Simultaneous phase and size manipulation in NaYF4: Er3+/Yb3+ upconverting nanoparticles for a non-invasion optical thermometer

被引:64
作者
Du, Peng [1 ]
Deng, An Meng [2 ]
Luo, Laihui [2 ]
Yu, Jae Su [1 ]
机构
[1] Kyung Hee Univ, Dept Elect Engn, Yangin Si 17104, Gyeonggi Do, South Korea
[2] Ningbo Univ, Dept Microelect Sci & Engn, Ningbo 315211, Zhejiang, Peoples R China
基金
新加坡国家研究基金会;
关键词
UP-CONVERSION LUMINESCENCE; TEMPERATURE SENSING BEHAVIOR; GLASS-CERAMICS; EMISSION; ER3+; YB3+; SENSITIVITY; NANOCRYSTALS; INTENSITIES; MECHANISM;
D O I
10.1039/c7nj03165c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of Er3+/Yb3+-codoped NaYF4 upconverting nanoparticles were synthesized via a hydrothermal method. By controlling the synthetic temperature, the phase transition and size manipulation of nanoparticles were simultaneously realized in the studied compounds. Upon the irradiation of near-infrared light, the prepared nanoparticles revealed dazzling visible emissions arising from the intra-4f transitions of Er3+ ions. Moreover, the pump power-dependent upconversion (UC) emission spectra were recorded to analyze the involved UC mechanism. Furthermore, the temperature sensing behaviors of the resultant compounds were investigated by analyzing the temperature- dependent green emission intensities from the thermally coupled levels of H-2(11/2) and S-4(3/2). It is found that the sensor sensitivity of the synthesized samples is dependent on the synthetic temperature which is further confirmed by the Judd-Ofelt theory. Additionally, the sensor sensitivity of the prepared nanoparticles is also found to be dependent on the laser pump power. The Er3+/Yb3+-codoped NaYF4 upconverting nanoparticles sintered at 160 degrees C exhibited the optimum thermometric properties with a maximum sensor sensitivity of 0044 K-1 at 637 K when the excitation pump power was 139 mW. The adjustment of the synthetic temperature and excitation pump power is a promising channel to manipulate the sensor sensitivity of the Er3+/Yb3+-codoped NaYF4 upconverting nanoparticles.
引用
收藏
页码:13855 / 13861
页数:7
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