Catalytic
combustion is a promising technology for removing unburnt
CH4 from natural gas vehicle exhaust gas under lean-burn
conditions. Supported Pd catalysts are widely applied and studied
for use in CH4 oxidation at <500–550 °C,
with their activities significantly affected by the interactions between
Pd and the support, depending on the dispersion, Pd valence state,
and properties of the support. However, whether metal–support
interactions are favorable in catalytic CH4 oxidation is
unclear. We therefore used YMn2O5 as a catalytically
active support to prepare a dual-site catalyst, Pd/YMn2O5, which shows high CH4 catalytic activities
in dry and wet atmospheres. Experimental and density functional theory
studies reveal that the CH4 adsorption and lattice oxygen
activity of the support are significantly enhanced due to the interactions
between PdO
x
and YMn2O5. In situ X-ray photoelectron spectroscopy shows that Pd
x+ (x = 2 and 4) and Mn
x+ (x = 3 and 4) species
undergo changes during CH4 oxidation. The PdO
x
sites are the main active sites, as the CH4 activation barrier is much lower than those at other sites. YMn2O5 and PdO
x
participate
in CH4 activation and oxidation via active oxygen transfer.