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Coexistence of light-induced photoluminescence enhancement and quenching in CH(3)NH(3)PbBr(3) perovskite films

Lead halide perovskites are promising semiconductors for various optoelectronic devices working in a wide photo-excitation density regime. However, photo-induced instability, attributed to illumination-activated mobile ions, has been an obstacle to their application. Herein, we use the time evolutio...

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Detalles Bibliográficos
Autores principales: Lou, Haoran, Lin, Chen, Fang, Zhishan, Jiang, Li, Chen, Xiaofeng, Ye, Zhizhen, He, Haiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050461/
https://www.ncbi.nlm.nih.gov/pubmed/35495358
http://dx.doi.org/10.1039/d0ra00605j
Descripción
Sumario:Lead halide perovskites are promising semiconductors for various optoelectronic devices working in a wide photo-excitation density regime. However, photo-induced instability, attributed to illumination-activated mobile ions, has been an obstacle to their application. Herein, we use the time evolution of photoluminescence (PL) to investigate the light illumination effects of CH(3)NH(3)PbBr(3) perovskite films under relatively high excitation (up to 4.5 W cm(−2)). We demonstrate that continuous illumination can lead to both PL enhancement and PL quenching simultaneously, with their weight ratios depending on the excitation density. The experimental data can be well described and interpreted by considering the coexistence of and competition between the photo-induced annihilation and the formation of long-living filled trap states. Our study may provide in-depth insight into the photo-induced instability of perovskite films and help to improve the performance of perovskite-based optoelectronic devices.