...
  • 主题
高级搜索  >
历史搜索 清空历史
首页> 外文期刊>Journal of Non-Crystalline Solids: A Journal Devoted to Oxide, Halide, Chalcogenide and Metallic Glasses, Amorphous Semiconductors, Non-Crystalline Films, Glass-Ceramics and Glassy Composites >Chemical co-precipitation of hybrid precursors to synthesize Eu3+/Dy3+ activated YNbxP1-xO4 and YNbxP1-xO4 microcrystalline phosphors
【24h】

Chemical co-precipitation of hybrid precursors to synthesize Eu3+/Dy3+ activated YNbxP1-xO4 and YNbxP1-xO4 microcrystalline phosphors

机译：化学共沉淀杂化前驱体以合成Eu3 + / Dy3 +活化的YNbxP1-xO4和YNbxP1-xO4微晶磷光体

获取原文
获取原文并翻译 | 示例
           
页面导航
  • 摘要
  • 著录项
  • 相似文献
  • 相关主题

摘要

A modified wet-chemical synthesis technology was put forward to fabricate Eu3+/Dy3+ doped with YNbxP1-xO4 and YNbxV1-xO4 phosphors with varying x from the assembly of multicomponent hybrid precursors. The morphologies have been found to be 1-2 mu m crystalline spheres using XRD and SEM. The red photoluminescence intensity reaches the strongest in YNb0.8P0.2O4:Eu3+ and YNb0.1-V0.9O4:Eu3+ phosphors and the red to orange intensity ratio (RO) values decrease with the content of P(V) increasing. Besides this, the optimum concentration for Dy3+ luminescence in YNb0.5P0.5O4 is 1 mol%, while that in YNb0.5V0.5O4 is 0.5 mol% or lower than 0.5 mol%. The yellow to blue intensity ratio (YB) value of Dy3+ increases when the Dy3+ concentration increases from 0.5 to 8 mol% in YNb0.5P0.5O4; however, that of Dy3+ does not vary much in YNb0.5V0.5O4 matrix. (c) 2006 Elsevier B.V. All rights reserved.
机译：提出了一种改进的湿化学合成技术，以制备多组分杂化前驱体组装而成的掺有x不同的YNbxP1-xO4和YNbxV1-xO4荧光粉的Eu3 + / Dy3 +。使用XRD和SEM已发现其形态为1-2μm的结晶球。在YNb0.8P0.2O4：Eu3 +和YNb0.1-V0.9O4：Eu3 +荧光粉中，红色光致发光强度最强，并且随着P（V）含量的增加，红色与橙色的强度比（RO）值降低。除此之外，YNb0.5P0.5O4中Dy3 +发光的最佳浓度为1mol％，而YNb0.5V0.5O4中Dy3 +发光的最佳浓度为0.5mol％或低于0.5mol％。当YNb0.5P0.5O4中Dy3 +的浓度从0.5 mol％增加到8 mol％时，Dy3 +的黄蓝强度比（YB）值增加;然而，在YNb0.5V0.5O4基质中Dy3 +的变化不大。 （c）2006 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱：kefu@zhangqiaokeyan.com

京公网安备：11010802029741号 ICP备案号：京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有

  • 客服微信

  • 服务号