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机构地区:[1]School of Science, Beijing Technology and Business University, Beijing 100048, China
出 处:《Journal of Rare Earths》2016年第1期12-16,共5页稀土学报(英文版)
基 金:supported by National Natural Science Foundation of China(20976002);the Beijing Natural Science Foundation(2122012);Key Projects for Science and Technology of Beijing Education Commission(KZ201310011013)
摘 要:Novel Sr3Gd(1-x)DyxNa(PO4)3F (SGNP:xDy3+, x=0.01, 0.03, 0.05, 0.07, 0.09, 0.11) phosphors were synthesized by a conventional solid-state reaction method at different compositions. The X-ray diffraction results confirmed that the as-prepared samples were pure phase. The phosphor had two intense emission bands centering at 481 and 574 nm which could be attributed to the 4F9/2→6H15/2 transition and the 4F9/2→6H13/2 transition, respectively. The chromaticity coordinates (x, y) of this phosphor were calculated to be (0.3054, 0.3354) located on the region of white light region when excited at 350 nm. The concentration quenching mechanism of Dy3+ was ascribed to the dipole-dipole interaction. The current research suggested that the phosphors might be potential application in the w-LEDs.Novel Sr3Gd(1-x)DyxNa(PO4)3F (SGNP:xDy3+, x=0.01, 0.03, 0.05, 0.07, 0.09, 0.11) phosphors were synthesized by a conventional solid-state reaction method at different compositions. The X-ray diffraction results confirmed that the as-prepared samples were pure phase. The phosphor had two intense emission bands centering at 481 and 574 nm which could be attributed to the 4F9/2→6H15/2 transition and the 4F9/2→6H13/2 transition, respectively. The chromaticity coordinates (x, y) of this phosphor were calculated to be (0.3054, 0.3354) located on the region of white light region when excited at 350 nm. The concentration quenching mechanism of Dy3+ was ascribed to the dipole-dipole interaction. The current research suggested that the phosphors might be potential application in the w-LEDs.
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