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    Hybrid Alkyl-Ethylene Glycol Side Chains Enhance Substrate Adhesion and Operational Stability in Accumulation Mode Organic Electrochemical Transistors

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    Type
    Article
    Authors
    Wang, Yazhou
    Zeglio, Erica
    Liao, Hailiang
    Xu, Jinqiu
    Liu, Feng
    Li, Zhengke
    Maria, Iuliana Petruta
    Mawad, Damia cc
    Herland, Anna
    McCulloch, Iain cc
    Yue, Wan cc
    KAUST Department
    Chemical Science Program
    KAUST Solar Center (KSC)
    Physical Science and Engineering (PSE) Division
    Date
    2019-11-11
    Online Publication Date
    2019-11-11
    Print Publication Date
    2019-12-10
    Embargo End Date
    2020-11-11
    Permanent link to this record
    http://hdl.handle.net/10754/660542
    
    Metadata
    Show full item record
    Abstract
    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.9b03798
    Sponsors
    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 Materials
    DOI
    10.1021/acs.chemmater.9b03798
    Additional Links
    https://pubs.acs.org/doi/abs/10.1021/acs.chemmater.9b03798
    ae974a485f413a2113503eed53cd6c53
    10.1021/acs.chemmater.9b03798
    Scopus Count
    Collections
    Articles; Physical Science and Engineering (PSE) Division; Chemical Science Program; KAUST Solar Center (KSC)

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