Fuel cell cathode catalyst with heme-like structure formed from nitrogen of glycine and iron

被引:60
作者
Maruyama, Jun [1 ]
Abe, Ikuo [1 ]
机构
[1] Osaka Municipal Tech Res Inst, Dept Environm Technol, Joto Ku, Osaka 5368553, Japan
关键词
D O I
10.1149/1.2409865
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
It is known that heme is closely related to chemical reactions involving oxygen, especially cathodic oxygen reduction, and that carbon materials with an Fe-N-4 moiety mimicking the heme center and embedded on the surface function as cathode catalysts for fuel cells, which would be one of the promising candidates for precious-metal-free catalysts and would lead to the realization of the widespread use of fuel cells. In this study, we found that a heat-treatment of a mixture of Fe(II) lactate, glucose, and glycine, which is the starting material of heme biosynthesis, generated a carbon material with the Fe-N-4 moiety by self-organization of Fe and N from glycine during pyrolysis. A polymer electrolyte fuel cell formed using the carbon material in the cathode generated electricity, confirming its function as the cathode catalyst, although the performance was inferior to that of a conventional Pt-based fuel cell. However, the increase in the structural regularity caused by an increase in the glycine content in the starting mixture improved the activity and durability. (c) 2007 The Electrochemical Society.
引用
收藏
页码:B297 / B304
页数:8
相关论文
共 69 条
[1]   REDUCTION OF OXYGEN IN AN ACIDIC METHANOL OXYGEN (AIR) FUEL-CELL - AN ONLINE MS STUDY [J].
BITTINSCATTANEO, B ;
WASMUS, S ;
LOPEZMISHIMA, B ;
VIELSTICH, W .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1993, 23 (06) :625-630
[2]   On active-site heterogeneity in pyrolyzed carbon-supported iron porphyrin catalysts for the electrochemical reduction of oxygen: An in situ Mossbauer study [J].
Bouwkamp-Wijnoltz, AL ;
Visscher, W ;
van Veen, JAR ;
Boellaard, E ;
van der Kraan, AM ;
Tang, SC .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (50) :12993-13001
[3]   The selectivity of oxygen reduction by pyrolysed iron porphyrin supported on carbon [J].
Bouwkamp-Wijnoltz, AL ;
Visscher, W ;
van Veen, JAR .
ELECTROCHIMICA ACTA, 1998, 43 (21-22) :3141-3152
[4]   EXAFS, XPS and electrochemical studies on oxygen reduction catalysts obtained by heat treatment of iron phenanthroline complexes supported on high surface area carbon black [J].
Bron, M ;
Radnik, J ;
Fieber-Erdmann, M ;
Bogdanoff, P ;
Fiechter, S .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2002, 535 (1-2) :113-119
[5]   Origin of the large N is binding energy in X-ray photoelectron spectra of calcined carbonaceous materials [J].
Casanovas, J ;
Ricart, JM ;
Rubio, J ;
Illas, F ;
JimenezMateos, JM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (34) :8071-8076
[6]   REDUCTION OF OXIDES OF IRON, COBALT, TITANIUM AND NIOBIUM BY LOW-ENERGY ION-BOMBARDMENT [J].
CHOUDHURY, T ;
SAIED, SO ;
SULLIVAN, JL ;
ABBOT, AM .
JOURNAL OF PHYSICS D-APPLIED PHYSICS, 1989, 22 (08) :1185-1195
[7]   EXAMINATION OF THE IONOMER ELECTRODE INTERFACE USING THE FERRIC FERROUS REDOX COUPLE [J].
CHU, D ;
TRYK, D ;
GERVASIO, D ;
YEAGER, EB .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1989, 272 (1-2) :277-284
[8]   MOLECULAR CATALYSTS FOR MULTIELECTRON REDOX REACTIONS OF SMALL MOLECULES - THE COFACIAL METALLODIPORPHYRIN APPROACH [J].
COLLMAN, JP ;
WAGENKNECHT, PS ;
HUTCHISON, JE .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1994, 33 (15-16) :1537-1554
[9]   Quantum jumps in the PEMFC science and technology from the 1960s to the year 2000 Part I. Fundamental scientific aspects [J].
Costamagna, P ;
Srinivasan, S .
JOURNAL OF POWER SOURCES, 2001, 102 (1-2) :242-252
[10]   Influence of nitrogen-containing precursors on the electrocatalytic activity of heat-treated Fe(OH)2 on carbon black for O2 reduction [J].
Cote, R ;
Lalande, G ;
Guay, D ;
Dodelet, JP ;
Denes, G .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1998, 145 (07) :2411-2418