已入深夜,您辛苦了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!祝你早点完成任务,早点休息,好梦!

Optical properties of Ce3+ and Tb3+ co-doped ZnS quantum dots

光致发光 X射线光电子能谱 兴奋剂 材料科学 掺杂剂 量子点 分析化学(期刊) 发光 晶体结构 光致发光激发 纳米技术 化学 光电子学 结晶学 化学工程 色谱法 工程类
作者
Nguyễn Xuân Ca,N.D. Vinh,Shivani Bharti,Pham Minh Tan,Nguyễn Thị Hiền,Xuan Hoa Vu,Yuxin Peng,Phan Văn Độ
出处
期刊:Journal of Alloys and Compounds [Elsevier BV]
卷期号:883: 160764-160764 被引量:62
标识
DOI:10.1016/j.jallcom.2021.160764
摘要

Ce3+ and Tb3+ co-doped ZnS quantum dots (QDs) were synthesized using a facile and effective wet chemical method. The effect of Tb3+ concentration on the structure and optical properties of the co-doped QDs was explored thoroughly using various characterization methods. The chemical composition and oxidation state of the elements in the synthesized QDs were examined by X-ray photoelectron spectroscopy (XPS). The crystal structure and luminescence properties of the synthesized QDs were investigated using X-ray diffraction (XRD) and photoluminescence (PL). The change in the crystal structure of the Ce3+ and Tb3+ co-doped QDs with an increase in the concentration of Tb3+ dopant from 1% to 8% was observed for the first time. The excitation spectra of Ce3+ and Tb3+ co-doped QDs were investigated using the photoluminescence excitation (PLE) technique. The energy transfer (ET) from Ce3+ to Tb3+ ions in the ZnS host lattice occurred effectively because of the large spectral overlap between the emission band of Ce3+ and the excitation band of Tb3+ ions. The observed properties revealed that doping with Ce3+ enhanced the energy transfer process and the interaction mechanism in energy transfer was dominated by dipole-dipole interaction. The thermal stability of the co-doped QDs was explored by studying their PL spectra in the temperature range of 15–300 K. Ce3+ and Tb3+ co-doped ZnS QDs exhibited a very long decay time on the order of ms. The valuable optical properties of Ce3+ and Tb3+ co-doped ZnS QDs make them potentially useful for photovoltaic, photocatalyst, and biosensing applications.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
思源应助科研通管家采纳,获得10
刚刚
ggghh应助科研通管家采纳,获得10
1秒前
Akim应助科研通管家采纳,获得10
1秒前
搜集达人应助科研通管家采纳,获得10
1秒前
1秒前
CipherSage应助科研通管家采纳,获得10
1秒前
cocaco应助科研通管家采纳,获得30
1秒前
小二郎应助科研通管家采纳,获得10
1秒前
1秒前
完美世界应助科研通管家采纳,获得10
1秒前
东方元语应助科研通管家采纳,获得20
1秒前
李爱国应助科研通管家采纳,获得10
1秒前
所所应助科研通管家采纳,获得10
1秒前
科研通AI6.4应助33采纳,获得10
1秒前
JamesPei应助科研通管家采纳,获得30
1秒前
Twonej应助淳于夜绿采纳,获得50
1秒前
田様应助科研通管家采纳,获得10
1秒前
Kao应助科研通管家采纳,获得10
1秒前
FashionBoy应助科研通管家采纳,获得10
2秒前
Akim应助科研通管家采纳,获得10
2秒前
2秒前
慕青应助文静的海采纳,获得10
2秒前
情怀应助科研通管家采纳,获得10
2秒前
Kao应助科研通管家采纳,获得10
2秒前
orixero应助科研通管家采纳,获得10
2秒前
今后应助科研通管家采纳,获得10
2秒前
思源应助科研通管家采纳,获得10
2秒前
酷波er应助科研通管家采纳,获得10
2秒前
搜集达人应助科研通管家采纳,获得10
2秒前
Hello应助科研通管家采纳,获得10
2秒前
香蕉觅云应助科研通管家采纳,获得10
2秒前
无花果应助科研通管家采纳,获得10
3秒前
在水一方应助科研通管家采纳,获得10
3秒前
所所应助科研通管家采纳,获得10
3秒前
BigTong应助科研通管家采纳,获得20
3秒前
星辰大海应助科研通管家采纳,获得10
3秒前
慕青应助科研通管家采纳,获得10
3秒前
深情安青应助科研通管家采纳,获得50
3秒前
wanci应助科研通管家采纳,获得10
3秒前
英俊的铭应助科研通管家采纳,获得10
3秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Gründe der Seele:Die Wiener Psychatrie im 20.Jahrhundert 1000
Development of a Bridge Weigh-In-Motion System: A technology to convert the bridge response to the passage of traffic into data on vehicle configurations, speeds, times of travel and weights 1000
Organic Reactions, Volume 116 1000
Current concepts in cutaneous toxicity : proceedings of the Fourth Conference on Cutaneous Toxicity, Washington, D.C., May 9-11, 1979 1000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7274029
求助须知:如何正确求助?哪些是违规求助? 8895158
关于积分的说明 18804700
捐赠科研通 6947774
什么是DOI,文献DOI怎么找? 3205583
关于科研通互助平台的介绍 2377151
邀请新用户注册赠送积分活动 2180474