A review on the state-of-the-art advances for CO2 electro-chemical reduction using metal complex molecular catalysts

H. Louis, O. Akakuru, Philip Monday, O. O. Funmilayo
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引用次数: 3

Abstract

Significantly, global warming which is caused by CO2 emission and energy shortage are global problems resulting from artificial photosynthesis because it required many functions (light harvesting, Z water, and oxidation scheme). Therefore, photocatalytic systems development for CO2 reduction is germane in this field. Metal complexes molecular catalyst have become prevalent homogeneous catalysts for carbon dioxide (CO2) photocatalytic reduction since it was initially known as CO2 reduction catalysts in the 70s and the 80s, while utmost part involved macrocyclic cobalt(II) and nickel(II) complexes. This review article presents a broad understanding on some active catalysts recently reported as a metal complex molecular catalytic schemes for CO2 reduction, alongside catalytic activity, stability, selectivity under electro-reduction, and photoreduction circumstances. The progress of in situ spectroelectrochemical methods, typically supported via theoretical calculations, helped to access this know-how by providing information which enabled researchers to acquire more in-depth perception into unveiling the catalytic reaction and mechanisms intermediates.
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金属络合分子催化剂在CO2电化学还原中的研究进展
值得注意的是,二氧化碳排放和能源短缺导致的全球变暖是由人工光合作用引起的全球性问题,因为人工光合作用需要许多功能(光收集、Z水和氧化方案)。因此,开发用于二氧化碳还原的光催化系统在这一领域是密切相关的。金属配合物分子催化剂自上世纪七八十年代初被称为CO2还原催化剂以来,已成为二氧化碳光催化还原中普遍使用的均相催化剂,其中大部分是大环钴(II)和镍(II)配合物。本文综述了近年来报道的几种金属络合物分子催化方案的活性催化剂,以及电还原和光还原条件下的催化活性、稳定性、选择性。原位光谱电化学方法的进步,通常是通过理论计算来支持的,通过提供信息,使研究人员能够更深入地了解催化反应和中间体机制,从而帮助获得这些知识。
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