Diyali Nilankar, Diyali Sangharaj, Chettri Meena, Saha Subhajit, Agrawalla Suraj Kumar, Bagdwal Harshita, Purohit Chandra Shekhar, Singh Monika, Biswas Bhaskar
Laboratory for Structural Engineering and Sustainable Catalysis, Department of Chemistry, University of North Bengal, Darjeeling 734013, India.
School of Chemical Sciences, National School of Science Education and Research, Bhubaneswar 752050, India.
ACS Appl Mater Interfaces. 2025 Feb 12;17(6):9351-9363. doi: 10.1021/acsami.4c20152. Epub 2025 Jan 28.
The upsurging of cost-effective electrocatalysts through the operando electro-oxidation approaches holds great promise for the scalable production of green energy in the pursuit of energy sustainability. This work introduces an operando electro-oxidation reconstitution strategy in producing a smart electrocatalyst, cobalt "oxyhydroxide" derived from a newly designed 2D cobalt(II) metal-organic framework (-) directly grown on nickel foam (NF), . The electrocatalyst, , exhibits an outstanding overpotential of 76 mV for the hydrogen evolution reaction and 336 mV for the oxygen evolution reaction to achieve a current density of 10 mA/cm with remarkable Faradaic efficiencies of 97.1 and 93.4%, respectively, in 1 M aqueous KOH. Unveiling the bifunctionality of as the cathode and anode for overall water splitting in 1 M aqueous KOH, a low voltage of 1.65 V was needed to obtain 10 mA/cm current density. Nonetheless, displayed excellent stability for 12 h as evidenced from the chronopotentiometry recorded at 10 mA/cm. The outstanding bifunctional electrocatalytic performance and stability of the electrocatalyst for 50 h is attributed to the unique 2D hexagonal nanosheet morphology of and the microporous structure with zigzag flow channels of NF, facilitating a faster kinetics through the Co and Ni dual sites synergism.
通过原位电氧化方法开发具有成本效益的电催化剂,对于在追求能源可持续性的过程中大规模生产绿色能源具有巨大潜力。这项工作引入了一种原位电氧化重构策略,用于制备一种智能电催化剂,即由新设计的二维钴(II)金属有机框架(-)直接生长在泡沫镍(NF)上衍生而来的钴“羟基氧化物”。该电催化剂在1 M KOH水溶液中,对于析氢反应表现出76 mV的出色过电位,对于析氧反应表现出336 mV的出色过电位,以实现10 mA/cm²的电流密度,其法拉第效率分别高达97.1%和93.4%。揭示了该电催化剂在1 M KOH水溶液中作为阴极和阳极用于全水解的双功能特性,仅需1.65 V的低电压即可获得10 mA/cm²的电流密度。尽管如此,从在10 mA/cm²下记录的计时电位法可以证明,该电催化剂在12小时内表现出优异的稳定性。该电催化剂在50小时内具有出色的双功能电催化性能和稳定性,这归因于其独特的二维六方纳米片形态以及NF具有曲折流动通道的微孔结构,通过钴和镍双位点协同作用促进了更快的动力学过程。