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Cobalt nanoparticles embedded in N-doped carbon on carbon cloth as free-standing electrodes for electrochemically-assisted catalytic oxidation of phenol and overall water splitting

机译:钴纳米粒子嵌入在碳布上的N掺杂碳作为直立电极,用于电化学辅助酚类酚类和整体水分裂的催化氧化

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摘要

Nowadays, environmental pollution and energy depletion are two important problems. In this work, we report the synthesis of cobalt nanoparticles (Co NPs) embedded in nitrogen doped carbon (NC) on carbon cloth (CC) by a two-step method to obtain Co@NC/CC and the application for both electrochemical assisted catalytic oxidation of phenol and electrochemical water splitting. An ultra-high activity could be obtained for the electrochemical catalytic oxidation of phenol, with the rate constant at 1.340 min(-1), much larger than the catalytic oxidation process (0.21 min(-1)). Moreover, Co@NC/CC exhibits remarkable activities in both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). Especially, a very early HER overpotential of 118 mV is achieved at 10 mAcm(-2) in 1 M KOH. The synergistic effect between Co and NC and the intimate interface are proposed to be the main cause of the enhanced activity. The free-standing and multi-functional Co@NC/CC electrode contains no noble metal, and should have great potential both in wastewater remediation and water splitting. (C) 2019 Elsevier Ltd. All rights reserved.
机译:如今,环境污染和能源消耗是两个重要问题。在这项工作中,通过两步方法报告在碳布(CC)上嵌入氮掺杂碳(NC)中的钴纳米颗粒(CO NP)的合成,得到CO @ NC / CC,以及电化学辅助催化剂的应用苯酚和电化学水分裂的氧化。可以获得超高活性的苯酚的电化学催化氧化,速率恒定在1.340min(-1),远大于催化氧化过程(0.21 min(-1))。此外,CO @ NC / CC在氢进化反应(她)和氧气进化反应(OER)中表现出显着的活性。特别是,在1M KOH中,在10mCM(-2)中实现了118 mV的非常早期的过电位。 CO和NC之间的协同效应和亲密接口被提出为增强活动的主要原因。独立式和多功能CO @ NC / CC电极不含贵金属,并且在废水修复和水分裂中应该具有很大的潜力。 (c)2019年elestvier有限公司保留所有权利。

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