Tailoring the active phase of CoO-based thin-film catalysts in order to tune selectivity in CO2 hydrogenation.

Abstract

In this study, we prepared CoO-based thin films deposited on Kanthal steel wire gauze meshes by plasma-enhanced chemical vapor deposition. X-ray photoelectron spectroscopy (XPS) analysis revealed a structure characterized by a combination of cobalt oxide and metallic cobalt embedded within a carbon matrix. Our primary objective was to gain insights into the roles of Co0 and CoO in CO2 hydrogenation reactions. To achieve this, the performance of the thin-film CoO-based catalyst with an initial atomic ratio of CoO/Co0 at 10.2 was compared with two series of the thin-film catalysts that underwent pre-reduction processes at 350 °C for durations of 30 and 60 minutes, resulting in atomic ratios of CoO/Co0 at 3.1 and 1.1, respectively. Subsequently, catalytic tests were conducted in a continuous flow stirred tank reactor operating at temperatures ranging from 250 °C to 400 °C. Our findings indicate that CoO plays a significant role in activating the CO2 methanation reaction which can be due to the high hydrogen coverage of CoO, while Co0 is the active phase in the reverse water-gas shift reaction. Results highlight the importance of oxidized cobalt for hydrogen adsorption and dissociation in CO2 hydrogenation for CH4 formation.