Electroactivity of tin modified platinum electrodes for ethanol electrooxidation

被引:149
作者
Simoes, F. C.
dos Anjos, D. M.
Vigier, F.
Leger, J.-M.
Hahn, F.
Coutanceau, C.
Gonzalez, E. R.
Tremiliosi-Filho, G.
de Andrade, A. R.
Olivi, P.
Kokoh, K. B.
机构
[1] Univ Poitiers, CNRS, UMR 6503, Equipe Electrocatalyse, F-86022 Poitiers, France
[2] Univ Sao Paulo, Dept Quim, Fac Filosofia Ciencias & Letras Ribeirao Preto, BR-14040901 Ribeirao Preto, Brazil
[3] Univ Sao Paulo, Inst Quim Sao Carlos, BR-13560970 Sao Carlos, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
ethanol oxidation; DEFC; platinum-tin electrocatalyst;
D O I
10.1016/j.jpowsour.2006.12.113
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Different electrochemical techniques like cyclic voltammetry and chronoamperometry and tests in a single direct ethanol fuel cell (DEFC) were used to evaluate the catalytic activity of various compositions of PtSn electrodes prepared by thermal decomposition for ethanol electrooxidation. This oxidation process was also investigated by in situ infrared reflectance spectroscopy to determine the presence of adsorbed intermediates. The experimental results showed that PtSn can oxidize ethanol mainly to acetaldehyde and acetic acid. Adsorbed CO was also found, which demonstrates that the rupture of the C-C bond in the ethanol molecule can also take place during the oxidation process. This intermediate species was oxidized to CO2 which was detected by IR spectroscopy and chromatography. With Pt90Sn10/C as anode catalyst, single DEFC tests carried out using MEAs with a geometric electrode area of 5 cm(2) allowed to produce a power density of ca. 72 mW cm(-2) at 110 degrees C. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 36 条
[1]   Formation, microstructural characteristics and stability of carbon supported platinum catalysts for low temperature fuel cells [J].
Antolini, E .
JOURNAL OF MATERIALS SCIENCE, 2003, 38 (14) :2995-3005
[2]   Carbon-supported Pt-Sn electrocatalysts for the anodic oxidation of H2, CO, and H2/CO mixtures.: Part II:: The structure-activity relationship [J].
Arenz, M ;
Stamenkovic, V ;
Blizanac, BB ;
Mayrhofer, KJJ ;
Markovic, NM ;
Ross, PN .
JOURNAL OF CATALYSIS, 2005, 232 (02) :402-410
[3]   New mechanistic aspects of methanol oxidation [J].
Batista, EA ;
Malpass, GRP ;
Motheo, AJ ;
Iwasita, T .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2004, 571 (02) :273-282
[4]   Nanoscale colloidal metals and alloys stabilized by solvents and surfactants - Preparation and use as catalyst precursors [J].
Bonnemann, H ;
Braun, G ;
Brijoux, W ;
Brinkmann, R ;
Tilling, AS ;
Seevogel, K ;
Siepen, K .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1996, 520 (1-2) :143-162
[5]   Parallel pathways of ethanol oxidation: The effect of ethanol concentration [J].
Camara, GA ;
Iwasita, T .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2005, 578 (02) :315-321
[6]   Preparation of metal nanoparticles in water-in-oil (w/o) microemulsions [J].
Capek, I .
ADVANCES IN COLLOID AND INTERFACE SCIENCE, 2004, 110 (1-2) :49-74
[7]   METAL CRYSTALLINITY EFFECTS IN ELECTROCATALYSIS AS PROBED BY REAL-TIME FTIR SPECTROSCOPY - ELECTROOXIDATION OF FORMIC-ACID, METHANOL, AND ETHANOL ON ORDERED LOW-INDEX PLATINUM SURFACES [J].
CHANG, SC ;
LEUNG, LWH ;
WEAVER, MJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1990, 94 (15) :6013-6021
[8]   Electrooxidation of methanol on PtMyOx (M = Sn, Mo, Os or W) electrodes [J].
de Oliveira, MB ;
Profeti, LPR ;
Olivi, P .
ELECTROCHEMISTRY COMMUNICATIONS, 2005, 7 (07) :703-709
[9]   Characterisation of DSA®-type coatings with nominal composition Ti/Ru0.3Ti(0.7-x)SnxO2 prepared via a polymeric precursor [J].
Forti, JC ;
Olivi, P ;
de Andrade, AR .
ELECTROCHIMICA ACTA, 2001, 47 (06) :913-920
[10]   Ethanol oxidation on PtRu electrodes studied by differential electrochemical mass spectrometry [J].
Fujiwara, N ;
Friedrich, KA ;
Stimming, U .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1999, 472 (02) :120-125