Nanoscale Resolution of Electric-field Induced Motion in Ionic Diblock Copolymer Thin Films

• Published in: ACS applied materials & interfaces Vol. 10; no. 38; pp. 32678 - 32687
• Main Authors: Dugger, Jason W, Li, Wei, Chen, Mingtao, Long, Timothy E, Welbourn, Rebecca J. L, Skoda, Maximilian W.A, Browning, James F, Kumar, Rajeev, Lokitz, Bradley S
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 26.09.2018; American Chemical Society (ACS)
• Subjects: electric field; interfacial tension; ionic block copolymer; MATERIALS SCIENCE; molecular dynamics; neutron reflectometry; ionic block copolymer; interfacial tension; electric field; molecular dynamics; neutron reflectometry
• ISSN: 1944-8244; 1944-8252
• DOI: 10.1021/acsami.8b11220

Understanding the responses of ionic block copolymers to applied electric fields is crucial when targeting applications in areas such as energy storage, microelectronics, and transducers. This work shows that the identity of counterions in ionic diblock copolymers substantially affects their responses to electric fields, demonstrating the importance of ionic species for materials design. In situ neutron reflectometry measurements revealed that thin films containing imidazolium based cationic diblock copolymers, tetrafluoroborate counteranions led to film contraction under applied electric fields, while bromide counteranions drove expansion under similar field strengths. Coarse-grained molecular dynamics simulations were used to develop a fundamental understanding of these responses, uncovering a nonmonotonic trend in thickness change as a function of field strength. This behavior was attributed to elastic responses of microphase separated diblock copolymer chains resulting from variations in interfacial tension of polymer–polymer interfaces due to the redistribution of counteranions in the presence of electric fields.