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用于电化学析氧的核壳结构CoMoO•nH₂O@CoFeOOH纳米催化剂。

A core-shell structured CoMoO•nHO@CoFeOOH nanocatalyst for electrochemical evolution of oxygen.

作者信息

Wang Jiajun, Yin Hui, Chen Zhengjun, Cao Guoxuan, Xu Ning, Wu Hui, Wang Ping

机构信息

School of Materials Science and Engineering, Key Laboratory of Advanced Energy Storage Materials of Guangdong Province, South China University of Technology, Guangzhou, 510641, PR China.

NIST Center for Neutron Research, National Institute of Standards and Technology, Gaithersburg, MD, 20899-6102, USA.

出版信息

Electrochim Acta. 2020;345. doi: 10.1016/j.electacta.2020.136125.

Abstract

Nickel-iron oxyhydroxide (NiFeOOH) is well recognized as the best-performing oxygen evolution reaction (OER) catalyst in alkaline electrolytes, however its analogue cobalt-iron oxyhydroxide (CoFeOOH) is surprisingly less explored despite their structural similarity. Inspired by our recent study on high-performance HER catalyst using the nanostructured CoMoO•nHO precursor, herein, we report a facile synthesis of CoFeOOH catalyst derived from the same precursor and its excellent electrocatalytic properties towards the OER in alkaline electrolytes. A core-shell structured nanocatalyst consisting of disordered CoFeOOH layer over the surface of crystalline CoMoO•nHO nanosheets was synthesized using a simple hydrothermal method followed by anodic electrooxidation. Thus-prepared catalyst exhibited extraordinarily high and stable activity towards the OER in alkaline electrolyte, which outperformed most Co-based OER catalysts. Combined with the HER catalyst derived from the same CoMoO•nHO precursor as the cathode, we further developed and tested a simple water-splitting cell, which significantly surpasses the benchmarking IrO-Pt/C couple (1.63 V) and requires a voltage of only 1.517 V to afford 10 mA cm in 1.0 M KOH solution. Density functional theory calculations were conducted to gain insight into the Fe-doping induced improvement of OER activity.

摘要

羟基氧化镍铁(NiFeOOH)被公认为是碱性电解质中性能最佳的析氧反应(OER)催化剂,然而,其类似物羟基氧化钴铁(CoFeOOH)尽管结构相似,却出人意料地较少被研究。受我们近期关于使用纳米结构的CoMoO•nH₂O前驱体合成高性能析氢反应(HER)催化剂的研究启发,在此我们报道了一种由相同前驱体衍生而来的CoFeOOH催化剂的简便合成方法及其在碱性电解质中对OER的优异电催化性能。采用简单的水热法随后进行阳极电氧化,合成了一种核壳结构的纳米催化剂,其由结晶态的CoMoO•nH₂O纳米片表面无序的CoFeOOH层组成。如此制备的催化剂在碱性电解质中对OER表现出极高且稳定的活性,优于大多数钴基OER催化剂。结合作为阴极的由相同CoMoO•nH₂O前驱体衍生而来的HER催化剂,我们进一步开发并测试了一种简单的水电解槽,其显著超越了基准的IrO₂-Pt/C电极对(1.63 V),在1.0 M KOH溶液中提供10 mA cm⁻²的电流仅需1.517 V的电压。进行了密度泛函理论计算以深入了解铁掺杂对OER活性的促进作用。

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