Cobalt and Iron Oxides Co-supported on Carbon Nanotubes as an Efficient Bifunctional Catalyst for Enhanced Electrocatalytic Activity in Oxygen Reduction and Oxygen Evolution Reactions

被引:23
作者
Zhao, Ye-Min [1 ]
Wang, Fei-Fei [1 ]
Wei, Ping-Jie [1 ]
Yu, Guo-Qiang [1 ]
Cui, Shi-Cong [1 ]
Liu, Jin-Gang [1 ]
机构
[1] East China Univ Sci & Technol, Sch Chem & Mol Engn, Key Lab Adv Mat, Shanghai 200237, Peoples R China
关键词
cobalt oxides; iron oxide; metal-organic frameworks; oxygen evolution reaction; oxygen reduction reaction; METAL-ORGANIC-FRAMEWORK; WATER OXIDATION; GRAPHENE OXIDE; AIR BATTERIES; NITROGEN; NANOPARTICLES; PERFORMANCE; NANOSHEETS; ALKALINE; NANOCRYSTALS;
D O I
10.1002/slct.201702231
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Developing efficient non-precious metal electrocatalysts for the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) in energy conversion and storage devices is highly desirable but challenging. This report describes a general approach for preparing cobalt and iron oxide nanoparticles co-supported on nitrogen-doped carbon materials as an efficient oxygen electrode catalyst with an improved catalytic activity toward OER and ORR; these nanoparticles were obtained through pyrolysis of Co- and Fe-based metal-organic frameworks grown directly on the surface of polyvinylimidazole-functionalized carbon nanotubes (CNTs). The Fe/Co-CNTs-800 catalyst pyrolyzed at 800 degrees C exhibited high electrocatalytic activity for ORR, with only approximate to 50mV lesser activity than that of Pt/C at the half-wave potential, and for OER, with only approximate to 70mV lesser activity than that of RuO2 at a current density of 10mAcm(-2) in a 0.1M KOH solution. The potential difference between OER and ORR for Fe/Co-CNTs-800 (EOER-ORR) was 0.905V, which was significantly lower than that for noble-metal catalysts (20wt% Pt/C (1.137V) and RuO2 (1.341V)). The preparation temperature and value of Fe/Co in the catalyst composite are crucial for achieving high electrocatalytic activity for both ORR and OER.
引用
收藏
页码:207 / 213
页数:7
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