Authors
Ruonan Wang, Jingjing Liu, Qin Zhong, Jianfeng Yao
Published in
ChemSusChem. Pages e2501468. Aug 28, 2025. Epub Aug 28, 2025.
Abstract
Artificial photosynthesis presents a highly promising approach for addressing global energy and environmental challenges. However, its efficiency remains constrained by rapid charge recombination and inefficient CO2 activation. To overcome these limitations, cobalt-nickel layered double hydroxide (CN-LDH) is decorated onto BiOBr nanosheets to enhance Lewis alkaline sites and facilitate charge separation. The resultant composite, denoted as BxCy, exhibits a stronger internal electric field than its individual components, promoting efficient migration of photogenerated carriers. This engineered structure directs photoinduced electrons accumulated in CN-LDH for CO2 reduction, as verified by in situ Kelvin probe force microscopy. Furthermore, in situ diffuse reflectance infrared Fourier transform spectroscopy combined with pulsed chemisorption studies identifies the critical activated carbonate intermediates (*CO2- and *COOH) as essential precursors for CO production. Consequently, the optimized B5C1 catalyst achieves a remarkable CO evolution rate of 88.92 μmol g-1 with 100% selectivity. This work provides pivotal insights into the charge transfer dynamics and intermediate evolution pathways during photocatalytic CO2 reduction.
PMID:
40875916
Bibliographic data and abstract were imported from PubMed on 29 Aug 2025.
Read full publication at:
Please sign in
to see all details.
Advertisement
Stats
- Recommendations n/a n/a positive of 0 vote(s)
- Views 28
- Comments 0