Enhanced 1.53 μm emission of Er3+ ions in phosphate glass via energy transfer from Cu+ ions

被引:26
|
作者
Jimenez, Jose A. [1 ]
Sendova, Mariana [2 ]
机构
[1] Univ N Florida, Dept Chem, Jacksonville, FL 32224 USA
[2] New Coll Florida, Opt Spect & Nanomat Lab, Sarasota, FL 34243 USA
关键词
TUNABLE WHITE LUMINESCENCE; PHOTOLUMINESCENCE PROPERTIES; OPTICAL-PROPERTIES; INFRARED-EMISSION; SILICATE-GLASSES; SYSTEM; COPPER; ERBIUM; NANOPARTICLES; FLUORESCENCE;
D O I
10.1063/1.4890716
中图分类号
O59 [应用物理学];
学科分类号
摘要
Optimizing the efficiency of Er3+ emission in the near-infrared telecommunication window in glass matrices is currently a subject of great interest in photonics research. In this work, Cu+ ions are shown to be successfully stabilized at a high concentration in Er-containing phosphate glass by a single-step melt-quench method, and demonstrated to transfer energy to Er3+ thereby enhancing the near-infrared emission about 15 times. The spectroscopic data indicate an energy conversion process where Cu+ ions first absorb photons broadly around 360 nm and subsequently transfer energy from the Stokes-shifted emitting states to resonant Er3+ absorption transitions in the visible. Consequently, the Er3+ electronic excited states decay and the I-4(3/2) metastable state is populated, leading to the enhanced emission at 1.53 mu m. Monovalent copper ions are thus recognized as sensitizers of Er3+ ions, suggesting the potential of Cu+ co-doping for applications in the telecommunications, solar cells, and solid-state lasing realizable under broad band near-ultraviolet optical pumping. (C) 2014 AIP Publishing LLC.
引用
收藏
页数:6
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