| Literature DB >> 31462795 |
Yu Yamashita1,2,3, Junto Tsurumi1,2,3, Masahiro Ohno1,2, Ryo Fujimoto1,2, Shohei Kumagai1,2, Tadanori Kurosawa1,2, Toshihiro Okamoto1,2,4,5, Jun Takeya1,2,3,4, Shun Watanabe6,7,8,9.
Abstract
The efficiency with which polymeric semiconductors can be chemically doped-and the charge carrier densities that can thereby be achieved-is determined primarily by the electrochemical redox potential between the π-conjugated polymer and the dopant species1,2. Thus, matching the electron affinity of one with the ionization potential of the other can allow effective doping3,4. Here we describe a different process-which we term 'anion exchange'-that might offer improved doping levels. This process is mediated by an ionic liquid solvent and can be pictured as the effective instantaneous exchange of a conventional small p-type dopant anion with a second anion provided by an ionic liquid. The introduction of optimized ionic salt (the ionic liquid solvent) into a conventional binary donor-acceptor system can overcome the redox potential limitations described by Marcus theory5, and allows an anion-exchange efficiency of nearly 100 per cent. As a result, doping levels of up to almost one charge per monomer unit can be achieved. This demonstration of increased doping levels, increased stability and excellent transport properties shows that anion-exchange doping, which can use an almost infinite selection of ionic salts, could be a powerful tool for the realization of advanced molecular electronics.Entities:
Year: 2019 PMID: 31462795 DOI: 10.1038/s41586-019-1504-9
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962