Co3O4 is an attractive alternative to precious
metal catalyst for CO oxidation due to its low cost and earth abundance,
but its high catalytic activity is severely degraded in the presence
of water. Here, we show that doping La into Co3O4 surfaces significantly enhances CO oxidation activity under moisture-rich
condition. While bare Co3O4 is deactivated under
moisture, the La-doped Co3O4 catalysts exhibit
greatly improved activity and water resistance. The higher ratio of
active Co3+ on the La-doped Co3O4 surface results in the enhanced activity. Especially, the La doping
greatly reduces the formation of surface OH on the Co3O4 surface, which causes the poor water resistance. Density
functional theory calculations reveal that the La doping suppresses
the vacancy-assisted dissociative adsorption of H2O, resulting
in less formation of surface OH and thereby mitigating water poisoning
on the Co3O4 surface. This work can provide
an insight into the surface restructuring for highly active and water-resistant
Co3O4 catalysts.