Sulfur doping induced 3D hierarchical porous BiOI–Bi2S3 S-scheme heterojunction with regulated oxygen vacancies for a four-pronged enhanced photocatalytic degradation towards four representative pollutants

IF 6.7 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Xiangdong Shi, Xiaoyun Qin, Xuanyu Yang, Xiangyu Wei, Ying Liu, Sihui Li, Guixia Liu, Jinxian Wang, Xiangting Dong, Fenghua Chen
{"title":"Sulfur doping induced 3D hierarchical porous BiOI–Bi2S3 S-scheme heterojunction with regulated oxygen vacancies for a four-pronged enhanced photocatalytic degradation towards four representative pollutants","authors":"Xiangdong Shi, Xiaoyun Qin, Xuanyu Yang, Xiangyu Wei, Ying Liu, Sihui Li, Guixia Liu, Jinxian Wang, Xiangting Dong, Fenghua Chen","doi":"10.1016/j.mtchem.2024.102283","DOIUrl":null,"url":null,"abstract":"It is challenging and still difficult to adjust and boost the catalytic performance of photocatalysts via the synergistic achievement of heteroatom doping, vacancies engineering, morphology regulation, and appropriate structural design. Herein, we developed an efficient method to synthesize 3D hierarchical porous BiOI–BiS S-scheme heterojunction with oxygen vacancies (Ov-BBS) induced by sulfur doping and systematically investigated regulation of oxygen vacancies by sulfur doping and their effects on photocatalytic performance. Results showed that sulfur species promoted the formation of S-scheme heterojunction but depleted oxygen vacancies in Ov-BiOI. The optimal sulfur doped catalyst (Ov-BBS-0.1) exhibited excellent UV–vis light photocatalytic activity towards four representative pollutants, affording removal rate of 97.1 % for MB, 97.6 % for RhB, 99.4 % for Cr(VI), and 92.0 % for TC, respectively, which were higher than those of pristine BiS, BiOI, Ov-BiOI, Ov-BiOI/BiS mixture, Ov-BBS-0.05, and Ov-BBS-0.2. Deep characterizations and theoretical studies certified that the four-pronged enhancement strategy of 3D hierarchical porous structure, oxygen vacancies, sulfur doping and the constructed S-scheme heterojunction, not only enriched accessible active sites, but also promoted electronic polarization and modulated electronic structure, resulting in rapid separation and migration of photogenerated carriers. Moreover, considering the excellent stability and cyclic photocatalytic performance, the film prepared by pumping Ov-BBS dispersion was also satisfactory in the practical application of circulating sewage treatment. Overall, the present work provides a novel approach for the design of more photocatalysts with high efficiency.","PeriodicalId":18353,"journal":{"name":"Materials Today Chemistry","volume":"13 1","pages":""},"PeriodicalIF":6.7000,"publicationDate":"2024-09-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Today Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1016/j.mtchem.2024.102283","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

It is challenging and still difficult to adjust and boost the catalytic performance of photocatalysts via the synergistic achievement of heteroatom doping, vacancies engineering, morphology regulation, and appropriate structural design. Herein, we developed an efficient method to synthesize 3D hierarchical porous BiOI–BiS S-scheme heterojunction with oxygen vacancies (Ov-BBS) induced by sulfur doping and systematically investigated regulation of oxygen vacancies by sulfur doping and their effects on photocatalytic performance. Results showed that sulfur species promoted the formation of S-scheme heterojunction but depleted oxygen vacancies in Ov-BiOI. The optimal sulfur doped catalyst (Ov-BBS-0.1) exhibited excellent UV–vis light photocatalytic activity towards four representative pollutants, affording removal rate of 97.1 % for MB, 97.6 % for RhB, 99.4 % for Cr(VI), and 92.0 % for TC, respectively, which were higher than those of pristine BiS, BiOI, Ov-BiOI, Ov-BiOI/BiS mixture, Ov-BBS-0.05, and Ov-BBS-0.2. Deep characterizations and theoretical studies certified that the four-pronged enhancement strategy of 3D hierarchical porous structure, oxygen vacancies, sulfur doping and the constructed S-scheme heterojunction, not only enriched accessible active sites, but also promoted electronic polarization and modulated electronic structure, resulting in rapid separation and migration of photogenerated carriers. Moreover, considering the excellent stability and cyclic photocatalytic performance, the film prepared by pumping Ov-BBS dispersion was also satisfactory in the practical application of circulating sewage treatment. Overall, the present work provides a novel approach for the design of more photocatalysts with high efficiency.
掺硫诱导的三维分层多孔 BiOI-Bi2S3 S 型异质结具有调节氧空位,可对四种代表性污染物进行四管齐下的增强型光催化降解
如何通过异质原子掺杂、空位工程、形态调控和适当的结构设计等协同作用来调整和提高光催化剂的催化性能,是一项具有挑战性的工作,目前仍很困难。在此,我们开发了一种在硫掺杂诱导下合成具有氧空位(Ov-BBS)的三维分层多孔BiOI-BiS S型异质结的有效方法,并系统研究了硫掺杂对氧空位的调控及其对光催化性能的影响。结果表明,硫元素促进了 S 型异质结的形成,但却耗尽了 Ov-BiOI 中的氧空位。最佳硫掺杂催化剂(Ov-BBS-0.1)对四种代表性污染物具有优异的紫外可见光光催化活性,对 MB、RhB、Cr(VI) 和 TC 的去除率分别为 97.1%、97.6%、99.4% 和 92.0%,均高于原始 BiS、BiOI、Ov-BiOI、Ov-BiOI/BiS 混合物、Ov-BBS-0.05 和 Ov-BBS-0.2。深入的表征和理论研究证明,三维分层多孔结构、氧空位、硫掺杂和构建的 S 型异质结这四管齐下的增强策略不仅丰富了可访问的活性位点,还促进了电子极化和电子结构调制,使光生载流子快速分离和迁移。此外,考虑到其优异的稳定性和循环光催化性能,泵送 Ov-BBS 分散制备的薄膜在循环污水处理的实际应用中也令人满意。总之,本研究为设计更多高效光催化剂提供了一种新方法。
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
CiteScore
8.90
自引率
6.80%
发文量
596
审稿时长
33 days
期刊介绍: Materials Today Chemistry is a multi-disciplinary journal dedicated to all facets of materials chemistry. This field represents one of the fastest-growing areas of science, involving the application of chemistry-based techniques to the study of materials. It encompasses materials synthesis and behavior, as well as the intricate relationships between material structure and properties at the atomic and molecular scale. Materials Today Chemistry serves as a high-impact platform for discussing research that propels the field forward through groundbreaking discoveries and innovative techniques.
×
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