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首页> 外文期刊>Optical Materials >Gold nanoparticles assisted structural and spectroscopic modification in Er~(3+)-doped zinc sodium tellurite glass
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Gold nanoparticles assisted structural and spectroscopic modification in Er~(3+)-doped zinc sodium tellurite glass

机译:金纳米粒子辅助掺Er〜(3+)锌钠碲酸盐玻璃的结构和光谱修饰

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摘要

Achieving enhanced spectroscopic properties of rare earth doped inorganic glasses by embedding metallic nanoparticles of controlled sizes is a challenging task. We report the gold (Au) NPs assisted modifications in structural and spectroscopic properties of melt-quench synthesized Er~(3+) doped zinc sodium tellurite glass. The growth of NPs is stimulated via time varying heat treatment at 300 ℃. XRD patterns confirm the amorphous nature of glasses and TEM images manifest the growth of gold NPs with sizes between 6.1 and 10.7 nm. The heat treatment time dependent variations in physical properties are ascribed to the alteration in bonding of non-bridging oxygen ions. The UV-VIS-NIR spectra reveal six absorption peaks centered at 488, 523, 655, 800, 973 and 1533 nm corresponding to the transition from ground state of ~4I_(15/2) to ~4F_(7/2), ~2H_(11/2), ~4F_(9/2), ~4I_(9/2), ~4I_(11/2),. and ~4I_(13/2) excited states of Er~(3+) ions, respectively. Surface plasmon resonance (SPR) bands are observed in the range of 618-632 nm. Judd-Ofelt analyses demonstrate a significant increase of spectroscopic quality factors (0.86-1.05) and branching ratio (0.62-92.38%). The up-conversion emission spectra of Er~(3+) exhibit three prominent peaks of reasonable green (502 nm), a moderate green (546 nm) and a strong red (629 nm). An enhancement in the red band luminescence intensity by a factor of 8.19 and 8.54 times are achieved for 2 and 4 h of heat treatments, respectively. This enhancement is attributed to the SPR effects of gold NPs producing an intense local field in the proximity of Er~(3+) ions and subsequent energy transfer between RE ions and NPs. The FTIR spectra display the presence of vibrational modes for ZnO_4 bonds, Te-O bond in TeO_3 (tp) and TeO_4 (tbp) units and the hydroxyl groups. Excellent features of the results suggest that our method constitute a basis for tunable growth of gold NPs which is exceedingly useful for the optimization of optical and structural properties.
机译:通过嵌入大小受控的金属纳米粒子来实现稀土掺杂无机玻璃的增强光谱性能是一项艰巨的任务。我们报道了金(Au)NPs辅助熔融淬火合成的Er〜(3+)掺杂锌钠碲酸盐玻璃的结构和光谱性质的修饰。 NPs的生长是通过在300℃时变热处理来刺激的。 XRD图谱证实了玻璃的无定形性质,TEM图像显示了金纳米颗粒的生长,其尺寸在6.1至10.7nm之间。取决于热处理时间的物理性质的变化归因于非桥接氧离子键的改变。 UV-VIS-NIR光谱显示了六个吸收峰,分别位于488、523、655、800、973和1533 nm,对应于从〜4I_(15/2)到〜4F_(7/2),〜 2H_(11/2),〜4F_(9/2),〜4I_(9/2),〜4I_(11/2)等。和〜4I_(13/2)激发态的Er〜(3+)离子。在618-632 nm范围内观察到表面等离振子共振(SPR)带。 Judd-Ofelt分析表明,光谱质量因子(0.86-1.05)和分支比(0.62-92.38%)显着增加。 Er〜(3+)的上转换发射光谱显示出三个突出的峰,分别是合理的绿色(502 nm),中等的绿色(546 nm)和强红色(629 nm)。对于2小时和4小时的热处理,红波段发光强度分别提高了8.19倍和8.54倍。这种增强归因于金NP的SPR效应,在Er〜(3+)离子附近产生了强烈的局部电场,并随后在RE离子和NP之间进行了能量转移。 FTIR光谱显示了ZnO_4键,TeO_3(tp)和TeO_4(tbp)单元中的Te-O键以及羟基的振动模式的存在。结果的出色特征表明,我们的方法构成了金纳米颗粒可调谐生长的基础,这对于优化光学和结构性能极为有用。

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