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
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