Electro-oxidation of methanol and ethanol using a Pt-RuO2/C composite prepared by the sol-gel technique and supported on boron-doped diamond

被引:52
作者
Suffredini, H. B.
Tricoli, V.
Vatistas, N.
Avaca, L. A.
机构
[1] Univ Sao Paulo, Inst Fis & Quim Sao Carlos, BR-13560970 Sao Carlos, SP, Brazil
[2] Univ Pisa, Dipartimento Ingn Chim, I-56126 Pisa, Italy
基金
巴西圣保罗研究基金会;
关键词
modified carbon powder electrodes; methanol electro-oxidation; ethanol electro-oxidation; boron-doped diamond; fuel cells; sol-gel;
D O I
10.1016/j.jpowsour.2005.09.040
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
A detailed description of the preparation, characterization and electrochemical performance towards methanol and ethanol oxidation in acid medium of a platinum-ruthenium oxide carbon powder composite is presented here. The composite was prepared by the sol-gel technique and fixed on the surface of a boron-doped diamond (BBD) electrode. The physical characterization by XRD and EDX revealed the crystalline nature of the catalysts particles having an average size of 7.2nm and a mass ratio of practically 1:1 for Pt and Ru, in accordance with the preparation conditions. Initial electrochemical experiments using also glassy carbon as the substrate for the composite showed that BDD has a superior performance, probably related to the very low capacitive currents of that material. The oxidation of methanol and ethanol in H2SO4 solutions was studied by cyclic voltammetry, Tafel plots and chronoamperometry and the results were compared to those obtained using a commercial Pt/C powder composite under the same conditions. In all cases, the Pt-RuO2/C composite showed larger anodic current densities and increased stability than the other material thus confirming the suitability of the simple and straightforward preparation technique for the catalysts. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:124 / 128
页数:5
相关论文
共 38 条
[1]   Optimization of operating parameters of a direct methanol fuel cell and physico-chemical investigation of catalyst-electrolyte interface [J].
Arico, AS ;
Creti, P ;
Antonucci, PL ;
Cho, J ;
Kim, H ;
Antonucci, V .
ELECTROCHIMICA ACTA, 1998, 43 (24) :3719-3729
[2]   EMERGING TECHNOLOGY OF DIAMOND THIN-FILMS [J].
BACHMANN, PK ;
MESSIER, R .
CHEMICAL & ENGINEERING NEWS, 1989, 67 (20) :24-&
[3]   HIGHLY DISPERSED METAL-CLUSTERS AND COLLOIDS FOR THE PREPARATION OF ACTIVE LIQUID-PHASE HYDROGENATION CATALYSTS [J].
BONNEMANN, H ;
BRIJOUX, W ;
BRINKMANN, R ;
DINJUS, E ;
FRETZEN, R ;
JOUSSEN, T ;
KORALL, B .
JOURNAL OF MOLECULAR CATALYSIS, 1992, 74 (1-3) :323-333
[4]   Electrochemical behaviour of ceramic sol-gel coatings on mild steel [J].
Fallet, M ;
Mahdjoub, H ;
Gautier, B ;
Bauer, JP .
JOURNAL OF NON-CRYSTALLINE SOLIDS, 2001, 293 :527-533
[5]   The efficiency of methanol conversion to CO2 on thin films of Pt and PtRu fuel cell catalysts [J].
Gao, L ;
Huang, HL ;
Korzeniewski, C .
ELECTROCHIMICA ACTA, 2004, 49 (08) :1281-1287
[6]   TEMPERATURE-DEPENDENT METHANOL ELECTROOXIDATION ON WELL-CHARACTERIZED PT-RU ALLOYS [J].
GASTEIGER, HA ;
MARKOVIC, N ;
ROSS, PN ;
CAIRNS, EJ .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1994, 141 (07) :1795-1803
[7]   Kinetic study of methanol oxidation on carbon-supported PtRu electrocatalyst [J].
Gojkovic, SL ;
Vidakovic, TR ;
Durovic, DR .
ELECTROCHIMICA ACTA, 2003, 48 (24) :3607-3614
[8]   Electrodeposition of Pt-Ru nanoparticles on carbon nanotubes and their electrocatalytic properties for methanol electrooxidation [J].
He, ZB ;
Chen, JH ;
Liu, DY ;
Zhou, HH ;
Kuang, YF .
DIAMOND AND RELATED MATERIALS, 2004, 13 (10) :1764-1770
[9]   Current-time behavior of smooth and porous PtRu surfaces for methanol oxidation [J].
Hoster, H ;
Iwasita, T ;
Baumgärtner, H ;
Vielstich, W .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2001, 148 (05) :A496-A501
[10]   Simultaneous oxygen reduction and methanol oxidation on a carbon-supported Pt catalyst and mixed potential formation-revisited [J].
Jusys, Z ;
Behm, RJ .
ELECTROCHIMICA ACTA, 2004, 49 (22-23) :3891-3900