Paper
24 August 2010 Catalytic conversion of carbon dioxide to methanol and higher order alcohols at a photoelectrochemical interface
Kate Keets, Amanda Morris, Elizabeth Zeitler, Prasad Lakkaraju, Andrew Bocarsly
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Abstract
There is increasing interest in photochemical schemes for converting CO2 into a useful product as a means of mitigating atmospheric levels of this gas. Although photoelectrochemical schemes have been considered for this application, typically very high overpotentials are observed, and thus, semiconductor-electrolyte interfaces have not been observed to actually convert light energy to chemical energy in the aqueous CO2 redox system. We report here on a catalytic system that efficiently converts CO2 to methanol and other alcohols. The system couples a III-V p-type semiconductor electrode with a pyridinium catalyst. The conversion of CO2 to alcohols can be driven solely with light to yield faradaic efficiencies approaching 100% at potentials well below the thermodynamic potential. Mechanistic studies on the formation of methanol indicate that the observed six-electron reduction occurs via a series of one electron reductions mediated by pyridinium.
© (2010) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Kate Keets, Amanda Morris, Elizabeth Zeitler, Prasad Lakkaraju, and Andrew Bocarsly "Catalytic conversion of carbon dioxide to methanol and higher order alcohols at a photoelectrochemical interface", Proc. SPIE 7770, Solar Hydrogen and Nanotechnology V, 77700R (24 August 2010); https://doi.org/10.1117/12.860024
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Cited by 4 scholarly publications.
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KEYWORDS
Carbon dioxide

Electrodes

Semiconductors

Interfaces

Carbon monoxide

Metals

Platinum

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