Facile synthesis of MgS/Ag2MoO4 nanohybrid heterojunction: Outstanding visible light harvesting for boosted photocatalytic degradation of MB and its anti-microbial applications

光催化 可见光谱 降级(电信) X射线光电子能谱 材料科学 激进的 光化学 辐照 纳米复合材料 纳米技术 纳米颗粒 化学工程 核化学 化学 催化作用 光电子学 有机化学 工程类 核物理学 物理 电信 计算机科学
作者
S. Kokilavani,Asad Syed,Bijandra Kumar,Abdallah M. Elgorban,Ali H. Bahkali,Bilal Ahmed,Arunava Das,S. Sudheer Khan
出处
期刊:Colloids and Surfaces A: Physicochemical and Engineering Aspects [Elsevier BV]
卷期号:627: 127097-127097 被引量:29
标识
DOI:10.1016/j.colsurfa.2021.127097
摘要

In this paper, a novel MgS/Ag2MoO4 nanocomposite (NCs) was synthesized for the evaluation of photocatalytic performance and anti-microbial activity. The particle was characterized using FT-IR, PL, HR-TEM, EDAX, XRD, XPS, SAED, UV–vis DRS, ESR, and EIS. The performance of the photocatalyst was improved by shift in band gap to 2.76 eV compared to its individual counter parts. The photocatalytic performance of MgS/Ag2MoO4 NCs was much better than MgS and Ag2MoO4 as individual particles. The reaction rate constant for degrading MB by MgS/Ag2MoO4 was 0.011 min−1. The degradation efficiency of MgS/Ag2MoO4 (90%) was about 1.5 and 2.2 times greater than bare Ag2MoO4 (62%) and MgS (41%). The photocatalytic degradation efficiency remains same with 90% efficiency after performing the reusability test for six consecutive cycles under visible light irradiation and the particles maintained photo stability even after 6 cycles. The strong interactions between the interfacial surfaces are responsible for the increase in charge separation owing to the superior activity of MgS/Ag2MoO4 NCs. The mechanism was established for this enhanced activity and the key reactive species, such as hydroxyl and superoxide radicals plays a major role in the photocatalytic process. The antimicrobial activity was evaluated against E. coli and B. subtilis and the activity of Ag2MoO4 was good compared to NCs and MgS. The synthesized NCs are found to be good alternative as a visible light driven photocatalyst.

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
1秒前
2秒前
lee完成签到 ,获得积分10
2秒前
郑可馨完成签到 ,获得积分10
3秒前
4秒前
阳光的绿竹完成签到,获得积分20
4秒前
4秒前
开朗猫咪完成签到,获得积分10
6秒前
Lucas应助Doctor Tang采纳,获得10
6秒前
mmm完成签到,获得积分20
6秒前
晨儿发布了新的文献求助10
7秒前
7秒前
严宇耕发布了新的文献求助10
8秒前
zhu发布了新的文献求助10
8秒前
量子星尘发布了新的文献求助10
9秒前
9秒前
equinox发布了新的文献求助10
10秒前
10秒前
nnn完成签到,获得积分10
11秒前
12秒前
12秒前
kingwsws发布了新的文献求助10
12秒前
斐然完成签到,获得积分20
12秒前
13秒前
13秒前
一十六发布了新的文献求助10
14秒前
科研通AI6.2应助qingmoheng采纳,获得10
15秒前
s5228201完成签到 ,获得积分10
15秒前
悬铃木发布了新的文献求助10
16秒前
Latti完成签到,获得积分10
16秒前
16秒前
16秒前
ZHANG发布了新的文献求助10
17秒前
18秒前
朱孟研发布了新的文献求助10
18秒前
瞎忙活完成签到 ,获得积分10
18秒前
Owen应助无聊的爆米花采纳,获得10
18秒前
奋斗的俊驰完成签到,获得积分10
18秒前
19秒前
小马甲应助Aurora采纳,获得10
19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
Burger's Medicinal Chemistry, Drug Discovery and Development, Volumes 1 - 8, 8 Volume Set, 8th Edition 1800
Cronologia da história de Macau 1600
Contemporary Debates in Epistemology (3rd Edition) 1000
International Arbitration Law and Practice 1000
文献PREDICTION EQUATIONS FOR SHIPS' TURNING CIRCLES或期刊Transactions of the North East Coast Institution of Engineers and Shipbuilders第95卷 1000
BRITTLE FRACTURE IN WELDED SHIPS 1000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 纳米技术 计算机科学 化学工程 生物化学 物理 复合材料 内科学 催化作用 物理化学 光电子学 细胞生物学 基因 电极 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6163416
求助须知:如何正确求助?哪些是违规求助? 7991320
关于积分的说明 16615507
捐赠科研通 5270889
什么是DOI,文献DOI怎么找? 2812166
邀请新用户注册赠送积分活动 1792236
关于科研通互助平台的介绍 1658469