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Self-assembly of binder-free 3D NiMoO4/ZnCo-LDH/NF core/shell architecture for efficient oxygen evolution reaction
被引:0
|作者:
Krishnamachari, Moorthy
[1
,2
]
Kumar, Mohanraj
[1
]
Pandian, Muthu Senthil
[3
]
Vijayakumar, Paranthaman
[4
,5
]
Chang, Jih-Hsing
[1
]
机构:
[1] Chaoyang Univ Technol, Dept Environm Engn & Management, Taichung 413310, Taiwan
[2] Chaoyang Univ Technol, Dept Appl Chem, Taichung 413310, Taiwan
[3] Sri Sivasubramaniya Nadar Coll Engn, SSN Res Ctr, Kalavakkam 603110, Tamil Nadu, India
[4] SIMATS, Saveetha Sch Engn, Dept Electrochem, Chennai 602105, Tamil Nadu, India
[5] Univ Tenaga Nas, Inst Sustainable Energy, Jalan Ikram UNITEN, Kajang 43000, Selangor, Malaysia
来源:
关键词:
Core-shell structure;
Binder free electrodes;
Synergistic coupling effect;
Layered Double Hydroxides;
Oxygen Evolution Reaction;
Electrochemical water splitting;
ELECTROCATALYSTS;
D O I:
10.1016/j.fuel.2025.135350
中图分类号:
TE [石油、天然气工业];
TK [能源与动力工程];
学科分类号:
0807 ;
0820 ;
摘要:
Developing cost-effective, robust, and low over-potential exhibiting Oxygen Evolution Reaction (OER) electrocatalysts has been highly desirable for large-scale energy conversion technologies. Herein, we have constructed binder-free 3D core/shell NiMoO4/ZnCo-LDH/NF nanostructural arrays via a facile two-step solvothermal process. These construction of the core/shell structure induced a synergistic electronic coupling effect and efficiently upgraded the rapid charge transfer characteristics, increasing active sites as well as oxygen vacancies on the surface of an electrode material. As a result, core/shell NiMoO4/ZnCo(1:2)-LDH/NF electrode material delivered superior OER over potential value of 252 mV and minimal Tafel slope value of 85.2 mV dec-1 at current density of 10 mA cm-2 in 1 M KOH electrolyte medium. Moreover, due to the strong electronic coupling among the counterparts, which delivered outstanding robust stability over 48 h. These above results advocates that core/ shell NiMoO4/ZnCo(1:2)-LDH/NF electro catalysts owned great potential for future energy conversion technologies.
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