Amorphous-crystalline heterostructures enable energy-level matching of cobalt sulfide/nickel iron layered double hydroxide for efficient oxygen evolution reaction

被引:15
|
作者
Zang, Shiqi [1 ]
Hou, Yan [1 ,2 ]
Chang, Jiuli [2 ]
Xu, Fang [2 ]
Wu, Dapeng [1 ]
Jiang, Kai [1 ]
Gao, Zhiyong [2 ]
机构
[1] Henan Normal Univ, Sch Environm, Key Lab Yellow River & Huai River Water Environm &, Henan Key Lab Environm Pollut Control,Int Joint La, Xinxiang 453007, Henan, Peoples R China
[2] Henan Normal Univ, Collaborat Innovat Ctr Henan Prov Green Mfg Fine C, Sch Chem & Chem Engn, Key Lab Green Chem Media & React,Minist Educ, Xinxiang 453007, Henan, Peoples R China
关键词
Oxygen evolution reaction; Heterojunction; Amorphous-crystalline phase; Catalytic mechanism; Water electrolysis; ELECTROCATALYSTS;
D O I
10.1016/j.jcis.2023.11.124
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
Interface engineering of heterostructures has emerged as a promising approach to enhance the catalytic activity of nonprecious electrocatalysts. Herein, a novel amorphous cobalt sulfide-crystalline nickel iron layered double hydroxide (a-CoS@NiFe-LDH) hybrid material is presented for application as an electrocatalyst for oxygen evolution reaction (OER). Benefitting from the well-matched energy level structures, the a-CoS@NiFe-LDH catalyst delivers a low overpotential of 221 symbolscript 14 mV at an OER current density of 20 mA cm-2 and a small Tafel slope of 83.1 mV dec-1, showing good OER properties. First-principle computations reveal that the electronic interaction between amorphous cobalt sulfide (a-CoS) and crystalline nickel iron layered double hydroxide (NiFe-LDH) components within a-CoS@NiFe-LDH promotes the adsorbate evolution mechanism and reduces the adsorption energies for oxygen intermediates, thereby enhancing the activity and stability for OER. This work opens up a new avenue to enhance the OER catalytic efficiency via the construction of amorphous-crystalline heterostructures.
引用
收藏
页码:485 / 494
页数:10
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