| Literature DB >> 30643236 |
David Kiefer1, Renee Kroon2, Anna I Hofmann2, Hengda Sun3, Xianjie Liu4, Alexander Giovannitti5, Dominik Stegerer2,6, Alexander Cano2, Jonna Hynynen2, Liyang Yu2, Yadong Zhang7, Dingqi Nai8, Thomas F Harrelson8, Michael Sommer6, Adam J Moulé8, Martijn Kemerink9, Seth R Marder7, Iain McCulloch5,10, Mats Fahlman4, Simone Fabiano3, Christian Müller11.
Abstract
Molecular doping is a crucial tool for controlling the charge-carrier concentration in organic semiconductors. Each dopant molecule is commonly thought to give rise to only one polaron, leading to a maximum of one donor:acceptor charge-transfer complex and hence an ionization efficiency of 100%. However, this theoretical limit is rarely achieved because of incomplete charge transfer and the presence of unreacted dopant. Here, we establish that common p-dopants can in fact accept two electrons per molecule from conjugated polymers with a low ionization energy. Each dopant molecule participates in two charge-transfer events, leading to the formation of dopant dianions and an ionization efficiency of up to 200%. Furthermore, we show that the resulting integer charge-transfer complex can dissociate with an efficiency of up to 170%. The concept of double doping introduced here may allow the dopant fraction required to optimize charge conduction to be halved.Entities:
Year: 2019 PMID: 30643236 DOI: 10.1038/s41563-018-0263-6
Source DB: PubMed Journal: Nat Mater ISSN: 1476-1122 Impact factor: 43.841