Methanol and ethanol electroxidation using Pt electrodes prepared by the polymeric precursor method

被引:53
作者
Freitas, R. G.
Santos, M. C.
Oliveira, R. T. S.
Bulhoes, L. O. S.
Pereira, E. C.
机构
[1] Univ Fed Sao Carlos, Dept Quim, Lab Interdisciplinar Electroquim & Ceram, Ctr Multidisciplinar Para Desenvolvimento Mat Cer, BR-13565970 Sao Carlos, SP, Brazil
[2] UNICEP, CENIP, BR-13563470 Sao Carlos, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Pt electrodes; Pt thin films; polymeric precursor method; methanol oxidation; ethanol oxidation;
D O I
10.1016/j.jpowsour.2005.10.002
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
The results of methanol and ethanol oxidation in acidic medium on Pt electrodes deposited on Ti substrate using the Pechini method are presented. In this route the metallic salts were dissolved in a mixture of ethylene glycol (EG) and citric acid (CA) forming a polyester network, which is painted onto a Ti substrate and then heat treated at 600 degrees C in order to obtain the metallic Pt thin films. The X-ray diffraction analysis showed the presence of Pt pattern peaks. The presence of the (420) plane in a higher amount compared to bulk Pt was observed and the peak position of the planes (200) and (420) were displaced by approximately -0.3 degrees. The roughness data presented almost the same values for Ti and Ti/Pt. The electrochemical characterization of the electrodes in 0.1 M HClO4 showed a typical Pt voltammetric profile. Although the voltammetric profiles of Ti/Pt and bulk Pt were the same, the electrocatalytical behavior for methanol oxidation showed an enhancement of the oxidation current density peak, which increased by 170% compared to bulk platinum. Although, the current density peak for ethanol oxidation on Ti/Pt is smaller than for Pt, it began at 0.11 V less positive than the same process on bulk Pt. The chronoamperometric experiments for methanol and ethanol oxidation on Ti/Pt increased by almost 934% and 440%, respectively, compared with Pt bulk. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:164 / 168
页数:5
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