Ni on graphene oxide: a highly active and stable alkaline oxygen evolution catalyst

被引:0
|
作者
Fruehwald, Holly M. [1 ]
Moghaddam, Reza B. [1 ]
Melino, Peter D. [1 ]
Ebralidze, Iraklii I. [1 ]
Zenkina, Olena V. [1 ]
Easton, E. Bradley [1 ]
机构
[1] Faculty of Science, Ontario Tech University (University of Ontario Institute of Technology), 2000 Simcoe Street North, Oshawa,ON, Canada
来源
Catalysis Science and Technology | 2021年 / 11卷 / 12期
基金
加拿大自然科学与工程研究理事会;
关键词
Graphene - Chemical modification - Oxygen - Catalyst activity - Electron microscopy - Nickel oxide - Electron microscopes - Morphology;
D O I
暂无
中图分类号
学科分类号
摘要
A novel oxygen evolution (OER) catalyst was prepared by reacting NiCl2·6H2O (Ni precursor) with electrochemically exfoliated graphene oxide (EGO) at mild reaction conditions, where the formation of Ni oxide nanoparticles and their deposition onto EGO occurs simultaneously. The resulting Ni@EGO catalyst was tested for OER in base, where it produced high stability and superior performances. Electron microscopy indicated that Ni@EGO had a uniform morphology, which together with the excellent electronic conductivity of the EGO support, must have contributed to the outstanding OER performance of the catalyst. The Ni@EGO catalyst showed superior OER activity with very low overpotential of 250 mV, which gave rise to the substantial current density of 750 A g−1at 1.6 V. Upon performing long term exhaustive galvanostatic stability tests at 10 mA cm−2, the Ni@EGO was highly stable and it improved over the course of the polarization. During performance studies, significant morphological changes of the material occur within the material as judged by electron microscopy. We believe the notable enhancement of the catalytic activity observed for the system during durability testing could be attributed to electrochemical cleaning of the surface from catalytically inactive nickel aggregates and due to chemical modification of the EGO material by NiOOH species. © The Royal Society of Chemistry 2021.
引用
收藏
页码:4026 / 4033
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