Pure red visible emission via three-photon excitation of colloidal Na3ZrF7:Er nanoparticles using a telecom-band laser

被引:10
作者
Ye, Shuai [1 ,2 ]
Wang, Guangsheng [1 ]
Xiong, Maozhen [1 ]
Song, Jun [1 ]
Qu, Junle [1 ]
Xie, Weixin [2 ]
机构
[1] Shenzhen Univ, Coll Optoelect Engn, Minist Educ Guangdong Prov, Key Lab Optoelect Devices & Syst, Shenzhen 518060, Peoples R China
[2] Shenzhen Univ, Coll Informat Engn, Shenzhen 518060, Peoples R China
基金
中国国家自然科学基金;
关键词
UP-CONVERSION EMISSION; NANOCRYSTALS; LUMINESCENCE; MICROSCOPY;
D O I
10.3788/COL201715.011601
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We provide the first demonstration of pure red emission in the visible light region via three-photon excitation in monodisperse Na3ZrF7:Er nanoparticles (NPs) by using a laser operating in the telecommunication band. NPs of similar to 22 nm in diameter are synthesized at 260 degrees C by the thermal decomposition method. The experimental results reveal that the Na3ZrF7: Er NPs exhibit pure red emission in the visible region under 1480 nm laser excitation, and the emission intensity is significantly influenced by the Er3+ ion concentration. The decay times of the S-4(3/2) -> F-4(15/2) and F-4(9/2) -> F-4(15/2) transitions of the Er3+ ions at 540 and 655 nm, respectively, are reduced by increasing the Er3+ ion concentration in the Na3ZrF7: Er NPs. The suppressed emission intensity result from the defect-related quenching effect: when trivalent Er3+ ions replac tetravalent Zr4+ ions, extra Na+ ions and F- vacancies are formed to re-balance the charge in the Na3ZrF7 matrix. The emission color of the Na3ZrF7: Er NPs is related to the cross relaxation between Er3+ ions. These results provide an important step toward more effective biological imaging and photodynamic therapy by minimizing the scattering of the excitation light and increasing the penetration depth.
引用
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页数:4
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