塔菲尔方程
双功能
过电位
析氧
分解水
材料科学
氧化物
无机化学
电化学
电极
化学工程
介电谱
制氢
金属
碱性水电解
石墨烯
贵金属
电催化剂
碱性电池
过渡金属
化学
氧化锡
可逆氢电极
氢
电化学动力学
作者
José Antonio Fontes de Carvalho Ribeiro Rodrigues,Thomaz de Oliveira Barros,João Victor Madureira Correia Moraes,R. Suresh Babu,A. L. F. de Barros
出处
期刊:Ionics
[Springer Science+Business Media]
日期:2026-04-21
卷期号:32 (5): 5825-5837
标识
DOI:10.1007/s11581-026-07132-8
摘要
Abstract Herein, we demonstrated nickel- and cobalt-based metal oxide electrocatalysts were synthesized on fluorine-doped tin oxide substrates via a simple, low-cost potentiostatic electrodeposition method at room temperature and evaluated as bifunctional electrodes for alkaline water splitting. Despite their straightforward synthesis and absence of noble metals, the prepared electrodes exhibit competitive electrocatalytic activity toward both half-reactions. For the hydrogen evolution reaction (HER), the CoO/NP electrode delivered − 10 mA cm⁻² at an overpotential (η) of − 398 mV, while the NiO/NP electrode required − 427 mV and exhibited faster reaction kinetics with a lower Tafel slope of 142 mV dec⁻¹. Both electrodes maintained stable performance during 15 h of continuous operation. For the oxygen evolution reaction (OER), CoO/NP reached 10 mA cm⁻² at 1.86 V (η = 630 mV), slightly outperforming NiO/NP, which required 1.89 V (η = 660 mV), whereas NiO/NP showed more favourable OER kinetics with a lower Tafel slope of 61 mV dec⁻¹. Electrochemical impedance spectroscopy confirmed efficient interfacial charge-transfer behaviour for both electrodes. Structural and morphological analyses revealed uniformly distributed nanoparticulate oxide films providing abundant active sites for both half-reactions. The complementary HER–OER performance highlights a complementary bifunctional behaviour between the nickel- and cobalt-based oxides. Combined with good durability and a facile, scalable synthesis route, these materials represent promising low-cost electrocatalysts for sustainable hydrogen production in alkaline media.
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