journal article·1989-06-01

Electrochemical and Surface Studies of Carbon Dioxide Reduction to Methane and Ethylene at Copper Electrodes in Aqueous Solutions

David W. DeWulf, Tuo Jin, Allen J. Bard

Publisher page

Abstract

The electrochemical reduction of to and in aqueous alkaline solutions at Cu electrodes was studied under potentiostatic conditions at −2.00V vs. SCE. The current at the Cu electrodes and the rate of hydrocarbon formation were monitored as a function of time over a temperature range from 0 to 48°C. Solutions of formate, formaldehyde, and methanol, possible intermediates in the reduction process, were also electrolyzed. Surface analyses (XPS and AES) were also performed on the Cu electrodes following electrolysis to identify surface intermediates. In addition to hydrocarbon formation, a poisoning process occurred, causing a deposit of a black film on the surface of the Cu cathode. XPS and AES studies indicated that the black film was graphitic carbon, probably the result of a side reaction, the reduction of through formate to graphite. A tentative reaction mechanism for reduction, based upon the data here and those of previous investigators, involving the reaction path , is proposed.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: CO2 Reduction Techniques and Catalysts · Electrocatalysts for Energy Conversion · Electrochemical Analysis and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry, University of Texas at Austin, Austin, Texas 78712

References

Reference metadata was not supplied for this record.