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An Organic Borate Salt with Superior p‐Doping Capability for Organic Semiconductors

Authors :
Berthold Wegner
Dominique Lungwitz
Ahmed E. Mansour
Claudia E. Tait
Naoki Tanaka
Tianshu Zhai
Steffen Duhm
Michael Forster
Jan Behrends
Yoshiaki Shoji
Andreas Opitz
Ullrich Scherf
Emil J. W. List‐Kratochvil
Takanori Fukushima
Norbert Koch
Source :
Advanced Science, Vol 7, Iss 17, Pp n/a-n/a (2020)
Publication Year :
2020
Publisher :
Wiley, 2020.

Abstract

Abstract Molecular doping allows enhancement and precise control of electrical properties of organic semiconductors, and is thus of central technological relevance for organic (opto‐) electronics. Beyond single‐component molecular electron acceptors and donors, organic salts have recently emerged as a promising class of dopants. However, the pertinent fundamental understanding of doping mechanisms and doping capabilities is limited. Here, the unique capabilities of the salt consisting of a borinium cation (Mes2B+; Mes: mesitylene) and the tetrakis(penta‐fluorophenyl)borate anion [B(C6F5)4]− is demonstrated as p‐type dopant for polymer semiconductors. With a range of experimental methods, the doping mechanism is identified to comprise electron transfer from the polymer to Mes2B+, and the positive charge on the polymer is stabilized by [B(C6F5)4]−. Notably, the former salt cation leaves during processing and is not present in films. The anion [B(C6F5)4]− even enables the stabilization of polarons and bipolarons in poly(3‐hexylthiophene), not yet achieved with other molecular dopants. From doping studies with high ionization energy polymer semiconductors, the effective electron affinity of Mes2B+[B(C6F5)4]− is estimated to be an impressive 5.9 eV. This significantly extends the parameter space for doping of polymer semiconductors.

Details

Language :
English
ISSN :
21983844
Volume :
7
Issue :
17
Database :
Directory of Open Access Journals
Journal :
Advanced Science
Publication Type :
Academic Journal
Accession number :
edsdoj.b961f4a44199bf77847432310f13
Document Type :
article
Full Text :
https://doi.org/10.1002/advs.202001322