We synthesised copper octahedrons by two electrode electrodeposition, to selectively reduce CO2RR into CO2+H2 (synthesis gas) to use it as starting material in well known Fischer-tropsch reaction. In a representative experiment, copper was dissolved from a sacrificial copper anode and collected as micro-octahedrons on the surface of a platinum foil. The structures were simply tapped off the surface, cleaned, dried and used as catalyst ink to reduce CO2 into value-added fuels. A set of experimental parameters were varied to study the effect of them on morphology, size and activity of the obtained copper powders. A pulse method involving anodic and cathodic waves passed through the copper anode was found to have a determining capability - be it shape, topology or size of the crystallites.
In a catholyte composed of 0.2 M KHCO3, cyclo-voltammograms (CVs) were recorded in N2 saturated and CO2 catholyte in a 3-electrode, 2-chambered cell. From preliminary results, it was shown that CuOcta showed activity towards CO2RR as was evident in enhanced faradaic response in CO2 saturated catholyte. To confirm the path of fixing and valorization, a thorough gas chromatography (GC) analysis was done on the gases that were collected in a Tedlar bag. CO was found to be major reduction product in gaseous phase overcoming the inherit HER (hydrogen evolution reaction) competition on metal surfaces. A significant amount of CH4 was also measured. The array of obtained products signal role of morphology, the surface topography of catalytic structures on the mechanism and kinetics of CO2RR.