One-Step Scalable Synthesis of 3D Self-Supported Superaerophobic Ce-Coupled Ni3S2/NiS@NF Nanobud Catalyst for Efficient Oxygen Evolution Reaction

被引:0
作者
Lu, Mengjie [1 ]
Cheng, Run [1 ]
Wang, Li [1 ]
Liang, Dandan [1 ]
Qin, Meng [1 ]
Wang, Bili [1 ]
Song, Rui [1 ]
Chen, Duo [2 ]
机构
[1] Army Engn Univ PLA, Dept Gen Educ, Nanjing 211101, Peoples R China
[2] Nanjing Univ Aeronaut & Astronaut, Coll Mat Sci & Technol, Jiangsu Key Lab Electrochem Energy Storage Technol, Nanjing 210016, Peoples R China
关键词
electrocatalysts; oxygen evolution reaction; superaerophobic; water splitting; BIFUNCTIONAL ELECTROCATALYSTS; HIGH-PERFORMANCE; NANOWIRES; ARRAYS; DESIGN; FOAMS;
D O I
10.3390/catal14110752
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
The elaborate design of inexpensive, high-performance electrocatalysts from earth-abundant elements toward oxygen evolution reaction (OER) is critical in various (electro)chemical processes. Herein, a novel binder-free catalyst of Ce-coupled Ni3S2/NiS supported on Ni foam (Ce-Ni3S2/NiS@NF) is successfully synthesized via a facile one-step hydrothermal method that enables practical feasibility with a significant enhancement of OER activity through anchoring Ce dopants on an Ni3S2/NiS nanobud host. Ce species coupling can modulate electronic structure, which reduces the reaction energy barrier and optimizes OER catalytic activity. More profoundly, the superhydrophilic and superaerophobic properties of the Ce-Ni3S2/NiS@NF electrode further promote mass transfer. As a result, the Ce-Ni3S2/NiS@NF electrode exhibits excellent OER activity with a low overpotential of 236 and 350 mV to achieve current densities of 10 and 100 mA cm-2, respectively, and long-term durability for 24 h in alkaline medium. These results could supply valuable guidelines for the design of other OER catalysts and beyond.
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页数:13
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