It is widely recognized that CO oxidation
effectively proceeds
over Au nanoparticles supported on a reducible oxide, such as TiO2 and Fe2O3, in which the support supplies
oxygen during the reaction (Mars–van Krevelen (MvK) type mechanism).
Here we examine the stable electride, [Ca24Al28O64]4+(e–)4 (C12A7:e–), with a low work function (2.4 eV), as a Ru catalyst
support for CO oxidation. Ru-loaded C12A7:e– exhibited
more than a 3-fold higher turnover frequency (TOF) and a lower activation
energy than Ru-loaded TiO2, Al2O3, and [Ca24Al28O64]4+(O2–)2 (C12A7:O2–)
catalysts. The high catalytic performance of Ru/C12A7:e– is not due to the MvK type mechanism but to efficient electron transfer
from C12A7:e– to the species adsorbed on the Ru
catalyst, in which the association reaction between adsorbed CO molecules
and O adatoms is promoted on the Ru surface.