Supported metal catalysts
are one of the major classes of heterogeneous catalysts, which demand
good stability in both the supports and catalysts. Herein, layered
protonated titanate-derived TiO2 (LPT-TiO2)
nanowire arrays were synthesized to support platinum catalysts using
different loading processes. The Pt ion-exchange loading on pristine
LPTs followed by thermal annealing resulted in superior Pt catalysts
supported on the LPT-TiO2 nanoarrays with excellent hydrothermal
stability and catalytic performance toward CO and NO oxidations as
compared to the Pt catalysts through wet-impregnation on the anatase
TiO2 (ANT-TiO2) nanoarrays resulted from thermal
annealing of LPT nanoarrays. Both loading processes resulted in highly
dispersed Pt nanoparticles (NPs) with average sizes smaller than 1
nm at their pristine states. However, after hydrothermal aging at
800 °C for 50 h, highly dispersed Pt NPs were only retained on
the ion-exchanged LPT-TiO2 nanoarrays with the support
structure consisting of a mixture of 74% anatase and 26% rutile TiO2. For the wet-impregnation loading directly on anatase TiO2 nanoarrays derived from LPT, the Pt catalysts experienced
severe agglomeration after hydrothermal aging, with the nanoarray
supports consisting of 86% anatase and 14% rutile TiO2.
Spectroscopy analysis suggested that Pt2+ cations intercalated
into the interlayers of the titanate frameworks through ion-exchange
impregnation procedure, which altered the chemical and electronic
structures of the catalysts, resulting in the shifts of the electronic
binding energy, Raman bands, and optical energy bandgap. The ion-exchangeable
nature of LPT nanoarrays clearly provides a structural modification
in Pt-doped LPT that has resulted in a strong interaction between
the Pt catalysts and LPT-TiO2 nanoarray supports, leading
to the enhanced hydrothermal stability of the catalysts. Considering
the wide applications of the LPT and TiO2 nanomaterials
as supports for catalysts, this finding provides a new pathway to
design highly stable supported metal catalysts for different reactions.