Afterglow Luminescence in Wet-Chemically Synthesized Inorganic Materials: Ultra-Long Room Temperature Phosphorescence Instead of Persistent Luminescence

被引:20
作者
Sontakke, Atul D. [1 ]
Ferrier, Alban [1 ,2 ]
Burner, Pauline [3 ,4 ]
Guimaraes, Vinicius F. [3 ,4 ]
Salaun, Mathieu [3 ,4 ]
Maurel, Vincent [5 ]
Gautier-Luneau, Isabelle [3 ,4 ]
Ibanez, Alain [3 ,4 ]
Viana, Bruno [1 ]
机构
[1] PSL Res Univ, Chim ParisTech CNRS, Inst Rech Chim Paris, F-75005 Paris, France
[2] Paris 06, Sorbonne Univ, UPMC Univ, F-75005 Paris, France
[3] CNRS, Inst NEEL, F-38042 Grenoble, France
[4] Univ Grenoble Alpes, Inst NEEL, F-38042 Grenoble, France
[5] Univ Grenoble Alpes, CNRS, CEA, INAC,SyMMES, F-38000 Grenoble, France
关键词
TUNABLE PHOTOLUMINESCENCE; WHITE PHOSPHORS; EFFICIENT;
D O I
10.1021/acs.jpclett.7b01702
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Wet-chemically synthesized amorphous yttrium aluminum-borates (a-YAB) exhibit intense visible photoluminescence (PL). Preliminary investigations revealed a correlation of PL with the presence of carbon-related impurities; however, their exact nature is still under investigation. These powders also exhibit afterglow luminescence that lasts for several seconds at room-temperature (RT). A comparison with persistent phosphors and phosphorescent dye revealed that the afterglow in a-YAB is a phosphorescence phenomenon and not the persistence luminescence, which is more common in inorganic solids. The unusual RT phosphorescence in a-YAB could be achieved due to triplet-state stabilization of trapped luminescent organic moieties in glassy matrix. This is indeed an important step forward in understanding the complex luminescence mechanism in such promising wet-chemically synthesized functional materials. Moreover, phosphorescence is detectable for over 10 s at RT, suggesting rigid glassy inorganic matrix is more efficient in preserving phosphorescence at elevated temperatures, opening the path for several attractive applications including time-resolved bioimaging and thermometry.
引用
收藏
页码:4735 / 4739
页数:5
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