4.6 Article

Structural Phase Formation and Tunable Luminescence of Eu2+-Activated Apatite-Type (Ca,Sr,Ba)5(PO4)2(SiO4)

Journal

JOURNAL OF THE ELECTROCHEMICAL SOCIETY
Volume 158, Issue 11, Pages J334-J340

Publisher

ELECTROCHEMICAL SOC INC
DOI: 10.1149/2.026111jes

Keywords

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Funding

  1. National Research Foundation of Korea (NRF)
  2. Ministry of Education, Science and Technology (MEST) [2009-0078682]
  3. Jiangsu Higher Education Institutions

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The samples on the base of the substitutions on Sr-cation in apatite Sr-5(PO4)(2)(SiO4) were prepared by conventional solid-state reaction method: I) Sr4.75-5xCa5x(PO4)(2)(SiO4):Eu-0.25(2+) (0.01 <= x <= 0.95) and II) Sr4.75-5yBa5y(PO4)2(SiO4):Eu0.252+ (0.01 <= z <= 0.5). The crystal phase formations were investigated by the X-ray powder diffraction patterns. The tunable green-yellow color was detected due to the substitution of cation Sr2+ in the host lattice by either Ca2+ or Ba2+. The relationship between the structure and luminescence properties was reported. The site-occupation of Eu2+ ions and energy transfer were discussed on the base of crystal structure. Partial substitution of Sr2+ by either Ca2+ or Ba2+ all results in a blue-shifted Eu2+ emission. The luminescence blue-shift is a common phenomenon in Ba2+-substition for Sr2+ due to a decreased crystal field splitting for Eu2+ on the bigger Ba2+ cation site. However, in the Ca2+-substitution for Sr2+, the luminescence blue-shifted Eu2+ emission is unusual. The detailed luminescence spectra of Eu2+ ions in relation with the micro-structure were first reported in one of the end compound Ca-5(PO4)(2)(SiO4). This is helpful to improve this series of materials for a potential application as a biomaterial or a phosphor for the lighting. (C) 2011 The Electrochemical Society. [DOI: 10.1149/2.026111jes] All rights reserved.

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