Abstract
Architecting Z-scheme heterojunction can restrain the recombination of photoinduced carriers to improve the photocatalytic performance. However, it still lacks high-efficiency catalysts for sustainable photoreduction of CO2. Herein, an Ag-bridged Z-scheme Bi4O5Br2/AgBr heterostructure is successfully developed, which enables room-temperature CO2 reduction driven by solar energy. In this catalyst, the Ag mediator acts as a bridge to shuttle electrons between Bi4O5Br2 and AgBr, separating the electron-hole pairs efficiently and maintaining the original strong reduction reaction. As a result, Z-scheme Bi4O5Br2/AgBr heterostructures show obviously promoted performance of photocatalytic CO2 reduction in contrast with pristine Bi4O5Br2, delivering a high CO2 conversion activity of 6.6 and 1.8 μmol g-1h−1 for CO and CH4 products, respectively. This study reports an effective reference of Z-scheme Bi4O5Br2/AgBr heterojunction for satisfactory photocatalytic solar energy conversion and synthesis of high value-added products from CO2.
| Original language | English |
|---|---|
| Article number | 153758 |
| Journal | Applied Surface Science |
| Volume | 598 |
| DOIs | |
| State | Published - 1 Oct 2022 |
| Externally published | Yes |
Keywords
- CO reduction
- Carrier separation
- Photocatalysis
- Solar energy
- Z-scheme heterojunction
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