Structure/Processing/Properties Relationships in Nanoporous Nanoparticles As Applied to Catalysis of the Cathodic Oxygen Reduction Reaction

被引:256
作者
Snyder, Joshua [1 ,2 ]
McCue, Ian [1 ,2 ]
Livi, Ken [3 ]
Erlebacher, Jonah [1 ,2 ]
机构
[1] Johns Hopkins Univ, Dept Mat Sci & Engn, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Dept Chem & Biomol Engn, Baltimore, MD 21218 USA
[3] Johns Hopkins Univ, Dept Earth & Planetary Sci, Baltimore, MD 21218 USA
关键词
PLATINUM-MONOLAYER ELECTROCATALYSTS; SHAPE-CONTROLLED SYNTHESIS; BIMETALLIC NANOPARTICLES; NANOCRYSTAL SYNTHESIS; ALLOY NANOPARTICLES; COLLOIDAL SYNTHESIS; METAL NANOCRYSTALS; COPT3; NANOCRYSTALS; CARBON NANOTUBES; HOT-INJECTION;
D O I
10.1021/ja3019498
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We present a comprehensive experimental study of the formation and activity of dealloyed nanoporous Ni/Pt alloy nanoparticles for the cathodic oxygen reduction reaction. By addressing the kinetics of nucleation during solvothermal synthesis we developed a method to control the size and composition of Ni/Pt alloy nanoparticles over a broad range while maintaining an adequate size distribution. Electrochemical dealloying of these size-controlled nanoparticles was used to explore conditions in which hierarchical nanoporosity within nanoparticles can evolve. Our results show that in order to evolve fully formed porosity, particles must have a minimum diameter of similar to 15 nm, a result consistent with the surface kinetic processes occurring during dealloying. Nanoporous nanoparticles possess ligaments and voids with diameters of approximately 2 nm, high surface area/mass ratios usually associated with much smaller particles, and a composition consistent with a Pt-skeleton covering a Ni/Pt alloy core. Electrochemical measurements show that the mass activity for the oxygen reduction reaction using carbon-supported nanoporous Ni/Pt nanoparticles is nearly four times that of commercial Pt/C catalyst and even exceeds that of comparable nonporous Pt-skeleton Ni/Pt alloy nanoparticles.
引用
收藏
页码:8633 / 8645
页数:13
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