Published July 2014
| public
Journal Article
Heterogenization of a Water-Insoluble Molecular Complex for Catalysis of the Proton-Reduction Reaction in Highly Acidic Aqueous Solutions
Chicago
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Abstract
Our long-held interest in the resiliency of electrochemical functionalities upon surface immobilization has herded us from directly chemisorbed electroactive moieties, to anchor group-leashed redox-active couples and to surface-tethered enzyme-inspired molecular catalysts. The latter represent the most intricate because the electrocatalytic activities involve mixed-valence states and may require certain entatic (fractionally rotated) configurations. In this regard, we recently investigated the proton-reduction electrocatalysis by hydrogenase-inspired di-iron complexes at polycrystalline and (111)-faceted Au electrodes.
Additional Information
© 2014 Springer Science+Business Media New York. Published online: 26 April 2014. This material is based upon work performed by the Joint Center for Artificial Photosynthesis, a DOE Energy Innovation Hub, as follows: except for the synthesis of the di-iron complexes which was funded by the National Science Foundation (CHE-091679 and CHE-1266097) (MYD), all the work was supported through the Office of Science of the US Department of Energy under Award No. DE-SC0004993.Additional details
- Eprint ID
- 45500
- DOI
- 10.1007/s12678-014-0200-7
- Resolver ID
- CaltechAUTHORS:20140505-132735594
- NSF
- CHE-091679
- NSF
- CHE-1266097
- Department of Energy (DOE)
- DE-SC0004993
- Created
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2014-05-05Created from EPrint's datestamp field
- Updated
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2021-11-10Created from EPrint's last_modified field
- Caltech groups
- JCAP