Synthesis and characterization of micro/nano-structured BaHPO4/Ba3(PO4)2/Ba5(PO4)3OH phases and their luminescence

被引:7
|
作者
Tong, Miaohui [1 ,2 ]
Zhao, Jianwen [2 ]
Liang, Yujun [1 ,2 ]
Zhu, Yingli [2 ]
Wu, Xingya [2 ]
Liu, Shiqi [2 ]
Yan, Chunjie [1 ,2 ]
Lia, Guogang [1 ,2 ]
机构
[1] China Univ Geosci, Minist Educ, Engn Res Ctr Nanogeomat, Wuhan 430074, Peoples R China
[2] China Univ Geosci, Fac Mat Sci & Chem, Wuhan 430074, Peoples R China
基金
中国国家自然科学基金;
关键词
CONTROLLABLE SYNTHESIS; OPTICAL-PROPERTIES; PHOTOLUMINESCENCE PROPERTIES; HYDROTHERMAL SYNTHESIS; CRYSTAL-GROWTH; MORPHOLOGY; FLUX; FABRICATION; MECHANISM; NETWORKS;
D O I
10.1039/c5ra01420d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Microspheres covered with microcuboids/nanorods and nanoparticles of BaHPO4/Ba-3(PO4)(2)/Ba-5(PO4)(3)OH phases have been successfully synthesized by a facile hydrothermal (HT) method using the citric acid as a surfactant at different pH values. X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM) and fluorescence spectrometry were used to characterize the samples. It was found that the pH value was a crucial factor for the phase formation and shape determination of the final products, which were discussed in detail. Attractively, the as-prepared BaHPO4/Ba-3(PO4)(2)/Ba-5(PO4)(3)OH samples emitted an intense blue light in a broad band from 380 to 625 nm, for which the mechanism was complex ions luminescence originating from the transition of T-3(1) -> (1)A(1) in PO43. Meanwhile, an obvious red shift for the emission band was observed between nano-and bulk-Ba-3(PO4)(2) synthesized by HT and conventional solid-state (CSS) reactions, respectively, which was due to the effect of the product being nanosized. The same effect was also revealed by the fact that the decay time of the latter was about 2.5 times that of the former. Moreover, the decay mode of Ba-5(PO4)(3)OH was different from those of BaHPO4 and Ba-3(PO4)(2), which was ascribed to the effect of the substitution of three OH- for one PO43- on their electronic structures.
引用
收藏
页码:27517 / 27525
页数:9
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