Unlocking enhanced photo-Fenton, night-Fenton, and photocatalytic activities of dual Z-scheme MoS2 /WO3-x /Ag2 S core-shell structure via defect engineering

被引:16
作者
Abbas, Muhammad [1 ]
Hussain, Kashif [2 ,3 ,4 ,5 ]
Shah, Navid Hussain [1 ]
Ilyas, Mubashar [6 ]
Batool, Rabia [7 ]
Ahmad, M. Ashfaq [9 ]
Cui, Yanyan [1 ]
Wang, Yaling [8 ]
机构
[1] Beijing Inst Technol, Beijing Engn Res Ctr Mixed Real & Adv Display, Sch Opt & Photon, Beijing 100081, Peoples R China
[2] Shenzhen Univ, THz Tech Res Ctr, Shenzhen 518060, Peoples R China
[3] Shenzhen Univ, Shenzhen Key Lab Micronano Photon Informat Technol, Shenzhen 518060, Peoples R China
[4] Shenzhen Univ, Coll Phys & Optoelect Engn, Key Lab Optoelect Devices & Syst, Minist Educ & Guangdong Prov, Shenzhen 518060, Peoples R China
[5] Shenzhen Univ, THz Tech Res Ctr, Shenzhen 518060, Peoples R China
[6] Beijing Inst Technol, Sch Chem, Key Lab Clusters Sci, Minist Educ, Beijing 100081, Peoples R China
[7] Univ Lahore, Dept Phys, Lahore, Pakistan
[8] Natl Ctr Nanosci & Technol China, CAS Key Lab Biomed Effects Nanomat & Nanosafety, Beijing 100190, Peoples R China
[9] COMSATS Univ Islamabad, Dept Phys, Lahore Campus, Lahore, Pakistan
来源
JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY | 2024年 / 197卷
基金
中国国家自然科学基金;
关键词
Fenton reaction; Photolysis; Core-shell; Dual Z-scheme; TC; WO3-x; DENSITY-FUNCTIONAL THEORY; LIGHT; NANOSHEETS; WO3; NANOPARTICLES; TETRACYCLINE; DEGRADATION; REDUCTION; EVOLUTION; SITES;
D O I
10.1016/j.jmst.2024.01.078
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Memory catalysis and conventional Fenton reactions are intended to counteract prevailing energy and environmental crises; however, poor performance and the need for UV irradiation question their sustainability. Herein, we demonstrate defect-engineered, dual Z-scheme MoS2 /WO3-x /Ag2 S exhibiting enhanced photo-Fenton (PFR), night-Fenton (NFR), and photocatalytic activities (PR) against tetracycline (TC) and Rhodamine B (RhB). Defects enable the catalyst to store ample electrons just like metals, which play a vital role by exciting H2 O2 during Fenton reactions. It removed 91.54 %, 76.43 %, and 83.39 % TC (40 mg L-1 ) in 100 min and registered degradation rate constants of 0.05379, 0.02858, and 0.04133 min-1 against RhB (20 mg L-1 ) during PFR, NFR, and PR respectively. The total organic carbon (TOC) removal rates reached 58.56 % and 60.88 % during TC and RhB degradations in PFR, respectively. Solid and Liquid EPR analysis shows it can excite H2 O2 to carry Fenton reactions with and without light. It demonstrates wide pH adaptability and tremendous potential to simultaneously counter energy and environmental crises. (c) 2024 Published by Elsevier Ltd on behalf of The editorial office of Journal of Materials Science & Technology.
引用
收藏
页码:160 / 170
页数:11
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