Efficient energy-saving hydrogen production on binder-free electrodeposited hierarchical Ni-Mn-P@Ni-Co nanostructure

被引:6
作者
Zhou, Bingjie [1 ]
Shao, Yuankai [1 ]
Li, Zhenguo [1 ]
Yang, Weisheng [2 ]
Ren, Xiaoning [1 ]
Hao, Yaodong [1 ]
机构
[1] China Automot Technol & Res Ctr Co Ltd, Natl Engn Lab Mobile Source Emiss Control Technol, Tianjin 300300, Peoples R China
[2] Nanjing Forestry Univ, Coll Mat Sci & Engn, Jiangsu Coinnovat Ctr Efficient Proc & Utilizat Fo, Nanjing 210037, Jiangsu, Peoples R China
关键词
Oxygen evolution reaction; Hydrogen evolution reaction; Overall water splitting; Electrocatalyst; HIGH-PERFORMANCE; EVOLUTION REACTION; UREA OXIDATION; OXYGEN EVOLUTION; NICKEL FOAM; ELECTROCATALYST; ELECTROLYSIS; NANOSHEETS; NANOARRAYS; CATALYST;
D O I
10.1016/j.ijhydene.2023.10.310
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Synthesis of optimized active and stable electrocatalyst represents a significant and crucial obstacle in producing green hydrogen. Additionally, the oxygen evolution reaction (OER) poses a significant challenge in the sustainable production of hydrogen, mainly because of its sluggish nature. In this research, the electrodeposition technique was used for synthesizing the hierarchical Ni-Mn-P@Ni-Co nanostructure and its electrocatalytic behavior was explored for hydrogen evolution and urea electro-oxidation reactions (HER and UOR). Electro-chemical analysis revealed that by utilizing a high surface area and favorable intrinsic activity, electrodes that demonstrated remarkable electrocatalytic activity and performance were created through the fabrication pro -cess. For delivering the 10 mA cm-2 current density, the Ni-Mn-P@Ni-Co electrode needed only 70 mV over-potential in HER and 1.309 V vs RHE in UOR. Furthermore, substituting the UOR with OER also resulted in an enhancement of hydrogen production efficiency. During overall urea electrolysis, the cell voltage in 10 mA cm-2 was only 1.395 V which, is 200 mV lower than the HER-OER process.
引用
收藏
页码:1022 / 1032
页数:11
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