Affiliation:
1. State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences Changchun 130022 China
2. School of Applied Chemistry and Engineering, University of Science and Technology of China Hefei 230026 China
3. Faculty of Materials Science and Chemistry China University of Geosciences 388 Lumo Road Wuhan 430074 P. R. China
4. Zhejiang Institute China University of Geosciences Hangzhou 311305 P. R. China
Abstract
AbstractMetal halide perovskites (MHPs) have shown great application prospects in the field of optoelectronics owing to their superior optical and optoelectronic properties. Bandgap engineering and impurity doping are effective ways to achieve regulation of luminous properties in the visible light region. However, realizing efficient deep red and wide‐range tunable near‐infrared (NIR) emission remains a challenge. Here, a series of rare earth (RE3+) ions (RE = Nd, Dy, Ho, Er, Tm, Yb) doped Cs4Cd1−xMnxSb2Cl12 (0 ≤ x ≤ 1) quadruple perovskites are designed. An efficient tunable luminescence from red to NIR light is achieved based on the energy transfer (ET) from Mn2+ to RE3+ by building the Mn2+ energy bridge, which covers the NIR‐I (650–900 nm) and NIR‐II (900–1700 nm) regions. Moreover, the ET efficiency is availably influenced by the doping concentration of Mn2+. Interestingly, the energy bridge from Mn2+ to RE3+ is cut off because of the increased bandgap when Bi3+ is introduced into the RE3+‐doped Cs4Cd0.4Mn0.6Sb2−yBiyCl12 (0 ≤ y ≤ 2) lattice. Through bandgap engineering, the ET from Mn2+ to RE3+ resembles an “optical energy shutter” which quenches the NIR emission of RE3+ owing to the mismatched energy level but enhances the emission of Mn2+.
Funder
National Science and Technology Major Project
National Natural Science Foundation of China
Natural Science Foundation of Zhejiang Province
China Postdoctoral Science Foundation
Subject
Atomic and Molecular Physics, and Optics,Electronic, Optical and Magnetic Materials
Cited by
11 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献