Abstract:The dynamic reduction behavior of a highly dispersed Pt 4? to Pt 0 particles on TiO 2 and Al 2 O 3 surfaces under the reductive atmosphere with an in situ timeresolved energy-dispersive X-ray absorption fine structure (DXAFS) analysis. A highly dispersed Pt 4? on TiO 2 was reduced to Pt 0 even at room temperature. In contrast, a highly dispersed Pt 4? on Al 2 O 3 was gradually reduced to Pt 0 even at 473 K. This result may suggest that the semiconductive behavior of TiO 2 promotes the low temperature adsorptio… Show more
“…A curve fitting suggested that ca. 25% fraction of Pt species was oxides and the remaining part was metal in the catalyst, using the spectra of Pt foil and PtO 2 [33]. As to Re L 3 -edge, intensity of the white line for Pt-Re/ZrO 2 corresponded to those for tetra-to hexa-valent oxides [34,35].…”
Section: Characterization Of Pt/zro 2 and Pt-re/zro 2 Catalystsmentioning
Abstract:Bimetallic Pt-Re/ZrO 2 catalysts were developed for the selective hydrodeoxygenation of 4-propylphenol as a lignin model to n-propylbenzene in water. The addition of Re to Pt/ZrO 2 improved the catalyst stability and product selectivity. Reaction temperature greatly affected not only reaction efficiency but also product distribution. n-Propylbenzene was obtained in up to 73% yield with ca. 80% selectivity. After the reaction, the catalyst was deactivated possibly due to waterinduced wrapping of Pt nanoparticles in ZrO 2 . The reaction may involve the hydrogenation of 4-propylphenol to 4-propylcyclohexanol, followed by the dehydration to give 4-propylcyclohexene and the subsequent dehydrogenation to n-propylbenzene.
“…A curve fitting suggested that ca. 25% fraction of Pt species was oxides and the remaining part was metal in the catalyst, using the spectra of Pt foil and PtO 2 [33]. As to Re L 3 -edge, intensity of the white line for Pt-Re/ZrO 2 corresponded to those for tetra-to hexa-valent oxides [34,35].…”
Section: Characterization Of Pt/zro 2 and Pt-re/zro 2 Catalystsmentioning
Abstract:Bimetallic Pt-Re/ZrO 2 catalysts were developed for the selective hydrodeoxygenation of 4-propylphenol as a lignin model to n-propylbenzene in water. The addition of Re to Pt/ZrO 2 improved the catalyst stability and product selectivity. Reaction temperature greatly affected not only reaction efficiency but also product distribution. n-Propylbenzene was obtained in up to 73% yield with ca. 80% selectivity. After the reaction, the catalyst was deactivated possibly due to waterinduced wrapping of Pt nanoparticles in ZrO 2 . The reaction may involve the hydrogenation of 4-propylphenol to 4-propylcyclohexanol, followed by the dehydration to give 4-propylcyclohexene and the subsequent dehydrogenation to n-propylbenzene.
“…Of these techniques, time resolved X-ray absorption fine structure (XAFS) spectroscopy is one of the most useful methods to observe metal nanoparticle formation process in situ because the chemical state and the structure of metal nanoparticles can be analyzed from the spectra. [44][45][46][47][48][49][50][51] Recently, a coupled in situ XANES and small-angle X-ray scattering (SAXS) spectroscopy was applied to elucidate the formation mechanism of gold nanoparticles from a solution of Au 3+ ions with citrate acid. 52 These studies helped describe the mechanism of nanoparticle formation, which was found to comprise different steps of particle growth via both the coalescence of nuclei and further monomer attachment.…”
Section: Formation Mechanism Of Gold Nanoparticlesmentioning
Recently, we studied and developed two useful synthesis methods of metal nanoparticles. The first system is wet chemical synthesis of gold nanoparticles using fast reduction. The second one is photodeposition of metal nanoparticles on TiO 2. The X-ray absorption fine structure (XAFS) study revealed their unique formation mechanisms different from the conventional mechanisms. Furthermore, we designed and synthesized new multidentate protecting ligand having sulfur functional groups to synthesize small gold nanoparticles efficiently.
“…Of these, quick X-ray absorption fine-structure (XAFS) spectroscopy is one of the most useful methods to observe AuNP formation process in situ because the chemical state and the structure of AuNP can be analyzed from the spectra. [15,16,17] Recently, Polte et al observed the formation process of AuNPs with citric acid by coupled in situ XANES and small-angle X-ray scattering (SAXS) spectroscopy. [18] This helped to describe the mechanism of nanoparticle formation, which was found to comprise different steps of particle growth via both the coalescence of nuclei and further monomer attachment.…”
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