Vishnu Prataap R K, Mohan S
EMFT Division, CSIR-Central Electrochemical Research Institute, Karaikudi-630 003, Tamil Nadu, India.
Chem Commun (Camb). 2017 Mar 16;53(23):3365-3368. doi: 10.1039/c7cc00712d.
Herein, we present the electrochemical fabrication of a hydroxide surface-covered nickel-cobalt alloy and its superior catalytic activity towards the electrochemical oxygen evolution reaction in alkaline media. Electrodes were fabricated via the galvanostatic and potentiostatic electrodeposition methods in various electrolytic compositions, in which a nanopyramid-like morphology was obtained under the galvanostatic conditions and a porous structure was obtained under the potentiostatic deposition conditions. The optimized porous electrode shows the overpotential of 1.537 V (η = 307 mV) vs. RHE for the current density of 10 mA cm in 1 M NaOH solution. Comparatively, the porous Ni-Co alloy electrode exhibits a better performance than the other morphologies obtained in this study. Owing to its highly active surface area with porous structures, it promotes the molecular oxygen evolution reaction.
在此,我们展示了一种表面覆盖氢氧化物的镍钴合金的电化学制备方法及其在碱性介质中对电化学析氧反应的卓越催化活性。通过在各种电解液组成中采用恒电流和恒电位电沉积方法制备电极,其中在恒电流条件下获得了纳米金字塔状形态,在恒电位沉积条件下获得了多孔结构。优化后的多孔电极在1 M NaOH溶液中,对于10 mA cm²的电流密度,相对于可逆氢电极(RHE)的过电位为1.537 V(η = 307 mV)。相比之下,多孔镍钴合金电极表现出比本研究中获得的其他形态更好的性能。由于其具有多孔结构的高活性表面积,它促进了分子析氧反应。