Beyond Metal-Hydrides: Non-Transition-Metal and Metal-Free Ligand-Centered Electrocatalytic Hydrogen Evolution and Hydrogen Oxidation

A new pathway for homogeneous electrocatalytic H2 evolution and H2 oxidation has been developed using a redox active thiosemicarbazone and its zinc complex as seminal metal-free and transition-metal-free examples. Diacetyl-bis­(N-4-methyl-3-thiosemicarbazone) and zinc diacetyl-bis­(N-4-methyl-3-thio...

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Bibliographic Details
Published in:Journal of the American Chemical Society 2016-06, Vol.138 (25), p.7844-7847
Main Authors: Haddad, Andrew Z, Garabato, Brady D, Kozlowski, Pawel M, Buchanan, Robert M, Grapperhaus, Craig A
Format: Article
Language:English
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Summary:A new pathway for homogeneous electrocatalytic H2 evolution and H2 oxidation has been developed using a redox active thiosemicarbazone and its zinc complex as seminal metal-free and transition-metal-free examples. Diacetyl-bis­(N-4-methyl-3-thiosemicarbazone) and zinc diacetyl-bis­(N-4-methyl-3-thiosemicarbazide) display the highest reported TOFs of any homogeneous ligand-centered H2 evolution catalyst, 1320 and 1170 s–1, respectively, while the zinc complex also displays one of the highest reported TOF values for H2 oxidation, 72 s–1, of any homogeneous catalyst. Catalysis proceeds via ligand-centered proton-transfer and electron-transfer events while avoiding traditional metal-hydride intermediates. The unique mechanism is consistent with electrochemical results and is further supported by density functional theory. The results identify a new direction for the design of electrocatalysts for H2 evolution and H2 oxidation that are not reliant on metal-hydride intermediates.
ISSN:0002-7863
1520-5126
DOI:10.1021/jacs.6b04441