Construction of stabilized bulk-nano interfaces for highly promoted inverse CeO2/Cu catalyst

Abstract

As the water-gas shift (WGS) reaction serves as a crucial industrial process, strategies for developing robust WGS catalysts are highly desiderated. Here we report the construction of stabilized bulk-nano interfaces to fabricate highly efficient copper-ceria catalyst for the WGS reaction. With an in-situ structural transformation, small CeO2 nanoparticles (2–3\u2009nm) are stabilized on bulk Cu to form abundant CeO2-Cu interfaces, which maintain well-dispersed under reaction conditions. This inverse CeO2/Cu catalyst shows excellent WGS performances, of which the activity is 5 times higher than other reported Cu catalysts. Long-term stability is also very solid under harsh conditions. Mechanistic study illustrates that for the inverse CeO2/Cu catalyst, superb capability of H2O dissociation and CO oxidation facilitates WGS process via the combination of associative and redox mechanisms. This work paves a way to fabricate robust catalysts by combining the advantages of bulk and nano-sized catalysts. Catalysts with such inverse configurations show great potential in practical WGS applications. Cu-CeO2 has been considered as promising alternative to Cu-Zn-Al catalyst for water-gas shift (WGS) reaction, but it still suffers from low activity caused by Cu sintering. Here, the authors develop inverse CeO2/Cu catalyst with remarkable activity and stability in WGS via construction of stabilized bulk-nano interfaces.