Synthesis and investigation of the optical characteristics of RE3+ activated Ca2Li2Si2O7 (Rare earth = Eu, Tb) phosphor for W-LED application

IF 3.8 Q2 CHEMISTRY, PHYSICAL
Pragati Tale , Ashok Mistry , Bharti Bawanthade , Ashish Mathur , S.J. Dhoble
{"title":"Synthesis and investigation of the optical characteristics of RE3+ activated Ca2Li2Si2O7 (Rare earth = Eu, Tb) phosphor for W-LED application","authors":"Pragati Tale ,&nbsp;Ashok Mistry ,&nbsp;Bharti Bawanthade ,&nbsp;Ashish Mathur ,&nbsp;S.J. Dhoble","doi":"10.1016/j.chphi.2024.100752","DOIUrl":null,"url":null,"abstract":"<div><div>Novel Eu<sup>3+</sup> and Tb<sup>3+</sup> ions-doped Ca<sub>2</sub>Li<sub>2</sub>Si<sub>2</sub>O<sub>7</sub> luminescent materials were prepared by a low-temperature solid-state reaction technique for LED application. The electronic transitions of <sup>5</sup>D<sub>0</sub> → <sup>7</sup>F<sub>2</sub> (Eu<sup>3+</sup>) and <sup>5</sup>D<sub>4</sub> → <sup>7</sup>F<sub>5</sub> (Tb<sup>3+</sup>) have caused the luminescent material to exhibit strong luminosity in 613 nm (red) and 545 nm (green), respectively. Fourier transform infrared (FT-IR) spectra were applied for the identification of functional groups, and powder X-ray diffraction (XRD) was used for structural analysis. Morphological data was gathered using scanning electron microscopy (SEM). Its color was also determined by calculating the CIE coordinates. The excitation, PL properties, and luminescence decay time of the emission transitions of Eu<sup>3+</sup> (<sup>5</sup>D<sub>0</sub> → <sup>7</sup>F<sub>2</sub>) and Tb<sup>3+</sup> (<sup>5</sup>D<sub>4</sub> → <sup>7</sup>F<sub>5</sub>) were measured in order to analyze luminosity spectra.</div></div>","PeriodicalId":9758,"journal":{"name":"Chemical Physics Impact","volume":null,"pages":null},"PeriodicalIF":3.8000,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Physics Impact","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667022424002962","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Novel Eu3+ and Tb3+ ions-doped Ca2Li2Si2O7 luminescent materials were prepared by a low-temperature solid-state reaction technique for LED application. The electronic transitions of 5D07F2 (Eu3+) and 5D47F5 (Tb3+) have caused the luminescent material to exhibit strong luminosity in 613 nm (red) and 545 nm (green), respectively. Fourier transform infrared (FT-IR) spectra were applied for the identification of functional groups, and powder X-ray diffraction (XRD) was used for structural analysis. Morphological data was gathered using scanning electron microscopy (SEM). Its color was also determined by calculating the CIE coordinates. The excitation, PL properties, and luminescence decay time of the emission transitions of Eu3+ (5D07F2) and Tb3+ (5D47F5) were measured in order to analyze luminosity spectra.

Abstract Image

用于 W-LED 的 RE3+活化 Ca2Li2Si2O7(稀土 = Eu、Tb)荧光粉的合成与光学特性研究
利用低温固态反应技术制备了掺杂 Eu3+ 和 Tb3+ 离子的新型 Ca2Li2Si2O7 发光材料,并将其应用于 LED。5D0 → 7F2 (Eu3+) 和 5D4 → 7F5 (Tb3+) 的电子跃迁分别使发光材料在 613 nm(红光)和 545 nm(绿光)波段表现出很强的发光强度。傅立叶变换红外光谱(FT-IR)用于识别官能团,粉末 X 射线衍射(XRD)用于结构分析。扫描电子显微镜(SEM)收集了形态数据。还通过计算 CIE 坐标确定了其颜色。为了分析发光光谱,测量了 Eu3+ (5D0 → 7F2) 和 Tb3+ (5D4 → 7F5) 发射跃迁的激发、PL 特性和发光衰减时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Chemical Physics Impact
Chemical Physics Impact Materials Science-Materials Science (miscellaneous)
CiteScore
2.60
自引率
0.00%
发文量
65
审稿时长
46 days
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信