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Active copper(Ⅱ) and copper(Ⅰ) reviving repeatedly in situ on copper wire electrode for full water splitting at ultra-low potential

机译:活性铜(Ⅱ)和铜(Ⅰ)在铜丝电极上反复原位复溶,以超低电位完全分解水

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摘要

Searching for inexpensive electrocatalysts for hydrogen and oxygen evolution reaction (HER, OER) with high activity has attracted considerable research interests in the past years. Herein, we report a self-supported electrode of the monolithic copper oxides directly on Cu wires [CW@Cu(I/II)NPs, as a working electrode] for full splitting water. In alkaline solution, with the electrode, OER occurs at the potential scope of 0.00 similar to +0.21 V and HER happens at the range of + 0.85 similar to +1.25 V with rough gas releasing. The activity of the electrode can be retrieved during the interactive electrochemical processes of OER and HER, which process shows decent stability. It is possible to save energy in industrial electrolysis water with the proposed electrode. The phenomena remind us of reassessing electrocatalytic ability of copper oxides or other metal oxides and provide a new design idea for metal wire-based electrodes for water splitting with low energy consumption.
机译:在过去的几年中,寻找用于氢和氧发生反应(HER,OER)的高活性的廉价电催化剂引起了相当大的研究兴趣。在这里,我们报告了直接在铜丝上的自支撑式整体氧化铜电极[CW @ Cu(I / II)NPs,作为工作电极],用于完全分解水。在碱性溶液中,对于电极,OER发生在与+0.21 V相似的0.00电位范围内,而HER发生在类似于+1.25 V的+ 0.85电位范围内,并释放出粗糙的气体。可以在OER和HER的相互作用电化学过程中恢复电极的活性,该过程显示出良好的稳定性。利用所提出的电极可以节省工业电解水中的能量。这种现象使我们想起了重新评估铜氧化物或其他金属氧化物的电催化能力,并为低能耗的水分解用金属线基电极提供了新的设计思路。

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