光激发
微秒
化学
纳秒
钙钛矿(结构)
化学物理
衍射
载流子
相变
通量
超快激光光谱学
激光器
超短脉冲
纳米颗粒
光电子学
结晶学
材料科学
光学
纳米技术
凝聚态物理
离子
原子物理学
物理
激发态
有机化学
作者
Yingqi Wang,Cunming Liu,Yang Ren,Xiaobing Zuo,Sophie E. Canton,Kaibo Zheng,Kuangda Lu,Xujie Lü,Wenge Yang,Xiaoyi Zhang
摘要
Metal halide perovskites have emerged as promising materials for optoelectronic applications in the last decade. A large amount of effort has been made to investigate the interplay between the crystalline lattice and photoexcited charge carriers as it is vital to their optoelectronic performance. Among them, ultrafast laser spectroscopy has been intensively utilized to explore the charge carrier dynamics of perovskites, from which the local structural information can only be extracted indirectly. Here, we have applied a time-resolved X-ray diffraction technique to investigate the structural dynamics of prototypical two-dimensional lead-free halide perovskite Cs3Bi2Br9 nanoparticles across temporal scales from 80 ps to microseconds. We observed a quick recoverable (a few ns) photoinduced microstrain up to 0.15% and a long existing lattice expansion (∼a few hundred nanoseconds) at mild laser fluence. Once the laser flux exceeds 1.4 mJ/cm2, the microstrain saturates and the crystalline phase partially transfers into a disordered phase. This photoinduced transient structural change can recover within the nanosecond time scale. These results indicate that photoexcitation of charge carriers couples with lattice distortion, which fundamentally affects the dielectric environment and charge carrier transport.
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