Activated CdS/ sulfur doped g-C3N4 photocatalyst for dye and antibiotic degradation: Experimental and DFT verification of S-scheme heterojunction.

IF 7.7 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES
Environmental Research Pub Date : 2025-02-01 Epub Date: 2024-11-29 DOI:10.1016/j.envres.2024.120487
Xu Duan, Jian Yang, Jiaqing Zhu, Hongbin Li, Yujie Fang, Runxue Liu, Chen Yang, Weizao Liu, Chunlian Ding, Qingcai Liu, Jiangling Li, Shan Ren
{"title":"Activated CdS/ sulfur doped g-C<sub>3</sub>N<sub>4</sub> photocatalyst for dye and antibiotic degradation: Experimental and DFT verification of S-scheme heterojunction.","authors":"Xu Duan, Jian Yang, Jiaqing Zhu, Hongbin Li, Yujie Fang, Runxue Liu, Chen Yang, Weizao Liu, Chunlian Ding, Qingcai Liu, Jiangling Li, Shan Ren","doi":"10.1016/j.envres.2024.120487","DOIUrl":null,"url":null,"abstract":"<p><p>To alleviate situation caused by azo dyestuff and antibiotics, a series of CdS/sulfur doped carbon nitride (GCNS) S-scheme heterojunction photocatalysts have been successfully fabricated by a pretty facile solid-state diffusion (SSD) method,. Under visible light, the optimal sample called CdS/GCNS-1:2 presented the best photodegradation rate of nearly 100% over methyl orange (MO), of which the reaction constant k was about 9.67 and 5.39 times higher than that of pure GCNS and CdS, respectively. Degradation rate of 91% over tetracycline hydrochloride (TCH) was achieved within 60 min as well. The DFT calculations, XPS and charge flow tracking tests clarified the surge of C-S linkages and the construction of interfacial S-scheme heterojunction. The former promoted the fixation and conversion of adsorbed oxygen, while the latter accelerated the separation/transport of charge carriers. These tuning eventually collaborates on the promotion of •O<sub>2</sub><sup>-</sup> reactive species, which confirmed as the predominant role of photoreaction. Furthermore, the plausible degradation pathways of MO/TCH and photocatalytic optimization mechanism were thoroughly elucidated.</p>","PeriodicalId":312,"journal":{"name":"Environmental Research","volume":" ","pages":"120487"},"PeriodicalIF":7.7000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental Research","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.1016/j.envres.2024.120487","RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/29 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

To alleviate situation caused by azo dyestuff and antibiotics, a series of CdS/sulfur doped carbon nitride (GCNS) S-scheme heterojunction photocatalysts have been successfully fabricated by a pretty facile solid-state diffusion (SSD) method,. Under visible light, the optimal sample called CdS/GCNS-1:2 presented the best photodegradation rate of nearly 100% over methyl orange (MO), of which the reaction constant k was about 9.67 and 5.39 times higher than that of pure GCNS and CdS, respectively. Degradation rate of 91% over tetracycline hydrochloride (TCH) was achieved within 60 min as well. The DFT calculations, XPS and charge flow tracking tests clarified the surge of C-S linkages and the construction of interfacial S-scheme heterojunction. The former promoted the fixation and conversion of adsorbed oxygen, while the latter accelerated the separation/transport of charge carriers. These tuning eventually collaborates on the promotion of •O2- reactive species, which confirmed as the predominant role of photoreaction. Furthermore, the plausible degradation pathways of MO/TCH and photocatalytic optimization mechanism were thoroughly elucidated.

活化CdS/硫掺杂g-C3N4光催化剂用于染料和抗生素降解:s -图式异质结的实验和DFT验证。
为了减轻偶氮染料和抗生素的影响,采用一种简单的固态扩散(SSD)方法成功制备了一系列CdS/硫掺杂氮化碳(GCNS) s型异质结光催化剂。在可见光下,最优样品CdS/GCNS-1:2对甲基橙(MO)的光降解率接近100%,其反应常数k分别比纯GCNS和CdS高9.67倍和5.39倍。60 min内对盐酸四环素(TCH)的降解率为91%。DFT计算、XPS和电荷流跟踪实验明确了C-S键的涌动和界面s型异质结的构建。前者促进了吸附氧的固定和转化,后者则加速了载流子的分离/输运。这些调整最终协同促进•O2-反应物质,这证实了光反应的主要作用。进一步深入探讨了MO/TCH的降解途径及光催化优化机理。
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
Environmental Research
Environmental Research 环境科学-公共卫生、环境卫生与职业卫生
CiteScore
12.60
自引率
8.40%
发文量
2480
审稿时长
4.7 months
期刊介绍: The Environmental Research journal presents a broad range of interdisciplinary research, focused on addressing worldwide environmental concerns and featuring innovative findings. Our publication strives to explore relevant anthropogenic issues across various environmental sectors, showcasing practical applications in real-life settings.
×
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