Construction of a cobalt-doped Ni3S2@NiFe-LDH heterojunction with enhanced local electric field for efficient oxygen evolution reaction

被引:6
作者
Wu, Jie [1 ]
Huang, Anqi [1 ]
Cao, Wen [1 ]
Gao, Xuehui [1 ]
Chen, Zhongwei [2 ,3 ]
机构
[1] Zhejiang Normal Univ, Coll Chem & Mat Sci, Key Lab Minist Educ Adv Catalysis Mat, Jinhua 321004, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis Energy, Dalian 116023, Peoples R China
[3] Chinese Acad Sci, Dalian Inst Chem Phys, Power Battery & Syst Res Ctr, Dalian 116023, Peoples R China
关键词
CATALYSTS;
D O I
10.1039/d4ta06830k
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
Alkaline oxygen evolution reaction (OER), involving a four-electron transfer process, is characterized by high overpotential and extremely sluggish reaction kinetics, posing a significant challenge for catalyst design. Herein, a strategy is proposed to modulate the electronic structure of electrocatalysts by constructing a cobalt-doped Ni3S2@NiFe-LDH (Co-Ni3S2@NiFe-LDH) hierarchical hollow heterojunction with enhanced local electric field (ELEF). The ELEF in the heterojunction induces band bending of the components, expediting electron transfer and accelerating OER kinetics. Furthermore, the hierarchical hollow structure offers a large specific surface area that ensures full exposure of adsorption and active sites. Benefiting from these synergetic advantages, Co-Ni3S2@NiFe-LDH shows remarkable performance and stability with a low overpotential of only 217 mV at 50 mA cm-2. Density functional theory (DFT) calculations further confirm that the ELEF can optimize the adsorption energy of intermediate reaction species, reduce reaction energy barriers, and modulate the d-band center of active sites, thereby improving the inherent catalytic activity.
引用
收藏
页码:1221 / 1229
页数:9
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