Enhanced tunable color emission in transparent Ag/Mn2+ codoped zinc borate glasses for broad band light source

被引:49
作者
Liu, X. Y. [1 ,2 ]
Guo, H. [3 ]
Ye, S. [1 ,2 ]
Peng, M. Y. [1 ,2 ]
Zhang, Q. Y. [1 ,2 ]
机构
[1] S China Univ Technol, State Key Lab Luminescent Mat & Devices, Guangzhou 510641, Guangdong, Peoples R China
[2] S China Univ Technol, Inst Opt Commun Mat, Guangzhou 510641, Guangdong, Peoples R China
[3] Zhejiang Normal Univ, Dept Phys, Jinhua 321004, Zhejiang, Peoples R China
关键词
ENERGY-TRANSFER; WHITE-LIGHT; AG NANOCLUSTERS; RED PHOTOLUMINESCENCE; SILVER NANOPARTICLES; OXYFLUORIDE GLASSES; ML-AG; LUMINESCENCE; NANOCRYSTALS; HOST;
D O I
10.1039/c5tc00641d
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Zinc borate oxyfluoride glasses containing silver ions (Ag+), Ag nanoclusters and manganese ions (Mn2+) have been successfully prepared using the melt-quenching method. Their structure and luminescent properties were evaluated using transmission electron microscopy (TEM), absorption measurements, steady and time-resolved photoluminescence spectra and fluorescence lifetime measurements. Benefitting from the unique excitation/emission characteristics of Ag nanoclusters in the matrix, the Ag singly doped glass exhibited intriguing wavelength dependent, broad band luminescent performance. After Mn2+ ions were built into the singly doped sample, the emission band was extended to white emission and the intensity was enhanced 13 times with a maximal quantum yield of 24.9%. It was demonstrated experimentally that dual-mode energy transfer does occur from isolated Ag+ and (or) Ag nanoclusters to Mn2+. At the same time, the addition of Mn2+ substantially promotes the formation of Ag nanoclusters. Direct spectroscopic evidence as well as the assumed mechanism have been presented for these processes. This research may help to devise a new perspective for the use of noble metal nanoclusters and transition metals in designing broad band tunable light source.
引用
收藏
页码:5183 / 5191
页数:9
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