Structural and XPS studies of polyhedral europium doped gadolinium orthovanadate (Eu3+:GdVO4) nanocatalyst for augmented photodegradation against Congo-red

光降解 X射线光电子能谱 光催化 掺杂剂 材料科学 刚果红 光化学 化学 兴奋剂 催化作用 发光 化学工程 物理化学 光电子学 有机化学 吸附 工程类
作者
Aftab A. Ansari,Dambarudhar Mohanta
出处
期刊:Physica E-low-dimensional Systems & Nanostructures [Elsevier BV]
卷期号:143: 115357-115357 被引量:16
标识
DOI:10.1016/j.physe.2022.115357
摘要

The present work demonstrates structural, valence band mapping (VBM) and photocatalytic activity of Eu3+ doped orthovanadate (GdVO4) nanosystem against an azo-dye, Congo-red. As evident from x-ray diffraction (XRD) studies, the nanosystem synthesized via a solid-state cum sintering route exhibited zircon-type crystal structure with space group I 41/amd. Imaging through transmission electron microscopy (TEM) has revealed polyhedral nanoaggregates, which are of polycrystalline nature. Introduction of Eu3+ into the host GdVO4 was substantiated from the energy dispersive x-ray (EDX) spectra, x-ray photoelectron spectra (XPS) and considering inclusion of dopants to binding energy correspondence in the VBM spectra. In this study, the azo-dye Congo-red has been opted as the target dye for photodegradation. After UV light illumination, Eu3+:GdVO4 nano-catalyst could degrade the organic dye quite effeciently (up to 91.8%), and offering a rate constant nearly doubled as compared with its undoped counterpart. The dopant ions being associated with the new localized states enabling promotion of additional photoexcited carriers taking advantage of the incident UV exposure. Structural, XPS, and optical studies of the rare-earth vanadate nano-systems as well as their photocatalytic activity would provide new insights to resolve existing concerns, viz., removal of organic contaminants, and environmentally harmful dyes and to carry multi-functional scope for industrial relevance. Moreover, such systems may have immense potential for displaying select emission response as well as photocatalysis even though both processes are mediated via opposite effects.
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
刚刚
善学以致用应助魏百悦采纳,获得10
刚刚
写个锤子完成签到,获得积分10
2秒前
2秒前
可靠寒云完成签到,获得积分10
2秒前
3秒前
33发布了新的文献求助10
3秒前
雪生在无人荒野完成签到,获得积分10
3秒前
Cookies完成签到,获得积分10
4秒前
Elma发布了新的文献求助10
5秒前
自然飞风完成签到 ,获得积分10
7秒前
加一发布了新的文献求助10
7秒前
光亮秋白发布了新的文献求助10
8秒前
迟迟不吃吃完成签到 ,获得积分10
9秒前
33完成签到,获得积分10
10秒前
小二_来篇一作完成签到 ,获得积分10
11秒前
勤恳马里奥完成签到,获得积分0
11秒前
宋宋完成签到 ,获得积分10
13秒前
16秒前
极品小亮完成签到,获得积分10
18秒前
付XR完成签到 ,获得积分10
19秒前
19秒前
aimynora完成签到 ,获得积分10
19秒前
无语的惜芹完成签到,获得积分10
20秒前
传奇3应助球球采纳,获得10
21秒前
21秒前
脑洞疼应助刻苦的冬易采纳,获得10
21秒前
fsm完成签到,获得积分10
25秒前
bab发布了新的文献求助10
26秒前
有人喜欢蓝完成签到,获得积分10
26秒前
27秒前
29秒前
30秒前
量子星尘发布了新的文献求助10
30秒前
孝顺的紫完成签到 ,获得积分10
30秒前
铭铭发布了新的文献求助10
31秒前
34秒前
聪慧紫菱完成签到,获得积分10
35秒前
务实蜻蜓完成签到,获得积分10
36秒前
张土豆发布了新的文献求助10
37秒前
高分求助中
(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
Kinesiophobia : a new view of chronic pain behavior 2000
Cronologia da história de Macau 1600
Developmental Peace: Theorizing China’s Approach to International Peacebuilding 1000
Traitements Prothétiques et Implantaires de l'Édenté total 2.0 1000
Earth System Geophysics 1000
Bioseparations Science and Engineering Third Edition 1000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6131771
求助须知:如何正确求助?哪些是违规求助? 7959199
关于积分的说明 16516151
捐赠科研通 5248884
什么是DOI,文献DOI怎么找? 2803038
邀请新用户注册赠送积分活动 1784064
关于科研通互助平台的介绍 1655150