Size- and Structure-specificity in Catalysis by Gold Clusters
نویسندگان
چکیده
منابع مشابه
Oxidation catalysis by supported gold nano-clusters
The historical notion regarding the inability of gold to catalyze reactions has been discarded in view of recent studies, which have clearly demonstrated the high catalytic efficiency of supported nano-gold catalysts. Although nano-Au catalysts are known to catalyze a variety of reactions, the major focus has been on CO oxidation catalysis. In this work we focus on the important aspects related...
متن کاملCatalysis by Supported Gold Nanoclusters
The physical and chemical properties of supported Au clusters are markedly sensitive to cluster size and morphology. To investigate the origin of the unique properties of nanosized Au clusters, model catalysts consisting of Au clusters of varying sizes have been prepared on single crystal TiO2(110) and ultrathin films of single crystalline TiO2, SiO2, and Al2O3. The morphology, electronic struc...
متن کاملThe promotional effect of gold in catalysis by palladium-gold.
Acetoxylation of ethylene to vinyl acetate (VA) was used to investigate the mechanism of the promotional effect of gold (Au) in a palladium (Pd)-Au alloy catalyst. The enhanced rates of VA formation for low Pd coverages relative to high Pd coverages on Au single-crystal surfaces demonstrate that the critical reaction site for VA synthesis consists of two noncontiguous, suitably spaced, Pd monom...
متن کاملSubstrate size-selective catalysis with zeolite-encapsulated gold nanoparticles.
Over the years, many strategies have been developed to address the problem of sintering of nanoparticle catalysts, including encapsulating metal nanoparticles in protective shells, and trapping nanoparticles in the cavities of certain zeolites in post-synthesis steps. In general, materials that contain metal nanoparticles that are only accessible via zeolite micropores are intriguing, specifica...
متن کاملSize-dependent structural evolution and chemical reactivity of gold clusters.
Ground-state structures and other experimentally relevant isomers of Au(15) (-) to Au(24) (-) clusters are determined through joint first-principles density functional theory and photoelectron spectroscopy measurements. Subsequent calculations of molecular O(2) adsorption to the optimal cluster structures reveal a size-dependent reactivity pattern that agrees well with earlier experiments. A de...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Chemistry Letters
سال: 2014
ISSN: 0366-7022,1348-0715
DOI: 10.1246/cl.131232