Methanol Oxidation in Alkaline Media with Pt-Au/fMWCNTs and Pt-Pd/fMWCNTs Electrocatalysts on an Exfoliated Graphite Electrode

被引:13
|
作者
Mpeta, L. S. [1 ]
Gwebu, S. S. [1 ]
Arotiba, O. A. [1 ]
Maxakato, N. W. [1 ]
机构
[1] Univ Johannesburg, Dept Appl Chem, POB 17011, ZA-2028 Johannesburg, South Africa
基金
新加坡国家研究基金会;
关键词
Exfoliated graphite electrode; Carbon nanotubes; Electrocatalysis; Methanol; Platinum; ELECTROCHEMICAL PROPERTIES; CATALYSTS; PLATINUM; ELECTROOXIDATION; PERFORMANCE; BEHAVIOR; ETHANOL; BIOMASS; OXIDE; ACID;
D O I
10.1007/s12678-019-00555-0
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 poisoning of pure platinum electrodes has propelled the improvement of platinum-based alloy catalysts. In this work, we report the application of exfoliated graphite electrode as an anode platform for binary platinum-based electrocatalysts for methanol oxidation in alkaline media. Platinum-based binary electrocatalysts comprising of Pt-Au and Pt-Pd nanoparticles on functionalized multi-walled carbon nanotubes (MWCNTs) support were synthesized via polyol process. The nanocomposite electrocatalysts (Pt-Au/fMWCNTs and Pt-Pd/fMWCNTs) were characterized by transmission electron microscopy (TEM) coupled with energy-dispersive X-ray spectroscopy (EDS) and X-ray diffractometer (XRD). The electrochemical activity of the Pt-Pd/fMWCNTs and the Pt-Au/fMWCNTs electrocatalysts was assessed utilizing cyclic voltammetry (CV), chronoamperometry (CA), and electrochemical impedance spectroscopy (EIS) in the presence of methanol. The nanoparticles were in the size regime of 3 to 5 nm and the XRD affirmed successful functionalization of the MWCNT and its impregnation with the binary Pt nanoparticles. The electrooxidation of methanol in alkaline conditions was seen with a high current density of about 26.1 mA cm(-2) on Pt-Au/fMWCNTs and 13.52 mA cm(-2) on Pt-Pd/fMWCNTs electrocatalysts deposited on exfoliated graphite working electrodes. The exfoliated graphite platform is a promising electrode for fuel cell application.
引用
收藏
页码:672 / 679
页数:8
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