激发态
激子
化学
化学物理
格子(音乐)
铋
钙钛矿(结构)
俘获
材料科学
基态
凝聚态物理
分子物理学
原子物理学
物理
结晶学
生物
声学
生态学
冶金
作者
Long Zhang,Shuoxue Li,Huaiyang Sun,Qiwen Jiang,Yue Wang,Yuanyuan Fang,Ying Shi,Defang Duan,Kai Wang,Hong Jiang,Laizhi Sui,Guorong Wu,Kaijun Yuan,Bo Zou
出处
期刊:Angewandte Chemie
[Wiley]
日期:2023-02-04
卷期号:62 (14): e202301573-e202301573
被引量:57
标识
DOI:10.1002/anie.202301573
摘要
Abstract Pressure‐induced emission (PIE) associated with self‐trapping excitons (STEs) in low‐dimensional halide perovskites has attracted great attention for better materials‐by‐design. Here, using 2D layered double perovskite (C 6 H 5 CH 2 CH 2 NH 3 + ) 4 AgBiBr 8 as a model system, we advance a fundamental physicochemical mechanism of the PIE from the perspective of carrier dynamics and excited‐state behaviors of local lattice distortion. We observed a pressure‐driven STE transformation from dark to bright states, corresponding a strong broadband Stokes‐shifted emission. Further theoretical analysis demonstrated that the suppressed lattice distortion and enhanced electronic dimensionality in the excited‐state play an important role in the formation of stabilized bright STEs, which could manipulate the self‐trapping energy and lattice deformation energy to form an energy barrier between the potential energy curves of ground‐ and excited‐state, and enhance the electron‐hole orbital overlap, respectively.
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