Dalle Kristian E, Warnan Julien, Leung Jane J, Reuillard Bertrand, Karmel Isabell S, Reisner Erwin
Christian Doppler Laboratory for Sustainable SynGas Chemistry, Department of Chemistry , University of Cambridge , Lensfield Road , Cambridge CB2 1EW , United Kingdom.
Chem Rev. 2019 Feb 27;119(4):2752-2875. doi: 10.1021/acs.chemrev.8b00392. Epub 2019 Feb 15.
The synthesis of renewable fuels from abundant water or the greenhouse gas CO is a major step toward creating sustainable and scalable energy storage technologies. In the last few decades, much attention has focused on the development of nonprecious metal-based catalysts and, in more recent years, their integration in solid-state support materials and devices that operate in water. This review surveys the literature on 3d metal-based molecular catalysts and focuses on their immobilization on heterogeneous solid-state supports for electro-, photo-, and photoelectrocatalytic synthesis of fuels in aqueous media. The first sections highlight benchmark homogeneous systems using proton and CO reducing 3d transition metal catalysts as well as commonly employed methods for catalyst immobilization, including a discussion of supporting materials and anchoring groups. The subsequent sections elaborate on productive associations between molecular catalysts and a wide range of substrates based on carbon, quantum dots, metal oxide surfaces, and semiconductors. The molecule-material hybrid systems are organized as "dark" cathodes, colloidal photocatalysts, and photocathodes, and their figures of merit are discussed alongside system stability and catalyst integrity. The final section extends the scope of this review to prospects and challenges in targeting catalysis beyond "classical" H evolution and CO reduction to C products, by summarizing cases for higher-value products from N reduction, C products from CO utilization, and other reductive organic transformations.
从丰富的水或温室气体CO合成可再生燃料是迈向创建可持续且可扩展的能量存储技术的重要一步。在过去几十年中,人们将大量注意力集中在开发非贵金属基催化剂上,近年来,又关注将其集成到在水中运行的固态载体材料和装置中。本综述调查了关于3d金属基分子催化剂的文献,并重点关注它们固定在多相固态载体上,用于在水性介质中进行电催化、光催化和光电催化合成燃料。第一部分重点介绍了使用质子和CO还原3d过渡金属催化剂的基准均相体系,以及常用的催化剂固定方法,包括对载体材料和锚定基团的讨论。随后的部分详细阐述了分子催化剂与基于碳、量子点、金属氧化物表面和半导体的各种底物之间的有效结合。分子-材料杂化体系被组织为“暗”阴极、胶体光催化剂和光阴极,并在讨论体系稳定性和催化剂完整性的同时讨论了它们的性能指标。最后一部分将本综述的范围扩展到除了“经典”的析氢和CO还原为C产物之外的靶向催化的前景和挑战,通过总结从N还原得到高价值产物、从CO利用得到C产物以及其他还原性有机转化的案例。