Dispersion and Stability Mechanism of Heterogeneous Catalysts

The dispersion and stability of noble-metal catalysts on transition-metal-oxide supports are considerably important for practical applications of the catalysts. Pt nanoparticles are uniformly and highly dispersed on transition-metal oxides when hydrogen peroxide (H₂O₂) is applied before calcination at 500 &lt;span style="font-size:10.8333px"&gt;^oC&lt;/span&gt;<b>.</b> The influence of H₂O₂ on the dispersion and the stability of Pt nanoparticles on titania-incorporated fumed silica (Pt/Ti-FS) supports was examined using in-situ X-ray absorption fine structure (XAFS) measurements at the Pt L₃ and Ti K edges as well as density functional theory (DFT) calculations. The local structural and chemical properties around Pt and Ti atoms of Pt/Ti-FS with and without H₂O₂ treatment were monitored using <i>in-situ</i> XAFS during heating from room temperature to 500 ^oC. XAFS revealed that the Pt nanoparticles of H₂O₂-Pt/Ti-FS are highly stable and that the Ti atoms of H₂O₂-Pt/Ti-FS support form into a distorted-anatase TiO₂. DFT calculations showed that Pt atoms bond more stably to oxidized-TiO₂ surfaces than they do to bare- and reduced-TiO₂ surfaces. XAFS measurements and DFT calculations clarified that the presence of extra oxygen atoms due to the H₂O₂ treatment plays a critical role in the strong bonding of Pt atoms to TiO₂ surfaces.