Efficient molecular doping of polymeric semiconductors driven by anion exchange
Efficient molecular doping of polymeric semiconductors driven by anion exchange
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DOI:
10.1038/s41586-019-1504-9
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发表时间:
2019-08
期刊:
影响因子:
64.8
通讯作者:
Yu Yamashita;J. Tsurumi;M. Ohno;Ryo Fujimoto;S. Kumagai;Tadanori Kurosawa;T. Okamoto;J. Takeya;S. Watanabe
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文献类型:
--
作者:
Yu Yamashita;J. Tsurumi;M. Ohno;Ryo Fujimoto;S. Kumagai;Tadanori Kurosawa;T. Okamoto;J. Takeya;S. Watanabe
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 species,. Thus, matching the electron affinity of one with the ionization potential of the other can allow effective doping,. 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 theory, 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.