Self-trapped exciton emission in an Sn(II)-doped all-inorganic zero-dimensional zinc halide perovskite variant
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Updated: Oct 21, 2025

Inkjet Printing All Inorganic Halide Perovskite Inks for Photovoltaic Applications
Published on: January 22, 2019
Xiaoyu Wang1, Qibin Shen1, Yansong Chen1
1Zhejiang Province Key Laboratory of Quantum Technology and Devices, Department of Physics, and State Key Laboratory of Silicon Materials, Zhejiang University, Hangzhou, 310027, PR China. hzwu@zju.edu.cn.
Abstract:
The toxicity of Pb in conventional perovskites impedes the commercialization of their optoelectronic devices. Therefore, the search for comparable Pb-free perovskites is vital and needs urgent attention. Herein, for the first time, we successfully synthesize the Sn(II)-doped Pb-free zinc-based perovskite variant Cs2ZnCl4. The influence of doping is investigated both experimentally and theoretically. Broad bright red emission with a large Stokes shift is observed and attributed to the self-trapped exciton (STE) emission of the doped disphenoidal [SnCl4]2- units in the host matrix, from 3P1 to 1S0. Temperature-dependent photoluminescence (PL) shows a peak split at cryogenic temperature, which is ascribed to the Jahn-Teller effect of the 3P1 state. Theoretical study reveals that the impurity states of Sn2+ shrink the bandgap and localize the band edges, and distortion of [SnCl4]2- under excitation ultimately leads to the STE emission. This work is significant for STE emission studies and will pave a way for Pb-free perovskite variants in illumination applications.
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