Coordination Geometry-Dependent Multi-Band Emission and Atypically Deep-Trap-Dominated NIR Persistent Luminescence from Chromium-Doped Aluminates

被引:81
作者
Lin, Xiaohui [1 ]
Zhang, Ruili [2 ]
Tian, Xiumei [5 ]
Li, Yang [1 ,4 ,6 ]
Du, Bingsheng [1 ]
Nie, Jianmin [6 ]
Li, Zhenzhang [1 ]
Chen, Li [1 ]
Ren, Jinjun [2 ]
Qiu, Jianrong [3 ]
Hu, Yihua [1 ]
机构
[1] Guangdong Univ Technol, Sch Phys & Optoelect Engn, Guangzhou 510006, Guangdong, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Opt & Fine Mech, Shanghai 201800, Peoples R China
[3] Zhejiang Univ, Coll Opt Sci & Engn, State Key Lab Modern Opt Instrumentat, Hangzhou 310058, Zhejiang, Peoples R China
[4] Univ Massachusetts, Sch Med, Dept Biochem & Mol Pharmacol, Worcester, MA 01605 USA
[5] Guangzhou Med Univ, Sch Basic Med Sci, Dept Biomed Engn, Guangzhou 510182, Guangdong, Peoples R China
[6] South China Univ Technol, Sch Mat Sci & Technol, State Key Lab Luminescent Mat & Devices, Guangzhou 510640, Guangdong, Peoples R China
来源
ADVANCED OPTICAL MATERIALS | 2018年 / 6卷 / 07期
基金
中国国家自然科学基金;
关键词
doping; light emission; luminescence; phosphorescence; structure-property relationships; PHOTO-STIMULATED LUMINESCENCE; LONG-PERSISTENT; PHOSPHORS; NMR; NANOPARTICLES; NANOPROBES; AL-27; GLASS; LA;
D O I
10.1002/adom.201701161
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
An abnormal trap distribution and coordination geometry-dependent multi-band emission are discovered in chromium-doped aluminates. The multi-band and broadband persistent luminescence from 650-1100 nm peaking at 688 and 793 nm from Cr3+-doped SrAl12O19 is systematically studied via structural and spectroscopic analysis. Solid state nuclear magnetic resonance allows the visualization of various coordination configurations in SrAl12O19, thus offering the possibility of tailoring the local geometry of the emission center to trigger the control of the spectral parameter. Deep tissue ex vivo and in vivo imaging in mice both demonstrate that multi-band-emissive SrAl12O19:Cr3+ shows superior, high-quality near-infrared (NIR) bio-imaging in the biological transparency window compared to single band-emissive (with emission only at 688 nm) SrAl2O4:Cr3+, although SrAl2O4:Cr3+ has a higher luminescent intensity and longer duration at 688 nm. Moreover, by measuring the thermoluminescence spectra the driving force of carrier release is discovered to be only from the deep trap (the depth is > 1 eV), which is different from the generally accepted shallow-dependent afterglow-emitting process. These findings pave the way for opening a vista of possible avenues for the enhancement of signal-to-noise ratio, the improvement of imaging quality, as well as the understanding of the trapping and de-trapping process in long-persistent phosphors.
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页数:10
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