Incorporating rare-Earth terbium(III) ions into :Bi nanocrystals toward tunable photoluminescence
- 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, Shenzhen University, Shenzhen, 518060 (China)
- 3. Department of Physics, Far Eastern State Transport University, Khabarovsk, 680021 (Russian Federation)
- 4. Department of Engineering Physics and Radioelectronics, Siberian Federal University, Krasnoyarsk, 660041 (Russian Federation)
- 5. Laboratory of Crystal Physics, Federal Research Center KSC SB RASs, Kirensky Institute of Physics, Krasnoyarsk, 660036 (Russian Federation)
- 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)
Description
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 NCs to impart and tune the optical performances in the visible light region. ions were incorporated into NCs and occupied sites as verified by both crystallographic analyses and first-principles calculations. Trace amounts of Bi doping endowed the characteristic emission () of ions with a new excitation peak at 368 nm rather than the single characteristic excitation at 290 nm of . By controlling ions concentration, the emission colors of Bi-doped /(Cs_2 Ag(In_{1-x}Tb_x)Cl_6/) NCs could be continuously tuned from green to orange, through the efficient energy-transfer channel from self-trapped excitons to 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 and Co. KGaA, Weinheim)
Additional details
Identifiers
Publishing Information
- Journal Title
- Angewandte Chemie (International Edition)
- Journal Volume
- 59
- Journal Issue
- 28
- Journal Page Range
- p. 11634-11640
- ISSN
- 1433-7851
- CODEN
- ACIEF5
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 51102011
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- BISMUTH ADDITIONS; CESIUM CHLORIDES; CONCENTRATION RATIO; DOPED MATERIALS; EMISSION SPECTRA; ENERGY TRANSFER; EXCITONS; INDIUM CHLORIDES; NANOCRYSTALS; PEROVSKITE; PHOTOLUMINESCENCE; SILVER CHLORIDES; TERBIUM IONS; TRACE AMOUNTS; TRANSMISSION ELECTRON MICROSCOPY; TUNING; VISIBLE SPECTRA; X-RAY DIFFRACTION; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- ALKALI METAL COMPOUNDS; ALLOYS; BISMUTH ALLOYS; CESIUM COMPOUNDS; CESIUM HALIDES; CHARGED PARTICLES; CHLORIDES; CHLORINE COMPOUNDS; COHERENT SCATTERING; CRYSTALS; DIFFRACTION; DIMENSIONLESS NUMBERS; ELECTRON MICROSCOPY; ELECTRON SPECTROSCOPY; EMISSION; HALIDES; HALOGEN COMPOUNDS; INDIUM COMPOUNDS; INDIUM HALIDES; IONS; LUMINESCENCE; MATERIALS; MICROSCOPY; MINERALS; NANOSTRUCTURES; OXIDE MINERALS; PEROVSKITES; PHOTOELECTRON SPECTROSCOPY; PHOTON EMISSION; QUASI PARTICLES; SCATTERING; SILVER COMPOUNDS; SILVER HALIDES; SPECTRA; SPECTROSCOPY; TRANSITION ELEMENT COMPOUNDS