MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry, Sun Yat-sen University, Guangzhou, 510275, China.
Nat Commun. 2023 Feb 25;14(1):1087. doi: 10.1038/s41467-023-36784-7.
The direct utilization of solar energy to convert CO into renewable chemicals remains a challenge. One essential difficulty is the development of efficient and inexpensive light-absorbers. Here we show a series of aminoanthraquinone organic dyes to promote the efficiency for visible light-driven CO reduction to CO when coupled with an Fe porphyrin catalyst. Importantly, high turnover numbers can be obtained for both the photosensitizer and the catalyst, which has not been achieved in current light-driven systems. Structure-function study performed with substituents having distinct electronic effects reveals that the built-in donor-acceptor property of the photosensitizer significantly promotes the photocatalytic activity. We anticipate this study gives insight into the continued development of advanced photocatalysts for solar energy conversion.
将太阳能直接转化为可再生化学品仍然是一个挑战。一个基本的困难是开发高效且廉价的光吸收剂。在这里,我们展示了一系列氨基蒽醌有机染料,当与铁卟啉催化剂结合时,可促进可见光驱动的 CO 还原为 CO 的效率。重要的是,在当前的光驱动系统中,敏化剂和催化剂都可以获得高的周转数。用具有不同电子效应的取代基进行的结构-功能研究表明,敏化剂的内置供体-受体性质显著促进了光催化活性。我们预计这项研究将为太阳能转换的先进光催化剂的进一步发展提供启示。