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Redox-Active Ligand Assisted Catalytic Water Oxidation by Ru-IV=O Intermediate

机译:Ru-IV = O中间体氧化还原活性配体辅助催化水氧化

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摘要

Water splitting is one of the most promising solutions for storing solar energy in a chemical bond. Water oxidation is still the bottleneck step because of its inherent difficulty and the limited understanding of the O-O bond formation mechanism. Molecular catalysts provide a platform for understanding this process in depth and have received wide attention since the first Ru-based catalyst was reported in 1982. Ru-V=O is considered a key intermediate to initiate the O-O bond formation through either a water nucleophilic attack (WNA) pathway or a bimolecular coupling (I2M) pathway. Herein, we report a Ru-based catalyst that displays water oxidation reactivity with Ru-IV=(O) with the help of a redox-active ligand at pH 7.0. The results of electrochemical studies and DFT calculations disclose that ligand oxidation could significantly improve the reactivity of Ru-IV=O toward water oxidation. Under these conditions, sustained water oxidation catalysis occurs at reasonable rates with low overpotential (ca. 183 mV).
机译:水分裂是在化学键中储存太阳能的最有希望的解决方案之一。由于其固有的难度和对O-O键形成机制的有限理解,水氧化仍然是瓶颈步骤。分子催化剂提供了一种用于理解该过程的平台,并在1982年报道了第一个Ru的催化剂以来,从ru基催化剂得到了广泛的关注.Ru-V = O被认为是通过水亲核攻击引发OO键形成的关键中间体。 (WNA)途径或双分子偶联(I2M)途径。在此,我们报告了一种基于Ru-IV =(O)的Ru-IV =(O)的Ru-IV =(O)催化剂,其在pH7.0下的氧化还原活性配体的帮助下。电化学研究和DFT计算的结果公开了配体氧化可以显着提高Ru-IV = O对水氧化的反应性。在这些条件下,持续的水氧化催化发生在合理的速率下,具有低过电位(约183mV)。

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