4.8 Article

Reversible Pb2+/Pb0 and I-/I3- Redox Chemistry Drives the Light-Induced Phase Segregation in All-Inorganic Mixed Halide Perovskites

期刊

ADVANCED ENERGY MATERIALS
卷 11, 期 12, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/aenm.202002934

关键词

complex lead halides; lead halide perovskites; light‐ induced halide phase separation; perovskite solar cells; photostability

资金

  1. Russian Science Foundation [19-73-30020]
  2. Ministry of Education and Science of Russian Federation [AAAA-A18-118020190098-5, FEUZ-2020-0060]

向作者/读者索取更多资源

Research shows that tunability of optoelectronic properties of lead halide perovskites can be achieved through halide mixing, but mixed halide perovskites are unstable under illumination due to halide phase segregation. Recent studies have found that iodoplumbate is selectively expelled from mixed halide perovskite grains, forming a separate I-rich phase, and proposed a mechanism based on reversible redox chemistry to explain this phenomenon.
Tunability of optoelectronic properties of lead halide perovskites achieved through halide mixing can potentially enable their multiple applications, for example, in tandem solar cells and light-emitting diodes. However, mixed halide perovskites are unstable under illumination due to their segregation to Br-rich and I-rich phases, which negatively affects the performance and the operational stability of devices. Research efforts over the past years provided a substantial understanding of the factors influencing light-induced halide phase segregation. While several mechanisms have been proposed, none of them could account for all available experimental data; and hence the origin of the effect is still under active debate. Herein, the photodegradation of CsPbI2Br and Cs1.2PbI2Br1.2 is thoroughly investigated using a set of complementary techniques. In situ atomic force microscopy provides a visualization of the real-time halide phase segregation dynamics demonstrating that iodoplumbate is selectively expelled from the mixed halide perovskite grains and nucleates as a separate I-rich phase at the grain boundaries. A mechanism based on the reversible Pb2+/Pb-0 and I-/I-3(-) redox (photo)chemistry is proposed, which explains the experimental findings and other previously reported results. Furthermore, it sheds new insights on the underlying mechanisms of multiple phenomena related to light- or electric field-induced degradation of various lead halide perovskites.

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