TY - JOUR
T1 - Poly(dimethylsiloxane-b-methyl methacrylate)
T2 - A Promising Candidate for Sub-10 nm Patterning
AU - Luo, Yingdong
AU - Montarnal, Damien
AU - Kim, Sangwon
AU - Shi, Weichao
AU - Barteau, Katherine P.
AU - Pester, Christian W.
AU - Hustad, Phillip D.
AU - Christianson, Matthew D.
AU - Fredrickson, Glenn H.
AU - Kramer, Edward J.
AU - Hawker, Craig J.
N1 - Publisher Copyright:
© 2015 American Chemical Society.
PY - 2015/6/9
Y1 - 2015/6/9
N2 - We report herein the modular synthesis and nanolithographic potential of poly(dimethylsiloxane-block-methyl methacrylate) (PDMS-b-PMMA) with self-assembled domains approaching sub-10 nm periods. A straightforward and modular coupling strategy, optimized for low molecular weight diblocks and using copper-catalyzed azide-alkyne "click" cycloaddition, was employed to obtain a library of PDMS-b-PMMA and poly(dimethylsiloxane-block-styrene) (PDMS-b-PS) diblock copolymers. Flory-Huggins interaction parameters, determined from small-angle X-ray scattering experiments, were high for PDMS-b-PMMA (χ ∼ 0.2 at 150 °C), suggesting this diblock copolymer system has promise for sub-10 nm lithographic applications when compared to the corresponding PDMS-b-PS diblock copolymers (χ ∼ 0.1 at 150 °C). Performance evaluation in thin film self-assembly experiments allowed domain periods as small as 12.1 nm to be obtained, which is among the smallest highly ordered nanoscale patterns reported hitherto for thermally annealed materials.
AB - We report herein the modular synthesis and nanolithographic potential of poly(dimethylsiloxane-block-methyl methacrylate) (PDMS-b-PMMA) with self-assembled domains approaching sub-10 nm periods. A straightforward and modular coupling strategy, optimized for low molecular weight diblocks and using copper-catalyzed azide-alkyne "click" cycloaddition, was employed to obtain a library of PDMS-b-PMMA and poly(dimethylsiloxane-block-styrene) (PDMS-b-PS) diblock copolymers. Flory-Huggins interaction parameters, determined from small-angle X-ray scattering experiments, were high for PDMS-b-PMMA (χ ∼ 0.2 at 150 °C), suggesting this diblock copolymer system has promise for sub-10 nm lithographic applications when compared to the corresponding PDMS-b-PS diblock copolymers (χ ∼ 0.1 at 150 °C). Performance evaluation in thin film self-assembly experiments allowed domain periods as small as 12.1 nm to be obtained, which is among the smallest highly ordered nanoscale patterns reported hitherto for thermally annealed materials.
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U2 - 10.1021/acs.macromol.5b00518
DO - 10.1021/acs.macromol.5b00518
M3 - Article
AN - SCOPUS:84931292189
SN - 0024-9297
VL - 48
SP - 3422
EP - 3430
JO - Macromolecules
JF - Macromolecules
IS - 11
ER -