Biornimetic hydrogen evolution:: MoS2 nanoparticles as catalyst for hydrogen evolution

被引:3513
作者
Hinnemann, B [1 ]
Moses, PG [1 ]
Bonde, J [1 ]
Jorgensen, KP [1 ]
Nielsen, JH [1 ]
Horch, S [1 ]
Chorkendorff, I [1 ]
Norskov, JK [1 ]
机构
[1] Tech Univ Denmark, Ctr Atom Scale Mat Phys, Dept Phys, NanoDTU, DK-2800 Lyngby, Denmark
关键词
D O I
10.1021/ja0504690
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The electrochemical hydrogen evolution reaction is catalyzed most effectively by the Pt group metals. As H2 is considered as a future energy carrier, the need for these catalysts will increase and alternatives to the scarce and expensive Pt group catalysts will be needed. We analyze the ability of different metal surfaces and of the enzymes nitrogenase and hydrogenase to catalyze the hydrogen evolution reaction and find a necessary criterion for high catalytic activity. The necessary criterion is that the binding free energy of atomic hydrogen to the catalyst is close to zero. The criterion enables us to search for new catalysts, and inspired by the nitrogenase active site, we find that MoS2 nanoparticles supported on graphite are a promising catalyst. They catalyze electrochemical hydrogen evolution at a moderate overpotential of 0.1-0.2 V. Copyright © 2005 American Chemical Society.
引用
收藏
页码:5308 / 5309
页数:2
相关论文
共 23 条
  • [1] Bockris J. O. M., 1998, MODERN ELECTROCHEM A, V2
  • [2] Density functional theory investigation of the active site of Fe-hydrogenases.: Systematic study of the effects of redox state and ligands hardness on structural and electronic properties of complexes related to the [2Fe]H subcluster
    Bruschi, M
    Fantucci, P
    De Gioia, L
    [J]. INORGANIC CHEMISTRY, 2004, 43 (12) : 3733 - 3741
  • [3] Modeling the active sites in metalloenzymes. 3. Density functional calculations on models for [Fe]-hydrogenase: Structures and vibrational frequencies of the observed redox forms and the reaction mechanism at the diiron active center
    Cao, ZX
    Hall, MB
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (16) : 3734 - 3742
  • [4] Chorkendorff I., 2003, Concepts of Modern Catalysis and Kinetics, V2a
  • [5] CO Desorption Rate Dependence on CO Partial Pressure over Platinum Fuel Cell Catalysts
    Davies, J. C.
    Nielsen, R. M.
    Thomsen, L. B.
    Chorkendorff, I.
    Logadottir, A.
    Lodziana, Z.
    Norskov, J. K.
    Li, W. X.
    Hammer, B.
    Longwitz, S. R.
    Schnadt, J.
    Vestergaard, E. K.
    Vang, R. T.
    Besenbacher, F.
    [J]. FUEL CELLS, 2004, 4 (04) : 309 - 319
  • [6] Alternative energy technologies
    Dresselhaus, MS
    Thomas, IL
    [J]. NATURE, 2001, 414 (6861) : 332 - 337
  • [7] Chemistry and the hydrogenases
    Evans, DJ
    Pickett, CJ
    [J]. CHEMICAL SOCIETY REVIEWS, 2003, 32 (05) : 268 - 275
  • [8] Chemical activity of the nitrogenase FeMo cofactor with a central nitrogen ligand: Density functional study
    Hinnemann, B
    Norskov, JK
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (12) : 3920 - 3927
  • [9] Lamle S. E., 2003, J CHEM SOC DA, V21, P4152
  • [10] Speculative synthetic chemistry and the nitrogenase problem
    Lee, SC
    Holm, RH
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) : 3595 - 3600