Rational syntheses of core-shell Fe@(PtRu) nanoparticle electrocatalysts for the methanol oxidation reaction with complete suppression of CO-poisoning and highly enhanced activity

被引:159
|
作者
Matin, Md. Abdul [1 ]
Lee, Eunjik [2 ]
Kim, Hyunchul [3 ]
Yoon, Won-Sub [3 ]
Kwon, Young-Uk [1 ,2 ]
机构
[1] Sungkyunkwan Univ, Dept Chem, Suwon 440746, South Korea
[2] Sungkyunkwan Univ, SKKU Adv Inst Nano Sci & Technol, Suwon 440746, South Korea
[3] Sungkyunkwan Univ, Dept Energy Sci, Suwon 440746, South Korea
关键词
OXYGEN REDUCTION REACTION; FUEL-CELL CATALYSTS; ALLOY ELECTROCATALYSTS; CARBON NANOTUBES; HIGH-PERFORMANCE; ANODE CATALYSTS; ELECTROOXIDATION; PTRU; FE; ETHANOL;
D O I
10.1039/c5ta03809j
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
We report the syntheses of ternary nanoparticles (NPs) of Fe-x@(PtRu)((1-x)/2) (x = 0.0, 0.30, 0.34, 0.38, and 0.44) with Fe cores and PtRu alloy shells, which exhibit greatly improved electrocatalytic properties for the methanol oxidation reaction (MOR). The syntheses were achieved by one-step sonochemical treatments of Pt(acac)(2), Ru(acac)(3), and Fe(acac)(3) in ethylene glycol. The NPs are characterized by X-ray diffractometry, transmission electron microscopy (TEM), and inductively coupled plasma-adsorption emission spectroscopy for the particle size, morphology, and composition, respectively. The formation of core-shell NPs has been proven by scanning TEM-energy dispersive X-ray spectroscopy, and the electronic structures of the elements have been investigated by X-ray photoelectron spectroscopy and X-ray adsorption near edge spectroscopy. The ternary NPs show enhanced MOR electrocatalytic activity compared to a commercial PtRu-alloy (PtRu) by a factor of up to 2.5 based on the forward current density data. More importantly, the ternary NPs show complete suppression of CO-poisoning. Chronoamperometry data for MOR on the ternary NPs show improved stability over Pt/C and PtRu references.
引用
收藏
页码:17154 / 17164
页数:11
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