Exploring haem-based alternatives for oxygen reduction catalysis in fuel cells - a status report of our first principles calculations

被引:9
作者
Dy, E. S.
Roman, T. A.
Kubota, Y.
Miyamoto, K.
Kasai, H.
机构
[1] Osaka Univ, Grad Sch Engn, Dept Precis Sci & Technol & Appl Phys, Suita, Osaka 5650871, Japan
[2] Kansai Elect Power Co Inc, Dept Res & Dev, Power Engn Res & Dev Ctr, Amagasaki, Hyogo 6610974, Japan
关键词
D O I
10.1088/0953-8984/19/44/445010
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
For hydrogen fuel cells to become commercially viable, an alternative catalyst to platinum surfaces that is both efficient and affordable must be discovered. We consider haem and haem derivatives as potentials substitutes. In this paper, we discuss the oxygen reduction reaction on both the platinum surface and on haem. We then introduce our suggestions based on density-functional studies on how to improve haem's oxygen-reduction capabilities, which can be summarized as follows: inducing the singlet state, inducing side-on interaction, mimicking cytochrome c oxidase by adding a copper-imidazole complex, using platinum deposited on tin porphyrin instead of haem, and using oxomolybdenum porphyrin instead of haem. We shall focus on the last three methods because of their experimental practicability.
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页数:12
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共 69 条
[1]  
Adzic R, 1998, FRONT ELECT, P197
[2]   Catalytic effect of platinum on oxygen reduction -: An ab initio model including electrode potential dependence [J].
Anderson, AB ;
Albu, TV .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2000, 147 (11) :4229-4238
[3]   VELOCITY DEPENDENCE OF COLLISIONAL ALIGNMENT OF OXYGEN MOLECULES IN GASEOUS EXPANSIONS [J].
AQUILANTI, V ;
ASCENZI, D ;
CAPPELLETTI, D ;
PIRANI, F .
NATURE, 1994, 371 (6496) :399-402
[4]   Orienting and aligning molecules for stereochemistry and photodynamics [J].
Aquilanti, V ;
Bartolomei, M ;
Pirani, F ;
Cappelletti, D ;
Vecchiocattivi, F ;
Shimizu, Y ;
Kasai, T .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2005, 7 (02) :291-300
[5]   ROTATIONAL ALIGNMENT IN SUPERSONIC SEEDED BEAMS OF MOLECULAR-OXYGEN [J].
AQUILANTI, V ;
ASCENZI, D ;
CAPPELLETTI, D ;
PIRANI, F .
JOURNAL OF PHYSICAL CHEMISTRY, 1995, 99 (37) :13620-13626
[6]   OBSERVATION OF 2 OXYGEN ISOTOPE SENSITIVE BANDS IN THE LOW-FREQUENCY RESONANCE RAMAN-SPECTRUM OF OXY(PHTHALOCYANATO)IRON(II) [J].
BAJDOR, K ;
OSHIO, H ;
NAKAMOTO, K .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1984, 106 (23) :7273-7274
[7]   REACTIONS OF COLLMAN COMPLEX WITH TIN(IV) AND GERMANIUM(IV) PORPHYRINS, FORMATION OF [TIN(II) AND GERMANIUM(II) PORPHYRINS] TETRACARBONYLIRON AND CRYSTAL-STRUCTURE OF [2,3,7,8,12,13,17,18-OCTAETHYLPORPHINATO TIN(II)] TETRACARBONYLIRON [J].
BARBE, JM ;
GUILARD, R ;
LECOMTE, C ;
GERARDIN, R .
POLYHEDRON, 1984, 3 (07) :889-894
[8]   Electrocatalysis under conditions of high mass transport rate: Oxygen reduction on single submicrometer-sized Pt particles supported on carbon [J].
Chen, SL ;
Kucernak, A .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (10) :3262-3276
[9]  
COLLMAN J P, 1974, Proceedings of the National Academy of Sciences of the United States of America, V71, P1326, DOI 10.1073/pnas.71.4.1326
[10]   A cytochrome c oxidase model catalyzes oxygen to water reduction under rate-limiting electron flux [J].
Collman, James P. ;
Devaraj, Neal K. ;
Decreau, Richard A. ;
Yang, Ying ;
Yan, Yi-Long ;
Ebina, Wataru ;
Eberspacher, Todd A. ;
Chidsey, Christopher E. D. .
SCIENCE, 2007, 315 (5818) :1565-1568