Gas-phase electrocatalytic conversion of CO 2 to chemicals on sputtered Cu and Cu–C catalysts electrodes

Citations of this article
Mendeley users who have this article in their library.


A novel gas-phase electrocatalytic cell containing a low-temperature proton exchange membrane (PEM) was developed to electrochemically convert CO 2 into organic compounds. Two different Cu-based cathode catalysts (Cu and Cu–C) were prepared by physical vapor deposition method (sputtering) and subsequently employed for the gas-phase electroreduction of CO 2 at different temperatures (70–90 °C). The prepared electrodes Cu and Cu–C were characterized by X-ray diffraction (XRD), X-ray photoemission spectroscopy (XPS) and scanning electron microscopy (SEM). As revealed, Cu is partially oxidized on the surface of the samples and the Cu and Cu–C cathodic catalysts were comprised of a porous, continuous, and homogeneous film with nanocrystalline Cu with a grain size of 16 and 8 nm, respectively. The influence of the applied current and temperature on the electro-catalytic activity and selectivity of these materials was investigated. Among the two investigated electrodes, the pure Cu catalyst film showed the highest CO 2 specific electrocatalytic reduction rates and higher selectivity to methanol formation compared to the Cu–C electrode, which was attributed to the higher particle size of the former and lower CuO/Cu ratio. The obtained results show potential interest for the possible use of electrical renewable energy for the transformation of CO 2 into valuable products using low metal loading Cu based electrodes (0.5 mg Cu cm −2 ) prepared by sputtering.




Gutiérrez-Guerra, N., González, J. A., Serrano-Ruiz, J. C., López-Fernández, E., Valverde, J. L., & de Lucas-Consuegra, A. (2019). Gas-phase electrocatalytic conversion of CO 2 to chemicals on sputtered Cu and Cu–C catalysts electrodes. Journal of Energy Chemistry, 46–53.

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free