Mitigating the Poisoning Effect of Formate during CO 2 Hydrogenation to Methanol over Co-Containing Dual-Atom Oxide Catalysts.
Nazmul Hasan M D DostagirCarlo Robert TomuschatKai OshiroMin GaoJun-Ya HasegawaAtsushi FukuokaAbhijit ShrotriPublished in: JACS Au (2024)
During the hydrogenation of CO 2 to methanol over mixed-oxide catalysts, the strong adsorption of CO 2 and formate poses a barrier for H 2 dissociation, limiting methanol selectivity and productivity. Here we show that by using Co-containing dual-atom oxide catalysts, the poisoning effect can be countered by separating the site for H 2 dissociation and the adsorption of intermediates. We synthesized a Co- and In-doped ZrO 2 catalyst (Co-In-ZrO 2 ) containing atomically dispersed Co and In species. Catalyst characterization showed that Co and In atoms were atomically dispersed and were in proximity to each other owing to a random distribution. During the CO 2 hydrogenation reaction, the Co atom was responsible for the adsorption of CO 2 and formate species, while the nearby In atoms promoted the hydrogenation of adsorbed intermediates. The cooperative effect increased the methanol selectivity to 86% over the dual-atom catalyst, and methanol productivity increased 2-fold in comparison to single-atom catalysts. This cooperative effect was extended to Co-Zn and Co-Ga doped ZrO 2 catalysts. This work presents a different approach to designing mixed-oxide catalysts for CO 2 hydrogenation based on the preferential adsorption of substrates and intermediates instead of promoting H 2 dissociation to mitigate the poisonous effects of substrates and intermediates.