Oxygen reduction reaction on carbon-supported CoSe2 nanoparticles in an acidic medium

被引:118
|
作者
Feng, Yongjun [1 ]
He, Ting [2 ]
Alonso-Vante, Nicolas [1 ]
机构
[1] Univ Poitiers, CNRS, Lab Electrocatalysis, UMR 6503, F-86022 Poitiers, France
[2] Honda Res Inst USA Inc, Columbus, OH USA
关键词
Cobalt selenide nanoparticles; Oxygen reduction reaction (ORR); Acid medium; Rotating disk electrode (RDE); Rotating ring-disk electrode (RRDE); RING-DISK ELECTRODE; NONPRECIOUS METAL-CATALYSTS; FUEL CELL CATHODE; MODEL CATALYSTS; THIN-FILMS; ELECTROCATALYSTS; MONOLAYER; STABILITY; PLATINUM; KINETICS;
D O I
10.1016/j.electacta.2009.03.052
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
We investigated the effect of CoSe2/C nanoparticle loading rate on oxygen reduction reaction (ORR) activity and H2O2 production using the rotating disk electrode and the rotating ring-disk electrode techniques. We prepared carbon-supported CoSe2 nanoparticles with different nominal loading rates and evaluated these samples by means of powder X-ray diffraction. All the catalysts had an OCP value of 0.81 V vs. RHE. H2O2 production during the ORR process decreased with an increase in catalytic layer thickness. This decrease was related to the CoSe2 loading on the disk electrode. H2O2 production also decreased with increasing catalytic site density, a phenomenon related to the CoSe2 loading rate on the carbon substrate. The cathodic current density significantly increased with increasing catalytic layer thickness, but decreased with increasing catalytic site density. In the case of 20 wt% CoSe2/C nanoparticles at 22 mu g cm(-2), we determined that the transfer process involves about 3.5 electrons. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5252 / 5256
页数:5
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