Pt-Ru catalysts prepared by high energy ball-milling for PEMFC and DMFC:: Influence of the synthesis conditions

被引:10
作者
Denis, M. C. [1 ]
Lefevre, M. [1 ]
Guay, D. [1 ]
Dodelet, J. P. [1 ]
机构
[1] INRS Energie Mat & Telecommun, Varennes, PQ J3X 1S2, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
fuel cell; CO tolerance; methanol oxidation; electrocatalyst; platinum; ruthenium;
D O I
10.1016/j.electacta.2008.02.045
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
High energy ball-milling was used to prepare several unsupported Pt-Ru anode catalysts for PEM- and direct methanol fuel cells. Pt and Ru with a 50:50 nominal Pt/Ru ratio were ball-milled at various ball-to-powder weight ratios (from 4/1 to 12/1) and with various Pt:Ru:MgH2 proportions (from 1:1:2 to 1:1:10), where MgH2 is a leacheable dispersive agent. The presence of MgH2 is necessary to obtain unsupported catalysts with a specific surface area of between 50 and 75 m 2 g(-1). The ball-milling parameters greatly affected the relative proportions of the three phases constituting the catalysts. These phases are:Pt(Ru) alloy nanocrystallites, unalloyed Ru crystallites and nanocrystallites. The best CO tolerant catalyst is obtained by using a 12/1 ball-to-powder ratio and a 1:1:8 Pt:Ru:MgH2 proportion of dispersive agent. It is made of 57at.% of a nanocrystalline (3 nm) Pt80Ru20 alloy, 42 at.% of a nanocrystalline (3 nm) Ru phase and I at.% of a crystalline (similar to 40 nm) Ru phase. This catalyst has the lowest Pt/Ru surface ratio (0.9), the highest content in nanocrystalline Ru, and the highest ratio of oxidized/metallic Ru (3.3). Both Pt-Ru alloy and nanocrystalline Ru participate to the CO tolerance. The best CO tolerant catalyst is, however, not the best catalyst in DMFC. The latter is obtained by using a 4/1 ball-to-powder ratio and a 1:1:6 Pt:Ru:MgH2 proportion. Within the starting 50:50 Pt-Ru nominal atomic ratio, no specific correlation was found between catalyst performance in DMFC and atomic surface Pt/Ru ratio, nor nanocrystalline Ru content, nor oxidized/metallic Ru ratio. Performances of the best ball-milled catalysts are compared to those of commercial unsupported catalysts in PEMFC and DMFC. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5142 / 5154
页数:13
相关论文
共 64 条
[31]  
Iwase M., 1995, P 1 INT S PROT COND, V1, P12
[32]  
Iwasita T., 2003, HDB FUEL CELLS, V2, P603, DOI DOI 10.1002/9780470974001
[33]   Composition and activity of high surface area PtRu catalysts towards adsorbed CO and methanol electrooxidation - A DEMS study [J].
Jusys, Z ;
Kaiser, J ;
Behm, RJ .
ELECTROCHIMICA ACTA, 2002, 47 (22-23) :3693-3706
[34]   Chemical state of ruthenium submonolayers on a Pt(111) electrode [J].
Kim, H ;
de Moraes, IR ;
Tremiliosi-Filho, G ;
Haasch, R ;
Wieckowski, A .
SURFACE SCIENCE, 2001, 474 (1-3) :L203-L212
[35]   X-RAY PHOTOELECTRON SPECTROSCOPIC STUDIES OF RUTHENIUM-OXYGEN SURFACES [J].
KIM, KS ;
WINOGRAD, N .
JOURNAL OF CATALYSIS, 1974, 35 (01) :66-72
[36]   Structural and surface characterizations of nanocrystalline Pt-Ru alloys prepared by high-energy ball-milling [J].
Lalande, G ;
Denis, MC ;
Guay, D ;
Dodelet, JP ;
Schulz, R .
JOURNAL OF ALLOYS AND COMPOUNDS, 1999, 292 (1-2) :301-310
[37]  
Larson A.C., 2000, GSAS GEN STRUCTURE A, P86
[38]   The function of ruthenium oxides in Pt-Ru catalysts for methanol electro-oxidation at low temperatures [J].
Lasch, K ;
Jörissen, L ;
Friedrich, KA ;
Garche, J .
JOURNAL OF SOLID STATE ELECTROCHEMISTRY, 2003, 7 (09) :619-625
[39]   The effect of metal oxides as co-catalysts for the electro-oxidation of methanol on platinum-ruthenium [J].
Lasch, K ;
Jörissen, L ;
Garche, J .
JOURNAL OF POWER SOURCES, 1999, 84 (02) :225-230
[40]   A review of anode catalysis in the direct methanol fuel cell [J].
Liu, HS ;
Song, CJ ;
Zhang, L ;
Zhang, JJ ;
Wang, HJ ;
Wilkinson, DP .
JOURNAL OF POWER SOURCES, 2006, 155 (02) :95-110