Stability Of Nanoclusters Research Articles

Is the kernel-staples match a key-lock match?

Metal nanoclusters provide excellent references for understanding metal nanoparticle surfaces, which remain mysterious due to the difficulty of atomically precise characterization. Although some remarkable advances have been achieved for understanding the structure of metal nanoclusters, it is still unknown if the inner kernel-outer staples match is a key-lock match and how the surface staples influence some of the properties of metal nanoclusters. Herein, we have developed an acid-induction method for synthesizing a novel gold nanocluster whose composition is determined to be Au42(TBBT)26 (TBBT: 4-tert-butylbenzenelthiolate) by ESI-MS and single-crystal X-ray crystallography (SCXC). SCXC also reveals that Au42(TBBT)26 has an identical kernel but different staples with an existing gold nanocluster Au44(TBBT)28, indicating that the kernel-staples match is not a key-lock match and the existence of homo-ligand-homo-kernel-hetero-staples phenomenon in metal nanoclusters provides some reference for understanding the growth or transformation of metal nanoclusters. Further experiments reveal that the staples greatly contribute to the stability of gold nanoclusters and influence their photoluminescence intensity and that minute differences in the interfacial structure can lead to enhanced stability and photoluminescence.

Stable and oxidant responsive zwitterionic nanoclusters.

Zwitterions are promising ligands for the fabrication of non-toxic and non-interacting biomaterials. Sulfonamide-based monothiol zwitterionic ligands on gold nanocluster (AuNC) surfaces provide nanomaterials with stable colloidal properties and intense red emission in biological environments. The fluorescence intensity of the nanocluster can be modulated by reactive oxygen species (e.g. ˙OH), allowing for quantitative and selective sensing of antioxidants (e.g. ascorbic acid) in real time.

Ag15(N-triphos)4(Cl4)](NO3)3: a stable Ag-P superatom with eight electrons (N-triphos = tris((diphenylphosphino)methyl)amine).

A first and stable Ag-P superatom nanocluster [Ag15(N-triphos)4(Cl4)](NO3)3 (1) has been successfully synthesized and characterized. X-ray analysis shows that this Ag15 cluster has a hexacapped body-centered cubic (bcc) framework which is consolidated by four tripodal N-triphos ligands. The identity of 1 is confirmed by high resolution ESI-MS. Cluster 1 has an electronic and geometric shell closure structure with 8 free electrons, matching the stability idea of superatom theory for a nanocluster. DFT calculation of this Ag15 cluster reveals the superatom feature with a 1S21P6 configuration. The chelation of multidentate phosphines enhances the stability of this Ag15 cluster. The AgAg distances between the centered and the vertical Ag atoms of this bcc (Ag@Ag8) are in the range of 2.57-2.71 Å, and the distances between the face-capped and the vertical silver atoms are in the range of 2.84-2.92 Å, showing strong AgAg interactions within this cluster core. This superatom complex exhibits a relatively high thermal and photolytic stability.

New stable isomorphous Ag34 and Ag33Au nanoclusters with an open shell electronic structure.

A novel atom-precise 3-electron homosilver nanocluster (Ag34) has been assembled for the first time by the oxidation of a thiol. When adding AuPPh3Cl in the reaction, we obtained an alloyed Ag33Au nanocluster, which shares a similar framework as that of Ag34, in which a doping Au atom replaced a core silver atom. Notably, both Ag34 and alloyed Ag33Au demonstrated exceptional stability in solution and solid state over 3 months, which is difficult to explain by using the superatom model. Such Ag34 and Ag33Au complexes complement the nanoclusters with an open shell electronic structure and unveil a new approach to synthesize monodisperse nanoclusters under mild conditions.

Polyglycerol grafting and RGD peptide conjugation on MnO nanoclusters for enhanced colloidal stability, selective cellular uptake and cytotoxicity

An efficient surface engineering strategy for MnO nanoparticles was developed to attain enhanced colloidal stability, selective uptake by and toxicity to specific cancer cells. Specifically, MnO nanoclusters prepared by polyol method were grafted with polyglycerol (MnO-PG), and then conjugated with arginine-glycine-aspartate peptide (MnO-PG-RGD) through stepwise organic reactions. The physicochemical properties of the surface engineered MnO nanoclusters were characterized by powder X-ray diffraction, Fourier transform infrared spectroscopy, thermogravimetric analysis, dynamic light scattering, zeta potential, transmission electron microscopy and high-resolution transmission electron microscopy. The grafted PG layer not only largely enhanced the dispersibility and colloidal stability of MnO nanoclusters in physiological media, but also effectively inhibited non-specific cellular uptake of MnO-PG. MnO-PG-RGD was selectively taken up by human glioblastoma U87MG cells overexpressing αvβ3 integrins through receptor-mediated endocytosis. The internalized MnO-PG-RGD was mainly located in the lysosomes of U87MG cells. The acidity of lysosomes accelerated Mn2+ ions releasing, which promoted intracellular oxidative stress and further led to cell damage and apoptosis. The results indicate that appropriate surface functionalization can enable MnO nanoparticles to act as a potential anticancer agent in addition to their MRI functionality.

Thermal stability of Pt nanoclusters interacting to carbon sublattice

The catalytic activity of Pt clusters is dependent not only on the nanoparticle size and its composition, but also on its internal structure. To determine the real structure of the nanoparticles used in catalysis, the boundaries of the thermal structure stability of Pt clusters to 8.0 nm in diameter interacting with carbon substrates of two types: a fixed α-graphite plane and a mobile substrate with the diamond structure. The effect of a substrate on the processes melting of Pt nanoclusters is estimated. The role of the cooling rate in the formation of the internal structure of Pt clusters during crystallization is studied. The regularities obtained in the case of “free” Pt clusters and Pt clusters on a substrate are compared. It is concluded that platinum nanoparticles with diameter D ≤ 4.0 nm disposed on a carbon substrate conserve the initial fcc structure during cooling.

Two-Way Transformation between fcc- and Nonfcc-Structured Gold Nanoclusters.

Precisely tuning the structure of nanomaterials, especially in a two-way style, is challenging but of great importance for regulating properties and for practical applications. The structural transformation from nonfcc to fcc (face center cubic) in gold nanoclusters has been recently reported; however, the reverse process, that is, the structural transformation from fcc to nonfcc, not to mention the two-way structural transformation between fcc and nonfcc, remains unknown. We developed a novel synthesis method, successfully fulfilled the two-way structure transformation, and studied the stability of gold nanoclusters with different structures. Additionally, a novel gold nanocluster was synthesized and structurally resolved by single-crystal X-ray crystallography. This work has important implications for structure and property tuning of gold nanoclusters and might open up some new potential applications for gold nanoclusters.

Diameter controlled growth of SWCNTs using Ru as catalyst precursors coupled with atomic hydrogen treatment

In this work, we present a practical approach for controlling single walled carbon nanotubes (SWCNTs) diameter distribution through thin film Ru catalyst, coupled with hydrogen pre-treatment. Uniform and stable Ru nanoclusters were obtained after dewetting the Ru thin films under atomic hydrogen pre-treatment. SWCNTs were synthetized by double hot filament chemical vapor deposition (d-HFCVD) on SiO2/Si substrates at different temperatures. We found that the temperature is an important synthesis parameter that influences the diameter distribution of the final SWCNTs. Statistical analysis of the Raman radial breathing modes evidences the growth of highly enriched semi-conducting SWCNTs (about 90%) with narrow diameter distribution that correlates directly with the catalyst particle size distribution. Electrical measurement results on as-grown SWCNTs show good thin-film transistor characteristics.

On the stability of noble-metal nanoclusters protected with thiolate ligands(a)(a)Contribution to the Focus Issue Self-assemblies of Inorganic and Organic Nanomaterials edited by Marie-Paule Pileni.

Noble metal nanoclusters (NCs) protected with thiolate ligands have been of interest because of their long-term stability that makes them suitable as building blocks for diverse assembled systems with emergent and improved functions. Despite the advances in synthesis and characterization, the mechanisms that contribute to their stability are still poorly understood. In this article, we review the different criteria that have been used to explain the experimental stability of NCs with a well-defined number of atoms that are protected with thiolate ligands. We discuss why these criteria are not enough to explain the stability. We conclude that there are other physical factors that should be included when explaining the stability of these systems and could be important for the discovery of new noble-metal NCs.

Growth and Stability of Titanium Dioxide Nanoclusters on Graphene/Ru(0001).

Titanium dioxide/graphene composites have recently been demonstrated to improve the photocatalytic activity of TiO2 in visible light. To better understand the interactions of TiO2 with graphene we have investigated the growth of TiO2 nanoclusters on single-layer graphene/Ru(0001) using scanning tunneling microscopy (STM) and Auger electron spectroscopy (AES). Deposition of Ti in the O2 background at 300 K resulted in the formation of nanoclusters nucleating on intrinsic defects in the graphene (Gr) layer. The saturation nanocluster density decreased as the substrate temperature was increased from 300 to 650 K, while deposition at 700 K resulted in the significant etching of the Gr layer. We have also prepared nanoclusters with Ti2O3 stoichiometry using lower O2 pressures at 650 K. Thermal stability of the TiO2 nanoclusters prepared at 300 K was evaluated with AES and STM. No change in oxidation state for the TiO2 nanoclusters or etching of the Gr layer was observed up to ∼900 K. Annealing studies revealed that cluster ripening proceeds via a Smoluchowski mechanism below 800 K. Above 800 K, the changes in cluster shapes indicate an onset of diffusion within the clusters. At even higher temperatures, the nanoclusters undergo reduction to TiOx (x ≈ 1-1.5) which is accompanied by oxidation and etching of the Gr. Our studies demonstrate that highly thermally stable TiOx nanoclusters of controlled composition and morphology can be prepared on Gr supports.

Supported Dendrimer-Encapsulated Metal Clusters: Toward Heterogenizing Homogeneous Catalysts.

Recyclable catalysts, especially those that display selective reactivity, are vital for the development of sustainable chemical processes. Among available catalyst platforms, heterogeneous catalysts are particularly well-disposed toward separation from the reaction mixture via filtration methods, which renders them readily recyclable. Furthermore, heterogeneous catalysts offer numerous handles-some without homogeneous analogues-for performance and selectivity optimization. These handles include nanoparticle size, pore profile of porous supports, surface ligands and interface with oxide supports, and flow rate through a solid catalyst bed. Despite these available handles, however, conventional heterogeneous catalysts are themselves often structurally heterogeneous compared to homogeneous catalysts, which complicates efforts to optimize and expand the scope of their reactivity and selectivity. Ongoing efforts in our laboratories are aimed to address the above challenge by heterogenizing homogeneous catalysts, which can be defined as the modification of homogeneous catalysts to render them in a separable (solid) phase from the starting materials and products. Specifically, we grow the small nanoclusters in dendrimers, a class of uniform polymers with the connectivity of fractal trees and generally radial symmetry. Thanks to their dense multivalency, shape persistence, and structural uniformity, dendrimers have proven to be versatile scaffolds for the synthesis and stabilization of small nanoclusters. Then these dendrimer-encapsulated metal clusters (DEMCs) are adsorbed onto mesoporous silica. Through this method, we have achieved selective transformations that had been challenging to accomplish in a heterogeneous setting, e.g., π-bond activation and aldol reactions. Extensive investigation into the catalytic systems under reaction conditions allowed us to correlate the structural features (e.g., oxidation states) of the catalysts and their activity. Moreover, we have demonstrated that supported DEMCs are also excellent catalysts for typical heterogeneous reactions, including hydrogenation and alkane isomerization. Critically, these investigations also confirmed that the supported DEMCs are heterogeneous and stable against leaching. Catalysts optimization is achieved through the modulation of various parameters. The clusters are oxidized (e.g., with PhICl2) or reduced (e.g., with H2) in situ. Changing the dendrimer properties (e.g., generation, terminal functional groups) is analogous to ligand modification in homogeneous catalysts, which affect both catalytic activity and selectivity. Similarly, pore size of the support is another factor in determining product distribution. In a flow reactor, the flow rate is adjusted to control the residence time of the starting material and intermediates, and thus the final product selectivity. Our approach to heterogeneous catalysis affords various advantages: (1) the catalyst system can tap into the reactivity typical to homogeneous catalysts, which conventional heterogeneous catalysts could not achieve; (2) unlike most homogeneous catalysts with comparable performance, the heterogenized homogeneous catalysts can be recycled; (3) improved activity or selectivity compared to conventional homogeneous catalysts is possible because of uniquely heterogeneous parameters for optimization. In this Account, we will briefly introduce metal clusters and describe the synthesis and characterizations of supported DEMCs. We will present the catalysis studies of supported DEMCs in both the batch and flow modes. Lastly, we will summarize the current state of heterogenizing homogeneous catalysis and provide future directions for this area of research.

Thermodynamic stability of ligand-protected metal nanoclusters

Despite the great advances in synthesis and structural determination of atomically precise, thiolate-protected metal nanoclusters, our understanding of the driving forces for their colloidal stabilization is very limited. Currently there is a lack of models able to describe the thermodynamic stability of these ‘magic-number’ colloidal nanoclusters as a function of their atomic-level structural characteristics. Herein, we introduce the thermodynamic stability theory, derived from first principles, which is able to address stability of thiolate-protected metal nanoclusters as a function of the number of metal core atoms and thiolates on the nanocluster shell. Surprisingly, we reveal a fine energy balance between the core cohesive energy and the shell-to-core binding energy that appears to drive nanocluster stabilization. Our theory applies to both charged and neutral systems and captures a large number of experimental observations. Importantly, it opens new avenues for accelerating the discovery of stable, atomically precise, colloidal metal nanoclusters.

Novel electrochemiluminescence of silver nanoclusters fabricated on triplex DNA scaffolds for label-free detection of biothiols

Electrochemiluminescence (ECL) of metal nanoclusters and their application have been widely reported due to the good biocompatibility, fascinating electrocatalytic activity and so on. Using DNA as synthesis template opens new opportunities to modulate the physical properties of AgNCs. Triplex DNA has been reported for the site-specific, homogeneous and highly stable silver nanoclusters (AgNCs) fabrication from our recent research. Here we further explore their extraordinary ECL properties and applications in biosensor utilization. By reasonable design of DNA sequence, AgNCs were obtained in the predefined position of CG.C+ sites of triplex DNA, and the ECL emission at a low potential was observed with this novel DNA template. Finally, a simple and label-free method was developed for biothiols detection based on the enhanced catalytic reaction and a robust interaction between the triplex-AgNCs and cysteine, by influencing the microenvironment provided by DNA template.

Au@Void@Ag Yolk-Shell Nanoclusters Visited by Molecular Dynamics Simulation: The Effects of Structural Factors on Thermodynamic Stability.

Au@void@Ag yolk-shell nanoclusters were studied by molecular dynamics simulation in order to study the effects of core and shell sizes on their thermodynamic stability and structural transformation. The results demonstrated that all of simulated nanoclusters with different core and shell sizes are unstable at temperatures lower than 350 K in such a way that Ag atoms are collapsed into the void space and fill it, which leads to creation of a more stable core-shell morphology, and at the melting point, only core-shell structures with altered thickness of the shell exist. Also, at higher temperatures, Au atoms tend to migrate toward the surface, and an increase of both the core and shell sizes leads to an increase of the thermodynamic stability. Moreover, a Au147@void@Ag252 nanocluster with the largest core and shell and minimum void space exhibited the most thermodynamic stability and highest melting point. Generally, the core and shell sizes affect the stability and thermal behavior of yolk-shell nanoclusters cooperatively.

Thermal stabilities of iron nanoparticles under hydrostatic pressure

The present study aimed to apply molecular dynamics simulation to study the thermal stability and melting behavior of bcc iron nanoclusters under the pressure of up to 40 GP. Several factors were calculated, including the bulk modulus, melting temperature, melting enthalpy changes, melting volume changes and radial distribution function. In addition, size effects were investigated in the melting process. The bulk modulus was observed to raise a thigh external pressure and decrease in enlarged sizes. Pressure and size were significant determinants of the melting temperature. In the melting process, rate of enthalpy changes increased with greater pressure and size, while the volume changes reduced at higher pressure and size. On the other hand, small nanocluster size augmented the ΔVm slope. Finally, g(r) values of the first shell declined with greater nanocluster sizes, and iron atoms appeared closer in the nanocluster structure at high pressure.

Stability of nanoclusters in an oxide dispersion strengthened alloy under neutron irradiation

Here, we report atom probe tomography results of the nanoclusters in a neutron-irradiated oxide dispersion strengthened alloy. Following irradiation to 5dpa at target temperatures of 300°C and 450°C, fewer large nanoclusters were found and the residual nanoclusters tend to reach an equilibrium Guinier radius of 1.8nm. With increasing dose, evident decrease in peak oxygen and titanium (but not yttrium) concentrations in the nanoclusters was observed, which was explained by atomic weight, solubility, diffusivity, and chemical bonding arguments. The chemical modifications indicate the equilibrium size is indeed a balance of two competing processes: radiation enhanced diffusion and collisional dissolution.

Insight from first principles into the stability and magnetism of alkali-metal superoxide nanoclusters

Alkali-metal superoxides are gaining increasing interest as 2p magnetic materials for information and energy storage. Despite significant research efforts on bulk materials, gaps in our knowledge of the electronic and magnetic properties at the nanoscale still remain. Here, we focused on the role that structural details play in determining stability, electronic structure, and magnetic couplings of (MO2)n (M = Li, Na, and K, with n = 2–8) clusters. Using first-principles density functional theory based on the Perdew-Burke-Ernzerhof and Heyd-Scuseria-Ernzerhof functionals, we examined the effect of atomic structure on the relative stability of different polymorphs within each investigated cluster size. We found that small clusters prefer to form planar-ring structures, whereas non-planar geometries become more stable when increasing the cluster size. However, the crossover point depends on the nature of the alkali metal. Our analysis revealed that electrostatic interactions govern the highly ionic M–O2 bonding and ultimately control the relative stability between 2-D and 3-D geometries. In addition, we analyzed the weak magnetic couplings between superoxide molecules in (NaO2)4 clusters comparing model Hamiltonian methods based on Wannier function projections onto πg states with wave function-based multi-reference calculations.

Enhancement of fluorescence brightness and stability of copper nanoclusters using Zn2 + for ratio-metric sensing of S2 −

It is acknowledged water soluble copper nanoclusters (Cu NCs) are extremely unstable in aqueous solutions, which limit their fluorescence applications to a great extent. In this work, it is found the fluorescence intensity and stability of water soluble Cu NCs could obviously be enhanced by the introduction of Zn2+. Then, the as modified Cu NCs will be stable enough to be applied as a ratio-metric sensor for S2−. This method may provide more broaden avenues for the application of fluorescent Cu NCs in the future.

Novel Preparation of Titania-Modified CMK-3 Nanostructured Material as Support for Ir Catalyst Applied in Hydrodenitrogenation of Indole

Iridium catalyst was prepared using a novel titanium oxide-CMK-3 support synthesized as a replica of Ti-SBA-15. The catalyst was applied in the hydrodenitrogenation of indole. The activity was compared with an iridium catalyst supported over a grafted titanium-CMK-3. Structural and textural characterization of the catalysts was performed by means of N2 adsorption, XRD, UV–Vis–DRS, Raman spectroscopy, XPS, TEM and H2 Chemisorption. Ir-Ti-CMK-3 was the most active catalyst for the hydrodenitrogenation reaction at mild conditions. Titanium oxide contained in carbon ordered mesoporous CMK-3 promotes a very good anchorage of iridium metallic clusters in the carbon framework reaching high active site distribution and more stable nanoclusters.

Parallel tempering Monte Carlo combined with clustering Euclidean metric analysis to study the thermodynamic stability of Lennard-Jones nanoclusters.

A basic requirement for an atom-level understanding of nanoclusters is the knowledge of their atomic structure. This understanding is incomplete if it does not take into account temperature effects, which play a crucial role in phase transitions and changes in the overall stability of the particles. Finite size particles present intricate potential energy surfaces, and rigorous descriptions of temperature effects are best achieved by exploiting extended ensemble algorithms, such as the Parallel Tempering Monte Carlo (PTMC). In this study, we employed the PTMC algorithm, implemented from scratch, to sample configurations of LJn (n=38, 55, 98, 147) particles at a wide range of temperatures. The heat capacities and phase transitions obtained with our PTMC implementation are consistent with all the expected features for the LJ nanoclusters, e.g., solid to solid and solid to liquid. To identify the known phase transitions and assess the prevalence of various structural motifs available at different temperatures, we propose a combination of a Leader-like clustering algorithm based on a Euclidean metric with the PTMC sampling. This combined approach is further compared with the more computationally demanding bond order analysis, typically employed for this kind of problem. We show that the clustering technique yields the same results in most cases, with the advantage that it requires no previous knowledge of the parameters defining each geometry. Being simple to implement, we believe that this straightforward clustering approach is a valuable data analysis tool that can provide insights into the physics of finite size particles with few to thousand atoms at a relatively low cost.