Boosting multi-center luminescence in Cs7Cd3Br13via synergistic defect passivation and sensitization of Cu(I)
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Updated: May 12, 2026

Low-energy Cathodoluminescence for (Oxy)Nitride Phosphors
Published on: November 15, 2016
Jianjie Zhang1, XinPeng Dai1, Baocheng Luo1
1Guangxi Key Laboratory of Advanced Rare Earth Materials, Guangxi Key Laboratory of Processing for Non-Ferrous Metals and Featured Materials, School of Resources, Environment and Materials, Guangxi University, Nanning, 530004, P.R. China. suliumei2020@gxu.edu.cn.
Abstract:
Driven by the demand for efficient and tunable lead-free optoelectronic materials, low-dimensional metal halides featuring multi-coordination structures have attracted widespread attention. Herein, a series of Cu+-doped Cs7Cd3Br13 phosphors featuring a unique mixed 0D/1D crystal structure were successfully synthesized. We demonstrate that the Cu+ dopant not only effectively passivates intrinsic defects to suppress non-radiative recombination, but also acts as an efficient sensitizer. It substantially promotes energy transfer from the 0D [CdBr4]2- sublattice to the 1D [CdBr6]4- self-trapped exciton (STE) states. Consequently, the phosphors exhibit distinct excitation-dependent photoluminescence: an ultrabroadband emission covering the entire visible spectrum under 320 nm excitation, a robust orange emission at 375 nm excitation, and a temperature-dependent multi-band emission under 282 nm excitation driven by Jahn-Teller distortion. Benefiting from the highly efficient single-component broadband emission and emission tunability, Cu+-doped Cs7Cd3Br13 reveals tremendous potential for applications in solid-state white lighting and advanced anti-counterfeiting.

