利用LHPG技术生长Er:YScO3混合倍半氧化物晶体光纤及其光学特性

IF 3.3 3区 物理与天体物理 Q2 OPTICS
Zhengyuan Jiang , Jian Liu , Longxin Liu , Jun Zhang , Peng Liu , Xiaodong Xu , Jun Xu , Kheirreddine Lebbou
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引用次数: 0

摘要

掺铒YScO3混合倍半氧化物晶体纤维,掺杂浓度为1 at。%, 4 at。%, 7%。%采用激光加热支架生长(LHPG)法生长。研究了Er:YScO3的光谱特性,发现其在983 nm处的吸收截面为2.05 × 10−21 cm2,在7 at处的半峰全宽为20.7 nm。% Er:YScO3晶体纤维。推导出judd - offelt参数(Ω2 = 1.50 × 10−20 cm2, Ω4 = 0.66 × 10−20 cm2, Ω6 = 0.96 × 10−20 cm2),计算出2729 nm处的发射截面为0.53 × 10−20 cm2, FWHM为65.0 nm。分析了不同掺杂浓度下4I11/2和4I13/2的荧光寿命。结果证明了Er:YScO3晶体光纤作为一种有前途的增益介质用于~ 2.7 μm激光应用的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Er:YScO3 mixed sesquioxide crystal fibers grown by the LHPG technique and optical characterization
Erbium-doped YScO3 mixed sesquioxide crystal fibers with doping concentrations of 1 at.%, 4 at.%, and 7 at.% were grown using the laser-heated pedestal growth (LHPG) method. The spectral properties of Er:YScO3 were investigated, revealing an absorption cross-section of 2.05 × 10−21 cm2 at 983 nm with full width at half maximum (FWHM) of 20.7 nm for 7 at.% Er:YScO3 crystal fiber. The Judd-Ofelt parameters (Ω2 = 1.50 × 10−20 cm2, Ω4 = 0.66 × 10−20 cm2, Ω6 = 0.96 × 10−20 cm2) were derived, and the emission cross-section at 2729 nm was calculated to be 0.53 × 10−20 cm2 with FWHM of 65.0 nm. The fluorescence lifetimes of the 4I11/2 and 4I13/2 levels were analyzed across doping concentration. The results demonstrate the potential of Er:YScO3 crystal fibers as a promising gain medium for ∼2.7 μm laser applications.
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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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