| Literature DB >> 32945031 |
Mahima Goel1, Marie Siegert2, Gert Krauss1, John Mohanraj1, Adrian Hochgesang1, David C Heinrich1, Martina Fried1, Jens Pflaum2, Mukundan Thelakkat1,3.
Abstract
Unlike the conventional p-doping of organic semiconductors (OSCs) using acceptors, here, an efficient doping concept for diketopyrrolopyrrole-based polymer PDPP[T]2 -EDOT (OSC-1) is presented using an oxidized p-type semiconductor, Spiro-OMeTAD(TFSI)2 (OSC-2), exploiting electron transfer from HOMOOSC-1 to HOMOOSC-2 . A shift of work function toward the HOMOOSC-1 upon doping is confirmed by ultraviolet photoelectron spectroscopy (UPS). Detailed X-ray photoelectron spectroscopy (XPS) and UV-vis-NIR absorption studies confirm HOMOOSC-1 to HOMOOSC-2 electron transfer. The reduction products of Spiro-OMeTAD(TFSI)2 to Spiro-OMeTAD(TFSI) and Spiro-OMeTAD is also confirmed and their relative amounts in doped samples is determined. Mott-Schottky analysis shows two orders of magnitude increase in free charge carrier density and one order of magnitude increase in the charge carrier mobility. The conductivity increases considerably by four orders of magnitude to a maximum of 10 S m-1 for a very low doping ratio of 8 mol%. The doped polymer films exhibit high thermal and ambient stability resulting in a maximum power factor of 0.07 µW m-1 K-2 at a Seebeck coefficient of 140 µV K-1 for a very low doping ratio of 4 mol%. Also, the concept of HOMOOSC-1 to HOMOOSC-2 electron transfer is a highly efficient, stable and generic way to p-dope other conjugated polymers.Entities:
Keywords: Mott-Schottky analysis; molecular doping; organic semiconductors; polymer thermoelectrics; ultraviolet photoelectron spectroscopy
Year: 2020 PMID: 32945031 DOI: 10.1002/adma.202003596
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849