节点文献

Photoluminescence of BaGdB9O16:Eu3+ co-doped Al3+ or Sc3+ under UV-VUV excitation

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 李小侠张占辉陈忠王育华黄新阳于泉茂吕兴栋

【Author】 LI Xiaoxia1,2, ZHANG Zhanhui, CHEN Zhong1, WANG Yuhua2, HUANG Xinyang1, YU Quanmao1, Lü Xingdong1(1.School of Electronics, Jiangxi University of Finance & Economics, Nanchang 330013, China;2.Department of Materials Science, School of Physical Science and Technology, Lanzhou University, Lanzhou 730000, China;3.School of Materials Science of Engineering, Wuhan Institute of Technology, Wuhan 430073, China)

【机构】 School of Electronics, Jiangxi University of Finance & EconomicsDepartment of Materials Science, School of Physical Science and Technology, Lanzhou UniversitySchool of Materials Science of Engineering, Wuhan Institute of Technology

【摘要】 Single phase of BaGd0.9-xMxEu0.1B9O16(M=Al or Sc, 0≤x≤0.3) powder was prepared by the solid-state reaction and its photoluminescence(PL) properties were investigated under ultraviolet(UV) and vacuum ultraviolet(VUV) excitation.Monitored with 613 nm emission, the excitation spectra of BaGd0.9-xMxEu0.1B9O16 consisted of three broad bands peaking at about 242, 208, and 142 nm, respectively.The one at about 242 nm originated from the charge transfer band(CTB) of O2-→Eu3+.The other two were assigned to the absorption of the host, which was overlapped with absorptions among borate groups, f→d transition of RE3+(RE=Gd, Eu), and the charge transfer transition of O2-→Gd3+.The maximum emission peak was observed at about 613 nm in the emission spectra of BaGd0.9-xMxEu0.1B9O16 under both 254 and 147 nm excitation, which originated from the electric dipole 5D0→7F2 transition of Eu3+.When excited with 254 nm, the integral emission intensity of Eu3+ increased after Al3+ or Sc3+ substituting Gd3+ partly in BaGd0.9Eu0.1B9O16.Under 147 nm excitation, the integral emission intensity of Eu3+ decreased after some Gd3+ was replaced by Sc3+, but increased after adding appropriate Al3+ into BaGd0.9Eu0.1B9O16.

【Abstract】 Single phase of BaGd0.9-xMxEu0.1B9O16(M=Al or Sc, 0≤x≤0.3) powder was prepared by the solid-state reaction and its photoluminescence(PL) properties were investigated under ultraviolet(UV) and vacuum ultraviolet(VUV) excitation.Monitored with 613 nm emission, the excitation spectra of BaGd0.9-xMxEu0.1B9O16 consisted of three broad bands peaking at about 242, 208, and 142 nm, respectively.The one at about 242 nm originated from the charge transfer band(CTB) of O2-→Eu3+.The other two were assigned to the absorption of the host, which was overlapped with absorptions among borate groups, f→d transition of RE3+(RE=Gd, Eu), and the charge transfer transition of O2-→Gd3+.The maximum emission peak was observed at about 613 nm in the emission spectra of BaGd0.9-xMxEu0.1B9O16 under both 254 and 147 nm excitation, which originated from the electric dipole 5D0→7F2 transition of Eu3+.When excited with 254 nm, the integral emission intensity of Eu3+ increased after Al3+ or Sc3+ substituting Gd3+ partly in BaGd0.9Eu0.1B9O16.Under 147 nm excitation, the integral emission intensity of Eu3+ decreased after some Gd3+ was replaced by Sc3+, but increased after adding appropriate Al3+ into BaGd0.9Eu0.1B9O16.

【关键词】 BaGdB9O16:Eu3+phosphorphotoluminescenceVUVrare earths
【Key words】 BaGdB9O16:Eu3+phosphorphotoluminescenceVUVrare earths
【基金】 supported by the Science Program of the Education Office, Jiangxi Province (GJJ08345);the Young Foundation of Jiangxi Univer-sity of Finance and Economy
  • 【文献出处】 Journal of Rare Earths ,稀土学报(英文版) , 编辑部邮箱 ,2009年01期
  • 【分类号】TB383.3
  • 【被引频次】4
  • 【下载频次】71
节点文献中: 

本文链接的文献网络图示:

本文的引文网络