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Evolution of Photoluminescence, Raman, and Structure of CH(3)NH(3)PbI(3) Perovskite Microwires Under Humidity Exposure

Self-assembled organic-inorganic CH(3)NH(3)PbI(3) perovskite microwires (MWs) upon humidity exposure along several weeks were investigated by photoluminescence (PL) spectroscopy, Raman spectroscopy, and X-ray diffraction (XRD). We show that, in addition to the common perovskite decomposition into Pb...

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Detalles Bibliográficos
Autores principales: Segovia, Rubén, Qu, Geyang, Peng, Miao, Sun, Xiudong, Shi, Hongyan, Gao, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5842165/
https://www.ncbi.nlm.nih.gov/pubmed/29516198
http://dx.doi.org/10.1186/s11671-018-2470-0
Descripción
Sumario:Self-assembled organic-inorganic CH(3)NH(3)PbI(3) perovskite microwires (MWs) upon humidity exposure along several weeks were investigated by photoluminescence (PL) spectroscopy, Raman spectroscopy, and X-ray diffraction (XRD). We show that, in addition to the common perovskite decomposition into PbI(2) and the formation of a hydrated phase, humidity induced a gradual PL redshift at the initial weeks that is stabilized for longer exposure (~ 21 nm over the degradation process) and an intensity enhancement. Original perovskite Raman band and XRD reflections slightly shifted upon humidity, indicating defects formation and structure distortion of the MWs crystal lattice. By correlating the PL, Raman, and XRD results, it is believed that the redshift of the MWs PL emission was originated from the structural disorder caused by the incorporation of H(2)O molecules in the crystal lattice and radiative recombination through moisture-induced subgap trap states. Our study provides insights into the optical and structural response of organic-inorganic perovskite materials upon humidity exposure. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s11671-018-2470-0) contains supplementary material, which is available to authorized users.