过电位
析氧
催化作用
制氢
纳米片
电化学
镍
材料科学
尿素
杂原子
兴奋剂
氢
分解水
化学工程
金属间化合物
纳米技术
电流密度
阳极
电催化剂
无机化学
介孔材料
氢燃料
热稳定性
纳米材料
多孔性
石墨烯
作者
Wenxiang Sheng,Xiaoxing Zhou,Yuanhang Ma,Irsa Tariq,Xu Dong,Ping Chen,Peng Li
标识
DOI:10.1021/acsaem.5c02679
摘要
The urea oxidation reaction (UOR) presents a sustainable pathway for energy-saving hydrogen production by replacing the sluggish oxygen evolution reaction (OER) in water electrolysis. However, developing efficient and stable UOR catalysts remains challenging. NiMoO 4 has emerged as a highly efficient UOR catalyst due to its synergistic intermetallic interactions and tunable electronic structure. Leveraging heteroatom doping, we engineered an Fe,P-codoped NiMoO 4 nanosheet array anchored on nickel foam (Fe,P-NiMnO 4 /NF) with dandelion-like hierarchical architecture via a facile hydrothermal-phosphorization approach. Systematic characterization demonstrates that Fe doping creates a porous hierarchical structure, facilitating mass transport and exposing abundant active sites, while P doping simultaneously optimizes the electronic configuration and enhancing hydrophilicity, leading to an expanding electrochemical active surface area. The resulting catalyst exhibits exceptional performance, achieving a current density of 100 mA cm –2 at just 1.345 V (vs RHE) for UOR, alongside a low HER overpotential of 270 mV at the same current density. When employed in a two-electrode overall urea splitting (OUS) system, it delivers 100 mA cm –2 at a cell voltage of 1.6 V with outstanding long-term stability of 50 h. This work introduces a design strategy for high-efficiency electrocatalysts in energy-efficient hydrogen production through urea-assisted electrolysis.
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