SO3 decomposition over silica-modified β-SiC supported CuFe2O4 catalyst: characterization, performance, and atomistic insights

Abstract

The sulfur–iodine (S–I) thermochemical water-splitting cycle is one of the potential ways to produce hydrogen on a large scale. CuFe₂O₄ was dispersed over modified silica or treated β-SiC and untreated β-SiC using the wet impregnation method for SO₃ decomposition, which is the most endothermic reaction of the S–I cycle. Various state-of-the-art techniques such as XRD, FT-IR, BET, XPS, TEM, HR-TEM, FESEM-EDS and elemental mapping were employed to characterize both the synthesized catalysts. CuFe₂O₄ catalyst supported on silica-modified β-SiC resulted in enhanced catalytic activity and stability due to better metal-support interaction. In order to get a better insight into the reaction mechanism over this bimetallic catalyst, the first principles based simulation under the framework of density functional theory was performed. We have found that the presence of Cu gives rise to an improved charge localization at the O-vacancy site alongside favourable reaction kinetics, which results in an enhanced catalytic activity for the CuFe₂O₄ nano-cluster compared to that of a single metallic catalyst containing Fe₂O₃ nano-cluster.