Mixed-morphology and mixed-orientation block copolymer bilayers

Block copolymers have attracted considerable attention due to their ability to self-assemble into highly regular structures, spanning length scales from several nanometers to over 100 nm. Block copolymers confined in thin films have been extensively utilized as soft templates for nanofabrication, bu...

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Detalhes bibliográficos
Autores: García, Nicolás, Davis, Raleigh L., Kim, So Youn, Chaikin, Paul M., Register, Richard A., Vega, Daniel Alberto
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2014
País:Argentina
Recursos:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/29775
Acesso em linha:http://hdl.handle.net/11336/29775
Access Level:acceso abierto
Palavra-chave:Nanotechnology
Block Copolymer
https://purl.org/becyt/ford/1.3
https://purl.org/becyt/ford/1
Descrição
Resumo:Block copolymers have attracted considerable attention due to their ability to self-assemble into highly regular structures, spanning length scales from several nanometers to over 100 nm. Block copolymers confined in thin films have been extensively utilized as soft templates for nanofabrication, but most applications have been restricted to single-layer templates with smectic and hexagonal symmetries. Here we show that a multi-step approach that includes shear alignment, thin film lift-off, and stacking can access novel three-dimensional block copolymer structures with long-range order and mixed symmetries. This technique allows control over the long-range order and also expands the range of nanolithographic templates accessible through guided self-assembly.