Seriatim ECSTM-ECPMIRS of the adsorption of carbon monoxide on Cu(100) in alkaline solution at CO_2-reduction potentials
Abstract
It was recently demonstrated that the sequential or seriatim application of electrochemical scanning tunneling microscopy (ECSTM) and differential electrochemical mass spectrometry (DEMS) enables the correlation, under actual reaction conditions, of a specific structure on a Cu electrode surface with the generation of a particular CO-reduction product. As an extension of the operando hyphenated-technique approach, we paired ECSTM with electrochemical polarization-modulation IR reflection-absorption spectroscopy (ECPMIRS) to identify a delineating potential that affected the coverage, the molecular orientation, and the adlattice structure of CO adsorbed on Cu(100) in 0.1 M KOH under CO_2-reduction conditions. The results may have significant ramifications on the theory-based reaction mechanism for the formation of C_2 compounds, as well as insights into the mode of coordination between CO and zerovalent Cu.
Additional Information
© 2018 Elsevier. Received 11 March 2018; Received in revised form 18 April 2018; Accepted 20 April 2018. Available online 22 April 2018. This material is based upon work performed by the Joint Center for Artificial Photosynthesis, a DOE Energy Innovation Hub, supported through the Office of Science of the U.S. Department of Energy under Award No. DE-SC0004993.Additional details
- Alternative title
- Seriatim ECSTM-ECPMIRS of the adsorption of carbon monoxide on Cu(100) in alkaline solution at CO2 -reduction potentials
- Eprint ID
- 86044
- Resolver ID
- CaltechAUTHORS:20180425-144714864
- Department of Energy (DOE)
- DE-SC0004993
- Created
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2018-04-25Created from EPrint's datestamp field
- Updated
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2021-11-15Created from EPrint's last_modified field
- Caltech groups
- JCAP