Surface- and Structure-Dependent Catalytic Activity of Au Nanoparticles for Oxygen Reduction Reaction

被引:131
作者
Lee, Youngmin [1 ]
Loew, Aviva [1 ]
Sun, Shouheng [1 ]
机构
[1] Brown Univ, Dept Chem, Providence, RI 02912 USA
基金
美国国家科学基金会;
关键词
SINGLE-CRYSTAL ELECTRODES; GOLD NANOPARTICLES; ELECTROCATALYSIS; ELECTROREDUCTION;
D O I
10.1021/cm9013046
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
Polycrystalline Au nanoparticles (NPs) of 3, 6, and 8 nm were synthesized via solution phase reaction of HAuCl4 center dot 3H(2)O With tert-butylamine borane and oleylamine in tetrahydronaphthalene. The sizes of the Au NPs were tuned by varying the reaction temperatures (40-3 degrees C). For polycrystalline Au NPs made at room temperature or above, smaller NPs showed more positive onset potential in catalyzing oxygen reduction reaction (ORR) in 0.5 M KOH media. However the most active Au NPs were the 8 nm ones that were synthesized at 3 degrees C. We rationalized the ORR activity of these Au NPs by the case of oleylamine surfactant removal and the degree of disorder in the polycrystalline structure. This was further confirmed by the low activity observed from the same Au NPs passivated with hexadecanethiol, or from the Au NPs with higher degree of crystallinity made from the etching of the composite Au-Fe3O4 NPs.
引用
收藏
页码:755 / 761
页数:7
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