Light-Induced Degradation of CH3NH3PbI3 Hybrid Perovskite Thin Film

The stability of CH3NH3PbI3 was investigated by observing the degradation in a coevaporated film irradiated by a blue laser in ultrahigh vacuum. X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) were employed to investigate the effects of irradiation on the surface. The c...

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Veröffentlicht in:Journal of physical chemistry. C 2017-02, Vol.121 (7), p.3904-3910
Hauptverfasser: Li, Youzhen, Xu, Xuemei, Wang, Congcong, Ecker, Ben, Yang, Junliang, Huang, Jinsong, Gao, Yongli
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container_issue 7
container_start_page 3904
container_title Journal of physical chemistry. C
container_volume 121
creator Li, Youzhen
Xu, Xuemei
Wang, Congcong
Ecker, Ben
Yang, Junliang
Huang, Jinsong
Gao, Yongli
description The stability of CH3NH3PbI3 was investigated by observing the degradation in a coevaporated film irradiated by a blue laser in ultrahigh vacuum. X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) were employed to investigate the effects of irradiation on the surface. The core levels of CH3NH3PbI3 were observed to shift toward a higher binding energy (BE) during the irradiation, suggesting that the surface became more n-type. A new metallic Pb component in the XPS spectrum appeared after 120 min of irradiation, indicating that the film had started to decompose. The decomposition saturated after about 480 min of irradiation when the ratio of metallic Pb to total Pb was about 33%. Furthermore, the film was no longer continuous after irradiation, as the elements gold and oxygen from the substrate were detected by XPS. SEM images also show a roughened surface after irradiation. The results strongly indicate that CH3NH3PbI3 is sensitive to the laser irradiation and that the light induced decomposition is a self-limiting process.
doi_str_mv 10.1021/acs.jpcc.6b11853
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X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) were employed to investigate the effects of irradiation on the surface. The core levels of CH3NH3PbI3 were observed to shift toward a higher binding energy (BE) during the irradiation, suggesting that the surface became more n-type. A new metallic Pb component in the XPS spectrum appeared after 120 min of irradiation, indicating that the film had started to decompose. The decomposition saturated after about 480 min of irradiation when the ratio of metallic Pb to total Pb was about 33%. Furthermore, the film was no longer continuous after irradiation, as the elements gold and oxygen from the substrate were detected by XPS. SEM images also show a roughened surface after irradiation. 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