Unraveling the synergy of interface engineering α-MnO2/Bi2WO6 heterostructures and defective active sites for superdurable photocatalysis: Mechanistic insights into charge separation/transfer

被引:23
作者
Arif, Muhammad [1 ]
Mahsud, Ayaz [2 ]
Ali, Amjad [3 ]
Liao, Shipeng [1 ]
Xia, Jiawei [1 ]
Xiao, Hai [4 ,5 ]
Azam, Mohammad [6 ]
Muhmood, Tahir [7 ]
Lu, Zhansheng [2 ]
Chen, Yinjuan [1 ]
机构
[1] Changzhou Univ, Adv Catalysis & Green Mfg Collaborat Innovat Ctr, Key Lab Adv Catalyt Mat & Technol, Changzhou 213164, Peoples R China
[2] Henan Normal Univ, Sch Phys, Xinxiang 453007, Peoples R China
[3] Linkoping Univ, Dept Sci & Technol, Lab Organ Elect, SE-60174 Norrkoping, Sweden
[4] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
[5] Tsinghua Univ, Key Lab Organ Optoelect & Mol Engn, Minist Educ, Beijing 100084, Peoples R China
[6] King Saud Univ, Coll Sci, Dept Chem, POB 2455, Riyadh 11451, Saudi Arabia
[7] Nanjing Forestry Univ, Jiangsu Coinnovat Ctr Efficient Proc & Utilizat Fo, Int Innovat Ctr Forest Chem & Mat, Coll Sci, Nanjing 210037, Peoples R China
基金
中国国家自然科学基金;
关键词
alpha-MnO2/Bi2WO6; heterostructure; Defect engineering; Built-in interface; Defective active sites; Z-scheme photocatalysis; TOTAL-ENERGY CALCULATIONS; Z-SCHEME; BI2WO6; NANOSHEETS; OXYGEN VACANCIES; DEGRADATION; WATER; HETEROJUNCTION; TETRACYCLINE; REDUCTION; COMPOSITE;
D O I
10.1016/j.cej.2023.146458
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The construction of visible-light-driven hybrid heterostructure photocatalysts is of great significance for environmental remediation, although the utilization of strong visible-light response photocatalysts with high efficiency and stability remains a major challenge. Defect engineering is an excellent way to introduce metal cation vacancies in materials, thereby ensuing in highly enhanced catalytic performance. Inspired by this, we effectively constructed a built-in interface alpha-MnO2/Bi2WO6 heterostructure with abundant intimate interfaces and defective Mn3+/Mn4+ active sites for photocatalytic tetracycline hydrochloride (TC-HCl), hexavalent chromium Cr6+ reduction, and Escherichia coli (E. coli) inactivation. The experimental results, such as the active species test and X-ray photoelectron spectroscopy, indicated that the defective sites Mn3+/Mn4+, surface oxygen vacancies, and Bi(3+x)+ boosted the visible light absorption, and highly enhanced the photoinduced charge separation/transfer. Furthermore, experimental and DFT calculations reveal the high charge density at the built-in interface heterostructure and the Z-scheme charge transfer mechanism during the photocatalytic process. The results further reveal that O-2(-) and O-1(2) are the main reactive active species contributing to the photocatalytic reaction. The exceptional TC-HCl decomposition activity of the alpha-MnO2/Bi2WO6 heterostructure (97.56%, 2.31, and 2.04 times higher than bulk), enhanced reaction kinetics (K-app = 0.041 min(-1), 6.4, and 5.2 times higher than bulk), removal rate of 80.3%, Cr6+ reduction to Cr3+ (98.56%, K-app = 0.0599 min(-1)), and almost 100% bacterial inactivation compared to bulk alpha-MnO2 (42.22%) and Bi2WO6 (47.76%), were mainly due to the enhanced charge separation/transfer at the built-in interface and high charge density. This study opens new horizons for constructing Z-scheme MnO-based interface heterostructures with abundant defect sites for exceptional photocatalytic applications.
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页数:18
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