Reduced graphene oxide supported FePt alloy nanoparticles with high electrocatalytic performance for methanol oxidation

被引:115
|
作者
Ji, Zhenyuan [1 ]
Zhu, Guoxing [1 ]
Shen, Xiaoping [1 ,3 ]
Zhou, Hu [2 ]
Wu, Chaomin [1 ]
Wang, Min [1 ]
机构
[1] Jiangsu Univ, Sch Chem & Chem Engn, Zhenjiang 212013, Peoples R China
[2] Jiangsu Univ Sci & Technol, Sch Mat Sci & Engn, Zhenjiang 212003, Peoples R China
[3] Nanjing Univ, State Key Lab Coordinat Chem, Nanjing 210093, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
EXFOLIATED GRAPHITE OXIDE; CARBON NANOTUBES; CATALYTIC PERFORMANCE; CHEMICAL-REDUCTION; OXYGEN; NANOSHEETS; RU; CO;
D O I
10.1039/c2nj40133a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Pt-based materials have been widely used as electrocatalysts in direct methanol fuel cells (DMFCs) due to their significant activity for methanol oxidation as well as their superior poison tolerance. In this study, a reduced graphene oxide (RGO) supported FePt alloy electrocatalyst is successfully synthesized by a facile in situ co-reduction route. The microstructure, composition and morphology of the synthesized materials are systematically investigated by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), Raman spectroscopy, energy dispersive X-ray spectroscopy (EDS), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). It is shown that the as-formed FePt nanoparticles with a size of 4 nm are well spread out on the RGO sheets and as a result, re-stacking of the RGO sheets is effectively inhibited. Their catalytic performance for electrocatalytic oxidation of methanol is investigated by cyclic voltammetry and amperometric method, which indicate that the RGO/FePt catalyst exhibits much higher catalytic activity and stability than the RGO/Pt nanocomposites. It is proposed that the addition of Fe, which increases the number of Pt active sites, is responsible for the improved catalytic performance. This result implies that the prepared RGO/FePt nanocomposites have great potential applications in DMFC.
引用
收藏
页码:1774 / 1780
页数:7
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