Issue 12, 2024

Temperature-dependent self-trapped models regulating energy transfer in rare earth double perovskites via 5s2 electron doping

Abstract

Due to their environmental friendliness, structural plasticity, and tunable emission, lead-free halide double perovskites offer a broad spectrum of applications in light-emitting diode (LED), photodetectors, infrared imaging, and temperature sensing. Herein, we synthesized rare earth-based Cs2NaYCl6 double perovskites using a solvothermal method, and Sb3+/Sm3+ co-doping can effectively modulate the luminescence by adjusting the band gap structure and channels of energy transfer. With the Sm3+-feeding concentration increasing, the emission could be adjusted from blue to white, attributed to an effective energy transfer from the self-trapped state to Sm3+. Temperature-dependent photoluminescence spectra indicate that the double self-trapped exciton emission at low temperatures originated from two minima in the excited state of 3P1. The relative sensitivity of the optical temperature sensor reached 1.08% K−1, which was better than that of other rare earth perovskites. The LED device based on Sb3+/Sm3+ co-doped Cs2NaYCl6@polymethylmethacrylate displays a chromaticity coordinate of (0.29, 0.28), a color rendering index of 87, and the correlated color temperature of 10 986 K. Our work explores an in-depth understanding of energy transfer in double self-trapped states and provides new material for advanced applications.

Graphical abstract: Temperature-dependent self-trapped models regulating energy transfer in rare earth double perovskites via 5s2 electron doping

Supplementary files

Article information

Article type
Research Article
Submitted
13 Mar 2024
Accepted
06 May 2024
First published
08 May 2024

Inorg. Chem. Front., 2024,11, 3607-3617

Temperature-dependent self-trapped models regulating energy transfer in rare earth double perovskites via 5s2 electron doping

C. Tan, S. Zhang, H. Wang, J. Yao, H. Liu, B. Zou and R. Zeng, Inorg. Chem. Front., 2024, 11, 3607 DOI: 10.1039/D4QI00649F

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