Effects of Side Chain Branch Point on Self Assembly, Structure, and Electronic Properties of High Mobility Semiconducting Polymers

Bridges, Colin R.; Ford, Michael J.; Thomas, Elayne M.; Gomez, Christian; Bazan, Guillermo C.; Segalman, Rachel A.

doi:10.1021/acs.macromol.8b01906

Title: Effects of Side Chain Branch Point on Self Assembly, Structure, and Electronic Properties of High Mobility Semiconducting Polymers

Journal Article · Mon Oct 22 00:00:00 EDT 2018 · Macromolecules

DOI:https://doi.org/10.1021/acs.macromol.8b01906· OSTI ID:1612528

Bridges, Colin R. ^[1];

^[1]; Thomas, Elayne M. ^[1]; Gomez, Christian ^[1];

^[1];

^[1]

University of California, Santa Barbara, CA (United States)

Semiconducting polymers exhibiting lyotropic liquid-crystalline (LC) mesophases allow for precise control over crystallinity and crystallite orientation using scalable equilibrium processing techniques. The ability to control morphologies from molecular to macroscopic scales is desirable for optimizing polymer electronic devices such as field-effect transistors. LC mesophases can form in semiconducting polymers with branched side chains, but steric repulsion from the side chain structure increases π-stacking distances. This change in unit cell negatively impacts electronic transport, negating any improvements gained by achieving more favorable mesostructures. Herein, we show that the π-stacking distance in cyclopentadithiophene-benzothiadiazole donor–acceptor copolymers is successively shortened by moving the branch point further away from the conjugated backbone. These materials retain their favorable LC properties, and the change in unit cell is accompanied by a monotonic increase in charge carrier mobility in field effect transistors. Mobility values span from ~10^–4 to 0.41 cm2 V^–1 s^–1, reaching their highest value when the branch point is furthest from the polymer backbone. Additionally, these LC materials can be aligned across large length scales on rubbed polyimide, resulting in an improvement of charge carrier mobility by a factor of 56 when comparing transistors fabricated parallel and perpendicular to the alignment direction.

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Research Organization:: Univ. of California, Santa Barbara, CA (United States)

Sponsoring Organization:: USDOE Office of Science (SC), Basic Energy Sciences (BES); National Science Foundation (NSF); National Science and Engineering Research Council of Canada (NSERC)

Grant/Contract Number:: SC0016390; AC02-05CH11231; DMR 1121053; DGE-1650114

OSTI ID:: 1612528

Journal Information:: Macromolecules, Vol. 51, Issue 21; ISSN 0024-9297

Publisher:: American Chemical SocietyCopyright Statement

Country of Publication:: United States

Language:: English

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Cited by: 33 works

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