过电位
碱性水电解
电解质
化学
电解
化学工程
制氢
电极
多孔性
氢
电解水
吸附
解吸
分解水
电子转移
传质
无机化学
涂层
可逆氢电极
电镀
电解槽
纳米孔
耐久性
催化作用
标准氢电极
纳米技术
工作电极
聚合物电解质膜电解
作者
Shang Jiang,Weiwei Hu,Shizheng Zhou,Linfeng Yu,Linfeng Yu,Liang Luo,Yunlong Zhang,Qiao Zhao,Zhibin Yu,Wei Liu,Xiaoming Sun,Liang Yu,Liang Yu,Yanting Liu,Dehui Deng
摘要
Developing highly active and durable electrodes for high-current-density alkaline water electrolysis is crucial for advancing cost-effective green hydrogen production. Herein, we report an atomic-to-macroscale assembly of an integrated Ni/MoO2 electrode possessing abundant atomic heterointerfaces with triscale (nano-micro-macro) porosity for high-performance hydrogen evolution. The electrode delivers an overpotential of 145 mV at 1 A cm–2 in 1 M KOH, markedly lower than the 300 mV of commercial Pt/C catalysts, while maintaining stable operation for over 3500 h. Practical application within an alkaline electrolyzer achieves a cell voltage of 1.80 V with an energy consumption of 4.3 kWh Nm–3 H2 at 1 A cm–2 under industrial conditions (30 wt % KOH at ≥85 °C), and operational durability exceeds 1000 h. Characterization and theoretical analysis elucidate a triple-enhancement effect on water electrolysis: (i) interfacial electron transfer from Ni to MoO2 moderately weakens H* adsorption and promotes the H2 desorption on the Ni sites, thereby boosting the intrinsic activity; (ii) triscale hierarchical porosity with hydrophilic MoO2 coating synergistically accelerates bubble detachment and electrolyte permeation, thereby enhancing mass transfer; and (iii) the strong Ni-MoO2 electronic interaction and their robust integration with the electrode skeleton significantly strengthen structural stability.
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