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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.
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页码:5183 / 5191
页数:9
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