Synthesis and characterization of PtCo nanowires for the electro-oxidation of methanol

被引:33
作者
Bertin, Erwan [1 ]
Garbarino, Sebastien [1 ]
Ponrouch, Alexandre [1 ]
Guay, Daniel [1 ]
机构
[1] INRS Energie Mat & Telecommun, Varennes, PQ J3X 1S2, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Electrodeposition; Thin film; Nanowire; Bimetallic CoPt; Electro-oxidation; Methanol; HIGH-SURFACE-AREA; OXYGEN-REDUCTION; PARTICLE-SIZE; FUEL-CELLS; UNDERPOTENTIAL DEPOSITION; ALLOY ELECTROCATALYSTS; CO; PLATINUM; OXIDATION; CATALYSTS;
D O I
10.1016/j.jpowsour.2012.01.015
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
PtxCo100-x (60 <= x <= 100) 10 nanostructures (nanowires) on titanium are prepared by direct electrodeposition throughout a porous anodic aluminum oxide membrane and analyzed for methanol electrooxidation. For comparison, thin films of the same composition are also prepared. The morphology and composition are characterized by scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). A model based on the simultaneous deposition of Pt and Co underpotential deposition (UPD) on Pt was devised to understand how the composition varies with the electrodeposition potential. The deposition rates were determined by means of an Electrochemical Quartz Crystal Microbalance (EQCM). PtxCo100-x alloy formation was confirmed by X-ray diffraction (XRD). Electrocatalytic properties for methanol oxidation are investigated by cyclic voltammetry (CV) in 1.0 M CH3OH + 0.5 M H2SO4. The results show that PtCo nanowires yield to an enhancement (by a factor of 5) of the exposed surface area (m(2) g(-1)). In the presence of CH3OH, l(f)/l(b) ratio of Pt rich nanowires is systematically higher than for thin films with the same composition. I-f/I-b ratio of Pt90Co10 nanowires is 1.59, larger than that of pure Pt (I-f/I-b = 0.76-0.87) and commercially available PtCo deposited on carbon support (I-f/l(b) = 1.32). (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:20 / 28
页数:9
相关论文
共 51 条
  • [1] The methanol oxidation reaction on platinum alloys with the first row transition metals - The case of Pt-Co and -Ni alloy electrocatalysts for DMFCs: A short review
    Antolini, E
    Salgado, JRC
    Gonzalez, ER
    [J]. APPLIED CATALYSIS B-ENVIRONMENTAL, 2006, 63 (1-2) : 137 - 149
  • [2] The effect of the particle size on the kinetics of CO electrooxidation on high surface area Pt catalysts
    Arenz, M
    Mayrhofer, KJJ
    Stamenkovic, V
    Blizanac, BB
    Tomoyuki, T
    Ross, PN
    Markovic, NM
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (18) : 6819 - 6829
  • [4] Supportless Pt and PtPd nanotubes as electrocatalysts for oxygen-reduction reactions
    Chen, Zhongwei
    Waje, Mahesh
    Li, Wenzhen
    Yan, Yushan
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2007, 46 (22) : 4060 - 4063
  • [5] THE ROLE OF MORPHOLOGY IN THE METHANOL ELECTROOXIDATION REACTION
    CHRISTENSEN, PA
    HAMNETT, A
    TROUGHTON, GL
    [J]. JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1993, 362 (1-2): : 207 - 218
  • [6] The degree and effect of methanol crossover in the direct methanol fuel cell
    Cruickshank, J
    Scott, K
    [J]. JOURNAL OF POWER SOURCES, 1998, 70 (01) : 40 - 47
  • [7] Cullity B. D., 1978, ELEMENTS XRAY DIFFRA
  • [8] Instability of Pt/C electrocatalysts in proton exchange membrane fuel cells - A mechanistic investigation
    Ferreira, PJ
    la O', GJ
    Shao-Horn, Y
    Morgan, D
    Makharia, R
    Kocha, S
    Gasteiger, HA
    [J]. JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2005, 152 (11) : A2256 - A2271
  • [9] In-situ vibrational spectroscopy on Pt electrocatalysts
    Friedrich, KA
    Henglein, F
    Stimming, U
    Unkauf, W
    [J]. ELECTROCHIMICA ACTA, 2001, 47 (05) : 689 - 694
  • [10] Size dependence of the CO monolayer oxidation on nanosized Pt particles supported on gold
    Friedrich, KA
    Henglein, F
    Stimming, U
    Unkauf, W
    [J]. ELECTROCHIMICA ACTA, 2000, 45 (20) : 3283 - 3293