Research on homogeneous and heterogeneous catalysis is indeed convergent and finds subnanometric particles to be at the heart of catalytically active species. Here, monodisperse gold clusters are deposited from the gas phase onto porous titania generating well-defined model systems and the resulting composite materials exhibit a sharp size-dependency on the number of gold atoms per cluster and exceptionally high-turnovers toward the bromination of 1,4-dimethoxybenzene are observed. This indicates that the deliberate generation of active centres is of utmost importance for the creation of the most "gold-efficient" catalysts.
Thins films are synthesized by deposition of size-selected Mo n À cluster anions on an inert substrate. Scanning tunneling microscopy pictures indicate that the deposited material consists of individual particles with diameters corresponding to the size of the preformed clusters from the gas phase. Previous attempts to manufacture cluster materials from metals failed since these clusters coalesced at room temperature. Our data suggest the possibility to synthesize new nanomaterials from clusters of high fusing metals. This may prove to be the key to harness size-dependent and tuneable properties of clusters for creating novel classes of functional tailor-made materials. V C 2014 AIP Publishing LLC. [http://dx.
studied here, no monolayer is formed. Instead, the clusters are randomly distributed as expected for particles with zero mobility. These results demonstrate the high potential of cluster deposition for the production of new types of nanostructured surfaces, thin films and nanomaterials.
We present a newly developed magnetic-bottle time-of-flight electron spectrometer suitable for continuous or quasicontinuous photoionization sources such as synchrotrons. A strong magnetic field collects almost all photoelectrons from a well-defined ionization volume and quantitatively suppresses background electrons which originate outside of this interaction region. Although it is a pulsed instrument, a relatively high duty cycle is achieved by storing the photoelectrons generated between two cycles in an electromagnetic trap. This makes the new instrument suitable for experiments with very low sample densities. Another advantage is the high energy resolution, 50 meV in the first version of the spectrometer described here, which simply depends on the length of the time-of-flight instrument.
Experimental results of the search for inorganic fullerenes are presented. MonSm− and WnSm− clusters are generated with a pulsed arc cluster ion source equipped with an annealing stage. This is known to enhance fullerene formation in the case of carbon. Analogous to carbon, the mass spectra of the metal chalcogenide clusters produced in this way exhibit a bimodal structure. The species in the first maximum at low mass are known to be platelets. Here, the structure of the species in the second maximum is studied by anion photoelectron spectroscopy, scanning transmission electron microscopy, and scanning tunneling microcopy. All experimental results indicate a two-dimensional structure of these species and disagree with a three-dimensional fullerene-like geometry. A possible explanation for this preference of two-dimensional structures is the ability of a two-element material to saturate the dangling bonds at the edges of a platelet by excess atoms of one element. A platelet consisting of a single element only cannot do this. Accordingly, graphite and boron might be the only materials forming nano-spheres because they are the only single element materials assuming two-dimensional structures.
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