Bavykin, Dmitry V., Lapkin, Alexei A., Plucinski, Pawel K., Torrente-Murciano, Laura, Friedrich, Jens M. and Walsh, Frank C.
Deposition of Pt, Pd, Ru and Au on the surfaces of titanate nanotubes
Topics in Catalysis, 39, (3-4), . (doi:10.1007/s11244-006-0051-4).
Full text not available from this repository.
Nanoparticles of different metals (Pt, Pd, Au) or a metal hydroxide (Ru) have been immobilized on the surface of mesoporous
titanate nanotubes produced by alkali hydrothermal treatment of TiO2, and have been characterized by HRTEM. Two different
approaches have been utilised for the deposition of metal particles into the internal pores of titanate nanotubes: (i) deposition from
solution confined inside the nanotubes and (ii) blocking the external surface of the nanotubes. A third method, ion-exchange of
protons onto metal cations in titanate nanotubes followed by reduction or alkali treatment (in the case of Ru hydroxide), has been
used for deposition of metal nano-particles on both the internal and external surfaces of the nanotubes. Nanoparticles of metal or
metal hydroxide deposited by the ion-exchange method are characterised by an average size in the range of 1.2–5 nm, and deposits are uniformly distributed on the surface, resulting in a very high loading density. An increase in the amount of deposited metal
resulted predominantly in a higher nanoparticle loading density, without growth in the particle size. This was correlated with the
retention of high specific catalytic activity of ruthenium hydrated oxide deposited on titanate nanotubes in the reaction of selective
oxidation of benzyl alcohol over a wide range (0.6–8.7 wt%) of ruthenium loading. The methods for metallization of titanate
nanotubes are critically discussed.
Actions (login required)