PtFe nanoparticles supported on electroactive AuPANI core@shell nanoparticles for high performance bifunctional electrocatalysis

被引:31
作者
Lee, Ji-Eun [1 ]
Jang, Yu Jin [1 ]
Xu, Wenqian [2 ]
Feng, Zhenxing [3 ]
Park, Hee-Young [4 ]
Kim, Jin Young [4 ]
Kim, Dong Ha [1 ]
机构
[1] Ewha Womans Univ, Coll Nat Sci, Div Mol Life & Chem Sci, Dept Chem & Nano Sci, 52 Ewhayeodae Gil, Seoul 03760, South Korea
[2] Argonne Natl Lab, Xray Sci Div, Lemont, IL 60439 USA
[3] Oregon State Univ, Sch Chem Biol & Environm Engn, Corvallis, OR 97331 USA
[4] Korea Inst Sci & Technol, Fuel Cell Res Ctr, 5 Hwarang Ro 14 Gil, Seoul 02792, South Korea
基金
新加坡国家研究基金会;
关键词
OXYGEN REDUCTION REACTION; FUNCTIONALIZED CARBON NANOTUBES; MEMBRANE FUEL-CELLS; ONE-POT SYNTHESIS; PLATINUM NANOPARTICLES; GOLD NANOPARTICLES; CATALYTIC-ACTIVITY; TRANSITION-METALS; PARTICLE-SIZE; POLYANILINE;
D O I
10.1039/c7ta02660a
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
The design of cost-effective and efficient catalysts requires not only reduced usage of precious metals such as Pt, but also enhanced catalytic activity and stability, which are immensely important for applications in fuel cells and metal-air batteries. Multimetallic core@shell nanoparticles (NPs) consisting of Au core and metal-containing polyaniline (PANI) shells were prepared. These PANI coated AuNPs were sequentially mixed with selected transition metal precursors and platinum precursor solutions followed by chemical reduction to obtain uniformly distributed metal NPs on a surface with reduced Pt usage. We systematically investigated structural alterations during the sequential synthetic process and compared performance of the resultant nanostructures with respect to Pt-decorated AuNP@PANI NPs and commercial Pt/C catalysts. The AuNP@PANI@PtFe with optimized configuration exhibited about 2.5 and 6.8 times enhanced mass activity for an oxygen reduction reaction and methanol oxidation reaction, respectively, compared to Pt/C. Durability of the AuNP@PANI@PtFe was also over 1.5 times better than of that of Pt/C. The success of this strategy indicates potential applications for designing bifunctional catalysts.
引用
收藏
页码:13692 / 13699
页数:8
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