"

Cookies ussage consent

Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our site without changing the browser settings you grant us permission to store that information on your device.

Facile synthesis and luminescence properties of Eu3+ doped BiPO4 powders by polyvinyl-alcohol mediated solid state reaction

LIYONG WANG1,* , YUANYUAN HAN2, HAIXIA ZHANG1, CHENLEI FENG1, YU DING3, LIHONG ZHANG1, CUIYE HAO1, NANA PEI1, XIAOYU WANG1

Affiliation

  1. College of Chemistry and Environmental Science of Hebei University, Baoding 071002, P. R. China
  2. Medical Experimental Centre of Hebei University, Baoding 071002, P. R. China
  3. Lucky Research Institute, Lucky Group Corporation of China

Abstract

Monoclinic phase Bi0.95Eu0.05PO4 was synthesized by polymer–mediated solid-state reaction employing polyvinyl alcohol (PVA). The powder X-ray diffraction revealed the phase purity and isostructural nature of both Eu3+-doped and undoped BiPO4. The role of PVA molecules in assisting the particle growth during the phase formation and enhancing the degree of crystallinity significantly by its combustion. The synthesized materials were characterized using different spectroscopic techniques such as FT-IR, Raman and Photoluminescence (PL). The methodology discussed here is fundamentally important, which may provide an excellent platform for the phase-controlled synthesis and further optimized materials performance..

Keywords

BiPO4, Solid state reaction, Eu3+ doping, Luminescence.

Citation

LIYONG WANG, YUANYUAN HAN, HAIXIA ZHANG, CHENLEI FENG, YU DING, LIHONG ZHANG, CUIYE HAO, NANA PEI, XIAOYU WANG, Facile synthesis and luminescence properties of Eu3+ doped BiPO4 powders by polyvinyl-alcohol mediated solid state reaction, Optoelectronics and Advanced Materials - Rapid Communications, 10, 5-6, May-June 2016, pp.368-372 (2016).

Submitted at: Jan. 7, 2015

Accepted at: June 9, 2016