Light-Induced Structural Dynamics and Charge Transport in Layered Halide Perovskite Thin Films

被引:7
|
作者
Tsai, Hsinhan [2 ]
Ghosh, Dibyajyoti [3 ,4 ,5 ]
Kinigstein, Eli [6 ]
Dryzhakov, Bogdan [7 ]
Driscoll, Honora [1 ]
Owczarek, Magdalena [1 ]
Hu, Bin [7 ]
Zhang, Xiaoyi [6 ]
Tretiak, Sergei [1 ]
Nie, Wanyi [1 ]
机构
[1] Los Alamos Natl Lab, Ctr Integrated Nanotechnol, Los Alamos, NM 87545 USA
[2] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[3] Los Alamos Natl Lab, Theoret Div, Los Alamos, NM 87545 USA
[4] Indian Inst Technol Delhi, Dept Mat Sci & Engn, New Delhi 110016, India
[5] Indian Inst Delhi, Dept Chem, New Delhi 110016, India
[6] Argonne Natl Lab, Xray Sci Div, Lemont, IL 60439 USA
[7] Univ Tennessee, Dept Mat Sci & Engn, Knoxville, TN 37996 USA
关键词
structural dynamics; 2D perovskites; charge transport; thin film; SOLID-STATE NMR; HYBRID PEROVSKITES; CATION DYNAMICS; CONDUCTIVITY; CH3NH3PBI3; MOBILITY; CARRIERS; RAMAN;
D O I
10.1021/acs.nanolett.2c03403
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The dynamic nature of the metal halide perovskite lattice upon photoexcitation plays a vital role in their properties. Here we report an observation of light-induced structure dynamics in quasi-2D Ruddlesden-Popper phase perovskite thin films and its impact on the carrier transport properties. By a time-resolved X-ray scattering technique, we observe a rapid lattice expansion upon photoexcitation, followed by a slow relaxation over the course of 100 ns in the dark. Theoretical modeling suggests that the expansion originates from the lattice's thermal fluctuations caused by photon energy deposition. Power dependent optical spectroscopy and photoconductivity indicate that high laser powers triggered a strong local structural disorder, which increased the charge dissociation activation energy that results in localized transport. Our study investigates the impact of laser energy deposition on the lattices and the subsequent carrier transport properties, that are relevant to device operations.
引用
收藏
页码:429 / 436
页数:8
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