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Superaerophobic Ni3N/Ni@W2N3 multi-heterointerfacial nanoarrays for efficient alkaline electrocatalytic hydrogen evolution reaction
被引:2
|作者:
Wang, Haidong
[1
]
Jiao, Yongxin
[1
]
Zhang, Guanghui
[1
]
Zhang, Zexi
[1
]
Ma, Weiguang
[1
]
Sun, Chenghua
[2
]
Zong, Xu
[1
]
机构:
[1] Dalian Maritime Univ, Marine Engn Coll, Linghai Rd 1, Dalian 116026, Peoples R China
[2] Swinburne Univ Technol, Sch Sci Comp Engn & Technol, Melbourne, Vic 3122, Australia
基金:
中国国家自然科学基金;
关键词:
Electrocatalytic water splitting;
Heterojunction interface;
Superaerophobic;
Hydrogen adsorption energy;
Hydrogen evolution reaction;
NICKEL-BASED ELECTROCATALYSTS;
OXIDATION;
D O I:
10.1016/j.cej.2024.154776
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
The hydrogen evolution performances of electrocatalysts are greatly restricted by their unfavorable hydrogen evolution kinetics and the undesirable accumulation of as-evolved gas bubbles on the electrocatalysts surface. Herein, we present the fabrication of self-supporting multi-heterointerfacial nanoarrays electrode toward addressing these challenges simultaneously. A monolith Ni3N/Ni@W2N3 electrode is prepared, which exhibits a multi-heterojunction interface between the different components. The construction of this multi-heterojunction interface allows for the redistribution of the electrons, thus alleviating the strong Ni-H bond and optimizing the hydrogen adsorption free energy toward more efficient HER catalysis. Moreover, by virtue of the distinct nanoarray structure, the Ni3N/Ni@W2N3 nanoarrays exhibit improved hydrophilicity and superaerophobicity compared with Ni/Ni3N, facilitating water contact and enabling more efficient detachment of the as-evolved H-2 bubbles from the surface. Benefiting from these attractive features, the Ni3N/Ni@W2N3 nanoarrays deliver an attractive alkaline HER catalytic activity with a low overpotential of 66 mV to achieve a current density of 10 mA cm(-2), which is comparable with that of the benchmark Pt/C electrode. Moreover, the electrode exhibits remarkable stability during long-term electrolysis. The simultaneous interface and nanostructure engineering provide a feasible pathway for obtaining high-performance electrodes and beyond for various electrochemical reactions.
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