Synergistic effect of Cu+ single atoms and Cu nanoparticles supported on alumina boosting water-gas shift reaction

The water-gas shift reaction (WGSR) is an important industrial process for H-2 production. Here, we rationally construct alumina supported dual-site copper catalysts, i.e. Cu+ single atoms (Cu-1(+)) surrounding Cu nanoparticles (Cu-NP(0) ), for WGSR. Our findings show that CO is tightly adsorbed on surface-enriched Cu-1(+) sites to inhibit competitive adsorption with H2O on Cu-NP(0) sites. The number of adsorbed CO is two orders of magnitude higher than that on conventional Cu-based catalysts. It significantly increases surface CO concentration, and forms a unique structure of Cu-NP(0) "islands " immerged in CO "pool ". Benefiting from synergy of Cu-1(+) and Cu-NP(0) sites, the catalyst with 12% Cu loading exhibits extraordinary and robust catalytic activity, compared to benchmark CuZn-Al catalyst, especially at low temperatures, e.g. 200 degrees C. The catalyst design strategy and facile synthesis methodology employed in this work could be potentially applied in other related industrial reactions.