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非晶态CoSe薄膜在强碱性条件下表现为一种活性且稳定的全水解电催化剂。

An amorphous CoSe film behaves as an active and stable full water-splitting electrocatalyst under strongly alkaline conditions.

作者信息

Liu Tingting, Liu Qian, Asiri Abdullah M, Luo Yonglan, Sun Xuping

机构信息

Chemical Synthesis and Pollution Control Key Laboratory of Sichuan Province, College of Chemistry and Chemical Engineering, China West Normal University, Nanchong 637002, Sichuan, China.

出版信息

Chem Commun (Camb). 2015 Dec 4;51(93):16683-6. doi: 10.1039/c5cc06892d. Epub 2015 Oct 2.

Abstract

It is attractive but still remains a big challenge to develop non-noble metal bifunctional electrocatalysts efficient for both oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) under alkaline conditions. Herein, an amorphous CoSe film electrodeposited on a Ti mesh (a-CoSe/Ti) is demonstrated to exhibit high electrocatalytic activity and stability for both reactions in 1.0 M KOH. It needs overpotentials of 292 and 121 mV to drive 10 mA cm(-2) for OER and HER, respectively. The two-electrode alkaline water electrolyzer affords a water-splitting current of 10 mA cm(-2) at a cell voltage of 1.65 V. This work offers an attractive cost-effective catalytic material toward full water splitting applications.

摘要

开发在碱性条件下对析氧反应(OER)和析氢反应(HER)均有效的非贵金属双功能电催化剂很有吸引力,但仍然是一个巨大的挑战。在此,证明了一种电沉积在钛网上的非晶态CoSe薄膜(a-CoSe/Ti)在1.0 M KOH中对这两种反应均表现出高电催化活性和稳定性。驱动10 mA cm(-2)的OER和HER分别需要292和121 mV的过电位。两电极碱性水电解槽在1.65 V的电池电压下提供10 mA cm(-2)的析氢电流。这项工作为全水解应用提供了一种有吸引力的具有成本效益的催化材料。

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