Affiliation:
1. Department of Chemical Engineering and Biotechnology University of Cambridge Cambridge CB3 0AS UK
2. Department of Physics Cavendish Laboratory University of Cambridge Cambridge CB3 0HE UK
3. Department of Materials Science and Metallurgy University of Cambridge Cambridge CB3 0FS UK
Abstract
AbstractHalide perovskites are excellent candidate materials for use in solar cell, LED, and detector devices, in part because their composition can be tuned to achieve ideal optoelectronic properties. Empirical efficiency optimization has led the field toward compositions rich in FA (formamidinium) on the A‐site and I on the X‐site, with additional small amounts of MA (methylammonium) or Cs A‐site cations and Br X‐site anions. However, it is not clear how and why the specific compositions of alloyed, that is, mixed component, halide perovskites relate to photo‐stability of the materials. Here, this work combines synchrotron grazing incidence wide‐angle X‐ray scattering, photoluminescence, high‐resolution scanning electron diffraction measurements and theoretical modelling to reveal the links between material structure and photostability. Namely, this work finds that increased octahedral titling leads to improved photo‐stability that is correlated with lower densities of performance‐harming hexagonal polytype impurities. These results uncover the structural signatures underpinning photo‐stability and can therefore be used to make targeted changes to halide perovskites, bettering the commercial prospects of technologies based on these materials.
Funder
European Research Council
Royal Society
Engineering and Physical Sciences Research Council
Royal Society of Chemistry
Cambridge Philosophical Society
Sir Richard Stapley Educational Trust
Royal Academy of Engineering
Tata Sons
Diamond Light Source
Cited by
2 articles.
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