Oxygen vacancy and heterointerface engineering of Ni3 Fe/NiFe2 O4 @N-GTs oxygen evolution reaction electrocatalyst for water splitting

被引:4
作者
Zou, Jiachen [1 ]
Song, Guanying [1 ]
Cui, Anguo [1 ]
Li, Zhenjiang [2 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Electromech Engn, Qingdao 266061, Shandong Provin, Peoples R China
[2] Qingdao Univ Sci & Technol, Coll Mat Sci & Engn, Qingdao 266042, Shandong Provin, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrochemical water splitting; Oxygen evolution reaction; Spinel NiFe 2 O 4; Oxygen vacancy; Heterointerface; NANOPARTICLES; NIFE2O4;
D O I
10.1016/j.diamond.2024.110999
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Developing highly efficient electrocatalysts for oxygen evolution reaction (OER) plays a key role in accelerating electrochemical water splitting green energy conversion systems. Herein, the dual strategy of incorporating oxygen vacancy and engineering heterointerface was employed for constructing N -doping graphene tubes (NGTs) supported Ni 3 Fe/NiFe 2 O 4 heterostructure with abundant oxygen vacancies (Ni 3 Fe/NiFe 2 O 4 @N-GTs). Benefit from accelerating reaction kinetics and optimizing adsorption strength for reaction intermediates resulting from the synergistic effect of vacancies introduction and heterointerface formation, the optimized Ni 3 Fe/NiFe 2 O 4 @N-GTs catalyst exhibits remarkably enhanced OER performance with an overpotential of 230 mV to achieve a current density of 10 mA cm -2 , a low Tafel slope of 33 mV dec - 1 and 330 h stability at the high current density of 100 mA cm -2 . Meanwhile, the full water splitting cell consisting of the Ni 3 Fe/NiFe 2 O 4 @NGTs-350 anode and a Pt/C cathode delivers a low cell voltage of 1.58 V at 10 mA cm -2 and presents excellent durability for over 330 h of continuous operation at the current density of 10 mA cm -2 , demonstrating it promising electrocatalyst for potential applications in the hydrogen production field.
引用
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页数:9
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