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Role of Water and Defects in Photo‐Oxidative Degradation of Methylammonium Lead Iodide Perovskite
Author(s) -
Ouyang Yixin,
Shi Li,
Li Qiang,
Wang Jinlan
Publication year - 2019
Publication title -
small methods
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.66
H-Index - 46
ISSN - 2366-9608
DOI - 10.1002/smtd.201900154
Subject(s) - perovskite (structure) , iodide , photochemistry , degradation (telecommunications) , halide , adsorption , oxygen evolution , oxygen , chemistry , density functional theory , inorganic chemistry , chemical engineering , catalysis , materials science , chemical physics , electrochemistry , computational chemistry , organic chemistry , telecommunications , electrode , computer science , engineering
Great progress has been made in improving power conversion efficiency of perovskite solar cells (PSCs), and now the pressing issue is the poor stability of organic–inorganic halide perovskites under ambient conditions. Degradation of MAPbI 3 induced by light and oxygen is a dominant factor limiting the lifetime of PSCs. Here, based on ab initio molecular dynamics simulations and first‐principles density functional theory calculations, the interactions between oxygen, water, and surface defects of MAPbI 3 are investigated. It is found that the photo‐oxidation of MAPbI 3 concentrates on the surface of the crystal, and this degradation can be accelerated by surface iodine vacancy and moisture. When oxygen coadsorbs with water molecules or oxygen adsorbs at the iodine vacancy on the MAPbI 3 surface, the energy levels of adsorbed O 2 are significantly lowered, facilitating the photoexcited electron transfer and the formation of reactive superoxide anions (O 2 − ). The understanding of the role of water and defects in MAPbI 3 photo‐oxidation from this study paves the way for further optimization of stable perovskite solar cells.

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