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Self-Trapped Exciton Emission in a Zero-Dimensional (TMA)2SbCl5·DMF Single Crystal and Molecular Dynamics Simulation
Qilin Wei1, Tong Chang1, Ruosheng Zeng1
1School of Physical Science and Technology, MOE Key Laboratory of New Processing Technology for Non-ferrous Metals and Materials, Guangxi Key Laboratory of Processing for Non-ferrous Metals and Featured Materials, Guangxi University, Nanning 530004, China.
Abstract:
Lead-free lower-dimensional organic-inorganic metal halide materials have recently triggered intense research because of their excellent photophysical properties and chemical stability. Herein, we report a novel zero-dimensional (0D) organic-inorganic hybrid single crystal (TMA)2SbCl5·DMF (TMA = N(CH3)3, DMF= HCON(CH3)2), which exhibits typical self-trapped exciton (STE) emission with an efficient yellow emission at 630 nm and high photoluminescence quantum yield (PLQY) of 67.2%. The dual STE emission is attributed to the singlet and triplet STEs in inorganic [SbCl5]2-, respectively. Further, an ab initio molecular dynamics simulation was performed to estimate the stability of crystal structure at room temperature. The calculated excited-state structure indicates that the deformation parameter (Δd) of the excited-state structure is larger than that of the ground state, illustrating the origin of a large Stokes shift. These results indicate that these new 0D lead-free organic-inorganic hybrid metal halides are promising luminescent materials for optoelectronic applications.
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