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Controlling the dimensionality of charge transport in organic thin-film transistors

机译:控制有机薄膜晶体管中电荷传输的维数

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摘要

Electrolyte-gated organic thin-film transistors (OTFTs) can offer a feasible platform for future flexible, large-area and low-cost electronic applications. These transistors can be divided into two groups on the basis of their operation mechanism: (i) field-effect transistors that switch fast but carry much less current than (ii) the electrochemical transistors which, on the contrary, switch slowly. An attractive approach would be to combine the benefits of the field-effect and the electrochemical transistors into one transistor that would both switch fast and carry high current densities. Here we report the development of a polyelectrolyte-gated OTFT based on conjugated polyelectrolytes, and we demonstrate that the OTFTs can be controllably operated either in the field-effect or the electrochemical regime. Moreover, we show that the extent of electrochemical doping can be restricted to a few monolayers of the conjugated polyelectrolyte film, which allows both high current densities and fast switching speeds at the same time. We propose an operation mechanism based on self-doping of the conjugated polyelectrolyte backbone by its ionic side groups.
机译:电解质门控有机薄膜晶体管(OTFT)可以为未来的灵活,大面积和低成本电子应用提供一个可行的平台。这些晶体管可以根据其工作机制分为两组:(i)场效应晶体管开关速度快,但电流要比(ii)电化学晶体管相反,而电化学晶体管的开关速度慢。一种有吸引力的方法是将场效应和电化学晶体管的优点结合到一个晶体管中,该晶体管既可以快速切换,又可以承载高电流密度。在这里,我们报道了基于共轭聚电解质的聚电解质门控OTFT的发展,并且我们证明了OTFT可以在场效应或电化学条件下可控地操作。而且,我们表明,电化学掺杂的程度可以限制在共轭聚电解质膜的几个单层中,这同时允许高电流密度和快速开关速度。我们提出了一种基于共轭聚电解质骨架的离子侧基自掺杂的操作机制。

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