Zn-facilitated surface reconstruction of Ni-MOF for an enhanced oxygen evolution reaction

被引:2
作者
Wu, Fang [1 ,2 ]
Jiao, Yuhong [1 ,2 ]
Ge, Jin-long [1 ,2 ]
Zhu, Yujun [3 ]
Feng, Chao [1 ,2 ]
Wu, Zhong [1 ,2 ]
Li, Qiu [1 ,2 ]
机构
[1] Bengbu Univ, Sch Mat & Chem Engn, Bengbu 233030, Anhui, Peoples R China
[2] Bengbu Univ, Silicon Based New Mat Engn Res Ctr Anhui Prov, Bengbu 233030, Anhui, Peoples R China
[3] Anhui Med Univ, Dept Pharm & Biomed Engn, Hefei 230000, Peoples R China
基金
美国国家科学基金会;
关键词
ELECTROCATALYSTS; NANOSHEETS; EFFICIENT;
D O I
10.1039/d4dt02040e
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Facilitating the surface reconstruction of pre-catalysts has been considered an effective strategy for constructing low-cost and highly efficient OER electrocatalysts. Metal doping is a feasible way to activate the surface reconstruction, thus enhancing the OER performance. Herein, we report a facile hydrothermal method to synthesize a series of Zn-doped Ni-MOF on nickel foam (NiZn-MOF/NF) as promising pre-catalysts toward the oxygen evolution reaction (OER). The Zn leaching of NiZn-MOF/NF can promote the surface self-reconstruction of NiZn-MOF/NF into oxygen-vacancy-rich NiOOH after electrochemical activation. Benefiting from the optimized electronic structure, abundant defects, more accessible active sites, and enhanced electrical conductivity, the reconstructed metal oxyhydroxide hybrids exhibit better electrocatalytic activity than the catalysts transformed from Ni-MOF/NF without Zn doping. The optimized NiZn-MOF/NF-OH as an OER catalyst has an overpotential of 336 mV at 100 mA cm-2, and a Tafel slope of 65.9 mV dec-1, as well as stability over 12 h. This work reveals that Zn cation-doping/leaching induces the surface reconstruction of pre-catalysts for enhanced oxygen catalytic activity, which provides a new approach for the development of advanced electrocatalysts. The Zn leaching of NiZn-BDC induces the surface self-reconstruction of NiZn-BDC into oxygen-vacancy-rich NiOOH with excellent OER performance.
引用
收藏
页码:15093 / 15100
页数:8
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