Formation of platinum-free fuel cell cathode catalyst with highly developed nanospace by carbonizing catalase

被引:70
作者
Maruyama, J [1 ]
Abe, I [1 ]
机构
[1] Osaka Municipal Tech Res Inst, Environm Technol Dept, Joto Ku, Osaka 5368553, Japan
关键词
D O I
10.1021/cm047944y
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
The amount of platinum in the catalyst for the electrodes of polymer electrolyte fuel cells must be minimized to widely substitute this new energy system for conventional ones. In this study, a platinum-free catalyst for the cathodic oxygen reduction was formed from a natural organic compound, catalase. We carbonized catalase to produce a catalyst active in the superacidic atmosphere of the polymer electrolyte. Nitrogen adsorption onto the carbonized material revealed that the material had highly developed internal nanospaces, which were essential for exposing active sites to oxygen reduction on the pore surface. The carbonized material was also characterized by X-ray photoelectron spectroscopy, X-ray diffraction, transmission electron microscopy, and Mossbauer spectroscopy. The activity for oxygen reduction was evaluated using rotating disk electrodes, forming a catalyst layer from the carbonized material and the polymer electrolyte on the electrode surface and immersing the layer in oxygen-saturated perchloric acid. The activity increased with the increase in the specific surface area and possibly the increase in the activity of the respective active sites. A preliminary fuel cell test using the material in the cathode confirmed the electricity generation, although the performance was inferior to a Pt-based fuel cell.
引用
收藏
页码:4660 / 4667
页数:8
相关论文
共 69 条
[1]  
Appleby A.J., 1989, FUEL CELL HDB
[2]   Graphite nanofibers as an electrode for fuel cell applications [J].
Bessel, CA ;
Laubernds, K ;
Rodriguez, NM ;
Baker, RTK .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (06) :1115-1118
[3]   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
[4]   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
[5]   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
[6]   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
[7]   MIXED-VALENCE STATE IN IRONPORPHYRIN AGGREGATES [J].
BURDA, K ;
HRYNKIEWICZ, A ;
KOLOCZEK, H ;
STANEK, J ;
STRZALKA, K .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 1995, 1244 (2-3) :345-350
[8]   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
[9]   HYDROPEROXIDE METABOLISM IN MAMMALIAN ORGANS [J].
CHANCE, B ;
SIES, H ;
BOVERIS, A .
PHYSIOLOGICAL REVIEWS, 1979, 59 (03) :527-605
[10]   Carbon nanotubule membranes for electrochemical energy storage and production [J].
Che, GL ;
Lakshmi, BB ;
Fisher, ER ;
Martin, CR .
NATURE, 1998, 393 (6683) :346-349