3D urchin like V-doped CoP in situ grown on nickel foam as bifunctional electrocatalyst for efficient overall water-splitting

被引:84
作者
Xue, Hongyao [1 ]
Meng, Alan [2 ]
Zhang, Haiqin [3 ]
Lin, Yusheng [4 ]
Li, Zhenjiang [1 ,4 ]
Wang, Chuansheng [5 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Electromech Engn, Qingdao 266061, Peoples R China
[2] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, MOE, Key Lab Opt Sensing & Analyt Chem Life Sci, Qingdao 266042, Peoples R China
[3] Shandong Shida Shenghua Chem Grp Co Ltd, Dongying 257503, Peoples R China
[4] Qingdao Univ Sci & Technol, Coll Mat Sci & Engn, Qingdao 266061, Peoples R China
[5] Qingdao Univ Sci & Technol, Natl Engn Lab Adv Equipments & Key Mat Tires, Qingdao 266042, Peoples R China
基金
中国国家自然科学基金;
关键词
overall water-splitting; V-doping; urchins like; density functional theory (DFT); density of states (DOS);
D O I
10.1007/s12274-021-3359-2
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
Cobalt phosphide (CoP) is considered to be a potential candidate in the field of electrocatalysis due to its low-cost, abundant resources and high electrochemical stability. However, there is a great space for further improvement of its electrocatalytic performance since its charge transfer rate and catalytic activity have not reached a satisfactory level. Herein, we design and fabricate a three dimensional urchins like V-doped CoP with different amounts of V-doping on nickel foam electrode. The V-doped CoP/NF electrode with optimized amounts of V-doping (10%) exhibits outstanding hydrogen evolution reaction (HER) performance under universal-pH conditions and preeminent oxygen evolution reaction (OER) performance in alkaline media. Notably, the assembled water-splitting cell displays a cell voltage of only 1.53 V at 10 mA center dot cm(-2) and has excellent durability, much better than many reported related bifunctional catalysts. The experiment results and theoretical analysis revealed that vanadium atoms replace cobalt atoms in CoP lattice. Vanadium doping can not only raise the density of electronic states near the Fermi level enhancing the conductivity of the catalyst, but can also optimize the free energy of hydrogen and oxygen-containing intermediates adsorption over CoP, thus promoting its catalytic activity. Moreover, the unique nanostructure of the catalyst provides the various shortened channels for charge transfer and reactant/electrolyte diffusion, which accelerates the electrocatalytic process. Also, the in situ growth strategy can improve the conductivity and stability of the catalyst.
引用
收藏
页码:4173 / 4181
页数:9
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