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Dual-Band-Tunable White-Light Emission from Bi3+ /Te4+ Emitters in Perovskite-Derivative Cs2 SnCl6 Microcrystals
Wei Zhang1,2, Wei Zheng1,3, Lingyun Li2
1CAS Key Laboratory of Design and Assembly of Functional Nanostructures, Fujian Key Laboratory of Nanomaterials, State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian, 350002, China.
Abstract:
Luminescent metal halides have attracted considerable attention in next-generation solid-state lighting because of their superior optical properties and easy solution processibility. Herein, we report a new class of highly efficient and dual-band-tunable white-light emitters based on Bi3+ /Te4+ co-doped perovskite derivative Cs2 SnCl6 microcrystals. Owing to the strong electron-phonon coupling and efficient energy transfer from Bi3+ to Te4+ , the microcrystals exhibited broad dual-band white-light emission originating from the inter-configurational 3 P0,1 →1 S0 transitions of Bi3+ and Te4+ , with good stability and a high photoluminescence (PL) quantum yield of up to 68.3 %. Specifically, a remarkable transition in Bi3+ -PL lifetime from milliseconds at 10 K to microseconds at 300 K was observed, as solid evidence for the isolated Bi3+ emission. These findings provide not only new insights into the excited-state dynamics of Bi3+ and Te4+ in Cs2 SnCl6 , but also a general approach to achieve single-composition white-light emitters based on lead-free metal halides through ns2 -metal ion co-doping.

