We have developed a composite catalyst featuring acid
and base
interface that enables the efficient conversion of ethanol to butanol.
Our catalyst, which possesses adjacent acid–base sites, exhibits
over a eightfold increase in dehydrogenation and condensation rates
per site compared to physical mixture of acid and base. This demonstrates
a remarkable acid–base synergistic effect in these two kinetically
relevant steps. Through isotope experiments, we have elucidated the
chemical origin of the strong activation of the C–H bond under
cooperative catalysis, which is the transformation of the dehydrogenation
mechanism from the “ethoxide pathway”, involving basic
sites, to the “enolate pathway”, involving dual-sites.
This work provides valuable insights into the design of catalysts
for C–H activation.