Effects of the molecular structure of fluorinated additives on the kinetics of cathodic oxygen reduction

被引:22
作者
Maruyama, J [1 ]
Inaba, M [1 ]
Morita, T [1 ]
Ogumi, Z [1 ]
机构
[1] Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Sakyo Ku, Kyoto 6068501, Japan
关键词
PEMFC; oxygen reduction; fluorinated alcohols; adsorption; gold; rotating ring-disk electrode;
D O I
10.1016/S0022-0728(01)00463-6
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The kinetics of oxygen reduction at a gold electrode was studied in 0.5 M sulfuric acid, in which different kinds of straight-chain [CF3(CF2)(2)CH2OH, CF3CF2CH2OH, and CF3CH2OH] and branched [(CF3)(2)CHOH] fluorinated alcohols were added. The adsorbed layers of the fluorinated alcohols were used as models of the fluorocarbon phase of the perfluorinated polymer electrolyte in gas-diffusion electrodes in proton-exchange membrane fuel cells. A rotating ring-disk electrode was used to determine kinetic parameters for O-2 reduction and to detect intermediate H2O2 formation. The kinetics of oxygen reduction were strongly dependent on the molecular structure of fluorinated additives. The addition of the straight-chain fluorinated alcohols enhanced the kinetic current density while addition of the branched alcohol did not. The linear C-3 fluorinated alcohol, CF3CF2CH2OH, gave the maximum enhancement effect. Oxygen is reduced predominantly via the two-electron series path in the range of 0.4 to 0.0 V at Au, on which no effect of fluorinated additives was observed. The rate constant for intermediate H2O2 reduction, k(3), was negligible in the range 0.40-0.25 V, whereas it increased with decreasing E-D in the range 0.25-0.0 V. In the lower potential range, k(3) decreased with an increase in the concentration of fluorinated alcohol and this decreasing tendency was greatly dependent on the molecular structure of the fluorinated alcohol. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:208 / 216
页数:9
相关论文
共 40 条
  • [11] ELECTROLYTE ADDITIVES FOR PHOSPHORIC-ACID FUEL-CELLS
    GANG, XA
    HJULER, HA
    OLSEN, C
    BERG, RW
    BJERRUM, NJ
    [J]. JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1993, 140 (04) : 896 - 902
  • [12] HYDROGEN PEROXIDE FORMATION IN OXYGEN REDUCTION AT GOLD ELECTRODES .I. ACID SOLUTION
    GENSHAW, MA
    DAMJANOV, A
    BOCKRIS, JO
    [J]. JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1967, 15 (2-3) : 163 - +
  • [13] GIERKE TD, 1982, ACS SYM SER, V180, P283
  • [14] THE MORPHOLOGY IN NAFION PERFLUORINATED MEMBRANE PRODUCTS, AS DETERMINED BY WIDE-ANGLE AND SMALL-ANGLE X-RAY STUDIES
    GIERKE, TD
    MUNN, GE
    WILSON, FC
    [J]. JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 1981, 19 (11) : 1687 - 1704
  • [15] Heat-treated iron(III) tetramethoxyphenyl porphyrin chloride supported on high-area carbon as an electrocatalyst for oxygen reduction: Part III. Detection of hydrogen-peroxide during oxygen reduction
    Gojkovic, SL
    Gupta, S
    Savinell, RF
    [J]. ELECTROCHIMICA ACTA, 1999, 45 (06) : 889 - 897
  • [16] OXYGEN REDUCTION KINETICS ON A PLATINUM RDE COATED WITH A RECAST NAFION1 FILM
    GOTTESFELD, S
    RAISTRICK, ID
    SRINIVASAN, S
    [J]. JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1987, 134 (06) : 1455 - 1462
  • [17] IBLE N, 1983, COMPR TREAT, V6, P239
  • [18] Hydrogen oxidation on partially immersed Nafion(R)-coated electrodes
    Inaba, M
    Uno, M
    Maruyama, J
    Tasaka, A
    Katakura, K
    Ogumi, Z
    [J]. JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1996, 417 (1-2): : 105 - 111
  • [19] Microelectrode simulation of anode in polymer electrolyte fuel cells
    Katakura, K
    Hinatsu, JT
    Inatomi, K
    Inaba, M
    Ogumi, Z
    Takehara, Z
    [J]. DENKI KAGAKU, 1996, 64 (06): : 711 - 717
  • [20] Kinoshita K., 1992, Electrochemical Oxygen Technology