Solar Fuels: Photoelectrosynthesis of CO from CO2 at p‐Type Si using Fe Porphyrin Electrocatalysts |
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Authors: | Khalaf Alenezi Dr. Saad K. Ibrahim Dr. Peiyi Li Prof. Dr. Christopher J. Pickett |
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Affiliation: | Energy Materials Laboratory, School of Chemistry, University of East Anglia, Norwich Research Park, Norwich NR4 7TJ (UK) |
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Abstract: | Photoelectrocatalytic conversion of CO2 to CO can be driven at a boron‐doped, hydrogen terminated, p‐type silicon electrode using a meso‐tetraphenylporphyrin FeIII chloride in the presence of CF3CH2OH as a proton source and 0.1 M [NBu4][BF4]/MeCN/5 % DMF (v/v) as the electrolyte. Under illumination with polychromatic light, the photoelectrocatalysis operates with a photovoltage of about 650 mV positive of that for the dark reaction. Carbon monoxide is produced with a current efficiency >90 % and with a high selectivity over H2 formation. Photoelectrochemical current densities of 3 mA cm?2 at ?1.1 V versus SCE are typical, and 175 turnovers have been attained over a 6 h period. Cyclic voltammetric data are consistent with a turnover frequency of ${k{{{rm Si}hfill atop {rm obs}hfill}}}$ =0.24×104 s?1 for the photoelectrocatalysis at p‐type Si at ?1.2 V versus SCE this compares with ${k{{{rm C}hfill atop {rm obs}hfill}}}$ =1.03×104 s?1 for the electrocatalysis in the dark on vitreous carbon at a potential of ?1.85 V versus SCE. |
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Keywords: | CO2 reduction iron photoelectrocatalysis porphyrins p‐type silicon |
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