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

被引:1764
作者
Hoke, Eric T. [1 ]
Slotcavage, Daniel J. [1 ]
Dohner, Emma R. [2 ]
Bowring, Andrea R. [1 ]
Karunadasa, Hemamala I. [2 ]
McGehee, Michael D. [1 ]
机构
[1] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
关键词
SOLAR-CELLS; SEQUENTIAL DEPOSITION; LEAD IODIDE; THIN-FILMS; EFFICIENT; CONDUCTIVITY; PERFORMANCE; PHOTOLYSIS; TRANSPORT; CUPBI3;
D O I
10.1039/c4sc03141e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report on reversible, light-induced transformations in (CH3NH3) Pb(BrxI1-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 similar to 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.
引用
收藏
页码:613 / 617
页数:5
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