Nickel-cobalt oxides supported on Co/N decorated graphene as an excellent bifunctional oxygen catalyst

被引:119
作者
Hao, Yongchao [1 ]
Xu, Yuqi [1 ]
Liu, Junfeng [1 ]
Sun, Xiaoming [1 ,2 ,3 ]
机构
[1] State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Beijing Univ Chem Technol, Coll Energy, Beijing 100029, Peoples R China
[3] Beijing Adv Innovat Ctr Soft Matter Sci & Engn, Beijing 100029, Peoples R China
关键词
POROUS NANOWIRE ARRAYS; IN-SITU; HIGHLY-EFFICIENT; CARBON SHEETS; REDUCTION; NITROGEN; EVOLUTION; NANOPARTICLES; ELECTROCATALYST; NICO2O4;
D O I
10.1039/c7ta00299h
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
The design of highly efficient electrocatalysts for the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) plays a key role in the development of various renewable energy storage and conversion devices. Recently, metal-organic framework (MOF) derived materials have shown great potential in ORR and OER; however, they may suffer from poor conductivity with limited electrochemical performance especially towards OER. In this work, nickel-cobalt oxides supported on Co/N decorated graphene were prepared by introducing nickel in a zeolitic imidazolate framework-67 (ZIF-67) as the precursor, which showed improved OER performance due to the as-derived NixCoyO4, and maintained the ORR performance of Co/N doped carbon at the same time. Meanwhile, graphene was utilized to further enhance the electrochemical surface area and charge transfer efficiency. The resulting composites show a potential of 0.796 V at 3 mA cm(-2) and superior stability to Pt/C towards ORR, as well as a potential of 1.629 V to achieve 10 mA cm(-2) current density for OER, which is much better than that of IrO2. In all, the overvoltage between ORR and OER was just 0.833 V, demonstrating the great potential of the composite in metal-air batteries as a bifunctional oxygen catalyst.
引用
收藏
页码:5594 / 5600
页数:7
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