Issue 2, 2017

Ground-state charge transfer for NIR absorption with donor/acceptor molecules: interactions mediated via energetics and orbital symmetries

Abstract

The interactions between electron donors (D) and acceptors (A) of organic semiconducting molecules are of great interest to organic electronics, e.g. electrical doping of organic semiconductors (OSCs), photo-generation of charges in organic solar cells, and light-emitting/detecting devices based on OSCs. A blend of D/A OSC is typically characterized by weak van der Waals interactions or integer charge transfer (ICT) between neighboring D/A molecules. In between these two scenarios of physical blends and ICT complexes, orbital hybridization between adjacent D/A molecules serves as a third alternative, characterized by an in situ formation of a ground state complex featuring partial charge transfer between participating donor and acceptor molecules. In this work is presented a comprehensive experimental study on partial charge-transfer complex (CPX) formed via orbital hybridization. Thiophenes and phthalocyanines are used as electron donors, while acceptor molecules of different geometries and electron affinities are employed with the aim to clarify how orbital symmetry, energy level alignment and steric hindrance affect orbital hybridization and subsequent tuning of the optical band-gap into the near infrared (NIR) region.

Graphical abstract: Ground-state charge transfer for NIR absorption with donor/acceptor molecules: interactions mediated via energetics and orbital symmetries

Supplementary files

Article information

Article type
Paper
Submitted
20 Nhl 2016
Accepted
24 Huk 2016
First published
24 Huk 2016

J. Mater. Chem. C, 2017,5, 275-281

Ground-state charge transfer for NIR absorption with donor/acceptor molecules: interactions mediated via energetics and orbital symmetries

Q. Zhang, X. Liu, F. Jiao, S. Braun, M. J. Jafari, X. Crispin, T. Ederth and M. Fahlman, J. Mater. Chem. C, 2017, 5, 275 DOI: 10.1039/C6TC04563D

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