Remarkable enhancement of the alkaline oxygen evolution reaction activity of NiCo2O4 by an amorphous borate shell

被引:34
作者
Ji, Xuqiang [1 ,2 ]
Ren, Xiang [1 ]
Hao, Shuai [1 ]
Xie, Fengyu [3 ]
Qu, Fengli [4 ]
Du, Gu [5 ]
Asiri, Abdullah M. [6 ]
Sun, Xuping [1 ]
机构
[1] Sichuan Univ, Coll Chem, Chengdu 610064, Sichuan, Peoples R China
[2] Qingdao Univ, Coll Chem & Environm Engn, Qingdao 266071, Shandong, Peoples R China
[3] Sichuan Normal Univ, Coll Chem & Mat Sci, Chengdu 610068, Sichuan, Peoples R China
[4] Qufu Normal Univ, Coll Chem & Chem Engn, Qufu 273165, Shandong, Peoples R China
[5] Chengdu Inst Geol & Mineral Resources, Chengdu 610081, Sichuan, Peoples R China
[6] King Abdulaziz Univ, Fac Sci, Chem Dept, Jeddah 21589, Saudi Arabia
基金
中国国家自然科学基金;
关键词
HIGHLY EFFICIENT ELECTROCATALYST; WATER OXIDATION; GENERATING HYDROGEN; CARBON NANOTUBES; NANOWIRE ARRAYS; SURFACE; OXIDE; NANOPARTICLES; TEMPERATURE; NANOSHEETS;
D O I
10.1039/c7qi00340d
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
It is highly desirable but still a challenging task to find a simple, fast and straightforward method to greatly improve the alkaline oxygen evolution reaction (OER) performance of a NiCo2O4 catalyst. In this communication, we demonstrate that developing an amorphous borate shell on a NiCo2O4 surface can boost its OER activity in alkaline media. As a 3D catalyst electrode, a NiCo2O4@Ni-Co-B nanoarray on carbon cloth needs an overpotential of only 270 mV to achieve a geometrical catalytic current density of 10 mA cm(-2) in 1.0 M KOH, which is 100 mV less than that for a NiCo2O4 nanoarray. Notably, this electrode also demonstrates strong electrochemical durability, maintaining its activity for at least 100 h. The superior activity of NiCo2O4@Ni-Co-B is attributed to the amorphous Ni-Co-B shell on NiCo2O4 favoring the in situ electrochemical generation of more active species during water oxidation.
引用
收藏
页码:1546 / 1550
页数:5
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