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铕对(钇,钆)氟纳米磷光体结构和光物理性质的影响。

Influence of Eu on the Structure and Photophysical Properties in (Y,Gd)F Nanophosphors.

作者信息

Nanda Sushri Sangita, Nayak Priyanka, Goutam U K, Dash S

机构信息

Department of Physics and Astronomy, National Institute of Technology Rourkela, Rourkela, Odisha, 769008, India.

Indus 2 Synchrotron Facility, Raja Ramanna Centre for Advanced Technology (RRCAT), Indore, Madhya Pradesh, 452013, India.

出版信息

J Fluoresc. 2021 Jan;31(1):129-139. doi: 10.1007/s10895-020-02642-8. Epub 2020 Nov 2.

Abstract

The scientific community has shown a growing interest in relating to the lanthanide based luminescent materials and it has made an effort to develop them. Among these several luminescent materials, we have proposed to developed (Y,Gd)F nanophosphors doped with distinct of Eu concentrations using modified hydrothermal process. The effect of co-doping of rare earth activators to the host lattice structure and morphology are investigated using different analytical techniques. The diffuse reflectance spectra reveal a tuning of optical band gap due to substitutions. From the extensive XPS analysis, Gd and Eu are found to be in a stable ionic state of +3 which is replacing Y in YF host. Photoluminescence emission spectra of the nanophosphors are excited by near ultraviolet (UV, 393 nm) excitation. From photoluminescence study, the intensity variation is observed for emission peak at 591 nm and fluorescence quenching occurs at higher doping level. This effect subsequently explained on the frame work of local symmetry and nonradiative transfer among multipole-multipole interaction. At 393 nm excitation Eu (2, 3, 5, 7, 10 at %) doped (Y, Gd) F show CIE chromaticity coordinates shifted to red regions with increase in Eu doping levels. Because of the longer decay time these phosphors can be used for bio-labeling and other similar applications.

摘要

科学界对基于镧系元素的发光材料越来越感兴趣,并致力于开发这些材料。在这些发光材料中,我们提出使用改进的水热法制备掺杂不同铕浓度的(Y,Gd)F纳米磷光体。使用不同的分析技术研究了稀土激活剂共掺杂对主体晶格结构和形貌的影响。漫反射光谱显示由于取代作用导致光学带隙发生了调整。通过广泛的XPS分析,发现Gd和Eu处于+3的稳定离子状态,它们在YF主体中取代了Y。纳米磷光体的光致发光发射光谱由近紫外(UV, 393 nm)激发。通过光致发光研究,观察到591 nm发射峰的强度变化,并且在较高掺杂水平下发生荧光猝灭。这种效应随后在局部对称性框架以及多极-多极相互作用之间的非辐射转移方面得到了解释。在393 nm激发下,掺杂Eu(2, 3, 5, 7, 10 at%)的(Y, Gd)F随着Eu掺杂水平的增加,CIE色度坐标向红色区域移动。由于这些磷光体具有较长的衰减时间,因此可用于生物标记和其他类似应用。

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