Back to Search Start Over

Peculiar β-Li2TiO3: Eu3+ red light emitting dominated by electric dipole transition: Asymmetric lattice point regulation and luminescence performance.

Authors :
Yu, Cheng-Long
Liu, Guan-Hua
Jin, Dang-Bo
Cheng, Hang
Qi, Yong
Liu, Zi-Hang
Wang, Zhi-Qi
Li, Hai
Gao, Dan-Peng
Wang, Xiu-Feng
Source :
Journal of Alloys & Compounds. Feb2024, Vol. 973, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

In order to obtain red phosphor with high color purity, β-Li 2 TiO 3 : Eu3+ dominated by electric dipole transition was prepared by the hydrothermal method. Eu3+ doping concentration (< 0.5 mol%) and calcination time (> 12 h) can regulate the phase purity, supercell development, asymmetric lattice point configuration and the luminescence performance. Under excitation at 394 nm, β-Li 2 TiO 3 : Eu3+ emits narrow band 618 nm red light due to that Eu3+ replaces Li+ at the relatively active Li1 position, and the 5D 0 → 7F 2 electric dipole transition dominates. Calcined at 600 °C for 36 h with Eu3+ doped concentration of 0.5 mol%, the luminescence performance of β-Li 2 TiO 3 : Eu3+ is superior, of which the lifetime is 0.64 ms, the color coordinates x = 0.63, y = 0.37, the color temperature of 987 K, the color rendering index of 82, and the red color purity of 99.7%. The electric dipole transition line intensity parameters Ω 2 and Ω 4 are 8.01 × 10−20 cm2 and 0.62 × 10−20 cm2, respectively, yielding Ω 2 /Ω 4 of 12.9. The fluorescence branch ratio of 5D 0 → 7F 2 is 82.9%, and the quantum efficiency can reach 92%, which is superior within similar materials. [Display omitted] • Peculiar red-light emitting β-Li 2 TiO 3 : Eu3+ with color purity of 99.7%. • Electric dipole transition can be regulated. • Electric dipole transition of Eu3+ is dominated in β-Li 2 TiO 3. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09258388
Volume :
973
Database :
Academic Search Index
Journal :
Journal of Alloys & Compounds
Publication Type :
Academic Journal
Accession number :
174034863
Full Text :
https://doi.org/10.1016/j.jallcom.2023.172917