Spectral shifting and NIR down-conversion in Bi3+/Yb3+ co-doped Zn2GeO4

被引:45
|
作者
Gao, Guojun [1 ]
Peng, Mingying [2 ,3 ]
Wondraczek, Lothar [1 ,3 ]
机构
[1] Univ Jena, Otto Schott Inst Mat Res, D-07743 Jena, Germany
[2] S China Univ Technol, Sch Mat Sci & Technol, State Key Lab Luminescent Mat & Devices, Guangzhou 510641, Guangdong, Peoples R China
[3] S China Univ Technol, Chinese German Res Ctr Photon Mat & Devices, Guangzhou 510641, Guangdong, Peoples R China
关键词
PHOTOSYNTHETIC ACTIVITY; OPTICAL-PROPERTIES; SOLAR-CELLS; PHOTOLUMINESCENCE; LUMINESCENCE; GLASSES; DOWNCONVERSION;
D O I
10.1039/c4tc01242a
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
We report on spectral modification through NIR down-conversion (DC) photoluminescence (PL) in Yb3+-Bi3+-co-doped Zn2GeO4. Energetic downshifting (DS) of UV-A irradiation occurs via intrinsic luminescence of the high-bandgap semiconductor Zn2GeO4 as well as via active Bi3+ centres. In parallel, both species act as sensitizers for Yb3+, strongly extending its excitation region to similar to 500 nm. In the absence of Bi3+, band-to-band absorption of Zn2GeO4 in the UV region results in PL at similar to 475-625 nm. Doping with Yb3+ initiates energy transfer from trapped defect states to two neighbouring Yb3+ ions in a cooperative DC process, resulting in Yb3+-related photoemission at similar to 1000 nm. The introduction of Bi3+ into Zn2GeO4:Yb3+ greatly extends the absorption band to the visible blue region. Then, energy transfer also occurs through cooperative DC from Bi3+ to Yb3+. As a result, a strong increase in the absolute Yb3+-related PL intensity is observed. This enables ultra-efficient harvesting of UV-A to visible radiation for energy conversion processes.
引用
收藏
页码:8083 / 8088
页数:6
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