Efficient red photoluminescence in holmium-doped Cs2NaInCl6 double perovskite

被引:61
|
作者
Nie, Jingheng [1 ]
Li, Henan [2 ]
Fang, Shaofan [2 ]
Zhou, Bo [2 ]
Liu, Zexiang [1 ]
Chen, Fuming [3 ]
Wang, Ye [4 ]
Shi, Yumeng [2 ]
机构
[1] Shenzhen Univ, Inst Microscale Optoelect, Int Collaborat Lab 2D Mat Optoelect Sci & Technol, Minist Educ, Shenzhen 518060, Peoples R China
[2] Shenzhen Univ, Sch Elect & Informat Engn, Shenzhen 518060, Peoples R China
[3] South China Normal Univ, Guangdong Prov Key Lab Quantum Engn & Quantum Mat, Guangzhou 510006, Peoples R China
[4] Zhengzhou Univ, Sch Phys & Microelect, Key Lab Mat Phys, Minist Educ, Zhengzhou 450052, Peoples R China
来源
CELL REPORTS PHYSICAL SCIENCE | 2022年 / 3卷 / 04期
基金
中国国家自然科学基金;
关键词
WHITE-LIGHT; LUMINESCENCE; EMISSION; DESIGN; BLUE; YB3+;
D O I
10.1016/j.xcrp.2022.100820
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Metal halide perovskites with efficient and stable self-trapped exciton emission have attracted considerable attention for next generation solid-state lighting owing to their ultrabroadband emission. However, it remains challenging to widen the color gamut and realize high color-rendering index due to the lack of highly saturated red color-emitting inorganic lead-free perovskite materials with narrow full width at half-maximum. Here, we report a lanthanide-co doped system (Cs2NaInCl6:Sb3+/Ho3+) that enables efficient blue and red emissions with photoluminescence quantum yields of up to 99% and 72%, respectively. The energy transfer efficiency in Ho3+-doped Cs2NaInCl6:Sb is up to 73%, which can overcome the weak absorption cross-section of the f-f transition of lanthanide ion and improve its luminescence performance. Benefitting from the efficient energy-transfer channel from the self-trapped excitons to Ho3+ , the emission color is continuously tuned from blue to red by controlling the Ho3+-doping concentration.
引用
收藏
页数:12
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