A facile synthesis of Cu catalysts with multiple high-index facets for the suppression of competing H2 evolution during electrocatalytic CO2 reduction. Issue 5 (29th January 2021) - Philip, Monday
Abstract : The formation of high-index facets were realized via the electropolishing process before and after annealing at different temperatures and exhibited the suppression of H2 evolution and C1 products during the electrochemical CO2 reduction. Abstract : The electrochemical CO2 reduction reaction (CO2 RR) over the high-index facets of Cu nanoparticles (NPs) is favourable towards the formation of multi-carbon products, such as hydrocarbons and oxygenates. However, the facile synthesis of Cu NPs with multiple high-index facets remains a great challenge in the research community. Herein, we have prepared numerous Cu catalysts with flat surfaces by electropolishing polycrystalline Cu foils before and after annealing at different temperatures ranging from 200 °C to 1000 °C under an argon atmosphere. The individual electrode crystal orientations were investigated via X-ray diffraction (XRD) and electron backscattering diffraction (EBSD) techniques. As confirmed by the EBSD technique, the formation of high-index facets increases with an increase in the annealing temperature and reaches a high quantity of high-index facets enclosed mainly by (211) and (431) facets with about 94% of those on the electrode annealed at 1000 °C. As a possible application, we have used the different electrodes for CO2 RR at −1.0 V vs. RHE with special emphasis on the formation of H2 gas and C1 products. Thus, the electrodes prepared at higher temperatures enable the suppression of competing H2 evolution due to the increased amount of high-index facets. Moreover, the formation rates of C1 products were inhibited as well at the electrodes with increased number of high-index facets. The drops in the formation rates of both H2 and C1 products indicate that they are consumed in the chemical reaction to commence the formation of multi-carbon products. However, further study is still required with superior attention on CO2 RR towards the C2+ product formation at a range of applied potentials.