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The Structure of a Water-oxidizing Cobalt Oxide Film and Comparison to the Photosynthetic Manganese Complex

机译:水氧化氧化钴膜的结构及其与光合锰配合物的比较

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In photosynthesis, water is oxidized at a proteinbound Mn4Ca complex. Artificial water-oxidation catalysts that are similarly efficient and based on inexpensive and abundant materials are of great interest. A recently reported inorganic cobalt catalyst (CoCat) forms by electrodeposition as an amorphous layer on inert anodes, starting from an aqueous solution of cobalt ions and buffered salts such as potassium phosphate (KPi). X-ray absorption spectroscopy (XAS) indicates that the central unit of the CoCat is a cluster of edge-sharing CoⅢ(μ-O)6 octahedra. We find that the apparent cluster nuclearity is higher for film formation at anode voltages below the water-oxidation threshold. These films exhibit only minimally lower cobalt oxidation states than the films of the same thickness but deposited at voltages supporting water-oxidation. The similarities in structure, function, and oxidative self-assembly of the all-inorganic CoCat and the photosynthetic Mn4Ca complex are striking, despite stark differences in the chemical environment.
机译:在光合作用中,水在蛋白质结合的Mn4Ca复合物中被氧化。类似地有效并且基于廉价和丰富的材料的人工水氧化催化剂引起了极大的兴趣。最近报道的无机钴催化剂(CoCat)是通过在惰性阳极上电沉积为非晶层而形成的,起始于钴离子和缓冲盐(如磷酸钾(KPi))的水溶液。 X射线吸收光谱(XAS)表明CoCat的中心单元是边缘共享的CoⅢ(μ-O)6八面体的簇。我们发现,在低于水氧化阈值的阳极电压下,成膜的表观核能更高。与相同厚度但在支持水氧化的电压下沉积的膜相比,这些膜仅显示出最低的钴氧化态。尽管化学环境存在明显差异,但全无机CoCat和光合Mn4Ca络合物在结构,功能和氧化自组装方面的相似性令人惊讶。

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