Remarkably enhanced catalytic performance in CoOx/Bi4Ti3O12 heterostructures for methyl orange degradation via piezocatalysis and piezo-photocatalysis

被引:54
|
作者
Wang, Kaiqi [1 ]
Guan, Ziying [1 ]
Liang, Xiaoya [1 ]
Song, Shuyue [1 ]
Lu, Pengyu [1 ]
Zhao, Chunran [1 ]
Yue, Lin [3 ]
Zeng, Zhihao [3 ]
Wu, Ying [3 ]
He, Yiming [1 ,2 ]
机构
[1] Zhejiang Normal Univ, Dept Mat Sci & Engn, Yingbin Rd 688, Jinhua 321004, Peoples R China
[2] Zhejiang Normal Univ, Key Lab Solid State Optoelect Devices Zhejiang Pro, Yingbin Rd 688, Jinhua 321004, Peoples R China
[3] Coll Chem & Mat Sci, Minist Educ Adv Catalysis Mat, Key Lab, Yingbin Rd 688, Jinhua 321004, Peoples R China
基金
中国国家自然科学基金;
关键词
Bi4Ti3O12; CoOx; piezocatalytic MO degradation; Piezo-photocatalysis; VISIBLE-LIGHT; OPTICAL-PROPERTIES; BENZYL ALCOHOL; NANOCOMPOSITE; MECHANISM; FILMS; DYE;
D O I
10.1016/j.ultsonch.2023.106616
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
A novel heterojunction composite of CoOx/Bi4Ti3O12 was synthesized through a combination of molten salt and photodeposition methods. The optimal sample exhibited superior performance in the piezocatalytic degradation of methyl orange (MO) dye with a degradation rate of 1.09 h(-1), which was 2.4 times higher than that of pristine Bi4Ti3O12. Various characterizations were conducted to reveal the fundamental nature accountable for the outstanding piezocatalytic performance of CoOx/Bi4Ti3O12. The investigation of the band structure indicated that the CoOx/Bi4Ti3O12 composite formed a type-I p-n heterojunction structure, with CoOx acting as a hole trapper to effectively separate and transfer piezogenerated carriers. Significantly, the MO degradation rate of the best CoOx/Bi4Ti3O12 sample further increased to 2.96 h(-1) under combined ultrasonic vibration and simulated sunlight. The synergy between piezocatalysis and photocatalysis can be ascribed to the following factors. The photoexcitation process ensures the sufficient generation of charge carriers in the CoOx/Bi4Ti3O12, while the piezoelectric field within Bi4Ti3O12 promotes the separation of electron-hole pairs in the bulk phase. Furthermore, the heterojunction structure between Bi4Ti3O12 and CoOx significantly facilitates the surface separation of charge carriers. This increased involvement of free electrons and holes in the reaction leads to a remarkable enhancement in catalytic MO degradation. This work contributes to the understanding of the coupling mechanism between the piezoelectric effect and photocatalysis, and also provides a promising strategy for the development of efficient catalysts for wastewater treatment.
引用
收藏
页数:13
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