期刊
JOURNAL OF MATERIALS CHEMISTRY A
卷 7, 期 5, 页码 2275-2282出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8ta12193a
关键词
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资金
- National Key R&D Program of China [2017YFA0204800]
- National Natural Science Foundation of China [21525311, 21773027, 11404056, 51502130]
- Jiangsu 333 project [BRA2016353]
- Scientific Research Foundation of Graduate School of Southeast University [YBJJ1772]
Although the power conversion efficiency of perovskite solar cells has exceeded 23%, the poor ambient stability of organic-inorganic halide perovskites poses a challenge for their commercialization. Comprehensive understanding of the underlying degradation mechanisms is a crucial step to seek approaches that can effectively suppress the degradation of perovskites. Herein, on the basis of extensive first-principles calculations, a three-step photo-oxidative degradation mechanism of MAPbI(3)d at the atomic level is revealed. We find that, in a dry ambient environment, the photo-generated superoxide anions (O-2(-)) first lead to fast surface oxidation. However, further oxidation of the perovskite interior is hindered by the solid oxidation product. The fresh water produced in surface oxidation leads to the hydration of the inner perovskite and eventual breakage of the MAPbI(3) lattice. We devise a practical strategy for protecting MAPbI(3) from photo-induced decomposition by anchoring hydrophobic 2-(4-fluorophenyl)propan-2-amine on the surface of MAPbI(3). The surface modification significantly retards the photo-induced decomposition.
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