C and O
Precursor
404 400408412 396 392 304 288 280284292296300
C(1s)N(1s)
TBTDET dose
TBTDET dose
SiO2
300K annealing
H2/H exposure
(a)
XPS
Inte
nsity
(Arb
itrar
y U
nits
)
Binding Energy (eV)
SiO2SiOx
(b)
Ta-OSiO2
SiO2
H2/H exposure
SiO2
H2/H exposure TaN
Ta2O5(c) TaOx
108 104 100 96 536 528 524532 3236 28 24 20
Si(2p) O(1s) Ta(4f)
16
TBTDET dose
300K annealing
300K annealing
TBTDET dose
TBTDET dose
SiO2
300K annealing
H2/H exposure
(a)
XPS
Inte
nsity
(Arb
itrar
y U
nits
)
Binding Energy (eV)
SiO2SiOx
(b)
Ta-OSiO2
SiO2
H2/H exposure
SiO2
H2/H exposure TaN
Ta2O5(c) TaOx
108 104 100 96 536 528 524532 3236 28 24 20
Si(2p) O(1s) Ta(4f)
16
TBTDET dose
300K annealing
300K annealing
TBTDET dose
TBTDET dose
TaN
SiO2
300K annealing
H2/H exposure
XPS
Inte
nsity
(Arb
itrar
y U
nits
)
Binding Energy (eV)
(d)Ta(4p3/2)
Precursor
SiO2
300K annealing
H2/H exposure
(e)
XPS
Inte
nsity
(Arb
itrar
y U
nits
)
Binding Energy (eV)
Adventitious C
Reaction of C and O
Precursor
404 400408412 396 392 304 288 280284292296300
C(1s)N(1s)
TBTDET dose
TBTDET dose
TaN
SiO2
300K annealing
H2/H exposure
XPS
Inte
nsity
(Arb
itrar
y U
nits
)
Binding Energy (eV)
(d)Ta(4p3/2)
Precursor
SiO2
300K annealing
H2/H exposure
(e)
XPS
Inte
nsity
(Arb
itrar
y U
nits
)
Binding Energy (eV)
Adventitious C
Reaction of C and O
Precursor
404 400408412 396 392 304 288 280284292296300
C(1s)N(1s)
TBTDET dose
TBTDET dose
53
higher binding energy at 295.5 eV (top of Fig. 3.2e), suggesting reactions with electron-
withdrawing groups, such as oxygen [18, 23]. The binding energies of all C(1s) peaks (Fig. 3.2e)
are above 284 eV, indicating no Ta carbide in the film. The later would yield C(1s) spectra near
281.9 eV [18, 24].
Formation of TaN upon exposure to H/H2 at 500 K might arguably be due to the rise in
temperature to 500K. In order to explore this possibility, a sequential experiment was carried out
as previously described, but with annealing to 500K in the absence of atomic hydrogen. Ta(4f)
and N(1s) XPS spectra (Fig. 3.3a and 3.3b respectively) show that annealing the adsorbed
precursor to 500 K without H/H2 induced more TaOx formation at binding energy of 24.7 eV and
negligible N change, indicating no TaN formation. Subsequent exposure to H/H2 at 500K,
however, immediately resulted in a significant Ta(4f7/2) feature at 23.2 eV and N(1s) intensity at
396.6 eV. It was reported that Ta nitride was formed by metal organic precursors and H2 only at
high temperature above ~650K [25]. The changes observed for Ta(4f) (Fig. 3.3a) and N(1s) (Fig.
3.3b) are therefore due specifically to interaction with the atomic hydrogen flux, rather than the
rise in temperature or H2 flux.
The evolution of Ta(4f) and N(1s) spectra upon repeated precursor
physisorption/warmup/H/H2 exposure cycles are displayed in Fig. 3.4. The increase in relative
intensities of the Ta(4f) feature at 23.2 eV and N(1s) peak at 396.6 eV corresponding to TaN [4]
is evident. Total average film thickness determined by Eq. (2.2), is 36Ǻ after the first cycle (Fig.
3.4a). After the second cycle, no Si(2p) intensity could be observed, indicating that the total
average thickness was >> 31.3 Ǻ - more like > ~100 Ǻ (assuming a Si(2p) photoelectron mean
free path of ~31.3 Ǻ). The ratio of Ta intensity in TaN to total Ta intensity (TaTaN/TaTotal)
54
increases from 0.09±0.01 for 36Ǻ film (first cycle) to 0.32±0.02 for the thick film (second
cycle), indicating the initial formation of Ta oxide at the overlayer/SiO2 interface, followed by
enhanced TaN during the second cycle.
Fig. 3.3 XPS spectra change after annealing without and with subsequent H2/H flux exposure on
SiO2 sample. (a) Ta(4f) and (b) N(1s).
H2/H exposure, 500K
300K annealing
500K annealing
(a)
Binding Energy (eV)
TaNTa2O5
TaOx
H2/H exposure, 500K
300K annealing
500K annealing
(b)
TaN
Binding Energy (eV)
Ta(4p3/2)
Precursor
Ta(4f) N(1s)
3236 28 24 20 404 396408412 392400 388
225 0
0 to
tal c
ount
s
7 000
tota
l co u
nts
55
Fig. 3.4 XPS spectra change with cycles of TBTDET dose and H2/H flux exposure on SiO2
sample. (a) Ta(4f) and (b) N(1s).
Ta(4f) spectra acquired with the sample aligned normal to the analyzer axis (normal
emission) and at 60º (from the surface normal - grazing emission) are shown in Fig. 3.5a and
3.5b for the thick film, respectively. The ratios of TaTaN/TaTotal are 0.32±0.02 in normal incidence
and 0.46±0.02 in grazing incidence, respectively. The increase in the relative intensity of TaN at
Ta-NTa-N/Ta total =0.32
Ta-N/Ta total =0.09
Ta2O5
TaOx
First Cycle~36Ă
Second Cycle
(a)
TaN
First Cycle~36Ă
Second Cycle
(b)Ta(4p3/2)
Binding Energy (eV)
404 400408412 396 388392
3236 28 24 20
Ta(4f)
N(1s)
16
2 250
0 to
tal c
ount
s7 0
00 to
t al c
oun t
s
56
grazing incidence [Fig. 3.5b] also indicates that TaN is associated with the surface region rather
than the film/substrate interface.
Fig. 3.5 Ta(4f) XPS spectra after TBTDET dose and H2/H flux exposure on SiO2. (a) Normal
incidence and (b) Grazing incidence.
3.3.2. TaN Formation on OSG
Typical Si(2p), O(1s) and C(1s) XPS spectra for an OSG sample are shown in Fig. 3.6,
along with the evolution of the Ta(4f) spectrum upon reaction with TBTDET. Since XPS on an
insulating OSG sample can result in sample charging that shifts the binding energies, spectra
Normal Emission
Grazing Emission
Ta-N
Ta-N/Ta total =0.32
Ta-N/Ta total =0.46
(a)
(b)Ta2O5
TaOx
Binding Energy (eV)3236 28 24 20 16
2 250
0 to
tal c
ount
s
57
were calibrated by referencing the peak from adventitious carbon at 284.5 eV [18]. The Si(2p)
spectrum (Fig. 3.6a) is well fit with a FWHM of 2.1 eV at binding energies of 103.2 eV and
102.1 eV, respectively. The peak at 103.2 eV can be assigned to the Si-O bond in SiO2, while the
feature at 102.1 eV indicates a different chemical environment, which can be assigned to the O-
Si-C bond formation [17, 18, 26]. The O(1s) spectrum (Fig. 3.6b) can be fit with two features
(FWHM = 2.1 eV) at binding energies of 532.1 eV and 531.1 eV, consistent with O-Si in SiO2
and O-Si-C bonding environments, respectively [18, 27]. In the C(1s) spectrum (Fig. 3.6e), the
peak at binding energy of 283.5 eV is consistent with a C-Si-O environment, and the feature at
284.5 eV is assigned to adventitious carbon [18, 28]. The XPS data indicate that this OSG
sample is an O-Si-C material with substantial amounts of SiO2 and a stoichiometry of SiC0.72O1.08
(Eq. (2.1)). As with SiO2, the TBTDET precursor was condensed on OSG at 120K, annealed to
300K, and exposed to H/H2 flux. After exposure to TBTDET precursor at 120K and annealing to
300K, considerable precursor interaction with OSG substrate occurred and resulted in Ta
suboxide formation with Ta(4f7/2) features at 24.7 eV and 25.8 eV (Fig. 3.6c), and the
corresponding O(1s) peaks at 529.8 eV (Fig. 3.6b) [4, 18, 20, 21]. The existence of the N(1s)
398 eV feature (Fig. 3.6d) and C(1s) 285 eV peak (Fig. 3.6e) at 300K indicates that some
precursor still remained in the film. Interaction with atomic hydrogen results in the formation of
a Ta(4f7/2) feature at 23.2 eV binding energy (top trace, Fig. 3.6c) and N(1s) feature at 396.6 eV
(top trace, Fig. 3.6d), with a Ta:N atomic ratio of 1:1 (Eq. (2.1)), indicating the formation of a
stoichiometric TaN phase on the OSG substrate [4]. Ta2O5 and additional Ta suboxide were
formed with atomic hydrogen exposure, characterized by the appearance of a Ta(4f) peak at 26.5
eV and increase of Ta(4f7/2) intensity at 24.7 eV, respectively (Fig. 3.6d) [18]. The atomic
hydrogen flux induced the shifting of C(1s) feature to higher binding energy at 295.5 eV (top of
58
Fig. 3.6e), suggesting reactions with electron-withdrawing groups, such as oxygen [18, 23]. The
binding energy of C(1s) (Fig. 3.6e) is above 284 eV, indicating no Ta carbide in the film on OSG
sample [18, 24].
Further evidence of the effects of H/H2 bombardment on precursor/substrate interactions
is displayed in figure 3.7. The data show changes in sample charging as a function of various
stages in precursor dose/annealing/reaction. Charging is frequently observed for photoemission
studies of insulating samples, due to the ejection of photoelectrons without compensating charge
flow from a conductive substrate layer. This net excess of charge usually leads to a uniform shift
of apparent photoelectron energies, as measured against the known energies of standard
transitions (in this case substrate C(1s) and Si(2p) transitions, as shown). Note that the
application of an H/H2 flux eliminates any significant charging, coincident with the formation of
a TaN overlayer. The elimination of sample charging is evidence that the TaN surface coverage
is sufficient to alter the electron emission of the sample so as to reduce the net charge imbalance.
This is in turn evidence that, at this point, the reacted overlayer covers a large proportion of the
surface area.
59
Fig. 3.6 XPS spectral changes upon reaction with TBTDET precursor. (Bottom traces) OSG
sample before precursor exposure; (middle traces) precursor adsorption at 120 K followed by
annealing to 300K; (top traces) after H/H2 exposure. (a) Si(2p); (b) O(1s); (c) Ta(4f); (d) N(1s)
and (e) C(1s).
Clean OSG
300K annealing
H2/H exposure
XPS
Inte
nsity
(Arb
itrar
y U
nits
)
Binding Energy (eV)
(a)
SiO2
C-Si-O
(b)
Ta-OSiO2
O-Si-C
H2/H exposure
300K annealing
Clean OSG
TaNTaOx
Ta2O5
H2/H exposure
300K annealing
Clean OSG
(c)Si(2p) O(1s) Ta(4f)
108 104 100 96 536 528 524532 3236 28 24 20 16
TaN
(d)
XPS
Inte
nsity
(Arb
itrar
y U
nits
)
Binding Energy (eV)
Ta(4p3/2)
Precursor
(e)
XPS
Inte
nsity
(Arb
itrar
y U
nits
)
Binding Energy (eV)
Reaction of C and O
Precursor
C-Si-OC-C
H2/H exposure
300K annealing
Clean OSG
H2/H exposure
300K annealing
Clean OSG
C(1s)N(1s)
404412420 396 388 284308 276292300
Clean OSG
300K annealing
H2/H exposure
XPS
Inte
nsity
(Arb
itrar
y U
nits
)
Binding Energy (eV)
(a)
SiO2
C-Si-O
(b)
Ta-OSiO2
O-Si-C
H2/H exposure
300K annealing
Clean OSG
TaNTaOx
Ta2O5
H2/H exposure
300K annealing
Clean OSG
(c)Si(2p) O(1s) Ta(4f)
108 104 100 96 536 528 524532 3236 28 24 20 16
Clean OSG
300K annealing
H2/H exposure
XPS
Inte
nsity
(Arb
itrar
y U
nits
)
Binding Energy (eV)
(a)
SiO2
C-Si-O
(b)
Ta-OSiO2
O-Si-C
H2/H exposure
300K annealing
Clean OSG
TaNTaOx
Ta2O5
H2/H exposure
300K annealing
Clean OSG
(c)Si(2p) O(1s) Ta(4f)
108 104 100 96 536 528 524532 3236 28 24 20 16
TaN
(d)
XPS
Inte
nsity
(Arb
itrar
y U
nits
)
Binding Energy (eV)
Ta(4p3/2)
Precursor
(e)
XPS
Inte
nsity
(Arb
itrar
y U
nits
)
Binding Energy (eV)
Reaction of C and O
Precursor
C-Si-OC-C
H2/H exposure
300K annealing
Clean OSG
H2/H exposure
300K annealing
Clean OSG
C(1s)N(1s)
404412420 396 388 284308 276292300
TaN
(d)
XPS
Inte
nsity
(Arb
itrar
y U
nits
)
Binding Energy (eV)
Ta(4p3/2)
Precursor
(e)
XPS
Inte
nsity
(Arb
itrar
y U
nits
)
Binding Energy (eV)
Reaction of C and O
Precursor
C-Si-OC-C
H2/H exposure
300K annealing
Clean OSG
H2/H exposure
300K annealing
Clean OSG
C(1s)N(1s)
404412420 396 388 284308 276292300
60
Fig. 3.7 XPS charge shift during various process stages of TaN formation, stage 1: OSG sample
as received; 2: cool down to 120K; 3: TBTDET dose at 120K; 4: anneal to 300K; 5: hydrogen
flux exposure for 90 min; 6: hydrogen flux exposure for 270 min.
The evolution of Ta and N core level spectra during sequential exposures to TBTDET at
120 K, followed by annealing to 300 K and H/H2 bombardment, are shown in figure. 3.8. The
increase in relative intensities of the Ta(4f) at 23.2 eV and N(1s) at 396.6 eV features
corresponding to TaN is evident. This suggests that a cyclic ALD or starved CVD process could
be used to form a TaN interfacial layer on an OSG dielectric substrate. The numbers to the left
of the Ta(4f) feature indicate the estimated total thickness (Eq. (2.2)) of the Ta-containing
overlayer (By the end of the third cycle, a substrate Si feature is no longer observed.).
0
2
4
6
8
10
0 1 2 3 4 5 6 7
Cha
rge
Shift
(eV)
H 2 /H
P r o c e s s S t a g e s
61
Fig. 3.8 XPS spectra change with cycles of TBTDET dose and H2/H flux exposure on OSG
sample. (a) Ta(4f) and (b) N(1s).
First Cycle
Second Cycle
Third Cycle
~37Ă
~79Ă
TaN(a)
Binding Energy (eV)
TaOxTa2O5
First Cycle
Third Cycle
~79Ă
TaN
(b)
Second Cycle
~37Ă
Ta(4p3/2)
3236 28 24 20 16
404412420 396 388Ta(4f)
N(1s)21
000
tota
l cou
nts
5500
tota
l cou
nts
62
3.4. Discussion
TBTDET condensed at 120K, annealed in UHV to 300K, and then exposed to an H/H2
flux at 500 K results in the formation of TaN on both OSG and SiO2 substrates, with Ta(4f7/2)
feature at binding energy 23.2 eV, N(1s) feature at 396.6 eV, and Ta:N atomic ratio of 1:1. No
TaN features were observed when similar experiments were carried out in the absence of atomic
hydrogen. TaN formation after subsequent atomic hydrogen exposure at 500K, indicates that
these features are formed only under atomic hydrogen flux. Temperature for TaN formation by
TBTDET CVD deposition without atomic hydrogen was reported to be ~720 K – 920 K [12, 13].
Such a high temperature limits its application involving low κ materials, as such materials often
degrade at temperature above ~600 K – 650 K. In this study, low-temperature of 500K TaN
CVD deposition on OSG with TBTDET and atomic hydrogen was developed. The intensities of
the Ta(4f) and N(1s) at 23.2 eV and 396.6 eV result in a atomic ratio of 1:1, indicating the
formation of TaN. TaN is an excellent diffusion barrier due to its low resistivity [3, 29].
Alternatively, attempt to grow TaN by CVD methods using Ta(NMe2)5 and ammonia resulted in
high resistivity Ta3N5, which hampers its usefulness as a diffusion barrier for advanced
metallization in IC applications [30].
By annealing to 300K, considerable TBTDET precursor interaction with SiO2 and OSG
substrate occurred and resulted in Ta-O bond formation, characterized by Ta(4f7/2) peaks at 24.7
and 25.8 eV, O(1s) at 529.8 eV for Ta suboxide. The atomic hydrogen flux induced new Ta2O5
and more Ta suboxide formation. Comparison of the relative intensity of Ta(4f7/2) at 23.2 eV at
normal incidence and grazing incidence on SiO2 (Fig. 3.5) indicates that TaN is associated with
the outer surface of the film, while the Ta oxide is associated with the interface. The formation of
63
Ta-O interfacial bonds strongly suggests good adhesion between the adlayer and the substrate.
The shifting of C(1s) feature to higher binding energies upon reaction with atomic hydrogen
suggests reactions with electron-withdrawing groups, such as oxygen. This aspect of the reaction
is not yet understood, but it is notable that an atomic hydrogen flux at low temperatures does not
readily remove organic species from the surface/interface region.
Ta(4f) XPS spectra resulting from a single TBTDET physisorption/300 K anneal/H/H2
cycle with ~36Ǻ Ta film thickness on SiO2 and OSG substrates are shown in figures. 3.9a and
3.9b, respectively. The TaTaN/TaTotal intensity ratios are 0.09±0.01 on SiO2 and 0.36±0.02 on
OSG. These data indicate more facile Ta-O bond formation on SiO2 than on OSG. The
formation of Ta oxide by reaction of Ta from the precursor and O from the substrate is also
corroborated by the fact that SiO2 is reduced, resulting in a Si(2p) substrate feature at 102.1 eV
(Fig. 3.2a) as the deposited Ta is oxidized at SiO2 substrate after atomic hydrogen exposure.
Fig. 3.9 Ta(4f) XPS spectra after TBTDET dose and H2/H flux exposure. (a) on SiO2 and (b) on
OSG.
On SiO2
On OSG
~36Ă
~37ĂTaN
TaOxTa2O5
Binding Energy (eV)
(a)
(b)
Ta-N/Ta total =0.36
Ta-N/Ta total =0.09
3236 28 24 20 161300
0 to
tal c
ount
s
64
Many factors are not understood, including the effects of H bombardment on
ligand/substrate interactions, precursor interaction with conductive surfaces (e.g., Cu), and
changes in reaction pathways for precursor deliveries at 300 K, rather than by
physisorption/annealing. The effects of higher hydrogen doses, exposure to NH3/NH2 fluxes,
etc., have not been examined. Nonetheless, these data demonstrate the potential for a
TBTDET/H process to yield conformal, ultra thin TaN barrier on low dielectric substrates.
3.5. Conclusions
TBTDET partially reacts with O atoms in both SiO2 and OSG substrate by 300 K to form
strong Ta-O interfacial bonds, characterized by the O(1s) feature at binding energy 529.8 eV,
Ta(4f7/2) at 24.7 eV and 25.8 eV. Reaction with atomic hydrogen at 500 K results in
stoichiometric TaN formation with the Ta(4f7/2) feature at binding energy 23.2 eV and N(1s) at
396.6 eV, leading to a TaN phase bonded to the substrate by Ta-O interactions. Ta is oxidized as
SiO2 is reduced, with the decrease of Si(2p) binding energy at 103.2 eV in SiO2 and appearance
of new feature at 102.1 eV in Si suboxide. The increase in the relative intensity of TaN on SiO2
at grazing incidence compared to normal incidence indicates that TaN is associated with the
surface region rather than the overlayer/substrate interface. Annealing of TBTDET on SiO2 to
500K without atomic hydrogen results in no TaN formation, indicating that the atomic hydrogen
induces the TaN formation. Sequential exposures of TBTDET at 120K, followed by annealing to
300K and exposure to H/H2 on the reacted layer on both SiO2 and OSG result in a gradual
increase in TaN formation. These data indicate precursor reaction with SiO2 and OSG at low
temperature (e.g. 300K) and TaN formation upon reaction with H/H2 flux at temperature < 500K.
65
The data therefore indicate that a low temperature TaN deposition process is possible on SiO2,
OSG or similar surfaces. The ready formation of Ta-O interfacial bonds strongly suggests good
adhesion between the adlayer and the SiO2 or OSG substrates. The data summarized here
indicate that TBTDET is a potential precursor for an atomic hydrogen driven ALD/CVD process.
3.6 Chapter References
[1] Kuo, Y.-L., Huang, J.-J., Lin, S.-T., Lee, C. and Lee, W.-H., Mater. Chem. Phys. 80 (2003)
690.
[2] Kim, H., Kellock, A. J. and Rossnagel, S. M., J. Appl. Phys. 92 (2002) 7080.
[3] Olowolafe, J. O., Mogab, C. J., Gregory, R. B. and Kottke, M., J. Appl. Phys. 72 (1992)
4099.
[4] Badrinarayanan, S. and Sinha, S., J. Appl. Phys. 69 (1991) 1141.
[5] Baba, K., Hatada, R., Udoh, K. and Yasuda, K., Nucl. Instrum. Methods in Phys. Res. B
127/128 (1997) 841.
[6] Lee, Y. K., Latt, K. M., Jaehyung, K. and Lee, K., Mater. Sci. Semicond. Processing 3
(2000) 179.
[7] Angelkort, C., Berendes, A., Lewalter, H., Bock, W. and Kolbesen, B. O., Thin Solid Films
437 (2003) 108.
[8] Wang, Q., Ekerdt, J. G., Gay, D., Sun, Y.-M. and White, J. M., Appl. Phys. Lett. 84 (2004)
1380.
[9] Ugolini, D., Kowalczyk, S. P. and McFeely, F. R., J. Appl. Phys. 72 (1992) 4912.
[10] Ugolini, D., Powalczyk, S. P. and McFeely, F. R., J. Appl. Phys. 70 (1991) 3899.
[11] Yokoyama, N., Hinode, K. and Homma, Y., J. Electrochem. Soc. 136 (1989) 882.
66
[12] Tsai, M. H., Sun, S. C., Chiu, H. T., Tsai, C. E. and Chuang, S. H., Appl. Phys. Lett. 67
(1995) 1128.
[13] Tsai, M. H., Sun, S. C., Lee, C. P., Chiu, H. T., Tsai, C. E., Chuang, S. H. and Wu, S. C.,
Thin Solid Films 270 (1995) 531.
[14] Park, J.-S., Lee, M.-J., Lee, C.-S. and Kang, S.-W., Electrochem. Solid-State Lett. 4 (2001)
C17.
[15] Eisenbraun, E., Straten, O. V. D., Zhu, Y., Dovidenko, K. and Kaloyeros, A., Proc. 2001
IITC (2001) 207.
[16] Ohshita, Y., Ogura, A., Hoshino, A., Hiiro, S. and Machida, H., J. Cryst. Growth (2000)
604.
[17] Tong, J., Martini, D., Magtoto, N. and Kelber, J., J. Vac. Sci. and Technol. B21 (2003) 293.
[18] Moulder, J. F., Stickle, W. F., Sobol, P. E., Bomben, K. D., Chastain, J. and King, R. C.,
Handbook of X-Ray Photoelectron Spectroscopy, Physical Electronics, Eden Prairie, MN.
[19] Barr, T. L., J. Vac. Sci. Technol. A 9 (1991) 1793.
[20] Atnassova, E. and Spassov, D., Appl. Surf. Sci. 135 (1998) 76.
[21] Nefedov, V. I., Firsov, M. N. and Shaplygin, I. S., J. Electron Spectrosc. Relat. Phenom. 26
(1982) 65.
[22] Engbrecht, E. R., Sun, Y.-M., Smith, S., Pfiefer, K., Bennett, J., White, J. M. and Ekerdt, J.
G., Thin Solid Films 418 (2002) 145.
[23] http://srdata.nist.gov/xps/Bind_e_spec_query.asp, retrieved the information on July 25,
2004.
[24] Kim, K. S., Jang, Y. C., Kim, H. J., Quan, Y.-C., Choi, J., Jung, D. and Lee, N.-E., Thin
Solid Films 377 (2000) 122.
67
[25] Machida, H., Hoshino, A., Suzuki, T., Ogura, A. and Ohshita, Y., J. Cryst. Growth 237-239
(2002) 586.
[26] Fisher, I., Kaplan, W. D., Eizenberg, M., Nault, M. and Weidman, T., Mat. Res. Soc. Symp.
Proc. 716 (2002) B7.20.1.
[27] Contarini, S., Howlett, S. P., Rizzo, C. and Deangelis, B. A., Appl. Surf. Sci. 51 (1991) 177.
[28] Chourasia, A. R., Surf. Sci. Spectra 8 (2001) 45.
[29] Holloway, K., Fryer, P. M., Cabral, C., Jr., Harper, J. M. E. and Bailey, P. J., J. Appl. Phys.
71 (1992) 5433.
[30] Fix, R. M., Gordon, R. G. and Hoffman, D. M., Chem. Mater. 5 (1993) 614.
68
CHAPTER 4
RUTHENIUM SPUTTER DEPOSITION ON ORGANOSILICATE GLASS AND ON
PARYLENE: AN XPS STUDY OF INTERFACIAL CHEMISTRY, NUCLEATION AND
GROWTH [1]*
4.1. Introduction
Ruthenium (Ru) is of growing interest as a diffusion barrier for copper (Cu) in low-k
integration, primarily because the semi-noble nature of the metal allows for facile
electrodeposition of Cu films, while the high melting point and immiscibility with Cu are
favorable for microelectronics applications [2]. In diffusion barrier applications, the adhesion of
Ru films to dielectric substrates is also important. The semi-noble nature of Ru is detrimental for
adhesion and conformal growth on dielectric substrates, and one would intuitively expect that Ru
would exhibit much less interfacial interaction with a silicon(Si)-oxygen(O)-carbon(C) low k
dielectric than would, e.g., tantalum (Ta) [3]. X-ray photoelectron spectroscopy (XPS) has been
demonstrated [3-5] to be an excellent method for characterizing the formation of metal-substrate
chemical bonds (or lack of same) during gradual metal deposition under controlled conditions.
In such experiments, it is usually helpful to transfer the sample from the deposition chamber to
the analysis chamber without exposure to atmosphere. This report documents results of XPS
core level spectra for sputter-deposited Ru on organosilicate glass (OSG) and on parylene, at
* Reproduced with permission from [Zhao, X., Magtoto, N. P., and Kelber, J. A., Mat. Res. Soc.
Symp. (MRS) Proc. 812 (2004) F2.5]. Copyright [2004] MRS.
69
coverages up to several monolayers. OSG is a leading low-k candidate for replacing SiO2 as an
interlayer dielectric, while parylene is a candidate for pore sealing of porous ultra-low k
materials [6]. The XPS results confirm generally weak Ru-substrate interactions, and this is
corroborated by results for a Scotch® tape (3M, Inc., St. Paul, Minnesota, www.3m.com) test of
an electrolessly deposited Cu film on Ru sputter-deposited onto OSG, showing failure at the
Ru/OSG interface.
4.2. Experiment Detail
Experiments were carried out in an ultrahigh vacuum (UHV) system attached to a dual
magnetron sputter deposition system. This system has been described previously in chapter 2.
Since XPS on insulating samples can result in sample charging that shifts the apparent
photoelectron energies, spectra were calibrated by referencing the peak from adventitious carbon
at 284.5 eV.
An elemental Ru sputter target was used, with target/sample distance adjusted so that a
minimum sputter deposition rate of 0.004 Å-sec-1 was observed, as determined by the attenuation
of core-level XPS intensity (Eq. (2.2)) during Ru deposition on clean Cu foil. Sample transfer
between deposition and analysis chambers occurred under UHV (< 10-8 torr). The ~ 1 cm2
samples consisted of either commercially prepared OSG deposited on Si, or 1000Å thick
parylene deposited on ~20Å silicon dioxide (SiO2) on a p-type Si(100) substrate.
4.3. Results XPS core-level spectra are displayed in figure 4.1 for the OSG sample after annealing
70
in UHV at 500 K for 30 minutes, which removed some adventitious carbon. This particular type
of OSG has been described in chapter 3. The main effect of annealing in UHV is to have
removed a significant amount of adventitious carbon from the sample, resulting in a post-anneal
stoichiometry of SiC0.72O1.08 (Eq. (2.1)).
XPS spectra of samples containing carbon and ruthenium are complicated by the overlap
between the C(1s) spectrum and the Ru(3d3/2) component of the Ru(3d) spectrum, as shown in
figure 4.2. For this reason, Ru coverage was determined from intensity of the Ru(3d5/2) feature.
Since the relative intensities of the Ru(3d3/2)/Ru(3d5/2) features are well known [7], the
estimation of the C(1s) signal intensity by subtraction of the determined Ru(3d3/2) intensity is
straightforward, as shown (Fig. 4.2).
Fig. 4.1 Core level XPS spectra for the OSG film before (bottom) and after (top) annealing at
500 K for 30 min. in UHV.
536 534 532 530 528288 286 284 282 280 106 104 102 100
C(1s)C-C(-284.5 eV) C-Si-O(-
283.5 eV)
O(1S)O-Si-C(-531.1 eV)
SiO2(-532.1 eV)
Si(2p)
C-Si-O(-102.1 eV)
Before Annealing
After Annealing
SiC0.86O1.11
SiC0.72O1.08
SiO2(-103.2 eV)
3500
tota
l cou
nts
1 30 0
0 to
t al c
o unt
s
3 55 0
tota
l cou
nts
Binding Energy (eV)536 534 532 530 528288 286 284 282 280 106 104 102 100
C(1s)C-C(-284.5 eV) C-Si-O(-
283.5 eV)
O(1S)O-Si-C(-531.1 eV)
SiO2(-532.1 eV)
Si(2p)
C-Si-O(-102.1 eV)
Before Annealing
After Annealing
SiC0.86O1.11
SiC0.72O1.08
SiO2(-103.2 eV)
3500
tota
l cou
nts
1 30 0
0 to
t al c
o unt
s
3 55 0
tota
l cou
nts
536 534 532 530 528288 286 284 282 280 106 104 102 100
C(1s)C-C(-284.5 eV) C-Si-O(-
283.5 eV)
O(1S)O-Si-C(-531.1 eV)
SiO2(-532.1 eV)
Si(2p)
C-Si-O(-102.1 eV)
Before Annealing
After Annealing
SiC0.86O1.11
SiC0.72O1.08
SiO2(-103.2 eV)
3500
tota
l cou
nts
1 30 0
0 to
t al c
o unt
s
3 55 0
tota
l cou
nts
Binding Energy (eV)
71
The Ru(3d5/2) binding energy of 280.0 eV is indicative of Ru in a metallic or zerovalent
state [8], and this binding energy was observed independent of Ru coverage, indicating
negligible charge transfer between the Ru and the substrate. The variation of
Ru(3d) intensity with deposition time on OSG is compared to the behavior on parylene in Fig.
4.3 (left), normalized to the substrate C(1s) intensity.
Fig. 4.2 Ru(3d)/C(1s) region, showing the partial overlap of the Ru(3d) and C(1s) core level
features. Spectrum corresponds to about 30 min Ru deposition (approximately 3 monolayers).
Ru(3d3/2) component indicated by dashed line was determined from the intensity and binding
energy of the Ru(3d5/2) component.
B in d in g E n erg y (eV )2 9 0 2 7 8
0
5 0 0 0
C (1 s) + R u (3 d 3 /2)
R u (3 d 5 /2)
Inte
nsity
(cou
nts)
B in d in g E n erg y (eV )2 9 0 2 7 8
0
5 0 0 0
C (1 s) + R u (3 d 3 /2)
R u (3 d 5 /2)
Inte
nsity
(cou
nts)
72
Fig. 4.3 The evolution of the Ru(3d5/2)/C(1s) intensity ratio as function of Ru deposition vs time
at 300 K. (Left) Deposition of Ru on OSG. The film thickness at 10 min corresponds to 1
monolayer. (Right) Deposition of Ru on parylene.
The data in figure 4.3 (left) indicate a linear increase in Ru intensity on OSG up to 10
minutes deposition time, followed by a change in slope. Such behavior is indicative of initial
conformal (2D) growth in the first layer, followed by a transition to 3D growth with the
formation of the second layer— SK growth [9]. Although such behavior—when observed for Cu
deposition— generally correlates with significant chemical interaction and charge exchange
between the metal overlayer and dielectric substrate [5, 10, 11], no evidence for Ru oxidation
was observed in the XPS spectra.
In contrast to Ru/OSG, similar data for Ru deposition on parylene shows different
behavior (Fig. 4.3, right). There is no sharp change in slope, as for deposition on OSG, and the
region where a gradual change is observed occurs well before an average thickness of 1
monolayer is achieved. The data in Fig. 4.3 therefore suggest a much less pronounced tendency
Ru(
3d5/
2)/C
(1s)
XPS
Inte
nsity
Rat
io
Ru Deposition Time(min)
00.10.20.30.40.50.60.7
0 10 20 30 40
~2.5Å Ru
PVD Ru on OSG
00.10.20.30.40.50.60.7
0 10 20 30 40
~2.5Å Ru
PVD Ru on OSG
0.1
0.3
0.5
0.7
0.9
0 10 20 30 400
~2.5ÅRu
PVD Ru on Parylene(a) (b)
73
for initial conformal growth on parylene than on OSG. A comparison of these results in turn
suggests a stronger interfacial interaction between Ru and OSG than between Ru and parylene.
In order to examine the suitability of sputter-deposited Ru films for Cu integration, a
Ru/OSG sample was prepared for Cu electroless deposition. A sample was prepared by 60
minutes sputter deposition of Ru onto an OSG substrate at 300 K—corresponding to an average
thickness of 6 Ru monolayers. The sample was removed from UHV and placed in a
formaldehyde-based electroless plating solution (6g/l copper sulfate, 32 g/l
ethylenediaminetetraacetic acid (EDTA), 4g/l formaldehyde and sodium hydroxide to adjust the
pH of the solution to 11). After 60 minutes, the sample was emersed from the solution, and air-
dried. A shiny Cu film was readily visible to the eye. The sample was then subjected to a simple
Scotch Tape test in order to provide a rough, qualitative assessment of film substrate adhesion.
The Scotch Tape test resulted in the loss of all visible Cu from the sample. XPS spectra of the
sample before Cu deposition (but after air exposure) and after Cu deposition and Scotch Tape
test, are shown in Fig. 4.4.
Fig. 4.4 XPS C(1s)/Ru(3d) spectra (left) and O(1s) spectra (right).
290 285 280 275
Before Cu
After Cu and Tape Test
C(1s)/Ru(3d)
536 532 528
O(1s)
O-Ru(-529.7eV)
O-Si-C(-531.1eV)
SiO2/OH(-532.1eV)
Ru-O(-281.4eV)
C-Si-O(-283.5eV)
Ru(-280eV)
Binding Energy (eV)
Inte
nsity
(arb
. uni
ts)
Inte
nsity
(arb
. uni
ts)
Binding Energy (eV)
290 285 280 275
Before Cu
After Cu and Tape Test
C(1s)/Ru(3d)
536 532 528
O(1s)
O-Ru(-529.7eV)
O-Si-C(-531.1eV)
SiO2/OH(-532.1eV)
536 532 528
O(1s)
O-Ru(-529.7eV)
O-Si-C(-531.1eV)
SiO2/OH(-532.1eV)
Ru-O(-281.4eV)
C-Si-O(-283.5eV)
Ru(-280eV)
Binding Energy (eV)
Inte
nsity
(arb
. uni
ts)
Inte
nsity
(arb
. uni
ts)
Binding Energy (eV)
74
The XPS spectra taken after air exposure but before Cu electroless deposition (bottom
traces) clearly show the presence of oxidized Ru, as evidenced by a broadening of the Ru(3d5/2)
feature (figure 4.4, bottom, left) which is well fit by a component at 281.4 eV—characteristic of
oxidized Ru [7, 8]. The presence of oxidized Ru is corroborated by the presence of a component
near 529.7 eV in the O(1s) spectrum [7](Fig. 4.4, bottom, right). After the Scotch tape test, the
Ru(3d5/2) intensity is reduced by 73% (Fig. 4.4, top, left). This is accompanied by a
corresponding loss in intensity of the O(1s) component near 529.7 eV (Fig. 4.4, top, right).
Cu(2p) spectra (not shown) indicated the presence of only trace amounts of Cu after the Scotch
tape test.
4.4. Discussion
The XPS data shown here indicate that sputter deposition of Ru on OSG at 300 K
results in the growth of a conformal interface (SK growth). In contrast, Ru deposition on
parylene shows less tendency towards SK behavior, indicative of a weaker interfacial interaction.
During deposition on OSG, there is no evidence for Ru oxidation, which would be evidenced by
a broadening of the Ru(3d5/2) component to higher binding energies. Such a broadening is only
observed after exposure of the sample to air (Fig. 4.4). Possible XPS evidence for the formation
of a Ru carbide interfacial layer is obscured by the overlap of Ru (3d) and C(1s) features in the
region of 283-281 eV (Fig. 4.2)—the region in which metal carbide features are often observed
[7]. The absence of interfacial carbide formation can be deduced from the fact that the
Ru(3d)/C(1s) intensity ratio (Fig. 4.3, left) increases linearly with Ru coverage up to the
completion of the first monolayer. Similar Ru/Si data (not shown) similarly strongly suggests an
absence of interfacial silicide formation. The weak chemical interaction between Ru and the
75
substrate is consistent with the results of the Scotch tape test on a Cu(electroless)/Ru/OSG
sample indicating failure mainly at the Ru/OSG interface.
The lack of interfacial chemical reaction between sputter-deposited Ru and OSG or
parylene is in contrast to what is observed for Ta. Ta sputter deposited onto a Si-O-C substrate,
where formation of interfacial Ta oxide and Ta carbide is observed [3]. Similarly, Ta deposited
on parylene results in the formation of interfacial carbide [12]. This would suggest that the use of
Ru on OSG or parylene sealed dielectric materials should be accompanied by the use of a Ta
“glue” layer between the Ru and the dielectric in order to increase interfacial adhesion. Such a
scheme, of course, replaces the deposition of a Cu seed on Ta with the deposition of a Ru layer,
which can then be used for direct electroless or electrodeposition of Cu. An alternative
approach, which would avoid the necessity for a glue layer, would be to hydroxylate the
substrate prior to Ru deposition. Such an approach has been shown to enhance the chemical
interaction of Cu with a variety of substrates [10, 11]. Other seminoble metals may exhibit
similar effects [13].
4.5 Conclusions
XPS has been used to characterize the chemical interactions of sputter-deposited Ru
with OSG and parylene at 300 K. The results indicate the lack of interfacial oxide, carbide or
silicide formation on OSG, and the lack of interfacial carbide formation on parylene. Ru exhibits
SK growth (conformal growth of the first layer) on OSG, but this tendency is much less clear-cut
on parylene. The formation of an electroless Cu layer on a Ru/OSG sample, followed by a
Scotch Tape test and subsequent XPS analysis, revealed failure at the Ru/OSG interface,
consistent with the weak interfacial chemical interactions observed by XPS. The results indicate
76
that the use of Ru as a diffusion barrier for Cu/low-k integration requires either the use of a
“glue” layer (e.g., Ta) between the Ru and dielectric substrate, or possibly some other chemical
modification, such as hydroxylation of the substrate.
4.6. Chapter References
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