Pt-Ruadatom nanoparticles as anode catalysts for direct methanol fuel cells

被引:48
作者
Cao, DX [1 ]
Bergens, SH [1 ]
机构
[1] Univ Alberta, Dept Chem, Edmonton, AB T6G 2G2, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
platinum; ruthenium; adatom; direct methanol fuel cell; anode electrocatalyst;
D O I
10.1016/j.jpowsour.2004.03.053
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 series of prototype direct methanol fuel cells (DMFCs) were constructed and operated under identical procedures and conditions except for the surface compositions of the anode electrocatalysts. The cathode electrocatalyst was Pt black (loading 2 mg/cm(2), specific surface area: ca. 27 m(2)/g), the electrolyte membrane was Nation(TM) 117, and the anode electrocatalysts were a series of Pt-Ru adatom (Pt-Ru-ad) nanoparticles (loading 2 mg/cm(2), specific surface area: ca. 27 m2/g) prepared by a direct surface reductive deposition of Ru-ad onto Pt black. The optimum surface coverage of Pt by Ruad was ca. 33% for DMFCs operating at 60degreesC. The optimum ranged from ca. 30 to 60% at 90degreesC. A DMFC using Pt-Ruad nanoparticles supported on carbon (Vulcan XC-72(TM)) as anode electrocatalyst was operated for 20 days at 8 h each day without loss of activity. These results, combined with those from an in situ cyclic voltammetry study, indicate that no significant Ruad dissolution and/or redistribution occurred during fabrication and operation of the prototype DMFCs. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:170 / 180
页数:11
相关论文
共 89 条
[81]   Reactivity and activation parameters in methanol oxidation on platinum single crystal electrodes 'decorated' by ruthenium adlayers [J].
Tremiliosi-Filho, G ;
Kim, H ;
Chrzanowski, W ;
Wieckowski, A ;
Grzybowska, B ;
Kulesza, P .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1999, 467 (1-2) :143-156
[82]  
VANDERWIEL A, 1952, CHEM WEEKBL, V48, P597
[83]   Electrochemical and spontaneous deposition of ruthenium at platinum electrodes for methanol oxidation:: an electrochemical quartz crystal microbalance study [J].
Vigier, F ;
Gloaguen, F ;
Léger, JM ;
Lamy, C .
ELECTROCHIMICA ACTA, 2001, 46 (28) :4331-4337
[84]   Methanol oxidation and direct methanol fuel cells:: a selective review [J].
Wasmus, S ;
Küver, A .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1999, 461 (1-2) :14-31
[85]   UHV and electrochemical studies of CO and methanol adsorbed at platinum/ruthenium surfaces, and reference to fuel cell catalysis [J].
Waszczuk, P ;
Lu, GQ ;
Wieckowski, A ;
Lu, C ;
Rice, C ;
Masel, RI .
ELECTROCHIMICA ACTA, 2002, 47 (22-23) :3637-3652
[86]   Methanol electrooxidation on platinum/ruthenium nanoparticle catalysts [J].
Waszczuk, P ;
Solla-Gullón, J ;
Kim, HS ;
Tong, YY ;
Montiel, V ;
Aldaz, A ;
Wieckowski, A .
JOURNAL OF CATALYSIS, 2001, 203 (01) :1-6
[87]   ELECTROCATALYSIS BY AD-ATOMS .2. ENHANCEMENT OF OXIDATION OF METHANOL ON PLATINUM BY RUTHENIUM AD-ATOMS [J].
WATANABE, M ;
MOTOO, S .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1975, 60 (03) :267-273
[88]   Direct methanol oxidation on platinum electrodes with ruthenium adatoms in hot phosphoric acid [J].
Watanabe, M ;
Genjima, Y ;
Turumi, K .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1997, 144 (02) :423-428
[89]  
WOODS R, 1974, J ELECTROANAL CHEM, V49, P217