Enhanced Methanol Electro-oxidation on Pt-Ru Decorated Self-Assembled TiO2-Carbon Hybrid Nanostructure

被引:7
|
作者
Nishanth, K. G. [1 ]
Sridhar, P. [1 ]
Pitchumani, S. [1 ]
Shukla, A. K. [2 ]
机构
[1] CSIR, Cent Electrochem Res Inst, Madras Unit, CSIR Madras Complex, Madras 600113, Tamil Nadu, India
[2] Indian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, India
来源
POLYMER ELECTROLYTE FUEL CELLS 11 | 2011年 / 41卷 / 01期
关键词
FUEL-CELLS; TIO2; ELECTROCATALYST; CARBON; NANOCOMPOSITE; OXIDATION; CATALYSTS;
D O I
10.1149/1.3635647
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Porous titanium oxide-carbon hybrid nanostructure (TiO2-C) is directly synthesized via supramolecular self-assembly with in situ crystallization process. TiO2-C supported Pt-Ru electrocatalyst (Pt-Ru/TiO2-C) is synthesized and investigated as an alternative anode catalyst for direct methanol fuel cells (DMFCs). TiO2-C with a specific surface area of 350m(2)/g and an average pore radius of 21.8 angstrom has been synthesized. X-ray diffraction, Raman spectroscopy and Transmission electron microscopy (TEM) have been employed to evaluate the crystalline nature and the structural properties of TiO2-C. TEM images reveal uniform distribution of Pt-Ru nanoparticles (d(Pt-Ru) = 1.5-3.5 nm) on TiO2-C. The methanol oxidation and accelerated durability (ADT) studies for Pt-Ru/TiO2-C show enhanced catalytic activity and durability, respectively compared to that for carbon supported Pt-Ru. DMFC employing Pt-Ru/TiO2-C as an anode catalyst delivers a peak-power density of 91mW/cm(2) at 65 degrees C as compared to the peak-power density of 60mW/cm(2) obtained with carbon supported Pt-Ru catalyst under similar conditions
引用
收藏
页码:1139 / 1149
页数:11
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