Switching charge states in quasi-2D molecular conductors

Author:

Huang Yulong1ORCID,Mitchell Travis2,Zheng Yixiong3,Hu Yong1,Benedict Jason B2,Seo Jung-Hun3,Ren Shenqiang124

Affiliation:

1. Department of Mechanical and Aerospace Engineering, University at Buffalo, The State University of New York , Buffalo, NY 14260, USA

2. Department of Chemistry, University at Buffalo, The State University of New York , Buffalo, NY 14260, USA

3. Department of Materials Design and Innovation, University at Buffalo, The State University of New York , Buffalo, NY 14260, USA

4. Research and Education in energy, Environment and Water (RENEW) Institute, University at Buffalo, The State University of New York , Buffalo, NY 14260, USA

Abstract

Abstract 2D molecular entities build next-generation electronic devices, where abundant elements of organic molecules are attractive due to the modern synthetic and stimuli control through chemical, conformational, and electronic modifications in electronics. Despite its promising potential, the insufficient control over charge states and electronic stabilities must be overcome in molecular electronic devices. Here, we show the reversible switching of modulated charge states in an exfoliatable 2D-layered molecular conductor based on bis(ethylenedithio)tetrathiafulvalene molecular dimers. The multiple stimuli application of cooling rate, current, voltage, and laser irradiation in a concurrent manner facilitates the controllable manipulation of charge crystal, glass, liquid, and metal phases. The four orders of magnitude switching of electric resistance are triggered by stimuli-responsive charge distribution among molecular dimers. The tunable charge transport in 2D molecular conductors reveals the kinetic process of charge configurations under stimuli, promising to add electric functions in molecular circuitry.

Funder

U.S. Department of Energy

National Science Foundation

Publisher

Oxford University Press (OUP)

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