Vacancies and interfaces engineering of core-shell heterostuctured NiCoP/NiO as trifunctional electrocatalysts for overall water splitting and zinc-air batteries

被引:0
|
作者
Xiaolin Hu [1 ]
Jichuan Fan [2 ]
Ronghua Wang [2 ]
Meng Li [3 ]
Shikuan Sun [4 ]
Chaohe Xu [1 ,5 ]
Fusheng Pan [2 ,5 ]
机构
[1] College of Aerospace Engineering, Chongqing University
[2] College of Materials Science and Engineering, Chongqing University
[3] MOE Key Laboratory of Low-grade Energy Utilization Technologies and Systems, CQU-NUS Renewable Energy Materials & Devices Joint Laboratory, School of Energy & Power Engineering, Chongqing University
[4] School of Materials Science and Energy Engineering, Foshan University
[5] National Engineering Research Center for Magnesium Alloys, Chongqing University
基金
中国国家自然科学基金;
关键词
D O I
暂无
中图分类号
TM911.41 [金属-空气电池];
学科分类号
0808 ;
摘要
The electronic structures and properties of electrocatalysts,which depend on the physicochemical structure and metallic element components,could significantly affect their electrocatalytic performance and their future applications in Zn-air battery(ZAB) and overall water splitting(OWS).Here,by combining vacancies and heterogeneous interfacial engineering,three-dimensional(3D) core-shell NiCoP/NiO heterostructures with dominated oxygen vacancies have been controllably in-situ grown on carbon cloth for using as highly efficient electrocatalysts toward hydrogen and oxygen electrochemical reactions.Theoretical calculation and electrochemical results manifest that the hybridization of NiCoP core with NiO shell produces a strong synergistic electronic coupling effect.The oxygen vacancy can enable the emergence of new electronic states within the band gap,crossing the Fermi levels of the two spin components and optimizing the local electronic structure.Besides,the hierarchical core-shell NiCoP/NiO nanoarrays also endow the catalysts with multiple exposed active sites,faster mass transfer behavior,optimized electronic strutures and improved electrochemical performance during ZAB and OWS applications.
引用
收藏
页码:601 / 611
页数:11
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