Hydrogen oxidation on PtRuPEM anodes -: Mechanism, effective mass transfer, and influence of CO2

被引:10
作者
Halseid, Rune [1 ]
Tunold, Reidar [1 ]
机构
[1] Norwegian Univ Sci & Technol, Grp Electrochem, Dept Mat Sci & Engn, NO-7491 Trondheim, Norway
关键词
D O I
10.1149/1.2360764
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 [应用化学];
摘要
The hydrogen oxidation reaction (HOR) on a PtRu anode catalyst has been investigated, and polarization curves for H-2 mixed with N-2, Ar, He, and CO2 have been measured in symmetrical H-2 vertical bar H-2 cells. HOR on the PtRu catalyst follows the Tafel-Volmer mechanism based on the observation of limiting currents that were not due to mass transfer but rather reaction limitations. The mass transfer rate in the gas diffusion layer was found to be very high. Transport through the ionomer in the catalyst layer covering the active catalyst also contributed to the mass transfer resistance, but it was not possible to estimate the relative importance of this compared to the reaction limiting current due to the Tafel step. The influence of CO2 on the performance of the PtRu anode was significant in symmetrical cells. Nitrogen did not have any effect on anode performance other than dilution. Recovery of the symmetrical H-2 vertical bar H-2 cell after exposure to CO2 was slow and not complete. To achieve complete recovery, it was required to electrochemically activate the electrodes by oxidation of adsorbed contaminants. (c) 2006 The Electrochemical Society.
引用
收藏
页码:A2319 / A2325
页数:7
相关论文
共 24 条
[1]
The proton exchange membrane fuel cell performance of a carbon supported PtMo catalyst operating on reformate [J].
Ball, S ;
Hodgkinson, A ;
Hoogers, G ;
Maniguet, S ;
Thompsett, D ;
Wong, B .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2002, 5 (02) :A31-A34
[2]
On-line mass spectrometry investigation of the reduction of carbon dioxide in acidic media on polycrystalline Pt [J].
Brisard, GM ;
Camargo, APM ;
Nart, FC ;
Iwasita, T .
ELECTROCHEMISTRY COMMUNICATIONS, 2001, 3 (11) :603-607
[3]
Catalyst microstructure examination of PEMFC membrane electrode assemblies vs. time [J].
Cheng, X ;
Chen, L ;
Peng, C ;
Chen, ZW ;
Zhang, Y ;
Fan, QB .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2004, 151 (01) :A48-A52
[4]
The influence of carbon dioxide on PEM fuel cell anodes [J].
de Bruijn, FA ;
Papageorgopoulos, DC ;
Sitters, EF ;
Janssen, GJM .
JOURNAL OF POWER SOURCES, 2002, 110 (01) :117-124
[5]
Giner J, 1963, Electrochim Acta, V8, P857, DOI [10.1016/0013-4686(63)80054-7, DOI 10.1016/0013-4686(63)80054-7]
[6]
Effect of reformate components on PEMFC performance - Dilution and reverse water gas shift reaction [J].
Gu, T ;
Lee, WK ;
Van Zee, JW ;
Murthy, M .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2004, 151 (12) :A2100-A2105
[7]
Halseid R., 2004, THESIS NORWEGIAN U S
[8]
ELECTROCATALYTIC PROCESS OF CO SELECTIVITY IN ELECTROCHEMICAL REDUCTION OF CO2 AT METAL-ELECTRODES IN AQUEOUS-MEDIA [J].
HORI, Y ;
WAKEBE, H ;
TSUKAMOTO, T ;
KOGA, O .
ELECTROCHIMICA ACTA, 1994, 39 (11-12) :1833-1839
[9]
ON THE STUDY OF ADSORBED SPECIES AT PLATINUM FROM METHANOL, FORMIC-ACID AND REDUCED CARBON-DIOXIDE VIA INSITU FT-IR SPECTROSCOPY [J].
IWASITA, T ;
NART, FC ;
LOPEZ, B ;
VIELSTICH, W .
ELECTROCHIMICA ACTA, 1992, 37 (12) :2361-2367
[10]
Modelling study of CO2 poisoning on PEMFC anodes [J].
Janssen, GJM .
JOURNAL OF POWER SOURCES, 2004, 136 (01) :45-54