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Efficient Homogeneous Electrocatalytic Water Oxidation by a Manganese Cluster with an Overpotential of Only 74 mV

机译:锰簇的高效均匀电催化水氧化仅为74 MV的过电位

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Water electrolysis is among the simplest method for generating hydrogen as an alternative renewable fuel. A major challenge associated with this process is the development of cheap, simple, and environmentally benign catalysts that lead to a minimum overpotential for water oxidation. Inspired by the Mn4CaOx cluster that catalyzes water oxidation in photosystemII, described here is the synthesis and characterization of the manganese cluster [Mn12O12(O2CC6H2(OH)(3))(16)(H2O)(4)] (Mn12TH) along with its electrocatalytic activity at pH 6. Electrochemical, spectroscopic, and electron microscopy studies show that Mn12TH is a homogeneous electrocatalyst for water oxidation and enables oxygen evolution with a reaction rate of 22 s(-1), high Faradic efficiency (93%), and an overpotential of only 74 mV, the lowest reported to date. Based on the electrochemical data, the organic ligands, which can be described as the second coordination sphere of the catalytic manganese core, play a key role in facilitating the oxidation process and accelerating the reaction.
机译:水电解是作为替代可再生燃料产生氢的最简单方法之一。与此过程相关的主要挑战是开发廉价,简单和环境良性催化剂,导致水氧化的最小过电位。由Mn4CaOx簇催化在这里描述的锰氧化的Mn4CaOx簇是锰簇[Mn12O12(O 2CC6H2(OH)(3))(16)(4)(4)](Mn12)以及其的合成和表征pH6的电催化活性电化学,光谱和电子显微镜研究表明,MN12TH是用于水氧化的均匀电催化剂,使氧气进化具有22 s(-1),高法拉效率(93%)和一个只有74英米的过电位,最低报告迄今为止。基于电化学数据,可以描述为催化锰核的第二配位球的有机配体在促进氧化过程和加速反应方面发挥关键作用。

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