Incorporating Rare-Earth Terbium(III) Ions into Cs2AgInCl6:Bi Nanocrystals toward Tunable Photoluminescence

被引:0
|
作者
Liu, Ying [1 ]
Rong, Ximing [2 ]
Li, Mingze [1 ]
Molokeev, Maxim S. [3 ,4 ,5 ]
Zhao, Jing [1 ]
Xia, Zhiguo [1 ,6 ]
机构
[1] The Beijing Municipal Key Laboratory of New Energy Materials and Technologies, School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing,100083, China
[2] Shenzhen Key Laboratory of Special Functional Materials, Shenzhen Engineering Laboratory for Advanced Technology of Ceramics, Guangdong Research Center for Interfacial Engineering of Functional Materials, College of Materials Science and Engineering, Shenz
[3] Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RASs, Krasnoyarsk,660036, Russia
[4] Federal University, Krasnoyarsk,660041, Russia
[5] Department of Physics, Far Eastern State Transport University, Khabarovsk,680021, Russia
[6] The State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, School of Materials Science and Technology, South China University of Technology, Guangzhou,510641, China
基金
中国国家自然科学基金; 俄罗斯基础研究基金会;
关键词
Calculations - Chlorine compounds - Energy transfer - Excitons - Indium compounds - Light - Metal ions - Nanocrystals - Optical properties - Photoluminescence - Rare earths - Silver compounds - Stability - Terbium compounds - Trapped ions;
D O I
10.1002/ANGE.202004562
中图分类号
学科分类号
摘要
The incorporation of impurity ions or doping is a promising method for controlling the electronic and optical properties and the structural stability of halide perovskite nanocrystals (NCs). Herein, we establish relationships between rare-earth ions doping and intrinsic emission of lead-free double perovskite Cs2AgInCl6 NCs to impart and tune the optical performances in the visible light region. Tb3+ ions were incorporated into Cs2AgInCl6 NCs and occupied In3+ sites as verified by both crystallographic analyses and first-principles calculations. Trace amounts of Bi doping endowed the characteristic emission (5D4→7F6-3) of Tb3+ ions with a new excitation peak at 368 nm rather than the single characteristic excitation at 290 nm of Tb3+. By controlling Tb3+ ions concentration, the emission colors of Bi-doped Cs2Ag-(In1−xTbx)Cl6 NCs could be continuously tuned from green to orange, through the efficient energy-transfer channel from self-trapped excitons to Tb3+ ions. Our study provides the salient features of the material design of lead-free perovskite NCs and to expand their luminescence applications. © 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
引用
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页码:11731 / 11737
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