Enhanced electrocatalytic performance for methanol oxidation on Pt-TiO2/ITO electrode under UV illumination

被引:78
|
作者
Zhang, Hongmei [1 ]
Zhou, Weiqiang [1 ,4 ]
Du, Yukou [1 ]
Yang, Ping [1 ]
Wang, Chuanyi [2 ,3 ]
Xu, Jingkun [4 ]
机构
[1] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China
[2] Chinese Acad Sci, Xinjiang Tech Inst Phys & Chem, Urumqi 830011, Peoples R China
[3] Tufts Univ, Dept Chem, Medford, MA 02155 USA
[4] Jiangxi Sci & Technol Normal Univ, Jiangxi Key Lab Organ Chem, Nanchang 330013, Peoples R China
基金
中国国家自然科学基金;
关键词
Methanol; Electrooxidation; UV illumination; Pt nanoparticles; Titanium oxide; PLATINUM ELECTROCATALYST; AUPT NANOPARTICLES; CARBON NANOTUBES; TIO2; CATALYSTS; ELECTROOXIDATION; ACID; RU; PD; PHOTOCATALYSTS;
D O I
10.1016/j.ijhydene.2010.09.025
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
Pt is one of the most important electrode materials employed in direct methanol fuel cell, and many efforts have been directed to improving its electrocatalytic performance. In this work, Pt-TiO2 nanocomposites are successfully prepared by a sol-gel method. As revealed by TEM, Pt nanoparticles with an average size of 2.6 nm are well uniformly dispersed on porous TiO2. XRD structural characterization indicates that Pt possesses a face centered cubic crystal structure while TiO2 is in the format of both rutile and anatase phases. The electrochemical performance of as-prepared nanocomposite electrode (Pt-TiO2/ITO) is evaluated by studying the electrocatalytic oxidation of methanol in an alkaline medium with or without UV illumination. Comparative experiments evince that the electrochemical performance of Pt-TiO2/ITO for methanol electrooxidation is markedly improved under UV illumination. Under UV illumination, moreover, the poisoning resistance of Pt-TiO2/ITO for methanol electrooxidation is significantly improved, as supported by the results of time-coursed current measurements. (C) 2010 Professor T. Nejat Veziroglu. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:13290 / 13297
页数:8
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