Carbon-Supported Palladium-Polypyrrole Nanocomposite for Oxygen Reduction and Its Tolerance to Methanol

被引:19
|
作者
Jeyabharathi, C. [1 ]
Venkateshkumar, P. [1 ]
Mathiyarasu, J. [1 ]
Phani, K. L. N. [1 ]
机构
[1] CSIR, Cent Electrochem Res Inst, Electrod & Electrocatalysis Div, Karaikkudi 630006, Tamil Nadu, India
关键词
PT-FE ALLOYS; FUEL-CELLS; BIMETALLIC NANOPARTICLES; ELECTROCATALYSTS; CATALYSTS; CO; DMFCS; FILM; O-2;
D O I
10.1149/1.3489266
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Carbon-supported palladium-polypyrrole (Pd-PPy/C) nanocomposite was synthesized by oxidative polymerization of pyrrole and reduction of palladium (II) precursor salt in the presence of Vulcan XC-72R. The Pd-PPy/C composites were characterized by X-ray diffraction (XRD), Fourier transform IR, X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TGA), and transmission electron microscopy (TEM) techniques. The XRD analysis of Pd-PPy/C shows the formation of the face-centered cubic structure of Pd particles and the mean particle size calculated from TEM was 5.3 + 2.0 nm. The electrochemical stability of Pd-PPy/C was examined by cyclic voltammetry in an acid solution. The thermal stability and Pd loading in the composite was assessed using TGA. The introduction of Pd in the conducting PPy/C matrix gives better catalytic activity toward oxygen reduction with resistance to methanol oxidation. This was further elucidated by the XPS analysis showing d-band vacancy that is attributed to metal-polymer interaction. From the polarization studies, it is observed that even in the presence of methanol there is no significant cathodic shift in the half-wave potential, revealing that Pd-PPy/C is tolerant to methanol. Rotating ring disk electrode studies show that there is only a negligible quantity of hydrogen peroxide produced in the potential region where its production is expected to be high. This confirms that Pd-PPy/C catalyzes reduction of oxygen directly to water through a four-electron pathway. (c) 2010 The Electrochemical Society. [DOI: 10.1149/1.3489266] All rights reserved.
引用
收藏
页码:B1740 / B1745
页数:6
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