Ultrafast relaxation of lattice distortion in two-dimensional perovskites

超快电子衍射 光激发 凝聚态物理 物理 材料科学 超短脉冲 电子衍射 分子物理学 衍射 光学 原子物理学 激发态 激光器
作者
Hao Zhang,Wenbin Li,Joseph Essman,Claudio Quarti,Isaac Metcalf,Wei‐Yi Chiang,Siraj Sidhik,Jin Hou,Austin Fehr,Andrew Attar,Ming‐Fu Lin,Alexander Britz,Xiaozhe Shen,Stephan Link,Xijie Wang,Uwe Bergmann,Mercouri G. Kanatzidis,Claudine Katan,Jacky Even,Jean‐Christophe Blancon
出处
期刊:Nature Physics [Nature Portfolio]
卷期号:19 (4): 545-550 被引量:63
标识
DOI:10.1038/s41567-022-01903-6
摘要

Direct visualization of ultrafast coupling between charge carriers and lattice degrees of freedom in photoexcited semiconductors has remained a long-standing challenge and is critical for understanding the light-induced physical behaviour of materials under extreme non-equilibrium conditions. Here we obtain a direct visualization of the structural dynamics in monocrystalline 2D perovskites. We achieve this by monitoring the evolution of wavevector-resolved ultrafast electron diffraction intensity following above-bandgap high-density photoexcitation. Our analysis reveals a light-induced ultrafast reduction in antiferro-distortion resulting from a strong interaction between the electron–hole plasma and perovskite lattice, which induces an in-plane octahedra rotation towards a more symmetric phase. Correlated ultrafast spectroscopy performed at the same carrier density as ultrafast electron diffraction reveals that the creation of a dense electron–hole plasma triggers the relaxation of lattice distortion at shorter timescales by modulating the crystal cohesive energy. Finally, we show that the interaction between carrier gas and lattice can be altered by tailoring the rigidity of the 2D perovskite by choosing an appropriate organic spacer layer. The ultrafast structural dynamics in 2D perovskites are an important part of their non-equilibrium properties. Now, their visualization reveals a light-induced reduction in the antiferro-distortion initiated by the electron–hole plasma.
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