A direct Z-scheme S-Co3O4/Bi2WO6 heterostructure for enhanced photoelectrocatalytic degradation of tetracycline under visible light. (23rd January 2023)
- Record Type:
- Journal Article
- Title:
- A direct Z-scheme S-Co3O4/Bi2WO6 heterostructure for enhanced photoelectrocatalytic degradation of tetracycline under visible light. (23rd January 2023)
- Main Title:
- A direct Z-scheme S-Co3O4/Bi2WO6 heterostructure for enhanced photoelectrocatalytic degradation of tetracycline under visible light
- Authors:
- Jia, Litao
Yu, Pei
Dong, Ying
Xing, Yonglei
Peng, Juan
Ni, Gang
Jin, Xiaoyong - Abstract:
- Abstract : Investigation of tetracycline degradation mechanism by calculation of material work function and free radical experiments. Abstract : The decomposition efficiency of refractory organic pollutants depends strongly on the characteristics of the photoanode semiconductors in the photoelectrocatalytic (PEC) process. The selection of superior materials with excellent PEC efficiency is a challenge in the practical application of PEC oxidation technology. Herein, a novel S-Co3 O4 /Bi2 WO6 heterojunction photoanode was fabricated using a simple hydrothermal procedure. Compared with Bi2 WO6 nanoflowers, the as-prepared S-Co3 O4 /Bi2 WO6 photoanode had a large electroactive surface area, low charge transfer resistance, strong light absorption ability, and high separation efficiency for induced photogenerated electron/hole pairs (e − /h + ). This relies on the fact that S doping not only controls the morphology of Co3 O4 but also changes its intrinsic electronic structure to improve the interlayer polarization. Notably, the Z-scheme heterojunction formed by the combination of S-Co3 O4 and Bi2 WO6 not only enhances the e − /h + separation efficiency but also results in a stronger redox ability than that of pure Bi2 WO6 . In addition, reactive species trapping experiments and electron spin resonance tests demonstrated that the S-Co3 O4 /Bi2 WO6 photoanode plays a dominant role in the degradation of tetracycline (TC) by ˙O2 − and ˙OH radicals. Therefore, the prepared S-Co3 O4Abstract : Investigation of tetracycline degradation mechanism by calculation of material work function and free radical experiments. Abstract : The decomposition efficiency of refractory organic pollutants depends strongly on the characteristics of the photoanode semiconductors in the photoelectrocatalytic (PEC) process. The selection of superior materials with excellent PEC efficiency is a challenge in the practical application of PEC oxidation technology. Herein, a novel S-Co3 O4 /Bi2 WO6 heterojunction photoanode was fabricated using a simple hydrothermal procedure. Compared with Bi2 WO6 nanoflowers, the as-prepared S-Co3 O4 /Bi2 WO6 photoanode had a large electroactive surface area, low charge transfer resistance, strong light absorption ability, and high separation efficiency for induced photogenerated electron/hole pairs (e − /h + ). This relies on the fact that S doping not only controls the morphology of Co3 O4 but also changes its intrinsic electronic structure to improve the interlayer polarization. Notably, the Z-scheme heterojunction formed by the combination of S-Co3 O4 and Bi2 WO6 not only enhances the e − /h + separation efficiency but also results in a stronger redox ability than that of pure Bi2 WO6 . In addition, reactive species trapping experiments and electron spin resonance tests demonstrated that the S-Co3 O4 /Bi2 WO6 photoanode plays a dominant role in the degradation of tetracycline (TC) by ˙O2 − and ˙OH radicals. Therefore, the prepared S-Co3 O4 /Bi2 WO6 photoanode exhibits better PEC performance than Co3 O4, S-Co3 O4 and Bi2 WO6 in the degradation of TC. The optimized S-Co3 O4 /Bi2 WO6 composite showed a degradation rate of 87.4% in 30 mg L −1 TC solution. This work provides a new strategy for the construction of efficient photoelectroanodes. … (more)
- Is Part Of:
- New journal of chemistry. Volume 47:Number 8(2023)
- Journal:
- New journal of chemistry
- Issue:
- Volume 47:Number 8(2023)
- Issue Display:
- Volume 47, Issue 8 (2023)
- Year:
- 2023
- Volume:
- 47
- Issue:
- 8
- Issue Sort Value:
- 2023-0047-0008-0000
- Page Start:
- 3745
- Page End:
- 3757
- Publication Date:
- 2023-01-23
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/d2nj05977k ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 25966.xml