Photo-induced halide redistribution in organic–inorganic perovskite films
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Author(s) • • • • • • • • •
deQuilettes, Dane W.
Zhang, Wei
Burlakov, Victor M.
Graham, Daniel J.
Leijtens, Tomas
Osherov-Beizerov, Anna
Bulovic, Vladimir
Snaith, Henry J.
Ginger, David S.
Stranks, Samuel David
Date Issued
May 2016
Journal
Nature Communications
Publisher
Springer Nature
Citation
deQuilettes, Dane W., Wei Zhang, Victor M. Burlakov, Daniel J. Graham, Tomas Leijtens, Anna Osherov, Vladimir Bulović, Henry J. Snaith, David S. Ginger, and Samuel D. Stranks. "Photo-induced halide redistribution in organic–inorganic perovskite films." Nature Communications 7, Article number: 11683 (2016), pp.1-9.
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Final published version
Abstract
Organic–inorganic perovskites such as CH3NH3PbI3 are promising materials for a variety of optoelectronic applications, with certified power conversion efficiencies in solar cells already exceeding 21%. Nevertheless, state-of-the-art films still contain performance-limiting non-radiative recombination sites and exhibit a range of complex dynamic phenomena under illumination that remain poorly understood. Here we use a unique combination of confocal photoluminescence (PL) microscopy and chemical imaging to correlate the local changes in photophysics with composition in CH3NH3PbI3 films under illumination. We demonstrate that the photo-induced ‘brightening’ of the perovskite PL can be attributed to an order-of-magnitude reduction in trap state density. By imaging the same regions with time-of-flight secondary-ion-mass spectrometry, we correlate this photobrightening with a net migration of iodine. Our work provides visual evidence for photo-induced halide migration in triiodide perovskites and reveals the complex interplay between charge carrier populations, electronic traps and mobile halides that collectively impact optoelectronic performance.
MIT Department
Massachusetts Institute of Technology. Research Laboratory of Electronics
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DOI of Published Version
https://doi.org/10.1038/ncomms11683