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Suppressed ion migration in powder-based perovskite thick films using an ionic liquid

Title data

Ramming, Philipp ; Leupold, Nico ; Schötz, Konstantin ; Köhler, Anna ; Moos, Ralf ; Grüninger, Helen ; Panzer, Fabian:
Suppressed ion migration in powder-based perovskite thick films using an ionic liquid.
In: Journal of Materials Chemistry C. Vol. 9 (2021) Issue 35 . - pp. 11827-11837.
ISSN 2050-7534
DOI: https://doi.org/10.1039/D1TC01554K

Official URL: Volltext

Project information

Project title:
Project's official title
Project's id
Stabile Perowskitsolarzellen durch kontrollierte Kristallisationsprozesse und durch grundlegendes Verständnis der optischen und elektrischen Eigenschaften sowie der Defektchemie
MO 1060/32-1
Trockenes Filmprozessieren hybrider Perowskite mit maßgeschneiderten optoelektronischen Eigenschaften
PA 3373/3-1
Festkörper-µ-MAS- und Dünnfilm-NMR-Spektroskopie an hybriden organisch/anorganischen, photovoltaischen Perowskit-Materialien
GR 5505/1-1

Project financing: Deutsche Forschungsgemeinschaft

Abstract in another language

While solution-processed halide perovskite thin films caused enormous attention when used in solar cells, thick films prepared by compressing perovskite powders are considered promising candidates for the next generation of X-ray detectors. However, X-ray detectors based on such powder-pressed perovskites typically suffer from relatively high dark currents, which were attributed to be caused by ion migration. Here we show that the dark current in 800 μm thick powder-pressed MAPbI3-pellets can be reduced by a factor of 25 when using a passivated powder. The passivation was achieved by adding 1 mol of the ionic liquid (IL) BMIMBF4 to the precursors MAI and PbI2 during the mechanochemical synthesis of the MAPbI3 powder. NMR verified the presence of the IL, and its impact on the excited state recombination dynamics was manifested in an increase in the photoluminescence (PL) intensity and a decrease in the monomolecular (trap-assisted) recombination rate, both by about one order of magnitude. By measuring the migration of a PL quenching front upon application of an electric field in a microscope, we determine an ionic diffusivity in the typical range of iodide vacancies in the non-passivated pellet. At the same time, we observe no such PL quenching front in the passivated pellet. Concomitantly, dark I–V curves are hysteresis-free, and light-soaking effects are absent, in contrast to non-passivated pellets. Thus, our work demonstrates the effect on the optical and electrical properties when passivating mechanochemically synthesized halide perovskite powders using an IL, which will facilitate the further development of powder-based perovskite X-ray detectors.

Further data

Item Type: Article in a journal
Refereed: Yes
Institutions of the University: Faculties
Faculties > Faculty of Mathematics, Physics und Computer Science
Faculties > Faculty of Mathematics, Physics und Computer Science > Department of Physics
Faculties > Faculty of Mathematics, Physics und Computer Science > Department of Physics > Chair Experimental Physics II - Optoelectronics of Soft Matter
Faculties > Faculty of Mathematics, Physics und Computer Science > Department of Physics > Chair Experimental Physics II - Optoelectronics of Soft Matter > Chair Experimental Physics II - Optoelectronics of Soft Matter - Univ.-Prof. Dr. Anna Köhler
Faculties > Faculty of Engineering Science
Faculties > Faculty of Engineering Science > Chair Functional Materials
Faculties > Faculty of Engineering Science > Chair Functional Materials > Chair Functional Materials - Univ.-Prof. Dr.-Ing. Ralf Moos
Profile Fields
Profile Fields > Advanced Fields
Profile Fields > Advanced Fields > Advanced Materials
Research Institutions
Research Institutions > Research Centres
Research Institutions > Research Centres > Bayreuth Center for Material Science and Engineering - BayMAT
Result of work at the UBT: Yes
DDC Subjects: 500 Science > 530 Physics
600 Technology, medicine, applied sciences > 620 Engineering
Date Deposited: 29 Jul 2021 06:24
Last Modified: 18 May 2022 07:17
URI: https://eref.uni-bayreuth.de/id/eprint/66704