Cover Feature: Visible Light‐Sensitized CO<sub>2</sub> Methanation along a Relaxed Heat Available Route (Chem. Eur. J. 63/2024)
The Cover Feature shows artificial photosynthesis to convert H2O vapour/CO2 into the value-added chemical CH4. Intermediate temperature-sensitive Ti−H species are generated by the photosensitized PDI dye component of the Pt/N−TiO2/PDI composite catalyst; this enables incident light energy that has relaxed into waste heat to locally heat a highly nucleophilic hydride for CO2 addition to a COOH* intermediate. (Until now it had been thought that photocatalysis and temperature were almost negatively dependent.) Shown top left is the photoexcitation process by which electrons are transferred to the TiO2 surface to generate Ti−H species; this converts 53 % of the relaxed incident light into a thermal effect to be re-used. Shown top right is the acceleration of the reaction rate through increasing the initial energy of the rate-limiting step as the catalyst surface temperature increases and it becomes easier to cross the activation barrier. More information can be found in the Research Article by D. Ma, H. Ji, W. Ma, and co-workers (DOI: 10.1002/chem.202402102).
Authors
- Jiazhen Li (ORCID: https://orcid.org/0000-0003-2716-6329)
- Jincai Zhao (ORCID: https://orcid.org/0000-0003-1449-4235)
- Dongge Ma (ORCID: https://orcid.org/0000-0002-6543-274X)
- Jianfei Ji (ORCID: https://orcid.org/0000-0003-3140-2902)
- Qiang Huang (ORCID: https://orcid.org/0000-0001-5269-4161)
- Qin He
- Hongwei Ji (ORCID: https://orcid.org/0000-0003-3128-714X)
- Wanhong Ma
- Yangyang Du (ORCID: https://orcid.org/0000-0002-5800-2717)
Institutions
- Beijing Technology and Business University (CN)
- Chinese Academy of Sciences (CN)
- Beijing National Laboratory for Molecular Sciences (CN)
- Institute of Chemistry (CN)
- University of Chinese Academy of Sciences (CN)
Publication Details
- Journal
- Chemistry - A European Journal
- Published
- 2024-11-12
- DOI
- https://doi.org/10.1002/chem.202486302
- Primary Topic
- Carbon dioxide utilization in catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.00