heating characterization of structural evolution and size-dependent melting point depression in gold nanoclusters: a comprehensive thermodynamic investigation.

The investigation of nanocluster behaviors at elevated temperatures is important because it encompasses temperature-dependent structural evolution and size-dependent melting points. Size-selected Au, Au, Au, and Au clusters were generated using a gas-phase condensation cluster beam source equipped with a lateral time-of-flight mass selector. Comprehensive heating characterization was conducted, revealing the structural evolution and size-dependent melting point depression of Au clusters at atomic resolution aberration-corrected scanning transmission electron microscopy (AC-STEM).

Coalescence behavior of size-selected gold and tantalum nanoclusters under electron beam irradiation: insights into nano-welding mechanisms.

The emerging technique of nano-welding (NW) precisely regulating the fusion of nanoclusters (NCs) in nanotechnology has attracted significant attention for its innovative approach. Employing the gas-phase condensation cluster source with a lateral time-of-flight (TOF) mass-selector, size-selected gold (Au), and tantalum (Ta) NCs were prepared. This study explores the coalescence behavior of size-selected Au and Ta NCs under electron beam irradiation, aiming to investigate the related mechanism governing the welding process.

Amorphous Metal-Organic Framework-Derived Electrocatalyst to Boost Water Oxidation.

Amorphous metal-organic framework (MOF) materials have drawn extensive interest in the design of high-performance electrocatalysts for use in the electrochemical oxygen evolution reaction. However, there are limitations to the utilization of amorphous MOFs due to their low electrical conductivity and unsatisfactory stability. Herein, a novel amorphous-crystalline (AC) heterostructure is successfully constructed by synthesizing a crystalline metal sulfide (MS)-embedded amorphous NiFe-MOF, namely an MS/NiFe-MOF.

Electrical devices designed based on inorganic clusters.

The idea of exploring the bottom brink of material science has been carried out for more than two decades. Clusters science is the frontmost study of all nanoscale structures. Being an example of 0-dimensional quantum dot, nanocluster serves as the bridge between atomic and conventionally understood solid-state physics.

Enhanced Methanol Electro-Oxidation Activity of Nanoclustered Gold.

Size-selected 3 nm gas-phase Au clusters dispersed by cluster beam deposition (CBD) on a conducting fluorine-doped tin oxide template show strong enhancement in mass activity for the methanol electro-oxidation (MEO) reaction compared to previously reported nanostructured gold electrodes. Density functional theory-based modeling on the corresponding Au clusters guided by experiments attributes this high MEO activity to the high density of exposed under-coordinated Au atoms at their faceted surface. In the description of the activity trends, vertices and edges are the most active sites due to their favorable CO and OH adsorption energies.

A Gd@C single-molecule electret.

Electrets are dielectric materials that have a quasi-permanent dipole polarization. A single-molecule electret is a long-sought-after nanoscale component because it can lead to miniaturized non-volatile memory storage devices. The signature of a single-molecule electret is the switching between two electric dipole states by an external electric field.

A platinum-nickel bimetallic nanocluster ensemble-on-polyaniline nanofilm for enhanced electrocatalytic oxidation of dopamine.

We report a new approach to design flexible functional material platforms based on electropolymerized polyaniline (PANI) polymer nanofilms modified with bimetallic nanoclusters (NCs) for efficient electro-oxidation of small organic molecules. Composition defined ligand free PtNi NCs were synthesized in the gas phase using the Cluster Beam Deposition (CBD) technology and characterized using RToF, HAADF-STEM, XAFS and XPS. NCs were then directly deposited on PANI coated templates to construct electrodes.

Unravelling the nucleation mechanism of bimetallic nanoparticles with composition-tunable core-shell arrangement.

The structure and atomic ordering of Au-Ag nanoparticles grown in the gas phase are determined by a combination of HAADF-STEM, XPS and Refl-XAFS techniques as a function of composition. It is shown consistently from all the techniques that an inversion of chemical ordering takes place by going from Au-rich to Ag-rich compositions, with the minority element always occupying the nanoparticle core, and the majority element enriching the shell. With the aid of DFT calculations, this composition-tunable chemical arrangement is rationalized in terms of a four-step growth process in which the very first stage of cluster nucleation plays a crucial role.

Atomic Resolution Observation of a Size-Dependent Change in the Ripening Modes of Mass-Selected Au Nanoclusters Involved in CO Oxidation.

Identifying the ripening modes of supported metal nanoparticles used in heterogeneous catalysis can provide important insights into the mechanisms that lead to sintering. We report the observation of a crossover from Smoluchowski to Ostwald ripening, under realistic reaction conditions, for monomodal populations of precisely defined gold particles in the nanometer size range, as a function of decreasing particle size. We study the effects of the CO oxidation reaction on the size distributions and atomic structures of mass-selected Au(561±13), Au(923±20) and Au(2057±45) clusters supported on amorphous carbon films.

Hybrid atomic structure of the Schmid cluster Au55(PPh3)12Cl6 resolved by aberration-corrected STEM.

We have investigated the atomic structure of the Au55(PPh3)12Cl6 Schmid cluster by using aberration-corrected scanning transmission electron microscopy (STEM) combined with multislice simulation of STEM images. Atom counting was employed, with size-selected clusters as mass standards, to "fractionate" the correct cluster size in the image analysis. Systematic structure analysis shows that a hybrid structure, predicted by density functional theory, best matches nearly half the clusters observed.

The effects of 1-pentyne hydrogenation on the atomic structures of size-selected Au(N) and Pd(N) (N = 923 and 2057) nanoclusters.

We report an investigation into the effects of the vapour-phase hydrogenation of 1-pentyne on the atomic structures of size-selected Au and Pd nanoclusters supported on amorphous carbon films. We use aberration-corrected high-angle annular dark field (HAADF) scanning transmission electron microscopy (STEM) to image populations of the nanoclusters at atomic resolution, both before and after the reaction, and we assign their atomic structures by comparison with multi-slice image simulations over a full range of cluster orientations. Gold nanoclusters consisting of 923 ± 20 and 2057 ± 45 atoms are found to be robust, exhibiting high structural stability.

Au40(SR)24 cluster as a chiral dimer of 8-electron superatoms: structure and optical properties.

We predict and analyze density-functional theory (DFT)-based structures for the recently isolated Au(40)(SR)(24) cluster. Combining structural information extracted from ligand-exchange reactions, circular dichroism and transmission electron microscopy leads us to propose two families of low-energy structures that have a chiral Au-S framework on the surface. These families have a common geometrical motif where a nonchiral Au(26) bi-icosahedral cluster core is protected by 6 RS-Au-SR and 4 RS-Au-SR-Au-SR oligomeric units, analogously to the "Divide and Protect" motif of known clusters Au(25)(SR)(18)(-/0), Au(38)(SR)(24) and Au(102)(SR)(44).