نتایج جستجو برای: tio2 supported au nanoparticle
تعداد نتایج: 320923 فیلتر نتایج به سال:
Electrocatalysis: A comparative study of the electrocatalytic activity LDHs (NiFe-LDH, CuFe-LDH) and TiO2 supported metal nanoparticles (Au−TiO2, Pd−TiO2) upon electroreduction a model compound, 4-nitrophenol(4-NP), potential environmental pollutant, in an aprotic solvent system (TBAPF6/ACN) was reported for first time. Hence its mitigation is interest science that applicable future technologies.
The unique catalytic activity of supported Au nanoparticles has been ascribed to various effects including thickness/shape, the metal oxidation state, and support effects. Previously, we reported the synthesis of ordered Au monolayers and bilayers on TiO(x), with the latter being significantly more active for CO oxidation than the former. In the present study, the electronic and chemical proper...
Au photosensitization can endow TiO2 visible-light-driven photocatalytic properties. Herein, via facet-optimized brookite TiO2 with tunable electronic band structures as the substrate, we found that intense visible light excitation of Au will result in the accumulation of hot-electrons, which will negatively shift the EF of Au and lower the Schottky barrier, thus ensuring their consecutive inje...
Introduction Bulk gold is a chemically inert metal, and had previously been disregarded as a candidate for catalytic applications [1]. Haruta’s pioneering work [2] showed exceptional reactivity on gold nanoparticles of 2-5 nm in diameter. Among reactions, the low temperature CO oxidation [3] on Au has created a strong interest. Model catalyst samples, which consist of planar metal oxide surface...
Poly(vinyl alcohol) (PVA)-stabilized Au nanoparticles (NPs) were synthesized by colloidal methods in which temperature variations (−75 to 75 °C) and mixed H2O/EtOH solvent ratios (0, 50, and 100 vol/vol) were used. The resulting Au NPs were immobilized on TiO2 (P25), and their catalytic performance was investigated for the liquid phase oxidation of glycerol. For each unique solvent system, ther...
Tuning the photonic band gap (PBG) to the electronic band gap (EBG) of Au/TiO2 catalysts resulted in considerable enhancement of the photocatalytic water splitting to hydrogen under direct sunlight. Au/TiO2 (PBG-357 nm) photocatalyst exhibited superior photocatalytic performance under both UV and sunlight compared to the Au/TiO2 (PBG-585 nm) photocatalyst and both are higher than Au/TiO2 withou...
Atom transfer radical polymerization (ATRP) of 4-vinylpyridine, t-butyl acrylate, and styrene in sequential order from a β-cyclodextrin core yielded an amphiphilic starlike triblock copolymer, poly(4-vinylpyridine)-block-poly(tbutyl acrylate)-block-polystyrene (P4VP-b-PtBA-b-PS). Subsequently, star-like triblock copolymer composed of inner hydrophilic P4VP blocks, central hydrophobic PtBA block...
This paper reports the synthesis of a new type of Au@TiO2 yolk-shell nanostructures by integrating ion sputtering method with atomic layer deposition (ALD) technique and its applications as visible light-driven photocatalyst and surface-enhanced Raman spectroscopy (SERS) substrate. Both the size and amount of gold nanoparticles confined in TiO2 nanotubes could be facilely controlled via properl...
Porous Ag/TiO2/Au coatings with excellent multipactor suppression were prepared by fabrication of porous Ag surface through two-step wet chemical etching, synthesis of TiO2 coatings by electroless-plating-like solution deposition and deposition of Au coatings via electroless plating. Porous structure of Ag surface, TiO2 coatings on porous Ag surface and Au coatings on porous Ag/TiO2 surface wer...
Polarization modulation infrared reflection absorption spectroscopy (PM-IRAS) was used to investigate the effects of water on CO oxidation catalyzed by TiO2 supported Au. The introduction of water into the reactant mixture caused two effects: (1) a decrease in the CO coverage; and (2) the appearance of a carbonate species. Since both effects inhibit CO oxidation, the promotional effects of wate...
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