Poly(dimethylsiloxane‑b‑methyl methacrylate): A Promising Candidate for Sub-10 nm Patterning
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 c...
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Veröffentlicht in: | Macromolecules 2015-06, Vol.48 (11), p.3422-3430 |
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creator | Luo, Yingdong Montarnal, Damien Kim, Sangwon Shi, Weichao Barteau, Katherine P Pester, Christian W Hustad, Phillip D Christianson, Matthew D Fredrickson, Glenn H Kramer, Edward J Hawker, Craig J |
description | 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. |
doi_str_mv | 10.1021/acs.macromol.5b00518 |
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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). 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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.</description><subject>Chemical Sciences</subject><subject>MATERIALS SCIENCE</subject><subject>morphology</subject><subject>organic compounds</subject><subject>Polymers</subject><subject>solvents</subject><subject>thin films</subject><subject>X-ray scattering</subject><issn>0024-9297</issn><issn>1520-5835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp9kEFPwyAYhonRxDn9Bx4aT-7QCRRo521Z1JkscYl6RkrBsbRgCjP25l_wL_pLpOn06IF8ycvzfoQHgHMEpwhidCWknzZCtq5x9ZSWEFJUHIARohimtMjoIRhBiEk6w7P8GJx4v4UQIUqyEXhZu7q7rEyjwqarvandh7Dq-_OrjGcIk37E7V0tgppcJ_NkHV8y3tjXZCFsZaqYJ9q1yeOuTBFMbJOsRQiqtRE5BUda1F6d7ecYPN_ePC2W6erh7n4xX6WCQhzSSqFSzXJWaKiRqKisCMaqzEtWiIwJrRUuSlLkWmksKWGZkjklAjOaK0QFzcbgYtjrfDDcSxOU3EhnrZKBI1SwGc4jNBmgjaj5W2sa0XbcCcOX8xXvM4hYRiBj7yiyZGCjV-9bpf8KCPJeO4_a-a92vtcea3Co9bdbt2tt_PX_lR_Xc4wf</recordid><startdate>20150609</startdate><enddate>20150609</enddate><creator>Luo, Yingdong</creator><creator>Montarnal, Damien</creator><creator>Kim, Sangwon</creator><creator>Shi, Weichao</creator><creator>Barteau, Katherine P</creator><creator>Pester, Christian W</creator><creator>Hustad, Phillip D</creator><creator>Christianson, Matthew D</creator><creator>Fredrickson, Glenn H</creator><creator>Kramer, Edward J</creator><creator>Hawker, Craig J</creator><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope><scope>1XC</scope><scope>OIOZB</scope><scope>OTOTI</scope><orcidid>https://orcid.org/0000-0003-3246-3467</orcidid></search><sort><creationdate>20150609</creationdate><title>Poly(dimethylsiloxane‑b‑methyl methacrylate): A Promising Candidate for Sub-10 nm Patterning</title><author>Luo, Yingdong ; Montarnal, Damien ; Kim, Sangwon ; Shi, Weichao ; Barteau, Katherine P ; Pester, Christian W ; Hustad, Phillip D ; Christianson, Matthew D ; Fredrickson, Glenn H ; Kramer, Edward J ; Hawker, Craig J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a502t-de1be9768f0f1ad5cd422eb7b68a36affe28b487fef2c5463ec754a2657e15a53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Chemical Sciences</topic><topic>MATERIALS SCIENCE</topic><topic>morphology</topic><topic>organic compounds</topic><topic>Polymers</topic><topic>solvents</topic><topic>thin films</topic><topic>X-ray scattering</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Luo, Yingdong</creatorcontrib><creatorcontrib>Montarnal, Damien</creatorcontrib><creatorcontrib>Kim, Sangwon</creatorcontrib><creatorcontrib>Shi, Weichao</creatorcontrib><creatorcontrib>Barteau, Katherine P</creatorcontrib><creatorcontrib>Pester, Christian W</creatorcontrib><creatorcontrib>Hustad, Phillip D</creatorcontrib><creatorcontrib>Christianson, Matthew D</creatorcontrib><creatorcontrib>Fredrickson, Glenn H</creatorcontrib><creatorcontrib>Kramer, Edward J</creatorcontrib><creatorcontrib>Hawker, Craig J</creatorcontrib><creatorcontrib>Argonne National Laboratory (ANL), Argonne, IL (United States)</creatorcontrib><collection>CrossRef</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>OSTI.GOV - Hybrid</collection><collection>OSTI.GOV</collection><jtitle>Macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Luo, Yingdong</au><au>Montarnal, Damien</au><au>Kim, Sangwon</au><au>Shi, Weichao</au><au>Barteau, Katherine P</au><au>Pester, Christian W</au><au>Hustad, Phillip D</au><au>Christianson, Matthew D</au><au>Fredrickson, Glenn H</au><au>Kramer, Edward J</au><au>Hawker, Craig J</au><aucorp>Argonne National Laboratory (ANL), Argonne, IL (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Poly(dimethylsiloxane‑b‑methyl methacrylate): A Promising Candidate for Sub-10 nm Patterning</atitle><jtitle>Macromolecules</jtitle><addtitle>Macromolecules</addtitle><date>2015-06-09</date><risdate>2015</risdate><volume>48</volume><issue>11</issue><spage>3422</spage><epage>3430</epage><pages>3422-3430</pages><issn>0024-9297</issn><eissn>1520-5835</eissn><abstract>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.</abstract><cop>United States</cop><pub>American Chemical Society</pub><doi>10.1021/acs.macromol.5b00518</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-3246-3467</orcidid><oa>free_for_read</oa></addata></record> |
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title | Poly(dimethylsiloxane‑b‑methyl methacrylate): A Promising Candidate for Sub-10 nm Patterning |
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