Tong Qing, Tang Yu, Zou Weixin, Ye Yu-Xin, Dong Lin, Ouyang Gangfeng
State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Key Laboratory of Mesoscopic Chemistry of MOE, School of Chemistry and Chemical Engineering, Jiangsu Key Laboratory of Vehicle Emissions Control, Center of Modern Analysis, Nanjing University, Nanjing, 210023, P. R. China.
School, of Chemical Engineering and Technology, IGCME, Sun Yat-sen University, Zhuhai, 519082, P. R. China.
Chemistry. 2024 Dec 18;30(71):e202402629. doi: 10.1002/chem.202402629. Epub 2024 Nov 10.
The utilization of CO, HO, and solar energy is regarded as a sustainable route for converting CO into chemical feedstocks, paving the way for carbon neutrality and reclamation. However, the simultaneous photocatalytic CO reduction and HO oxidation under non-sacrificial ambient conditions is still a significant challenge. Researchers have carried out extensive exploration and achieved dramatic developments in this area. In this review, we first primarily elucidate the principles of two half-reactions in the photocatalytic conversion of CO with HO, i. e., CO reduction by the photo-generated electrons and protons, and HO oxidation by the photo-generated holes without sacrificial agents. Subsequently, the strategies to promote two half-reactions are summarized, including the vacancy/facet/morphology design, adjacent redox site construction, and Z-scheme heterojunction development. Finally, we present the advanced in situ characterizations and future perspectives in this field. This review aims to provide fresh insights into effectively simultaneous photocatalytic CO reduction and HO oxidation under non-sacrificial ambient conditions.
一氧化碳、水和太阳能的利用被视为将一氧化碳转化为化学原料的可持续途径,为碳中和和回收利用铺平了道路。然而,在无牺牲剂的环境条件下同时进行光催化一氧化碳还原和水氧化仍然是一项重大挑战。研究人员已经进行了广泛的探索,并在这一领域取得了显著进展。在本综述中,我们首先主要阐明光催化一氧化碳与水转化中两个半反应的原理,即光生电子和质子还原一氧化碳,以及无牺牲剂时光生空穴氧化水。随后,总结了促进两个半反应的策略,包括空位/晶面/形貌设计、相邻氧化还原位点构建和Z型异质结开发。最后,我们介绍了该领域先进的原位表征和未来展望。本综述旨在为在无牺牲剂的环境条件下有效同时进行光催化一氧化碳还原和水氧化提供新的见解。