Pd-Ni electrocatalysts for efficient ethanol oxidation reaction in alkaline electrolyte

被引:293
作者
Zhang, Zhiyong [1 ]
Xin, Le [1 ]
Sun, Kai [2 ]
Li, Wenzhen [1 ]
机构
[1] Michigan Technol Univ, Dept Chem Engn, Houghton, MI 49931 USA
[2] Univ Michigan, Dept Mat Sci & Engn, Ann Arbor, MI 48109 USA
关键词
Electrocatalyst; Nanoparticle; Pd-Ni; Ethanol oxidation; Alkaline; Fuel cell; OXYGEN REDUCTION ACTIVITY; ANION-EXCHANGE MEMBRANES; RUTHENIUM ANODE CATALYST; FUEL-CELLS; IN-SITU; ALCOHOL OXIDATION; ELECTROOXIDATION; PALLADIUM; NANOPARTICLES; PERFORMANCE;
D O I
10.1016/j.ijhydene.2011.06.141
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
PdxNiy/C catalysts with high ethanol oxidation reaction (EOR) activity in alkaline solution have been prepared through a solution phase-based nanocapsule method. XRD and TEM show PdxNiy nanoparticles with a small average diameter (2.4-3.2 nm) and narrow size distribution (1-6 nm) were homogeneously dispersed on carbon black XC-72 support. The EOR onset potential on Pd4Ni5/C (-801 mV vs. Hg/HgO) was observed shifted 180 mV more negative than that of Pd/C. Its exchange current density was 33 times higher than that of Pd/C (41.3 x 10(-7) A/cm(2) us. 1.24 x 10(-7) A/cm(2)). After a 10,000-s chronoamperometry test at -0.5 V (us Hg/Hg0), the EOR mass activity of Pd2Ni3/C survived at 1.71 mA/mg, while that of Pd/C had dropped to 0, indicating PdxNiy/C catalysts have a better 'detoxification' ability for EOR than Pd/C. We propose that surface Ni could promote refreshing Pd active sites, thus enhancing the overall ethanol oxidation kinetics. The nanocapsule method is able to not only control over the diameter and size distribution of Pd-Ni particles, but also facilitate the formation of more efficient contacts between Pd and Ni on the catalyst surface, which is the key to improving the EOR activity. Copyright (C) 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:12686 / 12697
页数:12
相关论文
共 86 条
  • [1] Characterization and use of anionic membranes for alkaline fuel cells
    Agel, E
    Bouet, J
    Fauvarque, JF
    [J]. JOURNAL OF POWER SOURCES, 2001, 101 (02) : 267 - 274
  • [2] [Anonymous], 2007, BREAK CHEM ENG BARR
  • [3] [Anonymous], POTENTIALS COMMON RE
  • [4] [Anonymous], ELEMENT PT ELEMENT P
  • [5] Catalysts for direct ethanol fuel cells
    Antolini, Ermete
    [J]. JOURNAL OF POWER SOURCES, 2007, 170 (01) : 1 - 12
  • [6] Studies of the electrocatalytic activity of binary palladium ruthenium anode catalyst on Ni support for ethanol alkaline fuel cells
    Bagchi, Joyeeta
    Bhattacharya, Swapan Kumar
    [J]. TRANSITION METAL CHEMISTRY, 2008, 33 (01) : 113 - 120
  • [7] Electrocatalytic activity of binary Palladium Ruthenium anode catalyst on Ni-support for ethanol alkaline fuel cells
    Bagchi, Joyeeta
    Bhattacharya, Swapan Kumar
    [J]. TRANSITION METAL CHEMISTRY, 2007, 32 (01) : 47 - 55
  • [8] Ethanol Oxidation on Electrocatalysts Obtained by Spontaneous Deposition of Palladium onto Nickel-Zinc Materials
    Bambagioni, Valentina
    Bianchini, Claudio
    Filippi, Jonathan
    OberhauserIal, Werner
    Marchionni, Andrea
    Vizza, Francesco
    Psaro, Rinaldo
    Sordelli, Laura
    Foresti, Maria Luisa
    Innocenti, Massimo
    [J]. CHEMSUSCHEM, 2009, 2 (01) : 99 - 112
  • [9] Palladium-Based Electrocatalysts for Alcohol Oxidation in Half Cells and in Direct Alcohol Fuel Cells
    Bianchini, Claudio
    Shen, Pei Kang
    [J]. CHEMICAL REVIEWS, 2009, 109 (09) : 4183 - 4206
  • [10] Synthesis of FePt nanocubes and their oriented self-assembly
    Chen, Min
    Kim, Jaemin
    Liu, J. P.
    Fan, Hongyou
    Sun, Shouheng
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (22) : 7132 - 7133