高效氟磷酸盐玻璃白光荧光体制备及发光特性
详细信息    查看全文 | 推荐本文 |
  • 英文篇名:Preparation and Photoluminescence Properties of Fluorophosphate Glasses with High Efficient White Light Emission
  • 作者:郑加金 ; 陆强 ; 郑锐林 ; 邹辉 ; 余柯涵 ; 韦玮
  • 英文作者:ZHENG Jia-jin;LU Qiang;ZHENG Rui-lin;ZOU Hui;YU Ke-han;WEI Wei;College of Electronic and Optical Engineering,Nanjing University of Posts & Telecommunications;State Key Laboratory of Transient Optics and Photonics of Chinese Academy of Sciences,Xi'an;
  • 关键词:氟磷酸盐玻璃 ; 白光发射 ; 离子掺杂 ; 能量传递
  • 英文关键词:Fluorophosphate glass;;White light emitting phosphor;;Ions doping;;Energy transfer
  • 中文刊名:GUAN
  • 英文刊名:Spectroscopy and Spectral Analysis
  • 机构:南京邮电大学电子与光学工程学院微电子学院;中国科学院西安光学精密机械研究所瞬态光学与光子技术国家重点实验室;
  • 出版日期:2019-01-15
  • 出版单位:光谱学与光谱分析
  • 年:2019
  • 期:v.39
  • 基金:南京邮电大学国自基金孵化基金项目(NY215143);; 中国科学院西安光学精密机械研究所瞬态光学与光子技术国家重点实验室开放基金项目(SKLST201606)资助
  • 语种:中文;
  • 页:GUAN201901009
  • 页数:6
  • CN:01
  • ISSN:11-2200/O4
  • 分类号:45-50
摘要
采用熔融淬火方法制备了一系列Sn~(2+),Dy~(3+)单掺及Sn~(2+)-Dy~(3+)共掺氟磷酸盐玻璃荧光体。利用紫外-可见分光光度计分别对各玻璃荧光体的透过光谱、激发光谱、发射光谱及荧光寿命等进行了测试和分析。结果发现在紫外光激发下,对于Sn~(2+)、Dy~(3+)单掺氟磷酸盐玻璃可分别获得高效的蓝光与黄光发射,且Sn~(2+)单掺氟磷酸盐玻璃荧光体发光显色指数和量子效率最高;对于Sn~(2+)-Dy~(3+)共掺氟磷酸盐玻璃荧光体可实现高效的白光发射,且发现在Sn~(2+)和Dy~(3+)之间存在明显的能量传递,通过调节Dy~(3+)掺杂浓度,两离子之间的能量转移效率亦随之改变,从而可对其白光色度进行调节。当Dy~(3+)掺杂浓度为3Wt%时,利用280nm商用LED芯片激发可获得对应色坐标为(0.311,0.330),量子效率为56.3%,亮度为6 706cd·m-2的近纯白光发射。此外,对各类玻璃样品的DSC、导热及其他光学性能也进行了测试与计算,获得了各样品的热导率、量子效率、色坐标、显色指数等参数。研究结果表明,制备的高效氟磷酸盐玻璃完全有望作为可调谐白光发光荧光体应用于商用LED。
        A series of Sn~(2+),Dy~(3+) and Sn~(2+)-Dy~(3+) co-doped fluorophosphate glasses(FPGs)for white light emitting phosphor have been prepared by the melt quenching method.Under the UV light excitation,FPG:Sn~(2+)and FPG∶Dy~(3+) can obtain blue and yellow light,respectively.The emission color of FPG∶Sn~(2+)-Dy~(3+) can be tuned from blue to white color by properly adjusting the concentration of Dy~(3+) ions under the excitation of 280 nm UV light,which can be attributed to the energy transfer from Sn~(2+)to Dy~(3+) ions.The energy transfer mechanism was investigated and analyzed according to the photoluminescence,lifetime decay and CIE chromaticity coordinate.In addition,the FPG∶Sn~(2+)fluorophosphate glass shows the highest color rendering index of 94 and the quantum efficiency of 81.3%,and the Sn~(2+)-Dy~(3+) co-doped fluorophosphate glasses show better white color coordinates.By controlling the concentration of Dy~(3+) ,the FPGs can present a white light with a CIE chromaticity coordinate of(0.311,0.330),which is very close to the equal energy point.The corresponding quantum efficiency and the luminance are56.3% and 6 706cd·m-2,respectively.The results of this study demonstrate that the FPGs are promising candidate for commercial white light emitting applications.
引文
[1] Hamzaoui M,Soltani M T,Baazouzi M,et al.Physica Status Solidi,2012,249:2213.
    [2] Fan B,Xue B,Zhang X,et al.Optics Letters,2013,38:2280.
    [3] Sun C Y,Wang X L,Zhang X,et al.Nature Communications,2013,4:2717.
    [4] Babu B H,Kumar V V R K.Journal of Materials Science,2014,49:415.
    [5] Messing G L,Zhang S C,Jayanthi G V.Journal of the American Ceramic Society,1993,76:2707.
    [6] Yu Y,Liu Z,Dai N,et al.Optics Express,2011,19:19473.
    [7] Samsudin N F,Matori K A,Wahab Z A,et al.Optik-International Journal for Light and Electron Optics,2016,127:8076.
    [8] Kumar M V S,Rajesh D,Balakrishna A,et al.Journal of Molecular Structure,2013,1041:100.
    [9] Yuan Y,Zheng R,Lu Q,et al.Optics Letters,2016,41:3122.
    [10] Vincent A C,Scott P.Journal of Cosmology&Astroparticle Physics,2014,(4):19.
    [11] Babu P,Jang K H,Rao C,et al.Optics Express,2011,19(3):1836.
    [12] Kesavulu C R,Jayasankar C K.Materials Chemistry&Physics,2011,130(3):1078.
    [13] Okamoto H,Kasuga K,Kubota Y,et al.Optics Express,2013,21(19):22043.
    [14] Vijaya N,Upendra K K,Jayasankar C K.Spectrochimica Acta Part A Molecular&Biomolecular Spectroscopy,2013,113:145.
    [15] Rosemann N W,Eu?ner J P,Beyer A,et al.Science,2016,352:1301.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700