论文标题
杂化铅卤化物钙钛矿中动态极化应变场的可视化
Visualization of Dynamic Polaronic Strain Fields in Hybrid Lead Halide Perovskites
论文作者
论文摘要
涉及动态纳米级畸变的激发定位是光催化,量子材料和分子光电子的核心方面。这种扭曲的实验表征需要对实时形成类似点的局部结构重排的技术敏感。在这里,我们通过飞秒分辨率扩散X射线散射测量值可视化卤化物钙钛矿的原型成员中的激发诱导的应变场。这可以使局部延伸的结构的动量分辨的音子光谱法揭示了与光激发perovskites中极性子的形成和松弛相关的径向扩展的纳米尺度弹性应变场。获得了这种二极管失真的大小和形状的定量估计,从而直接洞悉了这些材料中争论的动态结构扭曲。光泵探针反射光谱验证证实了这些结果,并显示了这些巨大的二极管扭曲如何瞬时修改载体有效质量,从而提供了耦合的结构和电子动力学的统一图片,这些结构和电子动力学基于Hybrid Perovskites的独特光电子功能。
Excitation localization involving dynamic nanoscale distortions is a central aspect of photocatalysis, quantum materials and molecular optoelectronics. Experimental characterization of such distortions requires techniques sensitive to the formation of point-defect-like local structural rearrangements in real time. Here, we visualize excitation-induced strain fields in a prototypical member of the lead halide perovskites via femtosecond resolution diffuse x-ray scattering measurements. This enables momentum-resolved phonon spectroscopy of the locally-distorted structure and reveals radially-expanding nanometer-scale elastic strain fields associated with the formation and relaxation of polarons in photoexcited perovskites. Quantitative estimates of the magnitude and the shape of this polaronic distortion are obtained, providing direct insights into the debated dynamic structural distortions in these materials. Optical pump-probe reflection spectroscopy corroborates these results and shows how these large polaronic distortions transiently modify the carrier effective mass, providing a unified picture of the coupled structural and electronic dynamics that underlie the unique optoelectronic functionality of the hybrid perovskites.