Molybdenum (VI)‐oxo Clusters Incorporation Activates g‐C3N4 with Simultaneously Regulating Charge Transfer and Reaction Centers for Boosting Photocatalytic Performance. (7th July 2022)
- Record Type:
- Journal Article
- Title:
- Molybdenum (VI)‐oxo Clusters Incorporation Activates g‐C3N4 with Simultaneously Regulating Charge Transfer and Reaction Centers for Boosting Photocatalytic Performance. (7th July 2022)
- Main Title:
- Molybdenum (VI)‐oxo Clusters Incorporation Activates g‐C3N4 with Simultaneously Regulating Charge Transfer and Reaction Centers for Boosting Photocatalytic Performance
- Authors:
- Zhang, Sai
Liu, Yang
Ma, Ran
Jia, Dashuang
Wen, Tao
Ai, Yuejie
Zhao, Guixia
Fang, Fang
Hu, Baowei
Wang, Xiangke - Abstract:
- Abstract: Establishing local built‐in electric field of 2D semiconductors is one of the promising strategies to regulate the oriented charge delivery to active centers for enhancing photocatalytic performance. Herein, a novel heptamolybdate polyanions‐intercalated porous g‐C3 N4 ([Mo7 O24 ] 6− ‐ p CN) catalyst with integrating highly desirable visible‐light photocatalytic features is reported. After intercalation, the apparent reaction rate constants ( k app ) of [Mo7 O24 ] 6− ‐ p CN for bisphenol A (BPA) and 4‐chlorophenol (4‐CP) photodegradation are remarkably enhanced, which are 9.0 and 6.4 times faster than those of p CN, respectively. Analogously, the k app values of [Mo7 O24 ] 6– ‐CN for BPA and 4‐CP removal are also improved by contrast with CN. The experimental results and density functional theory calculations indicate that a local built‐in electric field is formed in [Mo7 O24 ] 6− ‐ p CN with a polarization direction from aromatic rings of g‐C3 N4 to the inserted [Mo7 O24 ] 6− clusters. Driven by the electric field, photogenerated carriers can be efficiently separated for better reactive oxidative species (ROSs) production. These O atoms are also proved as adsorption sites for phenols, greatly reducing the migration distance of ROSs and thus improving photocatalytic performances. This work offers a reliable strategy to construct local built‐in electric field via polyoxometalates intercalation for effective solar energy conversion and phenolic wastewaterAbstract: Establishing local built‐in electric field of 2D semiconductors is one of the promising strategies to regulate the oriented charge delivery to active centers for enhancing photocatalytic performance. Herein, a novel heptamolybdate polyanions‐intercalated porous g‐C3 N4 ([Mo7 O24 ] 6− ‐ p CN) catalyst with integrating highly desirable visible‐light photocatalytic features is reported. After intercalation, the apparent reaction rate constants ( k app ) of [Mo7 O24 ] 6− ‐ p CN for bisphenol A (BPA) and 4‐chlorophenol (4‐CP) photodegradation are remarkably enhanced, which are 9.0 and 6.4 times faster than those of p CN, respectively. Analogously, the k app values of [Mo7 O24 ] 6– ‐CN for BPA and 4‐CP removal are also improved by contrast with CN. The experimental results and density functional theory calculations indicate that a local built‐in electric field is formed in [Mo7 O24 ] 6− ‐ p CN with a polarization direction from aromatic rings of g‐C3 N4 to the inserted [Mo7 O24 ] 6− clusters. Driven by the electric field, photogenerated carriers can be efficiently separated for better reactive oxidative species (ROSs) production. These O atoms are also proved as adsorption sites for phenols, greatly reducing the migration distance of ROSs and thus improving photocatalytic performances. This work offers a reliable strategy to construct local built‐in electric field via polyoxometalates intercalation for effective solar energy conversion and phenolic wastewater remediation. Abstract : 2D porous g‐C3 N4 with heptamolybdate ([Mo7 O24 ] 6− ) clusters intercalation achieve the efficient removal of refractory phenols from wastewater via visible‐light photodegradation. The inserted [Mo7 O24 ] 6− clusters induce the formation of local built‐in electric field, and drive fast charge transfer from conjugated aromatic ring to O atoms, while rich O sites are provided to adsorb phenols, thus improving the photocatalytic performances. … (more)
- Is Part Of:
- Advanced functional materials. Volume 32:Number 38(2022)
- Journal:
- Advanced functional materials
- Issue:
- Volume 32:Number 38(2022)
- Issue Display:
- Volume 32, Issue 38 (2022)
- Year:
- 2022
- Volume:
- 32
- Issue:
- 38
- Issue Sort Value:
- 2022-0032-0038-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-07-07
- Subjects:
- built‐in electric field -- graphitic carbon nitride -- molybdenum (VI)‐oxo clusters -- phenols degradation -- visible‐light photocatalysis
Materials -- Periodicals
Chemical vapor deposition -- Periodicals
620.11 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1616-3028 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/adfm.202204175 ↗
- Languages:
- English
- ISSNs:
- 1616-301X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0696.853900
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23902.xml