Chem. J. Chinese Universities ›› 2013, Vol. 34 ›› Issue (1): 149.doi: 10.7503/cjcu20120364

• Physical Chemistry • Previous Articles     Next Articles

Effect of KOH Concentrations on Oxygen Reduction Reaction Catalyzed by CoPy/C Electrocatalyst and Active Site Studies

XU Li1, DING Lei1, DAI Xian-Feng1, ZHANG Jing1, TIAN Bing-Lun2, LIU Shi-Yao2, QIAO Jin-Li1   

  1. 1. College of Environmental Science and Engineering, Donghua University, Shanghai 201620, China;
    2. Pearl Hydrogen Technology Co., Ltd., Shanghai 201803, China
  • Received:2012-04-16 Published:2012-12-31

Abstract:

Nanostructure CoPy catalyst(15Co%25%Py/C, mass fraction) for the oxygen reduction reaction(ORR)was prepared by cobalt sulfate hepathydrate(CoSO4·7H2O) and pyridine(Py) as the Co and N precursors supported on Vulcan XC-72R, and followed by heat treatment in an inert atmosphere at 800℃. Electrochemical performances were evaluated using rotating disk electrode(RDE) technique in terms of its ORR activity in electrolytes containing various concentrations of KOH. The results show that the concentration of KOH has significant impact on the ORR performance of the CoPy/C catalyst. In 0.05 mol/L KOH, CoPy/C(in O2) can produce the obvious ORR current, giving the onset potential at 0.10 V(vs. SHE). The diffusion-limiting current density was 4.39 mA/cm2 at -0.381 V. RDE results reveal that CoPy/C catalyst in 0.05 and 0.1 mol/L KOH solution catalyze the ORR via four-electron pathway. XPS analysis indicates that both pyridinic-N and graphitic-N are responsible for the enhanced ORR activity.

Key words: CoPy/C catalyst, Oxygen reduction reaction, KOH concentration, Rotating disk electrode, Active site, Alkaline fuel cell

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