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:53
标识
DOI:10.1002/anie.202301573
摘要
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 (C6 H5 CH2 CH2 NH3 + )4 AgBiBr8 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.
科研通智能强力驱动
Strongly Powered by AbleSci AI