Carbon supported ruthenium chalcogenide as cathode catalyst in a microfluidic formic acid fuel cell

被引:38
作者
Gago, A. S. [1 ]
Morales-Acosta, D. [2 ]
Arriaga, L. G. [2 ]
Alonso-Vante, N. [1 ]
机构
[1] Univ Poitiers, CNRS, UMR 6503, Lab Electrocatalysis, F-86022 Poitiers, France
[2] SC Parque Tecnol Queretaro Sanfandila, Ctr Invest & Desarrollo Tecnol Electroquim, Pedro Escobedo 76703, Queretaro, Mexico
关键词
Ruthenium chalcogenide catalyst; Microfluidic fuel cell; Fuel cross-over; Ru(x)Se(y)/C; Pt/C; LAMINAR-FLOW; METHANOL TOLERANCE; DMFC; SE;
D O I
10.1016/j.jpowsour.2010.08.109
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
This work reports the electrochemical measurements of 20 wt.% Ru(x)Se(y)/C for oxygen reduction reaction (ORR) in presence of different concentration of HCOOH and its use as cathode catalyst in a microfluidic formic acid fuel cell (mu FAFC). The results were compared to those obtained with commercial Pt/C. Half-cell electrochemical measurements showed that the chalcogenide catalyst hs a high tolerance and selectivity towards ORR in electrolytes containing up to 0.1 M HCOOH. The deporlarization effect was higher on Pt/C than on Ru(x)Se(y)/C by a factor of ca. 23. Both catalysts were evaluated as cathode of a mu FAFC operating with different concentrations of HCOOH. When 0.5 M HCOOH was used, maximum current densities of 11.44 mA cm(-2) and 4.44 mA cm(-2) were obtained when the cathode was Ru(x)Se(y)/C and Pt/C, respectively. AT 0.5 M HCOOH, the peak power density of the mu FAFC was similar for both catalysts, ca. 1.9 mW cm(-2). At 5 M HCOOH the power density of the mu FAFC using Ru(x)Se(y), was 9.3 times higher than the obtained with Pt/C. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1324 / 1328
页数:5
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