Intermolecular charge transfer enhances the performance of molecular rectifiers

Author:

Sullivan Ryan P.1ORCID,Morningstar John T.2,Castellanos-Trejo Eduardo1,Bradford Robert W.1,Hofstetter Yvonne J.34ORCID,Vaynzof Yana34ORCID,Welker Mark E.2ORCID,Jurchescu Oana D.1ORCID

Affiliation:

1. Deparment of Physics and Center for Functional Materials, Wake Forest University, Winston-Salem, NC 27109, USA.

2. Deparment of Chemistry and Center for Functional Materials, Wake Forest University, Winston-Salem, NC 27109, USA.

3. Integrated Centre for Applied Physics and Photonic Materials, Technische Universität Dresden, Nöthnitzer Str. 61, 01187 Dresden, Germany.

4. Center for Advancing Electronics Dresden (cfaed), Technische Universität Dresden, Helmholtzstraße 18, 01089 Dresden, Germany.

Abstract

Molecular-scale diodes made from self-assembled monolayers (SAMs) could complement silicon-based technologies with smaller, cheaper, and more versatile devices. However, advancement of this emerging technology is limited by insufficient electronic performance exhibited by the molecular current rectifiers. We overcome this barrier by exploiting the charge-transfer state that results from co-assembling SAMs of molecules with strong electron donor and acceptor termini. We obtain a substantial enhancement in current rectification, which correlates with the degree of charge transfer, as confirmed by several complementary techniques. These findings provide a previously enexplored method for manipulating the properties of molecular electronic devices by exploiting donor/acceptor interactions. They also serve as a model test platform for the study of doping mechanisms in organic systems. Our devices have the potential for fast widespread adoption due to their low-cost processing and self-assembly onto silicon substrates, which could allow seamless integration with current technologies.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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