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Reversible photo-induced trap formation in mixed-halide hybrid perovskites for photovoltaics

We report on reversible, light-induced transformations in (CH(3)NH(3))Pb(Br(x)I(1–x))(3). Photoluminescence (PL) spectra of these perovskites develop a new, red-shifted peak at 1.68 eV that grows in intensity under constant, 1-sun illumination in less than a minute. This is accompanied by an increas...

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Detalles Bibliográficos
Autores principales: Hoke, Eric T., Slotcavage, Daniel J., Dohner, Emma R., Bowring, Andrea R., Karunadasa, Hemamala I., McGehee, Michael D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5491962/
https://www.ncbi.nlm.nih.gov/pubmed/28706629
http://dx.doi.org/10.1039/c4sc03141e
Descripción
Sumario:We report on reversible, light-induced transformations in (CH(3)NH(3))Pb(Br(x)I(1–x))(3). Photoluminescence (PL) spectra of these perovskites develop a new, red-shifted peak at 1.68 eV that grows in intensity under constant, 1-sun illumination in less than a minute. This is accompanied by an increase in sub-bandgap absorption at ∼1.7 eV, indicating the formation of luminescent trap states. Light soaking causes a splitting of X-ray diffraction (XRD) peaks, suggesting segregation into two crystalline phases. Surprisingly, these photo-induced changes are fully reversible; the XRD patterns and the PL and absorption spectra revert to their initial states after the materials are left for a few minutes in the dark. We speculate that photoexcitation may cause halide segregation into iodide-rich minority and bromide-enriched majority domains, the former acting as a recombination center trap. This instability may limit achievable voltages from some mixed-halide perovskite solar cells and could have implications for the photostability of halide perovskites used in optoelectronics.