Hybrid Alkyl-Ethylene Glycol Side Chains Enhance Substrate Adhesion and Operational Stability in Accumulation Mode Organic Electrochemical Transistors
Type
ArticleAuthors
Wang, YazhouZeglio, Erica
Liao, Hailiang
Xu, Jinqiu
Liu, Feng
Li, Zhengke
Maria, Iuliana Petruta
Mawad, Damia

Herland, Anna
McCulloch, Iain

Yue, Wan

KAUST Department
Chemical Science ProgramKAUST Solar Center (KSC)
Physical Science and Engineering (PSE) Division
Date
2019-11-11Online Publication Date
2019-11-11Print Publication Date
2019-12-10Embargo End Date
2020-11-11Permanent link to this record
http://hdl.handle.net/10754/660542
Metadata
Show full item recordAbstract
Donor-acceptor copolymers featuring electron-deficient isoindigo units and electron-rich 3,4-ethylenedioxy (EDOT) groups are presented as new materials for accumulation mode organic electrochemical transistors (OECTs). Grafting hybrid alkyl-ethylene glycol side chains on the isoindigo units of the copolymer leads to OECTs with outstanding substrate adhesion and operational stability in contact with an aqueous electrolyte, as demonstrated by their preserved performance after extensive ultrasonication (1.5 h) or after continuous on-off switching for over 6 h. Hybrid side chains outperform copolymers with alkyl only or ethylene glycol only side chains, which retain only 27% and 10% of the on currents after 40 min of on-off switching, respectively, under the same biasing conditions. These devices are promising candidates for in vitro and in vivo bioelectronics, applications where stability as well as robust adhesion of the conjugated polymer to the substrate are essential.Citation
Wang, Y., Zeglio, E., Liao, H., Xu, J., Liu, F., Li, Z., … Yue, W. (2019). Hybrid Alkyl–Ethylene Glycol Side Chains Enhance Substrate Adhesion and Operational Stability in Accumulation Mode Organic Electrochemical Transistors. Chemistry of Materials. doi:10.1021/acs.chemmater.9b03798Sponsors
The authors thank the National Natural Science Foundation of China (Grant Nos. 21875291 and 21702240) for the financial support. E.Z. thanks the Swedish Research Council (VR, International Postdoc Grant) and the Royal Swedish Academy of Sciences (Kungl. Vetenskapsakademiens stiftelser) for funding. A.H. thanks the Wallenberg foundation and Swedish Research Council (VR). This work was performed in part at the UNSW node of the Australian National Fabrication Facility, a company established under the National Collaborative Research Infrastructure Strategy to provide nano- and microfabrication facilities for Australia’s researchers.Publisher
American Chemical Society (ACS)Journal
Chemistry of MaterialsAdditional Links
https://pubs.acs.org/doi/abs/10.1021/acs.chemmater.9b03798ae974a485f413a2113503eed53cd6c53
10.1021/acs.chemmater.9b03798