卤化物
光致发光
钙钛矿(结构)
纳米晶
材料科学
铯
激子
光电子学
结合能
发光
化学物理
纳米技术
化学
无机化学
结晶学
凝聚态物理
原子物理学
物理
作者
Zhiwei Ma,Zhun Liu,Siyu Lu,Lingrui Wang,Xiaolei Feng,Dongwen Yang,Kai Wang,Guanjun Xiao,Lijun Zhang,Simon A. T. Redfern,Bo Zou
标识
DOI:10.1038/s41467-018-06840-8
摘要
Abstract Metal halide perovskites (MHPs) are of great interest for optoelectronics because of their high quantum efficiency in solar cells and light-emitting devices. However, exploring an effective strategy to further improve their optical activities remains a considerable challenge. Here, we report that nanocrystals (NCs) of the initially nonfluorescent zero-dimensional (0D) cesium lead halide perovskite Cs4PbBr6 exhibit a distinct emission under a high pressure of 3.01 GPa. Subsequently, the emission intensity of Cs4PbBr6 NCs experiences a significant increase upon further compression. Joint experimental and theoretical analyses indicate that such pressure-induced emission (PIE) may be ascribed to the enhanced optical activity and the increased binding energy of self-trapped excitons upon compression. This phenomenon is a result of the large distortion of [PbBr6]4− octahedral motifs resulting from a structural phase transition. Our findings demonstrate that high pressure can be a robust tool to boost the photoluminescence efficiency and provide insights into the relationship between the structure and optical properties of 0D MHPs under extreme conditions.
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