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    CITY UNIVERSITY OF HONG KONG

    DEPARTMENT OF

    PHYSICS AND MATERIALS SCIENCE

    BACHELOR OF ENGINEERING (HONS) IN MATERIALS ENGINEERING

    2006-2007

    DISSERTATION

    SYNTHESIS AND CHARACTERIZATION OF SILICON

    NANOWIRES AND SILICON NANOWIRE BASED FIELD

    EFFECT TRANSISTOR

    by

    XIANG Jing Lei

    March 2007

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    SYNTHESIS AND CHARACTERIZATION OF SILICON

    NANOWIRES AND SILICON NANOWIRE BASED FIELD

    EFFECT TRANSISTOR

    by

    XIANG Jing Lei

    Submitted in partial fulfilment of the

    Requirements for the degree of

    BACHELOR OF ENGINEERING (HONS)

    IN

    MATERIALS ENGINEERING

    from

    City University of Hong Kong

    March 2007

    Project Supervisor : Prof. S. T. Lee

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    A. Content

    A. Content I

    B. List of graphs III

    C. List of figures IV

    D.Acknowledgment V

    E. Abstract VI

    1. Introduction

    1.1 Silicon Nanowires 1

    1.2 Silicon based semiconductors and technology 2-3

    1.3 Silicon Nanowire-based nanoelectronics devices 4

    2. Literature Review

    2.1. Various methods in the synthesis of silicon nanowires

    2.1.1 Template-Directed Synthesis 5-6

    2.1.2 Vapor-Liquid-Solid growth 6-7

    2.1.3 Oxide-Assisted Growth 7-9

    2.1.4 Metal-Nano particl e-Catalyzed Chemical Etching 9-11

    3. Experimental Procedures 12

    3.1 Synthesis of silicon nanowires by MNCCE 12

    3.1.1 Characterization of SiNW 12

    3.1.1.1 SEM 12

    3.1.1.2 TEM 13

    3.1.1.3 EDX 13

    3.2 Simple Device Construction 13

    3.2.1 Wafer preparation 13

    3.2.2 Nanowire dispersion 14

    3.2.3 Electrode deposition 14

    I

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    3.2.3.1. Mechanical Mask Route (MMR) 14

    3.2.3.2 .Photolithography Route (PR) 14

    3.2.4. Positioning of SiNW 15

    3.3 Field Effect Transistor Construction 15

    3.3.1 Performance of SiNW in the ambient condition 15

    3.3.2 Surface passivation by coating an oxide layer 16

    3.4. Process of photolithography and experimental flow chart 17-18

    4. Results and discussions

    4.1 Properties of SiNW synthesized by MNCCE 19-20

    4.2. I-V of SiNW prepared by mechanical mask 21

    4.2.1. Effects of work function of the electrode material 21

    4.2.2 Exchange electrodes measurements for contact check 22-23

    4.3. I-V of SiNW prepared by photolithography 24-25

    4.4. Effect of contact resistance 26-27

    4.5. Gate construction for FET 28-32

    4.5.1 SiNW in the ambient atmosphere 28-32

    4.5.2 SiNW coated with a layer of SiO2 32-35

    4.6. Possible errors involved in calculation 35

    5. Conclusion 36-37

    6. Future Work 37

    7. List of Reference 38-41

    II

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    B List of graphs:

    Fig.2.1. Shadow sputtering against an array of V-grooves to form 1D nanomaterial

    Fig.2.2 Vapor-phase deposition of 1D nanomaterials into V-grooves

    Fig.2.3. Porous membrane used in the 1D structure synthesis

    Fig.2.4 Nanomaterial synthesized by VLS mechanism

    Fig.2.5 Phase diagram of Si-Au alloy

    Fig.2.6 Schematic graph showing the Ag particle is pinned

    Fig.2.7 Schematic graph showing the sinking track of Ag

    Fig.2.8 Cross-section of SiNW synthesized

    Fig.3.1. Electrode pattern on the wafer prepared by photolithography

    Fig.3.2 Magnified electrode with marks

    Fig.3.3. Schematic illustration of a two point probe station

    Fig.3.4 The configuration of the SiNW device

    Fig.3.5 Photolithography Technique

    Fig.3.6 Experimental flow chart

    Fig.4.1 SEM micrograph of SiNW synthesized by MNCCE

    Fig.4.2 EDX pattern showing the composition of the SiNW

    Fig.4.3 Band diagram for Schottky barrier

    Fig.4.4 I-V curve of a Schottky barrier

    Fig.4.5. Exchange electrode measurement of I-V

    Fig.4.6 SEM of Sample A prepared by shadow mask

    Fig.4.7.SEM of Sample B prepared by shadow mask

    Fig.4.8 I-V characteristics of 3 samples prepared by shadow mask

    Fig.4.9 Electrode pattern fabricated by photolithography without metal coating

    Fig.4.10 Electrode pattern fabricated by photolithography with metal coating

    Fig.4.11 SEM image of NW on electrode prepared by photolithography (Sp A)

    Fig.4.12 SEM image of NW on electrode prepared by photolithography (Sp B)

    Fig.4.13 Schematic illustration of contact area

    Fig.4.14 I-V characteristics of the FET deviceFig.4.15 Explanation of linear region in the curve

    III

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    Fig.4.16 Explanation of saturation region in the curve

    Fig.4.17 Ids vs. Vg plotted in the linear scale and log scale. Inset is the SEM image of

    the measured sample

    Fig.4.18 Transconductance measured at every gate voltage in air

    Fig.4.19 I-V characteristics of the FET device modified by SiO2

    Fig.4.20 Ids vs. Vg plotted in the linear scale and log scale with threshold voltage

    about 2 V. Inset is the SEM image of the measured sample

    Fig.4.21 Transconductance measured at every gate voltage with oxide coated

    C. List of Tables:

    Table.4.1 Resistivity of SiNW measured from the photolithographic samples and

    shadow mask samples

    Table 4.2 Mobility obtained in the ambient condition and in SiO2treated condition

    IV

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    D. Acknowledgement

    I would like to take this opportunity to express my gratitude and appreciation to my

    supervisor, Professor S.T. Lee for his constant encouragement and support. The

    enlightening discussion between Professor Lee and me has aroused great passion in

    me to explore the beauty of science and technology.

    I would also like to thank Dr.Jie for helping me get familiar with research

    environment in the lab while demonstrating to me so many experiments that kept me

    gravitated to the field of nanotechnology. The valuable advice he shared with me

    inspired me a lot throughout the project.

    I wish to thank all the Mphil students and PhD students in the Center of

    Super-Diamond and Advanced Films for giving me so many help during the

    experiment and sharing their research experience with me. Hereby, I would like to

    thank Mr. Tang Hao, Mr. Chen Zhenhua, Mr Jack Chung and Mr. Ye Qing and etc.

    particularly for their invaluable discussion with me on my project.

    Also, I would like to thank my parents and my friends for their encouragement and

    support without which the project will never be so successful. I treasure the kindness

    of all the people who have helped me in the project and I believe I will live up to your

    expectations.

    V

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    E. Abstract:

    Microelectronic technology has made a big difference in almost every corner of our

    lives thanks to the progressive development of semiconductor industry. Nowadays,

    people are making all those electronic devices smaller in size, and better in

    performance. Yet, challenges also come along since further miniaturization of devices

    require even better precision technology and the traditional planar fabrication

    technology will soon feel its confinement. 1D nanostructured materials have brought

    possibilities to overcome the difficulties and their potential to be applied in the

    electronic industry has created excitement in a lot of research labs all over the world.

    In this project, the SiNWs are used for all the experiments. They are synthesized by

    the Metal-Nanoparticle-Catalyzed-Chemical-Etching method which provides a better

    alignment of nanowires and easier controllability of its doping concentration as

    compared to the chemical vapor deposition, laser ablation and thermal evaporation.

    In order to measure the conductivity of the as-synthesized SiNWs, they were

    dispersed onto the silicon wafer randomly. Different masks for lithography were used

    to fabricate the electrodes. Shadow masking and photolithography defined the size and

    the pattern of electrode layout. The electrode material to be deposited was also

    carefully selected since either Schottky contact or ohmic contact would influence the

    charge flow in the SiNW due to the difference between the work function of the metal

    and that of the semiconductor. In order to achieve ohmic contact that allows the

    current flow in either direction, metals with work function higher than the

    semiconductor was used such as Au.

    Once the I-V characteristic of the SiNW was measured, gate voltage applied to the

    silicon substrate was also examined and the SiNW based field effect transistor was

    thus constructed (similar to a metal-oxide-semiconductor structure). The transport

    property of SiNW was manipulated by the application of different gate voltages. Since

    the SiNW is of p-type, positive gate voltage tends to expel the holes in the nanowire tothe negative electrode, thus forming a depletion region with high resistance and a

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    shallow conducting channel. The response of the SiNW FET shows an increase in the

    conductivity of the SiNW and higher saturation voltage with the negative increase of

    the gate voltage. Instead of scanning the source-drain voltage, the gate voltage was

    scanned while keeping the source-drain voltage fixed. The current flow in the source

    and drain and the corresponding gate voltage applied plotted in either linear or

    logarithmic scale shed light on the threshold voltage and the depletion threshold

    voltage of the device.

    To improve the performance of SiNW FET, silicon dioxide layer was used to cover the

    SiNW exposed in ambient environment. The surface was said to be isolated from

    external environment and the transport properties were observed to change quite a lot.

    The main mechanism accounting for the increase in hole mobility is the suppression

    of reaction between the surface and molecular species and reduction of scattering by

    the surface defects.

    VII

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    1. Introduction:

    1.1 Silicon Nanowires

    A nanowire is a wire of dimension of the order of a nanometer (109

    meters).

    Alternatively, nanowires can be defined as structures that have a lateral size

    constrained to tens of nanometers or less and an unconstrained longitudinal size. At

    these scales, quantum mechanical effects are important hence such wires are also

    known as "quantum wires". Many different types of nanowires exist, including

    metallic (e.g., Ni, Pt, Au), semiconducting (e.g., InP, Si, GaN, etc.), and insulating

    (e.g., SiO2, TiO2). Nanowires usually exhibit an aspect ratio of 1000 and more. As

    such they are often referred to as 1-Dimensional materials. Nanowires have many

    interesting properties that are not seen in bulk or 3-D materials. This is because

    electrons in nanowires are quantum confined laterally and thus occupy energy levels

    that are different from the traditional continuum of energy levels or bands found in

    bulk materials.

    As for the synthesis of SiNW, much effort has been made to prepare them by different

    methods, such as chemical vapor deposition,[1] laser ablation,[2,3] thermal

    evaporation decomposition,[4,5]supercritical fluid liquid solid (SFLS) synthesis,[6-7]

    and other methods. These methods are quite accessible and will be briefed in the

    second chapter.

    As the building blocks for future nanoelectronics, the 1D nanowire can be employed

    as active devices or interconnects that have great potential in improving the

    performance of the electronic devices prevailing in the market now because of their

    small size and reduced power consumption. Yet, everything has a trade off and the

    same for semiconducting nanowires. The conductivity of a nanowire is expected to be

    much less than the bulk material. The primary reason is that the scattering from the

    wire boundary will severely hinder the effective transport of carriers when the width

    of the nanowires is less than the mean free path of charge carriers. The so-called edge

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    effects come from atoms that lay at the nanowire surface and are not fully bonded to

    neighboring atoms like the atoms within the bulk of the nanowire. The unbonded

    atoms are often a source of defects within the nanowire, and may cause the nanowire

    to conduct electricity more poorly than the bulk material.

    1.2 Silicon based semiconductors and technology

    Silicon based semiconductor devices have been studied for more than 125 years. [8]

    The building blocks for semiconductor devices are showing better performance and

    adaptability to advance integrated circuits. The very primary components of

    semiconductor devices in chronological order in terms of its invention are the

    metal-semiconductor contact, the p-n junction, the heterojunction and the

    metal-oxide-semiconductor (MOS) structure. The development of semiconductor

    technology has made it possible for humans to fabricate more advanced integrated

    circuits with the combination of all these basic semiconductor devices and their

    derivatives.

    Semiconductor technology

    Crystal growth:From the starting material sand (silicon dioxide) to a silicon wafer,

    several chemical processes are involved to form a high-purity polycrystalline

    semiconductor from which single crystals are grown. The polycrystalline silicon is

    placed in the crucible with the furnace heated above the melting temperature of silicon.

    A suitably oriented seed crystal is suspended over the crucible in a seed holder and

    inserted into the melt. Part of it melts, but the tip of the remaining seed crystal still

    touches the liquid surface. It is then withdrawn. The progressive freezing at the

    solid-liquid interface yields a large, single crystal. This method is called Czochralski

    technique and virtually all the silicon used for fabricating integrated circuits is

    prepared by this technique. Then, the ingots are shaped to define the diameter of the

    material and sawed into wafers.

    Film formation: To fabricate discrete devices and integrated circuits, we may use

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    different kinds of thin films, namely, thermal oxides, dielectric layers, polycrystalline

    silicon, and metal films. Semiconductors can be oxidized by various methods; thermal

    oxidation is by far the most important for silicon devices. Thermal oxidation of silicon

    contains a reactor [9] consisting of a resistance-heated furnace, a cylindrical

    fused-quartz tube containing the silicon wafers held vertically in a slotted quartz boat,

    and a source of either pure dry oxygen or pure water vapor. The oxidation temperature

    is generally in the range of 900-1200C and the typical gas flow rate is about

    1liter/min.

    Lithography and etching: lithography is the process of transferring patterns of

    geometric shapes on a mask to a thin layer of radiation-sensitive material (called resist)

    covering the surface of a semiconductor wafer. These patterns define the various

    regions in an integrated circuit such as the implantation regions, the contact windows,

    and the bonding-pad areas. The resist patterns defined by the lithographic process are

    not permanent elements of the final device but only replicas of circuit features. To

    produce circuit features, these resist patterns must be transferred once more into the

    underlying layers comprising the device. The pattern transfer is accomplished by an

    etching process that selectively removes unmasked portions of a layer.

    Impurity doping:Diffusion and ion implantation are the two key methods of impurity

    doping. Until the early 1970s, impurity doping was done mainly by diffusion at

    elevated temperatures. In this method the dopant atoms are placed on or near the

    surface of the wafer by deposition from the gas phase of the dopant or by using

    doped-oxide sources. The doping concentration decreases monotonically from the

    surface, and the profile of the dopant distribution is determined mainly by the

    temperature and diffusion time. Since the early 1970s, many doping operation have

    been performed by ion implantation. The doping concentration has a peak distribution

    inside the semiconductor and the profile of the dopant distribution is determined by

    the ion mass and implanted-ion energy. Both diffusion and ion implantation are usedfor fabricating discrete devices because these processes complement each other.[10]

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    1.3 Silicon nanowire based nanoelectronic devices

    Since the composition and dimension of SiNWs can be controlled during the synthesis

    process, we can obtain a single SiNW with diameter less than 100nm for measuring

    the electrical properties of the wire by placing under two electrodes being source and

    drain respectively. The conductivity can be readily measured by 2 probe or 4 probe

    station. The poor conductance of SiNW can be attributed to a list of factors, such as

    the scattering effects of the boundary wire, the large contact resistance between the

    metal and semiconductor interface, and also the presence of surface defects along the

    wire. Furthermore, field effect transistor can be constructed by applying a back gate

    voltage to measure the response of the SiNW in terms of its change in conductivity.

    SiNW based field effect transistor can be turned on or off by the applied voltage

    making it possible to be used as a potential switching device in advanced circuits. The

    on/off ratio representing the performance of the FET device can be improved by

    proper surface modification of the SiNW so that the defects on the surface of the wire

    can be saturated; reducing the scattering sites of the charge carriers.

    SiNWs can also be used to construct p-n diode thanks to the better alignment

    technology including the Langmuir-Blodgett technique [11] and fluidic-directed

    assembly [12],p-type SiNW and n-type SiNW can be crossed to form a junction, the

    potential application also extends to other disciplines, revolutionizing the daily life of

    human beings.

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    2. Literature Review

    2.1. Various methods in the synthesis of silicon nanowires

    2.1.1 Template-Directed Synthesis

    Template-directed synthesis represents a straightforward route to 1D nanostructure.

    The template simply serves as a scaffold within (or around) which a different material

    is generated in situ and shaped into a nanostructure with its morphology

    complementary to that of the template. When the template is only involved physically,

    it is often necessary to selectively remove the template using post-synthesis treatment

    (such as chemical etching and calcination) in order to harvest the resultant

    nanostructures. In a chemical process, the template is usually consumed as the

    reaction proceeds and it is possible to directly obtain the nanostructures as a pure

    product.

    As shown by Jorritsma and co-workers [13], metal nanowires as thin as 15nm could

    be prepared by shadow sputtering a metal source against an array of V-grooves etched

    on the surface of a Si(100) wafer. Fig.2.1. In another procedure, metal or

    semiconductor was applied at normal incidence using techniques based on

    vapor-phase deposition or solution-phase electrochemical plating, and then allowed to

    reconstruct into 1D nanostructure at the bottom of each V-groove Fig.2.2.[14]Using

    these approaches, continuous thin nanowires with lengths up to hundreds of

    micrometers could be routinely prepared as parallel arrays on the surfaces of solid

    supports that could be subsequently released into the free-standing form or be

    transferred onto the surfaces of other substrates.

    Channels in porous membranes provide another class of templates for use in the

    synthesis of 1D nanostructure pioneered by Martin and several others. [15]Two types

    of porous membranes Fig.2.3 are commonly used in such synthesis: polymer films

    containing track-etched channels and alumina films containing anodically etched

    pores. For track-etching, a polymer film (6-20 microns) is irradiated with heavy ions

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    to generate damage spots in the surface of this film. The spots are amplified by

    chemical etching which facilitates the penetration of cylindrical pores into the films.

    [16]A variety of materials have been examined for use with this class of templates.

    The requirement for this method is that the material can be loaded into the pores using

    liquid phase injection, or solution-phase chemical or electrochemical deposition.

    Although the nanowires synthesized by this method are usually polycrystalline, the

    major advantage associated with membrane-based templates is that both the

    dimension and composition of nanowires can be easily controlled by varying

    experimental conditions.

    Fig. 2.1 Fig. 2.2

    Fig. 2.3

    Fig.2.1. Shadow sputtering against an array of V-grooves. Fig.2.2 Vapor-phase

    deposition of 1D nanomaterials into V-grooves. Fig.2.3. Porous membrane used in the

    1D structure synthesis.

    2.1.2 VLS growth of silicon nanowires

    The vapor-liquid-solid mechanism Fig.2.4 described in detail by Wagner and his

    co-workers [17-19] is one of the many common ways to synthesize the silicon

    nanowires catalyzed by gold nanoparticles. The name arises from the fact that thesilane [20]semiconductor vapor phase reactants usually taken as the source of silicon

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    will alloy with gold nanoparticles which are in a melted state when heated. As long as

    the temperature is higher than the eutectic temperature of the binary system Fig.2.5,

    the silane will decompose at the surface of the gold nanoparticle and the silicon will

    dissolve into the liquid gold nanoparticle. As silicon continues to dissolve in the gold,

    saturation will eventually occur as predicted by the phase diagram of the binary alloy

    system. After that, the silicon will precipitate out from the liquid phase to form the

    solid nanowire as we require. Since the eutectic temperature of Si-Au binary alloy

    system is around 363C [21], theoretically the temperature of synthesizing the silicon

    nanowire can be around 400 degrees which is not that high. The size of the as-grown

    silicon nanowires is controlled by the dimensions of gold nanoparticles and the growth

    rate is dependant on the partial pressure and temperature of the growing environment.

    Growth defects such as kinking and bending are observed from the experiment due to

    the different conditions used to grow the nanowires. The growth direction, as can be

    predicted by thermodynamic principles, is along family.[22-23]

    Fig. 2.4 Fig.2.5

    Fig.2.4 Nanomaterial synthesized by Fig.2.5 Phase diagram Si-Au alloy

    VLS mechanism

    2.1.3 Oxide Assisted Growth

    Another way to synthesize silicon nanowires in the absence of metal catalyst was

    proposed by Lee and co-workers [5]several years ago by laser ablating a mixture of

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    Si and SiO2. The vapor phase SixOgenerated by laser ablation seemed to be the key

    intermediate in this oxide assisted process. The formation of silicon was believed to

    occur through the following two steps:

    SixOSix-1 + SiO (x>1)

    2SiOSi + SiO2

    The TEM observations suggested that these decomposition reactions first led to the

    precipitation of Si nanoparticles encapsulated in shells of silicon oxide. Some of these

    particles might be piled up on the surface of the silicon oxide matrix, and served as

    seeds for the growth of nanowires in the following steps. SixO (x >1) layer at the tip of

    each nanowire seemed to have a catalytic effect. This layer might be in or near a

    molten state and thus capable of enhancing atomic absorption, diffusion, and

    deposition. The SiO2 component in the shell might help to retard the lateral growth of

    each nanowire. The precipitation, nucleation and growth of Si nanowires always

    occurred in the region closest to the cold finger suggesting that the temperature

    gradient was the driving force for the nanowire growth.[24-30]

    OAG growth with Au catalysts

    The diameter of the SiNWs grown by OAG method is determined by the ambient

    environment such as He, H2+Ar or N2 that controls the cluster migration and phase

    transformation of the tip of the SiNW. Lee and co-workers [31]proposed OAG with

    gold catalyst to grow SiNW with better dimensional control.

    The mechanism is just the combination of the VLS and OAG methods. The reduced

    growth temperature relative to that of metal-free OAG may be attributed to the Au

    catalytic effect in lowering SiO decomposition temperature. During growth, the

    arriving silicon atoms have to diffuse through the thin oxide layer to reach the Au

    particle. Thus, the growth temperature should be sufficiently high to allow silicon

    penetrating through the oxide layer to form the eutectic alloy so as to sustain thegrowth of SiNWs. The Au-SiO approach offered certain advantages over VLS growth

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    and OAG, such as the absence of toxic and flammable gases and the control of size

    and epitaxial growth of SiNW. The nanowires primarily grew along the and

    directions, similar to SiNWs grown by the OAG method without any catalysts.

    The side surfaces ofthe SiNW are made of the {1 1 1} and {1 1 0} facets for the

    nanowire grown along [1 1 2] direction. The presence of those crystal facets could

    minimize the total energyof the nanowire because the surface energy of the {1 1 1}

    facets is the lowest and the energy of the side surfaces dictates the total surface energy

    of a SiNW [32]

    2.1.4 Metal-nanoparticle catalyzed chemical etching

    Besides all the methods that I have introduced above in the synthesis of SiNWs, there

    is still one important mechanism which involves the electrochemical reaction in

    synthesizing nanomaterials. Since Si shows novel electrochemical properties in

    solutions containing hydrofluoric acid, Peng and co-workers [33]proposed electroless

    metal deposition (EMD) [34-37]and electroless etching in the synthesis of SiNW.

    The electroless metal deposition describes a galvanic displacement process that

    involves the spontaneous oxidation of Si and reduction of metal ions to metal particles

    without external electrical power source. In the case of electroless deposition of Ag in

    AgNO3/HF solution, the energy level of the system Ag+/Ag lies well below the Si

    valence band, simultaneous electrochemical processes including the reduction of Ag

    ions and the oxidation of silicon atoms occurs, silver ions are able to capture the

    electrons in the VB of silicon atoms and being reduced while the silicon atoms are

    being oxidized in the solution. As soon as the silicon oxide form below the Ag

    nanoparticle, the HF solution will etch it away and the Ag particle sinks into the hole

    which is kept immobile in the horizontal direction. Since the Ag nanoparticle is more

    electronegative to silicon, it continues to capture electrons from the silicon atoms and

    the Ag- ions formed will attract more Ag

    + from the solution, silicon beneath the Ag

    particle continues to supply the electrons needed for reduction of metal ions and thenanoparticle is becoming larger in size along with the deposition process. With longer

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    immersion time in the solution, the Ag particles that do not enter the pits will grow

    into the branched silver dendrites.

    In another system involving Fe (NO3)3/HF solution with Ag nanoparticles dispersed

    on the silicon substrate, the temperature is as low as 50 degrees, the redox reaction

    between the silicon atoms and Fe ions is very slow. Yet, the whole process can be

    speed up by covering the silicon substrate with a layer of Ag nanoparticle film. Metal

    contamination has a strong catalytic activity for the cathodic reaction. The Ag

    nanoparticle can act as local micro-cathodes which are for the reduction of Fe ions,

    owing to the more positive redox potential of Ag+

    /Ag system compared to Fe3+

    /Fe2+

    couple, the general reaction equation is presented below:

    Fe3+

    + e-Fe

    2+;

    Si (s) + H2OSiO2+ 4H++ 4e

    -;

    SiO2+ 6HFH2SiF6+ 2H2O;

    Therefore, in the Ag/Si/HF/Fe(NO3)3system, the Fe3+

    ions have a strong tendency to

    obtain electrons preferentially from Ag particles and be reduced to Fe2+

    ions, while the

    silicon underneath the Ag nanoparticles is locally oxidized into SiO2. The reaction

    proceeds as long as the Si atoms are able to dissolve into the solution, or until thick

    SiO2 forms, thereby halting electron transfer. In the present HF/ Fe (NO3)3 solution,

    the dissolution rate of SiO2by HF is higher than the Si oxidation rate by Fe (NO3)3.

    Therefore, the Si surface is always exposed to the solution.

    Since the Ag nanoparticle is pinned Fig.2.6 in the hole there is confinement in the

    horizontal movement. All Ag nanoparticles will just sink Fig.2.7in the holes and their

    sinking tracks will interconnect with each other and the silicon substrate looks porous

    in this sense. The walls of the pores Fig.2.8 that are left by the Ag nanoparticle

    constitute the 1D SiNWs as observed in the SEM. The galvanic displacement process

    will not come to a halt until the Fe3+

    ions are exhausted in the reaction solution. Byutilizing this method, single-crystalline SiNWs with desirable crystallographic

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    orientations can be readily and controllably created by the selection of Si wafers with

    the corresponding crystallographic orientations. [38]

    Fig.2.6 Fig.2.7

    SiNW

    synthesized

    Fig.2.8

    Fig.2.6 schematic graph showing the Ag particle is pinned. Fig.2.7 schematic graph

    showing the sinking track of Ag. Fig.2.8 cross-section of SiNW synthesized

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    3. Experimental

    3.1 Synthesis of silicon nanowires by metal-nanoparticle catalyzed chemical

    etching

    The synthesis of large-area oriented 1D silicon nanostructure arrays was conducted in

    a Teflon-lined stainless steel autoclave. The production process comprises 3 steps: 1)

    the silicon wafers were cleaned with acetone (5 min), ethanol (5 min), deionized water

    (2-3 times) and H2SO4/H2O2(3:1 H2SO4(97%)/H2O2(30%),10 min), then the wafers

    were thoroughly rinsed with deionized water (10 min) and dipped into a solution of

    HF (1 min); 2) electroplating the metal-nanoparticle films onto the cleaned silicon

    surface; and 3) immersion of the metal-nanoparticle-covered silicon wafers into

    HF-based aqueous chemical etching solutions contained in a sealed vessel and treated

    for the desired time (2060 degrees).

    All the experiments described here were performed at 50 degrees. The thickness of

    films (or the length of 1D silicon nanostructures) could be effectively controlled

    through adjusting the etching time, and film sizes could be readily made as large as

    needed and are ultimately limited only by the vessel dimensions. The concentrations

    of HF and AgNO3 for the deposition of Ag nanoparticle films were 4.6 and 0.01m,

    respectively.

    3.1.1 Characterization of SiNW

    3.1.1.1 SEM

    The morphology of the SiNWs were examined with a Philips XL30 scanning electron

    microscope (SEM) equipped with a field emission gun (FEG) which emits electrons to

    bombard the sample surface and the secondary electrons on the surface will recoil.

    Thornley-Everhard secondary electron detector is used to collect the recoiled

    secondary electrons and form the images of the sample through computer processing.

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    3.1.1.2 TEM

    Transmission electron microscope (TEM) was used to examine the crystal structure of

    SiNWs. TEM working principle is like a slide projector. The electron gun in the TEM

    projects a beam of electron through the sample. While the electron beam passes

    through the sample, the beam is deflected by the lattice structures and the materials of

    the sample. The transmitted beam is then projected onto the viewing screen, forming

    an enlarged image of the sample. The diffraction mode in TEM could clearly show the

    electron diffraction pattern of the SiNW showing the crystal structure of the material.

    3.1.1.3 EDX

    EDX is used in conjunction with SEM. An electron beam strikes the surface of a

    conducting sample. The energy of the beam is typically in the range of 10-20keV.

    This causes X-rays to be emitted from the point of the material. The energy of the

    X-rays emitted depends on the particular material. Therefore, EDX was used to

    characterize the composition of SiNWs.

    3.2 Simple Device Construction

    3.2.1. Wafer Preparation:

    After the silicon nanowires were successfully prepared by metal-nanoparticle

    catalyzed chemical etching method. They were carefully scratched off from the silicon

    substrate surface and dissolved into the ethanol. In order to have a better dispersion of

    the SiNW in the ethanol, the sample was ultra-sonicated for 15 minutes. At the same

    time, the Si/SiO2substrate with the oxide thickness of about 300nm was sterilized first

    by ethanol because the application of ethanol would kill organisms by denaturing their

    proteins and dissolving their lipids. Then the wafer was again sterilized by acetone

    which was used to remove the organic substances on the wafer. Deionized water was

    used so as to remove the possible remains of ethanol and acetone.

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    3.2.2. Nanowire dispersion:

    After the SiNWs have been immersed in the ethanol for a certain amount of time, it

    was ready for dispersion onto the silicon substrate which has already been placed on

    the heater for a better dispersive property. A sucker was used to suck a little bit of

    SiNW solution to drop on the substrate. The droplet, once it has contacted the surface

    of the wafer, would soon diffuse out and gradually covered the entire surface. This

    suck and drop process was repeated for 10 to 20 times to ensure that the SiNWs could

    be uniformly distributed onto the wafer surface having a concentration as expected.

    3.2.3. Electrode fabrication:

    3.2.3.1. Mechanical Mask Route (MMR)

    The first method was shadow mask: a shadow mask with through slots aligned

    properly on the mask was used and it was tightly pinned on the wafer. The slots were

    places where metal vapor could be successfully deposited on while leaving the

    covered area unexposed to the metal vapor. Gold electrodes were deposited on the

    silicon substrate by electron beam evaporation and gapped for further inspection of the

    electrical properties of SiNWs. In the last step, the shadow mask was removed.

    3.2.3.2 .Photolithography Route (PR)

    In stead of using the shadow mask, we used a Cr mask with electrode patterns. The

    wafer was initially heated to drive off the excessive moisture that might be present in

    it. Photoresist (AJ5206E) was then applied in its liquid form onto the substrate as it

    underwent rotation. The speed of rotation (3500 rev/min) determined the thickness of

    the photoresist dispersed on it. The photoresist-coated wafer was then transferred to a

    hot plate where a soft bake would be applied to drive off excessive solvent before the

    wafer was introduced into the exposure system. Light from a mercury arc lampwas

    focused through a complex system of lenses onto a "mask" (also called a reticle),

    containing the desired image. The light passed through the mask and was then focused

    to produce the desired image on the wafer through a reduction lens system.

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    Polymeric Developers were applied to remove the exposed photoresist. Gold was then

    deposited onto the windows etched away by the developer and lift-off technique was

    used to remove the unexposed photoresist.

    3.2.4. Positioning of SiNW for inspection

    After the SiNWs were successfully dispersed onto the wafer, in order to measure the

    conductivity of a single SiNW or a bunch of nanowires contacting the electrodes,

    microscopic examination was needed to ensure that the nanowires were electrically

    contacted. Proper reference was made that we could record the exact position of the

    qualified nanowires for further analysis. The electrode pattern Fig.3.1-2on the silicon

    wafer was shown below and the electrodes were marked with numbers. If nanowires

    were found to be lied across two, three or four electrodes, then probe could be placed

    on the appropriate electrodes for measurement of current through the nanowires.

    Fig.3.1 Fig.3.2

    1 3

    2 4

    Fig.3.1. Electrode pattern on the wafer Fig.3.2 Magnified electrode with marks

    3.3. Field Effect Transistor and two-point measurement

    3.3.1 Performance of SiNW in the ambient condition:

    Since the substrate was composed of a layer of silicon and a layer of silicon oxide, we

    could apply a voltage to the silicon substrate as the back gate. Due to the small size of

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    the substrate, it was rather difficult to apply the voltage directly. A piece of copper was

    attached to the conducting glue which directly contacted the bottom of the silicon

    substrate. A MOS structure was formed and the electrostatic potential could be altered

    by changing the gate voltage.

    A two point probe stationFig.3.3was used to measure the I-V characteristics of the

    device and data could be collected automatically by the computer to calculate the

    mobility of the charge carriers in the SiNW.

    Fig.3.3. Schematic illustration of a two point probe station

    3.3.2. Surface passivation by coating a layer of SiO2onto the SiNW:

    A layer of silicon oxide (200nm) was evaporated onto the SiNWs to cover all the

    surface of the substrate. Although the electrode material gold was also covered with a

    layer of oxide, it would not affect the measurement since the adhesion between the

    silicon oxide and gold was poor and could be scratched off easily by the probe tip. The

    FET characteristics were measured. Schematically, the graph is shown as in Fig.3.4

    Glass

    Conducting glueSilicon Wafer

    2 point probe

    Copper plate

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    GoldSiNW

    Silicon oxide

    Substrate

    Fig.3.4 the configuration of the SiNW device

    3.4.Process of photolithography and experimental flow chart:

    The following two graphs Fig.3.5and Fig.3.6 show the process of photolithography

    and the experimental flow chart:

    Fig.3.5 Photolithography Technique

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    Fig.3.6 Expe al flow chartriment

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    4. Results and discussion:

    4.1. Properties of silicon nanowires synthesized by MNCCE

    For the SiNWs synthesized by the VLS method, there are several problems that we

    have to address; firstly, the reactive gas used in this case is toxic and flammable,

    secondly, it is difficult for us to remove the metal particle on top of the nanowires and

    thirdly, doping of the SiNW involves a series of processes not that easily controlled.

    The same problem also exists in the OAG + VLS method although both methods

    involve the gold metal particle to help manipulate the size of the SiNW as synthesized.

    Yet the biggest advantage of using the silver particle catalyzed chemical etching

    method to synthesize the SiNW is the controllability of its doping density because the

    silicon wafer is pre-doped to be n-type or p-type with a certain doping concentration.

    The silver particles deposited on the silicon substrate will sink into the pits and the

    substrate is said to be etched. Actually, the SiNWs formed are the walls of the silver

    nanoparticle sinking tracks. So the morphology of the nanowires is of irregular shape

    and the interconnectedness of the sinking tracks has made the silicon substrate appear

    porous. Among other things, as long as the etching process continues, there will be a

    layer of silver dendrites deposited on the silicon substrate. The superfluous silver ions

    are reduced and grow on the dendrite to form a layer, which can effectively prevent

    the deposition of silver atoms on the small silver particles trapped in the pits.

    Schematically the synthesis process is illustrated as below and the morphology of the

    p-type SiNW is also shown in the SEM micrograph shown in Fig.4.1, element

    composition of the SiNW is examined by EDX shown in Fig.4.2and we found that

    the SiNW is composed of Si mainly. Since the material is prepared in the copper

    meshwork, the high intensity of copper signal is reasonable.

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    Fig.4.1 SEM micrograph of SiNW synthesized by MNCCE

    Fig.4.2 EDX pattern showing the composition of the SiNW

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    4.2. I-V characteristics of SiNW prepared by mechanical mask:

    4.2.1. Effects of work function of the electrode material:

    In order to measure the electrical conductivity of the SiNW, voltage was applied

    across the nanowire. The voltage was scanned from -2 volts to 2 volts and the

    corresponding current level was measured. The choices for different electrode

    materials will have a large impact on the current-voltage characteristics because of the

    different work functions. Whenever the work function of the electrode material is

    smaller than that of the p-type semiconductor, the Fermi level of the metal and

    semiconductor should line up and ensure that the vacuum level across the two

    materials is continuous. In the first case, the electrode material chosen is Ag and the

    work function is 4.63eV comparing to the p-type SiNW which is 4.99eV, so the

    semiconductor will bend downwards creating a potential barrier for holes to cross

    from semiconductor to the metal. The Schottky barrier serves to restrict the flow of

    charge carrier in one direction. The I-V characteristic has shown very clearly that the

    current will increase exponentially in the positive voltage range while maintaining a

    very small value in the negative range value. To explain this phenomenon by band

    diagram Fig.4.3, positive voltage will reduce the potential barrier, making it easy for

    holes to move, while potential barrier will be increased if a negative voltage is applied,

    restricting further the flow of holes. The I-V curve is shown in Fig.4.4

    Fig.4.3 Band diagram for Schottky barrier

    On the other hand, if the electrode material used is Au whose work function is larger

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    than that of p-type SiNW, since there are more energetic holes in the metal side, they

    will tunnel to the semiconductor in search of lower energy until the equilibrium is

    reached, i.e. the alignment of Fermi energy in both sides. The holes will accumulate at

    the contact region and the conducting holes in either side have about the same energy

    level and there is no barrier in between when they cross the junction in either direction

    under the influence of an applied field. In the case of ohmic contact, the linear region

    is used to calculate the resistance of the SiNW together with its contact resistance

    once the slope of the curve is obtained by OriginPro 7.5.

    Fig.4.4 I-V curve of a Schottky barrier

    4.2.2 Exchange electrodes measurements for contact check:

    In order to check whether the contact between the electrode and the semiconductor

    has constrained the flow of the charge carriers, I-V curve was measured twice while

    the electrodes were exchanged in the second time. One thing to be noted is that if the

    two I-V curves appear the same in the two cases, it is solid evidence that the contact is

    ohmic and the contact is not imposing a restriction on the direction of the charge flow.

    On the other hand, if the two curves appear symmetric with respect to the origin (0,0),

    the contact is not ohmic and a rectifying effect may take place. This technique is

    usually applied when the current is rather small and we can not simply decide whether

    the small current is caused by the contact effect or the pinch-off effect. Fig.4.5

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    Fig.4.5. Exchange electrode measurement of I-V

    SEM images Fig.4.6-7 show the configuration of the SiNW lying on the gap of the

    electrodes. Since the conductivity of the etched SiNW is the same as that of the silicon

    wafer, I can compare the values of the calculated results with the reference parameter

    of the silicon wafer given by the manufacturer. Three samples are measured and their

    I-V characteristics are shown in Fig.4.8

    The slope of the linear region estimated by linear fit is B=VI

    . The resistance R of the

    p-type SiNW is calculated according to Ohms Law by R=I

    V

    , the reciprocal of the

    slope. Also, intrinsically, the resistance R=A

    L , where is the resistivity of SiNW

    and L is the length of the SiNW; A is the cross-section area of the SiNW, respectively.

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    Fig.4.8 I-V characteristics of 3 samples prepared by shadow mask

    Fig.4.6 SEM of Sp A Fig.4.7.SEM of Sp B

    4.3. I-V characteristics of SiNW prepared by photolithography

    The process of photolithography was briefly introduced previously, and the major

    advantage is that the electrical property of single nanowire can be possibly measured

    due to the shorter length of the electrode in the central and the gap distance is also

    reduced to 2 micros. Such design has effectively increased the possibility of capturinga single nanowire crossing the electrode and it is far better than the mechanical mask

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    in which the gap length is long and the electrical property that we have measured may

    consist of a bundle of SiNWs instead of a single one. SEM images Fig.4.11-12show

    the sample A and B prepared by photolithography.

    SiNW found lying on the central

    Fig.4.9 Electrode pattern fabricated by Fig.4.10.Electrode pattern fabricated by

    PL without metal coating PL with metal coating

    Fig.4.11 SEM of nanowire lying on the Fig.4.12 SEM of nanowire lying

    electrode prepared by PL (Sp A) on the electrode prepared by PL (Sp B)

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    The table presents the results of the calculated resistivity of the SiNWs either through

    photolithography technique or shadow mask technique.

    Shadow Mask Length(cm) SectionalArea(cm2) B(slope) R(B-1) (cm)

    Sample A 3.0E-4 1.26E-9 3.80E-7 2.6E6 10.92

    Sample B 2.0E-4 1.14E-9 2.151E-7 4.65E6 26.5

    Sample C 5.3E-4 1.26E-9 5.031E-8 2.0E7 47.4

    Photolithography Length(cm) SectionalArea(cm2) B(slope) R(B

    -1) (cm)

    Sample A 2.0E-4 3.14E-10 9.86E-8 10E7 15.7

    Sample B 2.0E-4 2.15E-10 1.06E-7 9.4E6 10.11

    Table.4.1 Resistivity of SiNW measured from the photolithographic samples and

    shadow mask samples.

    The reference value of the silicon substrate is 9-13cm as compared with the results

    presented by the table, the photolithographic route yields better accuracy.

    4.4. Effect of contact resistance between the semiconductor and metal

    From the Table 4.1 shown above, the calculated resistivity of the SiNW deviates a lot

    from the reference value. The reason is that it is difficult to tell how many nanowires

    are lying across the electrode gap, yet the I-V curve is a reflection of the general

    profile of the nanowires successfully dispersed on the gap and may not be useful in

    calculating the resistance of a single nanowire as we have expected.

    The result shown by the photolithography improved due to the shorter strips of

    electrodes and the electrical property of single nanowires could be manageably

    obtained. Yet another important issue we could not afford to ignore is the large contact

    resistance of the metal-semiconductor interface. The contact resistance is inversely

    proportional to the contact area. In the case concerned, the SiNWs are surrounded by a

    layer of very thin Ti about 1nm. The reason why the Ti layer is deposited is that once

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    the developer etches the photoresist, the underlying oxide is exposed to the air. Gold

    can not be directed evaporated onto the silicon substrate because of its poor tackiness

    to the oxide. The layer of Ti acts as a buffer layer so that gold can contact well with

    the SiNW as well as the substrate. Due to the extreme thinness of Ti layer, the contact

    between the Au and the SiNW is still ohmic. The quality of metal evaporation and the

    coverage of gold film onto the nanowires are of great importance in calculating the

    resistance of the bulk SiNW. The surface of the interface might be very rough all the

    way along the contact, making the actual contact area much smaller than the apparent

    contact area illustrated in Fig.4.13. When the SiNW is synthesized by MNCCE and

    prior to electrode deposition, the surface of silicon oxide might be oxidized to a

    certain extent in the atmosphere. This layer of oxide film might be gapped between

    the metal and the semiconductor restricting the flow of charge carriers. The surface

    defects such as voids and pores and impurities could serve as scattering sites reducing

    the MFP of the charge carriers and the contact resistance could be very high in this

    case. Possible solution to reduce the contact resistance is to anneal the

    metal-semiconductor in high temperature for a while, the stress and strains could be

    annealed out with time and gold film could flow to cover the SiNW well in order to

    increase the contact area.

    Fig..4.13 schematic illustration of contact area

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    4.5. Gate construction for Field Effect Transistor

    4.5.1. SiNW in the ambient environment

    Measuring the I-V curve of a single SiNW under the source drain voltage gives us

    information about the intrinsic conductivity of the nanowire. Yet, the conductivity of

    the semiconductor wire can also be altered by applying a gate voltage on the silicon

    substrate. The effect of the gate voltage on the conductivity of the SiNW can be

    interpreted from the corresponding I-V measurements

    The original curve actually locates at the third quadrant and I convert the graph into

    the first quadrant for better observation. Among the I-V characteristics shown in

    Fig.4.14of the SiNW under different gate voltages marked by different colors, there is

    one thing in common, current increases with the negative increase of source-drain

    voltage, a linear relationship between I-V is observed. Yet, the current will not

    increase infinitely with voltage until saturation occurs which means that beyond

    certain voltage, the current remains almost the same. The principle of the existence of

    linear region in Fig.4.15and the saturation region in Fig.4.16can be explained by the

    expansion or shrinkage of conducting channel in the SiNW. As shown schematically

    in the draft, the drain is connected to the ground with zero potential, and the voltage is

    input from the source. The gate voltage is input from the silicon substrate. e.g. if the

    source input is -2 volts, then the potential along the SiNW should be from -2 volts to 0

    volt and assume no voltage is applied to the silicon substrate, then the potential

    difference at the source is the difference between the gate voltage and the source

    voltage, (in this case, the voltage will be 0-(-2) =2 volts) similar principle will apply to

    all the points along the SiNW. Since the majority of charge carrier in the p-type SiNW

    is hole, positive voltage will expel holes and a depletion region will form. The positive

    voltage along the SiNW is decreasing, so is the depletion region. Once the voltage at

    the source is large enough to deplete all the holes, pinch-off occurs and the current

    remains almost the same. Increase of the saturation voltage will enable the pinch-offpoint to move towards the drain, flatness of the I-V curve at higher voltage is

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    attributed to the fact that the pinch-off voltage remains the same, so do the number of

    holes that are attracted to the pinch-off point P.

    Conducting

    channel of SiNW

    (shaded)

    SiO2

    Si

    Fig.4.15 Explanation of linear region in the curve

    Depletion Region

    Fig.4.16 Explanation of saturation region in the curve

    When the gate voltage is applied on the silicon substrate, the potential along the

    SiNWs is changed, the negative voltage of the gate will attract more holes in the

    SiNW and the pinch-off (corresponding to saturation) occurs at a higher negative

    voltage given the fact that pinch-off voltage remains the same. The conductivity of the

    SiNW under the linear region increases with negative gate voltage as evidenced by the

    steeper slope of the linear region.

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    Fig.4.14 I-V characteristics of the FET device

    In order to inspect deeper into the device response to the gate voltage, the source-drain

    voltage is maintained while the gate voltage is scanned so as to examine the Idsversus

    the Vg, both linear scale and logarithmic scale is used to inspect the relationship

    between the current and the voltage. The source-drain voltage is fixed at -0.2 volts.

    From the Fig.4.17 the threshold voltage defined as the voltage to turn on or off the

    device is approximated as an intersecting point on the x-axis by the tangential line

    where the curve assumes best linearity. The on/off current ratio observed from the

    logarithmic plot is estimated to be about 103

    . The transconductance defined as the

    dIds/dVgis plotted against the gate voltage for every single Vgshown in Fig.4.18 and

    the largest value of transconductance is found which later will be used in the

    calculation of the hole mobility.

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    Fig.4.17 Ids vs Vg plotted in the linear scale and log scale. Inset is the SEM image of

    the measured sample

    Fig.4.18 Transconductance measured at every gate voltage

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    The capacitance of the SiNW is calculated from the following equation assuming the

    metal cylinder on an infinite metal plate model [39]:

    C= )/4ln(/2 0 dhL

    is the dielectric constant of SiO2 and 0 is the dielectric constant of vacuum. L is

    the source-drain nanowire length, h is the SiO2 thickness and d is the diameter of

    SiNW.

    The hole mobility of SiNW is obtained with the equation described below:

    VVsdgVsdL

    Cm 2.0

    1

    2 =

    ,

    C is capacitance of nanowire, L is the source-drain nanowire length, V sd is source

    drain voltage kept constant, gmis the transconductance of SiNW.

    Due to the limited time, I have only measured two samples. The results of the samples

    are presented in the Table 4.2below:

    4.5.2. SiNW coated with a layer of oxide

    Since the transport property can be affected by the ambient environment, the

    deposition of a layer of SiO2 can effectively passivate the surface and the molecular

    species in the atmosphere will have the least effect on the SiNW.

    As observed from the response of I-V under different gate voltages Fig.4.19, the

    current was obviously larger than the sample in the air. I shrank the range of V ds to

    -0.2V so that the device still remained in the linear region. The increase of

    conductivity could be easily interpreted from the slope of the I-V curve. Compared

    with the result of the experiment done in atmosphere without the shielding of the

    coating layer, the current is observed to increase phenomenally by almost two orders

    of magnitude in this case. In this case, the threshold voltage is about 2 volts and the

    on/off current ratio reaches 104

    as observed in the Fig.4.20. The maximum

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    transconductance is obtained from Fig.4.21corresponding to the gate voltage of -2V.

    The major mechanism accounting for the increase in conductance and mobility is that

    charge carriers will be protected from its external environment unlike the presence of

    oxygen in the ambient condition that will trap the holes compromises the conducting

    channel in the surface by forming a depletion region. Also, other species in the air will

    not have the direct route to contact the surface of the SiNW, maintaining the surface to

    be intact and free of external disturbance.

    Fig.4.19 I-V characteristics of the FET device modified by SiO2

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    Fig.4.20 Idsvs Vg plotted in the linear scale and log scale with threshold voltage about

    2 V. Inset is the SEM image of the measured sample

    Fig.4.21 Transconductance measured at every gate voltage

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    The results of the samples in the ambient condition and the result from the sample

    coated by a layer of oxide are presented in this table with key parameters highlighted:

    Table 4.2 mobility obtained in the ambient condition and SiO2 treated condition

    Air Diameter(m) Length(m) h(m) Vsd(V) gm C

    Sp A 1.5E-7 2.5E-6 3E-7 0.2 3.34E-8 2.61E-16 40.03

    Sp B 1.5E-7 4E-6 3E-7 0.2 8E-9 4.17E-16 15.34

    SiO2 Diameter(m) Length(m) h(m) Vsd(V) gm C(F)

    Sp A 1.5E-7 2.5E-6 3E-7 0.06 6.8E-8 2.61E-16 271.68

    4.6. Possible errors involved in calculation:

    The threshold voltage as determined from the Vg intersected by the tangential line in

    the maximum slope of the Ids vs. Vg may not be very accurate since certain mobile

    charges or fixed charges are already present in the interface of the silicon oxide and

    the silicon substrate. The positive charge they carry may contribute to the threshold

    voltage and Vthas found may be underestimated in the real case.

    Also, since the expression used for all calculation of nanowire capacity is based on the

    assumption that the nanowire is an equipotential surface like in metals. However, the

    SiNW as synthesized with a doping concentration (lower than a certain concentration)

    may not qualify it to assume a metallic nature. So the expression used may not be very

    accurate. Another error resulting from the calculation of nanowire capacitance is its

    irregular geometry. The expression only accounts for the calculation in the case of a

    cylindrical nanowire. The SiNWs produced by metal particle catalyzed chemical

    etching do not have proper shape that facilitates the calculation.

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    5. Conclusion

    In this project, p-type SiNWs are synthesized by metal-nanoparticle-catalyzed

    chemical etching method. The as-synthesized SiNWs have exhibited good alignment

    and easier control of doping concentration within the SiNW. It provides us a very

    convenient way to cast the SiNW with the desired doping concentration for practical

    application without going through the complicated process of doping the SiNW during

    its synthesis. The cross section of the as-synthesized SiNW is irregular due to the

    mechanism of etching and this may affect the charge transport in the SiNW devices

    and their overall performances.

    Simple devices can be constructed with the 1D nanowire through several processes,

    namely, preparation of silicon wafer, dispersion of nanowires randomly onto the wafer,

    lithography technique to transfer a pattern of a mask onto the silicon substrate,

    deposition of electrode contact material followed by measurement of transport

    properties of the particular nanowires. Among all these processes, deposition of

    electrode material into the open windows can be critical in device construction.

    Electrode materials with an appropriate work function should also be carefully

    selected to form ohmic contact with the semiconductor nanowire instead of a contact

    barrier. In addition, the contact resistance between the semiconductor and the metal

    also affect the behavior of devices due to the defects in the interface of the two

    materials serving the scattering sites for charge carrier and the real contact area is

    much less than the apparent one.

    To measure the transport characteristic of SiNW such as the conductance of SiNW and

    mobility of charge carriers, a gate voltage is applied to the silicon substrate to

    construct a SiNW-based FET. The response of SiNW in terms of its Idsvs. Vdscurve

    will show the effects of the gate. For p-type devices, negative gate voltage attracts

    more holes to the conducting channel so as to increase the carrier density while

    positive voltage expels the holes and form a depletion region. Current saturation will

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    occur when pinch-off point is reached meaning the depletion region is so wide as to

    cut off the conducting channel in the SiNW.

    Improvement is observed when the surface of SiNW is covered with a layer of

    insulating silicon oxide which has effectively eliminated the influence of external

    environment. The conductance and mobility increases quite compared with the result

    obtained in the ambient environment. This is a clear indication of the effect of

    molecular species on the surface property of SiNW. It is predicted that certain

    molecules in the atmosphere can trap the holes in the surface of the nanomaterials

    although the details of the mechanism is not clear yet.

    6. Future work

    Since the performance of SiNW FET, namely the conductance, the mobility is affected

    by the surface property a lot due to the large surface to volume ratio. Passivation of

    the surface defects seem to be very important. Once the defect in the surface region is

    saturated, its dangling bonds which may carry certain charge will be neutralized and

    form a stable chemical species, reducing the possibility of attracting charge carriers in

    the conducting channel. Certain chemicals can be used to react with the surface of

    SiNW, altering the nature of its property. In addition, the quality of contact area should

    further be improved so that resistance in the contact can be further reduced.

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