Improving the Electrocatalytic Activity of a Nickel-Organic Framework toward the Oxygen Evolution Reaction through Vanadium Doping

被引:17
|
作者
Yu, Hongbo [1 ]
Wang, Lixia [1 ]
Li, Huatong [1 ]
Luo, Zuyang [1 ]
Isimjan, Tayirjan Taylor [2 ]
Yang, Xiulin [1 ]
机构
[1] Guangxi Normal Univ, Sch Chem & Pharmaceut Sci, Guangxi Key Lab Low Carbon Energy Mat, Guilin 541004, Peoples R China
[2] King Abdullah Univ Sci & Technol KAUST, Saudi Arabia Basic Ind Corp SABIC, Thuwal 239556900, Saudi Arabia
基金
中国国家自然科学基金;
关键词
electrocatalysis; ion doping; metal-organic frameworks; oxygen evolution reaction; overall water splitting; EFFICIENT; CATALYST; HYDROGEN;
D O I
10.1002/chem.202201784
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Metal-organic frameworks (MOFs) have been considered as potential oxygen evolution reaction (OER) electrocatalysts owning to their ultra-thin structure, adjustable composition, high surface area, and high porosity. Here, we designed and fabricated a vanadium-doped nickel organic framework (V1-x-NixMOF) system by using a facile two-step solvothermal method on nickel foam (NF). The doping of vanadium remarkably elevates the OER activity of V1-x-NixMOF, thus demonstrating better performance than the corresponding single metallic Ni-MOF, NiV-MOF and RuO2 catalysts at high current density (>400 mA cm(-2)). V-0.09-Ni0.91MOF/NF provides a low overpotential of 235 mV and a small Tafel slope of 30.3 mV dec(-1) at a current density of 10 mA cm(-2). More importantly, a water-splitting device assembled with Pt/C/NF and V-0.09-Ni0.91MOF/NF as cathode and anode yielded a cell voltage of 1.96 V@1000 mA cm(-2), thereby outperforming the-state-of-the-art RuO2(+)||Pt/C(-). Our work sheds new insight on preparing stable, efficient OER electrocatalysts and a promising method for designing various MOF-based materials.
引用
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页数:9
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