N, P-doped multiphase transition metal sulfides are used for efficient electrocatalytic oxygen evolution reaction

被引:30
|
作者
Zhang, Zhiqiang [1 ]
Tang, Shuli [2 ]
Lin, Xiaofeng [1 ]
Liu, Chenghao [1 ]
Hu, Shirong [2 ]
Huang, Qitong [1 ]
机构
[1] Gannan Med Univ, Key Lab Prevent & Treatment Cardiovasc & Cerebrov, Key Lab Biomat & Biofabricat Tissue Engn Jiangxi, Minist Educ,Sch Med & Informat Engn,Sci Res Ctr,O, Ganzhou 341000, Peoples R China
[2] Minnan Normal Univ, Coll Chem Chem Engn & Environm, Zhangzhou 363000, Peoples R China
基金
中国国家自然科学基金;
关键词
Multiphase transition metal sulfides; Heteroatom doping; Oxygen evolution reaction; BIFUNCTIONAL CATALYSTS; NANOSHEETS; NITROGEN; HETEROSTRUCTURES; NANOPARTICLES; GRAPHENE; ARRAYS;
D O I
10.1016/j.apsusc.2022.152546
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
It is of great significance for the electrolysis of hydrogen and air-fuel cells to synthesize super active non-noble-metal electrocatalytic oxygen evolution reaction (OER). Due to the limitation of the OER process involving multiple electron transfer and multiple intermediates. Catalysts with a single active component can hardly exhibit high activity in this process. Here, we report an N, P-doped multiphase transition metal sulfide composite electrocatalyst (N, P-Co9S8/CoS2/Co1-xS) by an atmosphere conversion pyrolysis strategy. The multiple active components not only provide abundant catalytic active sites for the reaction at the catalytic interface but also the coupling tuning of the heterogeneous interface optimizes the valence orbital of the catalyst, which results in the catalyst exhibiting excellent catalytic activity. Both theoretical calculations and experimental investigations confirm the excellent adsorption kinetics of the intermediates at the interface. When used as an electrocatalyst for OER in alkaline environments, it exhibits robust activity (eta(10): 285 mV, Tafel slope: 70 mV dec(-1)) and long-term stability. Our study illustrates that compared with single-component cobalt-based sulfide, N, P-Co9S8/CoS2/ Co1-xS catalyst is favorable as highly efficient OER catalytic activity.
引用
收藏
页数:7
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