Effective enhancement of the yellow emission of Dy3+: Na5Lu9F32 fluoride single crystal by co-doping with Tb3+ ions

IF 3.3 3区 物理与天体物理 Q2 OPTICS
Enbo Zhao , Haiping Xia , Lizhi Fang , Xiong Zhou , Hongwei Song , Baojiu Chen
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引用次数: 0

Abstract

Bulk Na5Lu9F32 (NLF) single crystals doped with 0.5 mol% Dy3+ and χ Tb3+ (χ = 0, 0.5, 1.0, 2.0, and 3.0 mol%, respectively) ions were synthesized successfully via Bridgman method. The Dy3+/Tb3+ co-doped Na5Lu9F32 crystal structure was investigated by using X-ray diffraction (XRD) and Rietveld refinements, confirming that the Lu3+ sites in the crystal were successfully substituted by Dy3+ and Tb3+ ions. The fluorescence spectra of the doped NLF single crystals were investigated under excitation with 453 nm light. It was found that the intensity of the 573 nm yellow emission can be increased to about 132 % through co-doping of 1mol% Tb3+ ion. The energy transfer efficiency (ETE) from Dy3+ to Tb3+ was calculated, which effectively reduces the lifetime of Dy3+: 6H13/2 energy level. The depopulation of energy level by energy transfer from 6H13/2 of Dy3+ to 7F4 of Tb3+ ions mainly accounts for the enhancement of the yellow emission. The results suggest that the Dy3+/Tb3+ co-doped NLF single crystal is a prospective candidate for yellow solid-state laser material in related optical device.
与Tb3+离子共掺杂可有效增强Dy3+: Na5Lu9F32氟化单晶的黄色发光
采用Bridgman法成功合成了掺杂0.5 mol% Dy3+和χ Tb3+ (χ分别为0、0.5、1.0、2.0和3.0 mol%)离子的Na5Lu9F32 (NLF)块状单晶。采用x射线衍射(XRD)和Rietveld细化技术研究了Dy3+/Tb3+共掺杂Na5Lu9F32的晶体结构,证实了晶体中的Lu3+位点被Dy3+和Tb3+离子成功取代。研究了掺杂NLF单晶在453nm光激发下的荧光光谱。结果表明,共掺杂1mol%的Tb3+离子可将573 nm的黄色发射强度提高到132%左右。计算了Dy3+到Tb3+的能量传递效率(ETE),有效降低了Dy3+: 6H13/2能级的寿命。从Dy3+的6H13/2离子到Tb3+的7F4离子的能量转移导致能级下降是导致黄色发射增强的主要原因。结果表明,Dy3+/Tb3+共掺杂NLF单晶是相关光学器件中黄色固体激光材料的理想候选材料。
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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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