Abstract
This work compares the capacity of generating
the surface oxygen vacancies over SrTiO3, BaTiO3 and the
mixed Sr0.5Ba0.5TiO3. This aspect is elucidated
by significantly different chemical states of the elements on the surface of
the three materials. Along with the fundamental materials aspect, CO oxidation
studies complement the highest surface reducibility of the Sr0.5Ba0.5TiO3
catalyst. With detailed adsorption-desorption studies, we report that the A-site
cation substitution renders a better surface-reducibility induced catalytic
activity for CO oxidation.
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