过电位
制氢
吉布斯自由能
析氧
阳极
阴极
电解质
氢
电解
分解水
材料科学
电解水
化学工程
无机化学
碱性水电解
催化作用
化学
密度泛函理论
氢燃料
吸附
聚合物电解质膜电解
电化学
氢经济
氧化还原
高温电解
电流密度
高压电解
作者
Ning Zhao,Ningning Zhang,Kaiwei Liu,Shufen Liu,Yinghui Wang,Jia Ran,Yuxin Dai,Mei Xue,Gang Zhao
出处
期刊:
[Tsinghua University Press]
日期:2025-10-30
卷期号:4 (4): e9120206-e9120206
被引量:5
标识
DOI:10.26599/nre.2025.9120206
摘要
Hydrogen energy serves as a secondary energy carrier, and water electrolysis for hydrogen production is a core development direction. By combining the cathode hydrogen evolution reaction (HER) with the dual anode reactions—oxygen evolution reaction (OER) and urea oxidation reaction (UOR), it simultaneously achieves mainstream alkaline electrolytic hydrogen production and urea treatment. Here, Ni3S2(Fe, Mo)-NiFe LDH, a trifunctional electrocatalyst, is prepared via a two-step hydrothermal method. Density functional theory (DFT) calculations confirmed that co-doping with Mo and Fe optimizes Gibbs free energy of hydrogen adsorption of Ni3S2. The doping-modulated Ni3S2(Fe, Mo) and NiFe LDH form a hierarchical structure, not only achieving performance complementarity but also further enhancing the overall catalytic activity through interfacial electronic interactions. At 10 mA·cm–2, the HER overpotential is 91 mV, and the UOR overpotential is 74 mV, which is a reduction of 154 mV compared to OER (228 mV). Moreover, the constructed HER‖OER (HER‖UOR) electrolyzer operates at a voltage as low as 1.55 V (1.41 V), along with 100 h stability.
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