Structure and color-tunable luminescence properties of Sm3+ singly- and Dy3+/Sm3+ co-doped CaLaGa3O7 phosphors

IF 3.3 3区 物理与天体物理 Q2 OPTICS
Fei Pan , Yunyun Liu , Chaoyang Tu
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引用次数: 0

Abstract

Sm3+ singly- and Dy3+/Sm3+ co-doped CaLaGa3O7 phosphors were synthesized successfully by a traditional high-temperature solid-state reaction method. Their structure was determined by X-ray diffraction (XRD) measurements, confirming the tetragonal phase of the samples with space group P 4 21m. For Sm3+: CaLaGa3O7 samples, the excitation spectra show that the phosphors could be excited by 403 nm light. The strongest emission peak is at 598 nm, which is assigned to the transition from Sm3+: 4G5/2 level to 6H7/2 state. The CIE color coordinate with optimal Sm3+ doping concentration was calculated to be (0.5882, 0.4110), which is located in the orange-red area. For Dy3+/Sm3+: CaLaGa3O7 phosphors, the excitation spectra show that the obtained samples could be effective pumped by 348 nm or 403 nm. Regardless of the excitation wavelength, the emission spectrum contains the characteristic emission peaks of Dy3+ and Sm3+. The relative emission intensity of Dy3+ and Sm3+ could be adjusted by modifying the concentration of Sm3+ and the exciting wavelength, indicating that the luminescence color is tunable for Dy3+/Sm3+ co-doped samples. The luminescence performance and fluorescence lifetime jointly prove that mutual energy transfers between Dy3+ and Sm3+ take place in the Dy3+/Sm3+: CaLaGa3O7 phosphors. The CIE color coordinates and correlated color temperature were calculated for varying rare-earth concentration as well as excitation wavelength to ascertain their potential applications in light emission devices.
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来源期刊
Journal of Luminescence
Journal of Luminescence 物理-光学
CiteScore
6.70
自引率
13.90%
发文量
850
审稿时长
3.8 months
期刊介绍: The purpose of the Journal of Luminescence is to provide a means of communication between scientists in different disciplines who share a common interest in the electronic excited states of molecular, ionic and covalent systems, whether crystalline, amorphous, or liquid. We invite original papers and reviews on such subjects as: exciton and polariton dynamics, dynamics of localized excited states, energy and charge transport in ordered and disordered systems, radiative and non-radiative recombination, relaxation processes, vibronic interactions in electronic excited states, photochemistry in condensed systems, excited state resonance, double resonance, spin dynamics, selective excitation spectroscopy, hole burning, coherent processes in excited states, (e.g. coherent optical transients, photon echoes, transient gratings), multiphoton processes, optical bistability, photochromism, and new techniques for the study of excited states. This list is not intended to be exhaustive. Papers in the traditional areas of optical spectroscopy (absorption, MCD, luminescence, Raman scattering) are welcome. Papers on applications (phosphors, scintillators, electro- and cathodo-luminescence, radiography, bioimaging, solar energy, energy conversion, etc.) are also welcome if they present results of scientific, rather than only technological interest. However, papers containing purely theoretical results, not related to phenomena in the excited states, as well as papers using luminescence spectroscopy to perform routine analytical chemistry or biochemistry procedures, are outside the scope of the journal. Some exceptions will be possible at the discretion of the editors.
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