Electrochemical stability of carbon nanofibers in proton exchange membrane fuel cells

被引:36
作者
Alvarez, Garbine [1 ]
Alcaide, Francisco [1 ]
Miguel, Oscar [1 ]
Cabot, Pere L. [2 ]
Martinez-Huerta, M. V. [3 ]
Fierro, J. L. G. [3 ]
机构
[1] CIDETEC IK4, Dept Energy, San Sebastian 20009, Spain
[2] Univ Barcelona, Dept Quim Fis, Lab Electroquim Mat & Medi Ambient, E-08028 Barcelona, Spain
[3] Inst Catalisis & Petroleoquim CSIC, Madrid 28049, Spain
关键词
Catalyst support; Carbon nanofibers; Carbon corrosion; Durability; PEMFC; CATALYST DEGRADATION; DURABILITY; NANOTUBES; SUPPORT; OXIDATION; CORROSION; PERFORMANCE; SYSTEMS; ISSUES; ELECTROCATALYSTS;
D O I
10.1016/j.electacta.2011.08.022
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
070208 [无线电物理];
摘要
This fundamental study deals with the electrochemical stability of several non-conventional carbon based catalyst supports, intended for low temperature proton exchange membrane fuel cell (PEMFC) cathodes. Electrochemical surface oxidation of raw and functionalized carbon nanofibers, and carbon black for comparison, was studied following a potential step treatment at 25.0 degrees C in acid electrolyte, which mimics the operating conditions of low temperature PEMFCs. Surface oxidation was characterized using cyclic voltammetry. X-ray photoelectron spectroscopy (XPS), and contact angle measurements. Cyclic voltammograms clearly showed the presence of the hydroquinone/quinone couple. Furthermore, identification of carbonyl, ether, hydroxyl and carboxyl surface functional groups were made by deconvolution of the XPS spectra. The relative increase in surface oxides on carbon nanofibers during the electrochemical oxidation treatment is significantly smaller than that on carbon black. This suggests that carbon nanofibers are more resistant to the electrochemical corrosion than carbon black under the experimental conditions used in this work. This behaviour could be attributed to the differences found in the microstructure of both kinds of carbons. According to these results, carbon nanofibers possess a high potential as catalyst support to increase the durability of catalysts used in low temperature PEMFC applications. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:9370 / 9377
页数:8
相关论文
共 86 条
[1]
Electrogeneration of hydroperoxide ion using an alkaline fuel cell [J].
Alcaide, F ;
Brillas, E ;
Cabot, PL .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1998, 145 (10) :3444-3449
[2]
Pt supported on carbon nanofibers as electrocatalyst for low temperature polymer electrolyte membrane fuel cells [J].
Alcaide, Francisco ;
Alvarez, Garbine ;
Miguel, Oscar ;
Jesus Lazaro, Maria ;
Moliner, Rafael ;
Lopez-Cudero, Ana ;
Solla-Gullon, Jose ;
Herrero, Enrique ;
Aldaz, Antonio .
ELECTROCHEMISTRY COMMUNICATIONS, 2009, 11 (05) :1081-1084
[3]
Technical electrodes catalyzed with PtRu on mesoporous ordered carbons for liquid direct methanol fuel cells [J].
Alvarez, Garbine ;
Alcaide, Francisco ;
Miguel, Oscar ;
Calvillo, Laura ;
Jesus Lazaro, Maria ;
Quintana, Jacob J. ;
Carlos Calderon, Juan ;
Pastor, Elena .
JOURNAL OF SOLID STATE ELECTROCHEMISTRY, 2010, 14 (06) :1027-1034
[4]
Surface oxidation of carbon supports due to potential cycling under PEM fuel cell conditions [J].
Avasarala, Bharat ;
Moore, Richard ;
Haldar, Pradeep .
ELECTROCHIMICA ACTA, 2010, 55 (16) :4765-4771
[5]
Bagotsky, 2009, FUEL CELLS PROBLEMS, P45
[6]
Barbir F, 2006, ENG MAT PRO, P27
[7]
Temperature effects on PEM fuel cells Pt/C catalyst degradation [J].
Bi, Wu ;
Fuller, Thomas. F. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2008, 155 (02) :B215-B221
[8]
BOURRAT X, 2001, DESIGN CONTROL STRUC, pCH3
[9]
Study of the Surface Chemistry of Modified Carbon Nanofibers by Oxidation Treatments in Liquid Phase [J].
Calvillo, L. ;
Lazaro, M. J. ;
Suelves, I. ;
Echegoyen, Y. ;
Bordeje, E. G. ;
Moliner, R. .
JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, 2009, 9 (07) :4164-4169
[10]
Surface analysis for catalyst layer (PT/PTFE/C) and diffusion layer (PTFE/C) for proton exchange membrane fuel cells systems (PEMFCs) [J].
Chebbi, Rachid ;
Beicha, Abdellah ;
Daud, W. R. W. ;
Zaamouche, Radia .
APPLIED SURFACE SCIENCE, 2009, 255 (12) :6367-6371