4.5 Article

Characterization and luminescent properties of lanthanum borate prepared by solution combustion method

出版社

ELSEVIER
DOI: 10.1016/j.mseb.2023.116362

关键词

Solution combustion method; Luminescent material; Lanthanum borate; XPS analysis

向作者/读者索取更多资源

A series of LaBO3:Pr3+ luminescent materials were prepared using lanthanum nitrate hexahydrate and boric acid as raw materials, glycine as combustion agent and praseodymium nitrate hexahydrate as modifier. The phase structure, micro morphology and ionic valence of the materials were analyzed, and the fluorescence properties of the materials were characterized. The results showed that Pr3+ ions successfully entered the lattice of LaBO3 after calcination at 850 degrees C for 4 hours. The main luminescence peak of LaBO3:Pr3+ powder was located at 670 nm at the excitation wavelength of 448 nm, and the luminescence intensity was the highest when the doping ratio was 0.03.
A series of LaBO3:Pr3+ luminescent materials were prepared by using lanthanum nitrate hexahydrate (La (NO3)3.6H2O) and boric acid (H3BO3) as raw materials, glycine (C2H5NO2) as combustion agent and praseo-dymium nitrate hexahydrate (Pr(NO3)3.6H2O) as modifier. XRD, SEM, XPS, UV-vis DRS, PL and other charac-terization methods were used to analyze the phase structure, micro morphology and ionic valence of the luminescent materials, and the fluorescence properties of the materials were characterized in detail. The results showed that Pr3+ ions had entered into the lattice of LaBO3 after calcined at 850 degrees C for 4 h by solution com-bustion method. The macro particle size of the material was 790 nm, which belongs to submicron material. The valence state of rare earth ions was stable due to high temperature or other factors during the preparation process. The band gap of the powder was 6.62 eV. The fluorescence results showed that the main luminescence peak of LaBO3:Pr3+ powder was located at 670 nm at the excitation wavelength of 448 nm, and the luminescence intensity was the highest when the doping ratio was 0.03.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据