Modification of hydrophobic/hydrophilic properties of Vulcan XG72 carbon powder by grafting of trifluoromethylphenyl and phenylsulfonic acid groups

被引:47
作者
Weissmann, Martin [1 ]
Baranton, Steve [1 ]
Clacens, Jean-Marc [1 ]
Coutanceau, Christophe [1 ]
机构
[1] CNRS, UMR 6503, Catalyse Chim Organ Lab, F-86022 Poitiers, France
关键词
POLYMER ELECTROLYTE MEMBRANES; GAS-DIFFUSION LAYER; REDUCTION; PLATINUM; PERFORMANCE; CATALYSTS; NANOPARTICLES; OXIDATION; IMPROVEMENT; DEPOSITION;
D O I
10.1016/j.carbon.2010.04.003
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
Carbon supports (glassy carbon and Vulcan XC72 powder) were modified by electrochemical and spontaneous grafting of phenylsulfonic acid (PSA) or trifluoromethylphenyl (TFMP) groups via diazonium ion reduction. The effectiveness of the grafting was confirmed electrochemically, by XPS measurements and elemental analyses. The hydrophobic or hydrophilic character of carbon surfaces was evidenced by measuring the contact angles of drops of different liquids (water, ethylene glycol and glycerol) in heptane. The surface energy was calculated and it was found, for example, that spontaneous grafting of a glassy carbon surface by PSA groups led to an increase by a factor 20 of the surface energy compared with an unmodified glassy carbon surface. The study of the grafting of such groups on XC72 carbon powder indicated that a very low grafting ratio (in wt%) led to a significant change in the macroscopic properties of the powder. Thermogravimetric analysis coupled with mass spectroscopy measurements (TGA-MS) showed that these grafted layers were thermally stable even in the presence of dispersed platinum nanoparticles. It was shown by cyclic voltammetry that the carbon substrate modification did not affect the electrochemical behavior of platinum catalyst, since the same active surface area was determined on Pt-XC72, Pt-PSA-XC72 and Pt-TFMP-XG72 catalysts. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2755 / 2764
页数:10
相关论文
共 43 条
[1]   Carbon supports for low-temperature fuel cell catalysts [J].
Antolini, Ermete .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2009, 88 (1-2) :1-24
[2]   Electrochemical derivatization of carbon surface by reduction of in situ generated diazonium cations [J].
Baranton, S ;
Bélanger, D .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (51) :24401-24410
[3]  
BIEGLER T, 1971, J ELECTROANAL CHEM, V29, P269, DOI 10.1016/0368-1874(71)85078-5
[4]   Solid polymer fuel cell synthesis by low pressure plasmas:: a short review [J].
Brault, P ;
Roualdès, S ;
Caillard, A ;
Thomann, AL ;
Mathias, J ;
Durand, J ;
Coutanceau, C ;
Léger, JM ;
Charles, C ;
Boswell, R .
EUROPEAN PHYSICAL JOURNAL-APPLIED PHYSICS, 2006, 34 (02) :151-156
[5]   Influence of surfactant removal by chemical or thermal methods on structure and electroactivity of Pt/C catalysts prepared by water-in-oil microemulsion [J].
Brimaud, S. ;
Coutanceau, C. ;
Garnier, E. ;
Leger, J.-M. ;
Gerard, F. ;
Pronier, S. ;
Leoni, M. .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2007, 602 (02) :226-236
[6]   Increasing the activity of Fe/N/C catalysts in PEM fuel cell cathodes using carbon blacks with a high-disordered carbon content [J].
Charreteur, Fanny ;
Ruggeri, Stephane ;
Jaouen, Frederic ;
Dodelet, J. P. .
ELECTROCHIMICA ACTA, 2008, 53 (23) :6881-6889
[7]   Water distribution measurement for a PEMFC through neutron radiography [J].
Chen, Yong-Song ;
Peng, Huei ;
Hussey, Daniel S. ;
Jacobson, David L. ;
tran, Doanh T. ;
Abdel-Baset, Tarek ;
Biernacki, Mark .
JOURNAL OF POWER SOURCES, 2007, 170 (02) :376-386
[8]   Hydrophobic coatings on carbon electrodes for proton exchange membrane fuel cells [J].
Chiu, K. -F. ;
Wang, K. W. .
SURFACE & COATINGS TECHNOLOGY, 2007, 202 (4-7) :1231-1235
[9]   Review of different methods for developing nanoelectrocatalysts for the oxidation of organic compounds [J].
Coutanceau, C. ;
Brimaud, S. ;
Lamy, C. ;
Leger, J. -M. ;
Dubau, L. ;
Rousseau, S. ;
Vigier, F. .
ELECTROCHIMICA ACTA, 2008, 53 (23) :6865-6880
[10]   Electrocatalytic reduction of dioxygen at platinum particles dispersed in a polyaniline film [J].
Coutanceau, C ;
Croissant, MJ ;
Napporn, T ;
Lamy, C .
ELECTROCHIMICA ACTA, 2000, 46 (04) :579-588