期刊
CHEMICAL SOCIETY REVIEWS
卷 49, 期 18, 页码 6579-6591出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9cs00920e
关键词
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资金
- National Key RAMP
- D Program of China [2017YFA0207301]
- NSFC [21725102, 51902253, 91961106]
- CAS Key Research Program of Frontier Sciences [QYZDB-SSW-SLH018]
- Shannxi Key Research and Development Project [2019ZDLSF05-05-01]
- CAS Interdisciplinary Innovation Team
Solar-driven reduction of CO(2)into fuels/feedstocks is a promising strategy for addressing energy and CO(2)emission issues. Despite great research efforts, it still remains a grand challenge to achieve efficient and highly selective reduction of CO(2)owing to the large bond energy of CO(2)and the diversity of reduction products. In addition to the control of light harvesting and charge transfer like photocatalytic water splitting, the design of catalytically active sites is highly important to promote CO(2)reduction activity and selectivity (e.g., C-C coupling). In fact, we can learn a lot from conventional CO(2)hydrogenation and syngas conversion in terms of active site design. In this article, we demonstrate how to design catalytically active sites for efficient and highly selective photocatalytic reduction of CO(2)by sorting out the rules from the existing research on conventional CO(x)hydrogenation, with a focus on enhancing Cxe001;O activation and C-C coupling to form value-added products. This article aims to highlight the challenges in the field of photocatalytic CO(2)conversion and the connection of photocatalysis with conventional catalytic systems, providing the readers the opportunities to join the research.
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