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Electrochemical reduction of CO<sub>2</sub> on silver as probed by surface‐enhanced Raman scattering
67
Citations
22
References
1995
Year
EngineeringMetal NanoparticlesSurface-enhanced Raman ScatteringMetallic NanomaterialsChemistrySurface‐enhanced Raman ScatteringAg ElectrodeElectrochemical ReductionElectrode Reaction MechanismMaterials ScienceNanotechnologySurface ElectrochemistryCo 2HydrogenElectrochemical ProcessElectrochemistrySurface ScienceAbstract Surface‐enhanced RamanElectrochemical Surface Science
Abstract Surface‐enhanced Raman scattering (SERS) spectroscopy was used to explore the electrochemical reduction of CO 2 at a polycrystalline Ag electrode in KHCO 3 aqueous solution saturated with CO 2 at room temperature. Raman scattering from the oxidation‐reduction cycled Ag electrode suggests the formation of CO and HCOOH by CO 2 reduction. At an electrode potential of 0.08 V ( vs. Ag/AgCl), adsorbed CO gives rise to a C‐O stretch band at 2128 cm −1 . This band decreases in intensity and shifts to higher wavenumber with an increase of negative potential in the range from 0.0 to − 0.24 V. A different potential dependence is observed for the C‐H stretch mode of adsorbed HCOO − (2870 cm −1 at − 0.8 V). The O‐C‐O antisymmetric and symmetric stretch modes of HCOO − observed at near 1550 and 1350 cm −1 decrease in intensity with increasing negative potential, presenting a striking contrast to the C‐H stretch mode. The SERS experiment with a CO 2 ‐saturated KHCO 3 D 2 O solution is also described and discussed.
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