Polymer Synthesis CHEM 421 “Organic imaging materials: a view of the future” J. Phys. Org. Chem. 2000, 13, 767 “Advances in Patterning Materials for 193 nm Immersion Lithography” Chem. Rev. 2010, 110, 321–360 “Block Copolymer Nanolithography: Translation of Molecular Level Control to Nanoscale Patterns” Adv. Mater. 2009, 21, 4769–4792 “Tech Focus – Lithography” Nature Photonics 2010, 4, 19-30 More Reading Materials
31
Embed
Polymer Synthesis CHEM 421 “Organic imaging materials: a view of the future” J. Phys. Org. Chem. 2000, 13, 767 “Advances in Patterning Materials for 193.
This document is posted to help you gain knowledge. Please leave a comment to let me know what you think about it! Share it to your friends and learn new things together.
Transcript
Polymer SynthesisCHEM 421
“Organic imaging materials: a view of the future”J. Phys. Org. Chem. 2000, 13, 767
“Advances in Patterning Materials for 193 nm Immersion Lithography”Chem. Rev. 2010, 110, 321–360
“Block Copolymer Nanolithography: Translation ofMolecular Level Control to Nanoscale Patterns”Adv. Mater. 2009, 21, 4769–4792
Model for Constructing a Chemically Amplified Resist
Levinson, Harry J. Principles of Lithography. SPIE Press, 2001.
Etch Barrier
Backbone
Protecting Group
Acidic Group
CH CH2 CH CH2
OOH
O
O
Polymer SynthesisCHEM 421
Low- and High-Activation Energy Chemically Amplified Resists
CH CH2
O
O
O
CH CH2
OH
• Copolymer of hydroxy styrene and t-BOC protected hydroxy styrene• Good hydrophilic/hydrophobic balance• IBM’s Apex Resist• Low activation energy, very reactive• PAB below Tg
CH CH2
C
CH CH2
OH
O
O
• IBM’s ESCAP Resist• High activation energy, lower reactivity• Allows for high T bake• PAB above Tg
• removes stress• removes residual solvent• higher density films• Low diffusion of PAG
Polymer SynthesisCHEM 421“Transitions” in Optical Lithography
365 nm365 nm
248 nm248 nm
193 nm193 nm
157 nm157 nm
E-beamE-beam
X-rayX-ray
EUVEUV
?
Polymer SynthesisCHEM 421
How?
R: resolution or critical dimensionk1: Rayleigh coefficient of resolutionΛ0: vacuum wavelengthn: refractive index of the incident mediumθ: angular aperture of the lens n · sin θ is also referred to as the numerical aperture (NA) of the imaging system.
4141 5252 77 92923500 /3500 /1.421.42 Insol.Insol. To be To be
determineddetermined
CF2CF2 CF2 CF
OCF2 CF
CF3
OCF2
CF2
O
OMe
Polymer SynthesisCHEM 421
157/193 nm PhotoresistsTeflon® AF as Backbone Material
• Due to its amorphous structure and rigid backbone, Teflon® AF has unique Due to its amorphous structure and rigid backbone, Teflon® AF has unique properties that are desirable in a photoresist backboneproperties that are desirable in a photoresist backbone
Advantages Challenges
• very low absorbance • cost of PDD monomer
• rigid structure (good etch resistance)
• need functional monomer without significantly increasing absorbance
• forms smooth films
• broad range of Tgs available
Tetrafluoroethylene(TFE)
2,2-Bis(trifluoromethyl)-4,5-difluoro-1,3-dioxole
(PDD)
CF2 CF2 + CF2 CF2 / CF CF
O O
F3C CF3
i
CF CF
O O
F3C CF3
Teflon® AFTeflon® AF
Polymer SynthesisCHEM 421
157/193 nm PhotoresistsAbsorbance at 157 nm and 193 nm
• Values for Teflon® AF and Values for Teflon® AF and the CO2 synthesized the CO2 synthesized copolymer are very close copolymer are very close and well below 1 and well below 1 mm-1 -1 at at 157 nm 157 nm
• Values at 193 nm are Values at 193 nm are slightly different but both slightly different but both extremely lowextremely low
Sample 157.6 (nm)
193 (nm)
Teflon® AF 0.154 0.004
CO2 Synthesized Copolymer
0.153 0.019
Absorbance [Absorbance [mmOptical Density
0
0.5
1
1.5
2
2.5
145 155 165 175 185 195
wavelength (nm)
(m
-1)
Teflon AF CO2 Synthesized Copolymer
T
Polymer SynthesisCHEM 421
157/193 nm PhotoresistsTeflon® AF as Backbone Material
Protected Functional Monomer
Acidic Group
CF2 CF2 CF CF
OO
CF3F3C
CF2 CF2 CF CF
OO
CF3F3C
PAG
• In order for a Teflon® AF In order for a Teflon® AF derivative to serve as a derivative to serve as a photoresist, a functionalized photoresist, a functionalized monomer that can be monomer that can be cleaved by an acid must be cleaved by an acid must be incorporated into the incorporated into the backbonebackbone
• After cleaving with a photo After cleaving with a photo acid generator (PAG) the acid generator (PAG) the functional monomer will functional monomer will exhibit different solubility exhibit different solubility properties from unexposed properties from unexposed regionsregions
• Chose to explore Ester Vinyl Ether (EVE) Chose to explore Ester Vinyl Ether (EVE) as a prototype for potential EVE derived as a prototype for potential EVE derived functional monomersfunctional monomers
• Conducted a Plackett-Burman Conducted a Plackett-Burman experimental scheme varying five experimental scheme varying five parameters (composition, initiator parameters (composition, initiator concentration, temperature, pressure and concentration, temperature, pressure and reaction time) to study the reaction of EVE reaction time) to study the reaction of EVE with PDD and TFEwith PDD and TFE
Exp. # EVE/PDD/TFE (mol %)
Initiator (mol %)
Temp (oC) Pressure (psi)
Rxn Time (hr)
1 7/73/20 1 15 3500 4
2 25/55/20 0.2 35 3500 4
3 25/55/20 0.2 15 3500 0.5
4 25/55/20 1 15 1500 4
5 7/73/20 1 35 3500 0.5
6 7/73/20 0.2 35 1500 4
7 25/55/20 1 35 1500 0.5
8 7/73/20 0.2 15 1500 0.5
CF2 CF2 CF CF
OO
CF3F3C
F2C
O
CF
CF3
O CF2 CF2
O
OCH3
CF CF
poly(TFE-co-PDD-co-EVE)
Polymer SynthesisCHEM 421
157/193 nm Photoresists EVE/TFE/PDD - Absorbance
• Absorbance values at 157 nm increase with increasing EVE Absorbance values at 157 nm increase with increasing EVE content but still remain well below 1 content but still remain well below 1 mm
• Values at 193 nm are very low and vary only slightlyValues at 193 nm are very low and vary only slightly
157/193 nm PhotoresistsAbsorbance at 157 nm and 193 nm
• Values for Teflon® AF and the CO2 synthesized copolymer are very close and well below 1 m-1 at 157 nm
• Values at 193 nm are slightly different but both extremely low
Sample 157.6 (nm)
193 (nm)
Teflon® AF 0.154 0.004
CO2 Synthesized Copolymer
0.153 0.019
Absorbance [mOptical Density
0
0.5
1
1.5
2
2.5
145 155 165 175 185 195
wavelength (nm)
(m
-1)
Teflon AF CO2 Synthesized Copolymer
T
Polymer SynthesisCHEM 421
157/193 nm PhotoresistsTeflon® AF as Backbone Material
Protected Functional Monomer
Acidic Group
CF2 CF2 CF CF
OO
CF3F3C
CF2 CF2 CF CF
OO
CF3F3C
PAG
• In order for a Teflon® AF derivative to serve as a photoresist, a functionalized monomer that can be cleaved by an acid must be incorporated into the backbone
• After cleaving with a photo acid generator (PAG) the functional monomer will exhibit different solubility properties from unexposed regions
• Chose to explore Ester Vinyl Ether (EVE) as a prototype for potential EVE derived functional monomers
• Conducted a Plackett-Burman experimental scheme varying five parameters (composition, initiator concentration, temperature, pressure and reaction time) to study the reaction of EVE with PDD and TFE
Exp. # EVE/PDD/TFE (mol %)
Initiator (mol %)
Temp (oC) Pressure (psi)
Rxn Time (hr)
1 7/73/20 1 15 3500 4
2 25/55/20 0.2 35 3500 4
3 25/55/20 0.2 15 3500 0.5
4 25/55/20 1 15 1500 4
5 7/73/20 1 35 3500 0.5
6 7/73/20 0.2 35 1500 4
7 25/55/20 1 35 1500 0.5
8 7/73/20 0.2 15 1500 0.5
CF2 CF2 CF CF
OO
CF3F3C
F2C
O
CF
CF3
O CF2 CF2
O
OCH3
CF CF
poly(TFE-co-PDD-co-EVE)
Polymer SynthesisCHEM 421
157/193 nm Photoresists EVE/TFE/PDD - Absorbance
• Absorbance values at 157 nm increase with increasing EVE content but still remain well below 1 m
• Values at 193 nm are very low and vary only slightly
Sample Composition(mol %)
157.6(nm)
193(nm)
REH-004 7/73/20 EVE/PDD/TFE (Charged) 0.128 0.013
REH-013 12/59/29EVE/PDD/TFE 0.252 0.011
REH-005 18/54/28EVE/PDD/TFE 0.574 0.017
VASE® Absorbance [mMeasurements
Polymer SynthesisCHEM 421“Transitions” in Optical Lithography