The electrocatalytic activity of Cu electrode in the electrochemical reduct
ion of carbon dioxide (CO2) was investigated. Electroreduction mechanism of
CO2 was studied by the adsorption/desorption behaviors of reacting species
by using an in-situ electrochemical quartz crystal microbalance. (EQCM) an
d the surface changes measured by ex-situ SEM, AES, and XRD analysis. Durin
g cathodic reduction of CO2 on Cu, the adsorption of amorphous carbon was o
bserved. After electrolysis time of 1 h at constant cathodic potential, the
poisoning of amorphous carbon resulted in the decrease of the faradaic eff
iciency for the formation of hydrocarbons such as CH4 and C2H4. On the othe
r hand, the potential modulation method caused the change of the surface st
ructure of copper, i.e. the formation of cuprous oxide (Cu2O). This structu
ral change prevented the adsorption of amorphous graphite and the constant
production rate of methane was obtained in long-term electrolysis. (C) 2001
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