Polarity-switching top coats enable orientation of sub-10-nm block copolymer domains

Block copolymers (BCPs) must necessarily have high interaction parameters (χ), a fundamental measure of block incompatibility, to self-assemble into sub-10-nanometer features. Unfortunately, a high χ often results from blocks that have disparate interfacial energies, which makes the formation of use...

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Vydáno v:Science (American Association for the Advancement of Science) Ročník 338; číslo 6108; s. 775
Hlavní autoři: Bates, Christopher M, Seshimo, Takehiro, Maher, Michael J, Durand, William J, Cushen, Julia D, Dean, Leon M, Blachut, Gregory, Ellison, Christopher J, Willson, C Grant
Médium: Journal Article
Jazyk:angličtina
Vydáno: United States 09.11.2012
ISSN:1095-9203, 1095-9203
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Abstract Block copolymers (BCPs) must necessarily have high interaction parameters (χ), a fundamental measure of block incompatibility, to self-assemble into sub-10-nanometer features. Unfortunately, a high χ often results from blocks that have disparate interfacial energies, which makes the formation of useful thin-film domain orientations challenging. To mitigate interfacial forces, polymers composed of maleic anhydride and two other components have been designed as top coats that can be spin-coated from basic aqueous solution in the ring-opened, acid salt form. When baked, the anhydride reforms and switches polarity to create a neutral layer enabling BCP feature alignment not possible by thermal annealing alone. Top coats were applied to the lamella-forming block copolymers poly(styrene-block-trimethylsilylstyrene-block-styrene) and poly(trimethylsilylstyrene-block-lactide), which were thermally annealed to produce perpendicular features with linewidths of 15 and 9 nanometers, respectively.
AbstractList Block copolymers (BCPs) must necessarily have high interaction parameters (χ), a fundamental measure of block incompatibility, to self-assemble into sub-10-nanometer features. Unfortunately, a high χ often results from blocks that have disparate interfacial energies, which makes the formation of useful thin-film domain orientations challenging. To mitigate interfacial forces, polymers composed of maleic anhydride and two other components have been designed as top coats that can be spin-coated from basic aqueous solution in the ring-opened, acid salt form. When baked, the anhydride reforms and switches polarity to create a neutral layer enabling BCP feature alignment not possible by thermal annealing alone. Top coats were applied to the lamella-forming block copolymers poly(styrene-block-trimethylsilylstyrene-block-styrene) and poly(trimethylsilylstyrene-block-lactide), which were thermally annealed to produce perpendicular features with linewidths of 15 and 9 nanometers, respectively.Block copolymers (BCPs) must necessarily have high interaction parameters (χ), a fundamental measure of block incompatibility, to self-assemble into sub-10-nanometer features. Unfortunately, a high χ often results from blocks that have disparate interfacial energies, which makes the formation of useful thin-film domain orientations challenging. To mitigate interfacial forces, polymers composed of maleic anhydride and two other components have been designed as top coats that can be spin-coated from basic aqueous solution in the ring-opened, acid salt form. When baked, the anhydride reforms and switches polarity to create a neutral layer enabling BCP feature alignment not possible by thermal annealing alone. Top coats were applied to the lamella-forming block copolymers poly(styrene-block-trimethylsilylstyrene-block-styrene) and poly(trimethylsilylstyrene-block-lactide), which were thermally annealed to produce perpendicular features with linewidths of 15 and 9 nanometers, respectively.
Block copolymers (BCPs) must necessarily have high interaction parameters (χ), a fundamental measure of block incompatibility, to self-assemble into sub-10-nanometer features. Unfortunately, a high χ often results from blocks that have disparate interfacial energies, which makes the formation of useful thin-film domain orientations challenging. To mitigate interfacial forces, polymers composed of maleic anhydride and two other components have been designed as top coats that can be spin-coated from basic aqueous solution in the ring-opened, acid salt form. When baked, the anhydride reforms and switches polarity to create a neutral layer enabling BCP feature alignment not possible by thermal annealing alone. Top coats were applied to the lamella-forming block copolymers poly(styrene-block-trimethylsilylstyrene-block-styrene) and poly(trimethylsilylstyrene-block-lactide), which were thermally annealed to produce perpendicular features with linewidths of 15 and 9 nanometers, respectively.
Author Bates, Christopher M
Maher, Michael J
Cushen, Julia D
Dean, Leon M
Durand, William J
Ellison, Christopher J
Seshimo, Takehiro
Willson, C Grant
Blachut, Gregory
Author_xml – sequence: 1
  givenname: Christopher M
  surname: Bates
  fullname: Bates, Christopher M
  organization: Department of Chemistry, University of Texas at Austin, Austin, TX 78712, USA
– sequence: 2
  givenname: Takehiro
  surname: Seshimo
  fullname: Seshimo, Takehiro
– sequence: 3
  givenname: Michael J
  surname: Maher
  fullname: Maher, Michael J
– sequence: 4
  givenname: William J
  surname: Durand
  fullname: Durand, William J
– sequence: 5
  givenname: Julia D
  surname: Cushen
  fullname: Cushen, Julia D
– sequence: 6
  givenname: Leon M
  surname: Dean
  fullname: Dean, Leon M
– sequence: 7
  givenname: Gregory
  surname: Blachut
  fullname: Blachut, Gregory
– sequence: 8
  givenname: Christopher J
  surname: Ellison
  fullname: Ellison, Christopher J
– sequence: 9
  givenname: C Grant
  surname: Willson
  fullname: Willson, C Grant
BackLink https://www.ncbi.nlm.nih.gov/pubmed/23139327$$D View this record in MEDLINE/PubMed
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Snippet Block copolymers (BCPs) must necessarily have high interaction parameters (χ), a fundamental measure of block incompatibility, to self-assemble into...
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Title Polarity-switching top coats enable orientation of sub-10-nm block copolymer domains
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