| Literature DB >> 28240871 |
Meysam Pazoki1,2, T Jesper Jacobsson3, Jolla Kullgren2, Erik M J Johansson1, Anders Hagfeldt3, Gerrit Boschloo1, Tomas Edvinsson4.
Abstract
Organometallic halide perovskites (OMHPs) have recently emerged as a promising class of materials in photovoltaic technology. Here, we present an in-depth investigation of the physics in these systems by measuring the photoinduced absorption (PIA) in OMHPs as a function of materials composition, excitation wavelength, and modulation frequency. We report a photoinduced Stark effect that depends on the excitation wavelength and on the dipole strength of the monovalent cations in the A position of the ABX3 perovskite. The results presented are corroborated by density functional theory calculations and provide fundamental information about the photoinduced local electric field change under blue and red excitation as well as insights into the mechanism of light-induced ion displacement in OMHPs. For optimized perovskite solar cell devices beyond 19% efficiency, we show that excess thermalization energy of blue photons plays a role in overcoming the activation energy for ion diffusion.Entities:
Keywords: CH3NH3PbI3; Stark effect; cation-dependent ion movement; mixed halide perovskites; perovskite solar cells; photoinduced ion migration
Year: 2017 PMID: 28240871 DOI: 10.1021/acsnano.6b07916
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881