Please use this identifier to cite or link to this item: http://hdl.handle.net/1783.1/83831

Profiling the Organic Cation-dependent Degradation of Organolead Halide Perovskite Solar Cells

Authors Zhang, Teng HKUST affiliated (currently or previously)
Meng, Xiangyue HKUST affiliated (currently or previously).
Bai, Yang HKUST affiliated (currently or previously)
Xiao, Shuang HKUST affiliated (currently or previously)
Hu, Chen HKUST affiliated (currently or previously)
Yang, Yinglong HKUST affiliated (currently or previously)
Chen, Haining HKUST affiliated (currently or previously)
Yang, Shihe View this author's profile
Issue Date 2017
Source Journal of Materials Chemistry A , v. 5, (3), 2017, p. 1103-1111
Summary Operational stability is one of the main obstacles that may hold back the commercialization of perovskite solar cells (PVSCs). In this paper, we provide a detailed account of the ion migration accelerated PVSC degradation by comparatively studying perovskite materials with two different organic cations (methylammonium (MA+) and formamidinium (FA+)). Using time of flight secondary ion mass spectrometry (TOF-SIMS), we have uncovered the ion migration accelerated degradation of PVSCs at the device level. Not only did mobile iodide (I-) ions from the perovskite layer diffuse out, but Ag atoms/ions from the metal electrode also diffused into the perovskite layer, which resulted in severe device degradation. Besides, we identified I- species in the hole transport material (HTM) layer for even freshly prepared PVSC devices, which was responsible for the degradation of devices kept under inert conditions. This also testifies the existence of ion migration on the device level of PVSCs. Compared with MAPbI3, the ion migration process can slow down in FAPbI3 devices which accounts for a better stability of FAPbI3 devices. This work underscores the impact of organic cation substitution on PVSC degradation and provides solid evidence for mobile ion migration in perovskite materials and the consequent degradation in specific device settings such as the n-i-p type perovskite solar cells. © The Royal Society of Chemistry.
Subjects
ISSN 2050-7488
2050-7496
Language English
Format Article
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