Simultaneous oxygen reduction and methanol oxidation on a carbon-supported Pt catalyst and mixed potential formation-revisited

被引:54
作者
Jusys, Z [1 ]
Behm, RJ [1 ]
机构
[1] Univ Ulm, Dept Surface Chem & Catal, D-89069 Ulm, Germany
关键词
electrocatalysis; oxygen reduction; methanol oxidation; mixed potential formation; Pt catalyst; DEMS;
D O I
10.1016/j.electacta.2004.01.077
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The mutual effects of the oxygen reduction reaction (ORR) and methanol oxidation reaction (MOR) occurring simultaneously on a Pt/Vulcan fuel cell catalyst in O-2-saturated 0.5 M H2SO4 Solution containing 0.1 or 0.01 M methanol and the formation of a mixed potential were studied using differential electrochemical mass spectrometry (DEMS). This allows to separately monitor the partial reaction rates via CO2 formation (MOR) and O-2 consumption (ORR) and determine the partial Faradaic currents for the individual reactions. While the influence of methanol and of the MOR lead to significant changes in the ORR characteristics, e.g., a shift of the cathode potential by about 0.3 V in 0.1 methanol, the mutual effects on the reaction characteristics of the two partial reactions are much smaller. A fit of the sum of the partial currents to the measured net current results in electrons yield of 8.3 electrons (0.1 M methanol solution) and 6.3 electrons (0.01 M methanol solution) per CO2 molecule for the MOR, compared to values of 7.5 and six electrons in the absence of O-2, indicating an O-2-induced increase in incomplete methanol oxidation by-products. Slight deviations from a simple additive superposition of the ORR and MOR currents, the 'classic' picture for mixed potential formation, are mainly caused by O-2-induced changes in the MOR pathways, together with small changes in the O-2 transport, while the ORR selectivity, predominant oxygen reduction to water, is maintained at relevant potentials. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3891 / 3900
页数:10
相关论文
共 23 条
[1]   THE ADSORPTION OF UNSATURATED ORGANIC-SPECIES AT SINGLE-CRYSTAL ELECTRODES STUDIED BY DIFFERENTIAL ELECTROCHEMICAL MASS-SPECTROMETRY [J].
BALTRUSCHAT, H ;
SCHMIEMANN, U .
BERICHTE DER BUNSEN-GESELLSCHAFT-PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1993, 97 (03) :452-460
[2]   REDUCTION OF OXYGEN IN AN ACIDIC METHANOL OXYGEN (AIR) FUEL-CELL - AN ONLINE MS STUDY [J].
BITTINSCATTANEO, B ;
WASMUS, S ;
LOPEZMISHIMA, B ;
VIELSTICH, W .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1993, 23 (06) :625-630
[3]   THE INFLUENCE OF METHANOL ON O(2) ELECTROREDUCTION AT A ROTATING PT DISK ELECTRODE IN ACID ELECTROLYTE [J].
CHU, D ;
GILMAN, S .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1994, 141 (07) :1770-1773
[4]  
Gottesfeld S., 1997, ADV ELECTROCHEMICAL, V5
[5]   ONLINE MASS-SPECTROSCOPY OF VOLATILE PRODUCTS DURING METHANOL OXIDATION AT PLATINUM IN ACID-SOLUTIONS [J].
IWASITA, T ;
VIELSTICH, W .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1986, 201 (02) :403-408
[6]  
Jarvi TD, 1998, FRONT ELECT, P75
[7]   Methanol oxidation on a carbon-supported Pt fuel cell catalyst - A kinetic and mechanistic study by differential electrochemical mass spectrometry [J].
Jusys, Z ;
Behm, RJ .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (44) :10874-10883
[8]   Simulated 'air bleed' oxidation of adsorbed CO on carbon supported Pt - Part I. A differential electrochemical mass spectrometry study [J].
Jusys, Z ;
Kaiser, J ;
Behm, RJ .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2003, 554 :427-437
[9]   Methanol electrooxidation over Pt/C fuel cell catalysts: Dependence of product yields on catalyst loading [J].
Jusys, Z ;
Kaiser, J ;
Behm, RJ .
LANGMUIR, 2003, 19 (17) :6759-6769
[10]   Electrooxidation of COH2/CO and mixtures on a carbon-supported Pt catalyst -: a kinetic and mechanistic study by differential electrochemical mass spectrometry [J].
Jusys, Z ;
Kaiser, J ;
Behm, RJ .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2001, 3 (21) :4650-4660