Self-assembly of semicrystalline PE-b-PS diblock copolymers within AAO nanoporous templates

Strongly segregated polyethylene-b-polystyrene (PE-b-PS) diblock copolymers were infiltrated within anodic aluminum oxide nanoporous templates (AAO) (with 60 nm diameter). After carefully removing the nanofibers from the nanopores, TEM revealed their morphology. This is the first time that the morph...

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Detalles Bibliográficos
Autores: Casas Becerra, María Teresa|||0000-0002-5309-8246, Michell, Rose Mary, Blaszczyk-Lezak, Iwona, Puiggalí Bellalta, Jordi|||0000-0002-0640-4474, Mijangos, Carmen, Lorenzo, Arnaldo T., Müller, Alejandro
Tipo de recurso: artículo
Fecha de publicación:2015
País:España
Institución:Universitat Politècnica de Catalunya (UPC)
Repositorio:UPCommons. Portal del coneixement obert de la UPC
Idioma:inglés
OAI Identifier:oai:upcommons.upc.edu:2117/79549
Acceso en línea:https://hdl.handle.net/2117/79549
https://dx.doi.org/10.1016/j.polymer.2015.06.025
Access Level:acceso abierto
Palabra clave:Copolymers
Crystallization
Confined crystallization
Core–shell morphology
AAO templates
Block copolymers
Cristal·lització
Copolímers
Àrees temàtiques de la UPC::Enginyeria química
Descripción
Sumario:Strongly segregated polyethylene-b-polystyrene (PE-b-PS) diblock copolymers were infiltrated within anodic aluminum oxide nanoporous templates (AAO) (with 60 nm diameter). After carefully removing the nanofibers from the nanopores, TEM revealed their morphology. This is the first time that the morphology of semi-crystalline diblock copolymers infiltrated within AAO templates is observed. Regardless of their composition, the infiltrated nanofibers are constituted by core–shell or pseudo core–shell self-assembled nanocylinders. The affinity of PE to the AAO walls tailors the morphology towards PE shells with PS cores. The PS cores for some compositions have PE inclusions whose morphology is expected on the basis of previous computer simulation studies. Morphological observations successfully explain the confined crystallization of the PE block within the nanopores and the origin of novel double confinement effects (induced by glassy PS block and rigid AAO walls) on the PE block