A highly active and stable electrocatalyst for the oxygen reduction reaction based on a graphene-supported g-C3N4@cobalt oxide core-shell hybrid in alkaline solution

被引:109
作者
Jin, Jutao [1 ,2 ]
Fu, Xiaogang [1 ,3 ]
Liu, Qiao [1 ,2 ]
Zhang, Junyan [1 ]
机构
[1] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Solid Lubricat, Lanzhou 730000, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China
关键词
METAL-FREE ELECTROCATALYSTS; FREE ACTIVATION; AIR BATTERIES; FUEL-CELL; LI-AIR; CATALYSTS; EVOLUTION; NANOCRYSTALS; PERFORMANCE; OXIDATION;
D O I
10.1039/c3ta11144j
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
A novel hybrid, with g-C3N4 embedded CoO particles covalently supported on a two-dimensional graphene sheet, is synthesized by a facile and scalable method towards the oxygen reduction reaction (ORR) for fuel cells. The composite hybrid with a suitable loading of g-C3N4@cobalt oxide on graphene exhibits excellent electrocatalytic activity and a dominant four-electron oxygen reduction pathway in basic solution. The kinetic-limiting current density (J(k)) is 16.78 mA cm(-2) at -0.25 V, approaching that of 20% Pt-C (17.22 mA cm(-2)) at the same potential. The performance gap between the hybrid and 20% Pt-C in terms of the half-wave potential difference (Delta E-1/2) is 25 mV in alkaline solution. Furthermore, the hybrid is robust and methanol tolerant, making it a good candidate as a cathodic electrocatalyst in fuel cells.
引用
收藏
页码:10538 / 10545
页数:8
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