Perovskite Oxide Catalysts for Enhanced CO2 Reduction: Embroidering Surface Decoration with Ni and Cu Nanoparticles

Abstract

The imperative reduction of carbon dioxide into valuable fuels stands as a crucial step in the transition towards a more sustainable energy system. Perovskite oxides, with their high compositional and property adjustability, emerge as promising catalysts for this purpose, whether employed independently or as a supporting matrix for other active metals. In this study, an A-site-deficient La0.9FeO3 perovskite underwent surface decoration with Ni, Cu or Ni + Cu via a citric acid-templated wet impregnation method. Following extensive characterization through XRD, N2 physisorption, H2-TPR, SEM-EDX, HAADF STEM-EDX mapping, CO2-TPD and XPS, the prepared powders underwent reduction under diluted H2 to yield metallic nanoparticles (NPs). The prepared catalysts were then evaluated for CO2 reduction in a CO2/H2 = 1/4 mixture. The deposition of Ni or Cu NPs on the perovskite support significantly enhanced the conversion of CO2, achieving a 50% conversion rate at 500 °C, albeit resulting in only CO as the final product. Notably, the catalyst featuring Ni-Cu co-deposition outperformed in the intermediate temperature range, exhibiting high selectivity for CH4 production around 350 °C. For this latter catalyst, a synergistic effect of the metal–support interaction was evidenced by H2-TPR and CO2-TPD experiments as well as a better nanoparticle dispersion. A remarkable stability in a 20 h time-span was also demonstrated for all catalysts, especially the one with Ni-Cu co-deposition.