Ag Clusters Research Articles

Spatial Confinement of Li Metal in Hollow Microcapsule Hosts Enabled by Heteroatom-Driven Inward Growth

In recent years, the demand for advanced batteries with high energy densities has increased significantly, along with the growing demand for electric vehicles. Li metal has garnered considerable research attention as a promising anode material because of its high theoretical specific capacity (3860 mAh g−1) and low electrochemical equilibrium potential (−3.040 V vs. standard hydrogen electrode). However, Li metal batteries still have several hurdles in their practical application because Li metal anodes experience infinite volume expansion, which induces continuous rupture and formation of solid-electrolyte interphase (SEI) layers. This leads to electrolyte consumption and corrosion of Li metal, resulting in a low Coulombic efficiency and poor cycling performance. In addition, the uncontrollable dendrite growth of Li metal may cause early battery failure and safety issues. To address these problems, extensive research efforts have been made, including artificial SEI layers, optimized electrolyte formula, and rational design of three-dimensional (3D) host materials.Among the various 3D host materials under development, carbon-based materials with hollow structures have been investigated extensively because of their attractive features. The enlarged void space (cavity) of the hollow hosts can accommodate a significant amount of Li deposits, while inhibiting volume changes during plating–stripping cycles. In addition, hollow carbon possesses much lower density than metal-based materials, thereby increasing the specific capacity and energy density. However, the lithiophobic nature of carbon combined with its high resistance to Li+ transport through nanopores on the walls significantly hinders the formation of Li deposits inside the cavity. Li may nucleate on the outer surface of the carbon particles in a nonuniform manner, thereby causing the growth of Li dendrites and electrochemically inactive Li deposits.In this study, we synthesize metal-organic framework-derived carbon microcapsules with heteroatom clusters (Zn and Ag) on the capsule walls and demonstrate that Ag-assisted nucleation of Li metal alters the outward-to-inward growth in the microcapsule host. The cavity inside the microcapsule host, which was generated by etching with tannic acid, provides large void spaces for Li metal storage. Atomic Ag clusters decorated by a galvanic displacement reaction serve as preferential nucleation sites with a reduced energy barrier and promote the inward growth of Li metal in the cavity, while suppressing nonuniform Li plating on the outer surface. Through combined electrochemical, microstructural, and simulation studies, we verify the beneficial role of Ag-assisted Li nucleation in facilitating inward growth inside the cavity of the microcapsule host, resulting in enhanced electrochemical performance. This study provides new insights into the design of reversible host materials for practical Li-metal batteries.

Photophysical Properties of Silver Clusters in Faujasite Zeolites: Does the Crystal Size Matter?

Electrostatic interactions between the zeolite cavity and confined noble-metal nanoparticles govern the photophysical properties of these materials. A better understanding of these interactions can afford new perspectives in optoelectronics applications. We investigated this interplay by revealing the peculiar photophysical properties of Ag clusters embedded in nanosized faujasite zeolite structures. Crystal size and steady state optical properties were characterized via integrated light and electron microscopy (ILEM) and steady state spectroscopy. Extensive time-resolved spectroscopy experiments performed on femtosecond to millisecond time scales revealed excited state dynamics that are intriguingly different from those observed for their micrometer sized counterpart. Multiscale modeling investigations were performed to rationalize the effect of the crystal size on the photophysical properties. Our results indicate that for the nanosized crystals, the emissive properties as well as the radiative and nonradiative processes involving the Ag clusters are dramatically dependent on the surface charge density and surface charge balance.

Locating Interstitial Hydrides in MH2@Cu14 (M = Cu, Ag) Clusters by Single-Crystal X-ray Diffraction.

Two structures, [Cu15H2(S2CNnBu2)6(C≡CPh)6][CuCl2] (1) and [AgH2Cu14{S2P(OiPr)2}6(C≡CPh)6][PF6] (2), are characterized by X-ray crystallography with high-quality single crystals. The position of interstitial hydrides can be accurately located. In addition, the refinement of the hydrides with anisotropic displacement parameters (ADPs) was successful. The distances between the central atom and copper atoms, as well as the distances within the metal cages surrounding the hydrides, are analyzed and compared with similar MH2@Cu14 (M = Cu, Ag, Pd) compounds. This work provides a thoughtful and accurate assessment of the considerations and challenges associated with anisotropic refinement for H atoms, particularly in X-ray data collection.

Coalescing Dynamics between Ag55 and Cu55 Clusters as Well as Thermodynamics during Cooling the Coalesced Clusters from Atomic Simulations.

Molecular dynamics simulations are performed to investigate the coalescing processes between a Cu55 cluster with a liquid, FCC, or Ih structure and a Ag55 cluster in liquid, as well as the structural changes of the coalesced clusters during the cooling process. The simulation results show that the initial structure of the Ag and Cu clusters significantly affects the coalescence stages and the structures after coalescence. There are apparent rotations of the Ag cluster with the liquid structure relative to the Cu cluster with the liquid structure when they are approaching. Before the formation of a neck, the Cu cluster with the Ih structure is more stable and less likely to lose its structure compared to the Cu cluster with the FCC structure. During the cooling process, the coalesced clusters will form different packing structures, including Ih and metastable core/shell structures. The Lode-Nadai values reveal the loading states on the atoms when the two clusters collide. The thermodynamic behaviors during the cooling process were investigated to better understand the order degree of the packing structures and the structural transition processes.

Hydride Locations and Planar σ‐Aromaticity in Hydrido‐Coinage‐Metal Clusters

AbstractThe atomic‐scale analysis of hydrides within metal clusters remains challenging due to the difficulties in performing spatially resolved characterization experiments. One important issue is understanding how hydrogens bond to metal atoms and their positions. The classification of hydride as either a ligand or doped metal is a difficult problem due to its different impacts on electronic structures of coinage metal (Cu, Ag, and Au) clusters. Here, geometric characteristics, stability and electronic properties of MnH (M=Cu, Ag and Au; n=2–9) clusters are investigated in detail. We find that structure transitions of CunH and AgnH occur at n=5, while all AunH are more inclined to planar configurations, where H atoms prefer to be located on the bridge positions of M−M regardless of different sizes and configurations. Among them, the planar M5H clusters have the same structural framework and higher stability than their neighbors. The AIMD simulations demonstrate that these three clusters still show excellent thermal stability at 700 K. The molecular orbitals and AdNDP analyses reveal that the M5H clusters exhibit three six‐center two‐electron σ bonds throughout whole structural spaces and conform to σ aromaticity rule, which are also further confirmed by the ELF, LOL and NICSzz‐scan analyses.

Fabrication and Characterization of Hybrid and Tunable ZnO@Ag Flexible Thin Films Used as SERS Substrates

Flexible substrates have known increased popularity over rigid ones due to their use in surface-enhanced Raman scattering (SERS). They provide irregular surfaces, ideal for in situ sensing. In this context, we report the SERS performance of hybrid ZnO@Ag thin films deposited by magnetron sputtering (MS) on flexible, thermoplastic substrates. This physical deposition method is acknowledged for obtaining high-quality and reproducible ZnO films that can be embedded in (bio)sensing devices with various applications. Three types of thermoplastic-based, commercially available substrates with different glass transition temperatures (Tg) were chosen for the variation in flexibility, transparency, and thickness. Zeonor® (Tg = 136 °C, thickness of 188 μm) and two types of Topas (Topas®: Tg = 142 °C, thickness of 176 μm; Topas2: Tg = 78 °C, thickness of 140 μm) thermoplastic sheets are nonpolar and amorphous cyclo-olefin polymer (COP) and cyclo-olefin copolymers (COC), respectively. Their thicknesses and different values of Tg can greatly affect the topographical and roughness properties of films with small thicknesses and, thus, can greatly influence the enhancement of the Raman signal. The ZnO films deposited on top of Zeonor® or Topas® have identical morphological properties, as shown by the scanning electron microscopy (SEM) characterization. Subsequently, by using the MS technique, we tuned the thickness of the deposited silver (Ag) films in the range of 7–30 nm to assess the growth influence on the morphology and the SERS signal amplification of the substrates with and without the ZnO intermediate layer. The SEM analysis showed that the Ag atoms migrated both into the interstitial areas, filling the voids between the ZnO granular structures, and over the latter, forming, in this case, isolated Ag clusters. SERS analysis performed on the ZnO-Ag hybrid films using crystal violet (CV) molecule revealed a limit of detection (LOD) of 10−7 M in the case of 15 nm thick Ag/Zeonor® interlayer films ZnO and relative standard deviation (RSD) below 10%.

Lipid-driven interleaflet coupling of plasma membrane order regulates FcεRI signaling in mast cells

Interleaflet coupling—the influence of one leaflet on the properties of the opposing leaflet—is a fundamental plasma membrane organizational principle. This coupling is proposed to participate in maintaining steady-state biophysical properties of the plasma membrane, which in turn regulates some transmembrane signaling processes. A prominent example is antigen (Ag) stimulation of signaling by clustering transmembrane receptors for immunoglobulin E (IgE), FcεRI. This transmembrane signaling depends on the stabilization of ordered regions in the inner leaflet for sorting of intracellular signaling components. The resting inner leaflet has a lipid composition that is generally less ordered than the outer leaflet and that does not spontaneously phase separate in model membranes. We propose that interleaflet coupling can mediate ordering and disordering of the inner leaflet, which is poised in resting cells to reorganize upon stimulation. To test this in live cells, we first established a straightforward approach to evaluate induced changes in membrane order by measuring inner leaflet diffusion of lipid probes by imaging fluorescence correlation spectroscopy, by imaging fluorescence correlation spectroscopy (ImFCS), before and after methyl-α-cyclodexrin (mαCD)-catalyzed exchange of outer leaflet lipids (LEX) with exogenous order- or disorder-promoting phospholipids. We examined the functional impact of LEX by monitoring two Ag-stimulated responses: recruitment of cytoplasmic Syk kinase to the inner leaflet and exocytosis of secretory granules (degranulation). Based on the ImFCS data in resting cells, we observed global increase or decrease of inner leaflet order when outer leaflet is exchanged with order- or disorder-promoting lipids, respectively. We find that the degree of both stimulated Syk recruitment and degranulation correlates positively with LEX-mediated changes of inner leaflet order in resting cells. Overall, our results show that resting-state lipid ordering of the outer leaflet influences the ordering of the inner leaflet, likely via interleaflet coupling. This imposed lipid reorganization modulates transmembrane signaling stimulated by Ag clustering of IgE-FcεRI.

Designing of surface chemical enhanced Raman AgCu and AuCu clusters: Density functional theory

Designing of surface-enhanced Raman material with low cost and high enhancement ability become animportant research direction in the field of surface-enhanced Raman scattering. In this paper, the density functional theory calculations were utilized to investigated the Raman performances of stabled CuAg and CuAu clusters for 4-NBT probe molecule. Some suitable alloying designs in atomic level were found to reduce cost and enhance Raman signal of noble nanoparticles, such as, a small quantity introduction of Cu element into the tip of Ag nanoparticle surface and the core–shell structure. The designed Cu2Ag2, Cu1Ag12, Cu1Au12, Cu3Ag10, Cu3Au10, Cu14Ag9, Cu4Au9, Cu9Au4 and Cu10Au3 clusters exhibited enhanced Raman diffraction peak intensity beyond 11.0% compared to the 4-NBT molecule on the Ag4, Ag13 and Au13 clusters. This strategy could be applied to designing noble metal based surface-enhanced Raman materials with low cost and high enhancement ability by adjusting the atom site in atomic level.

Time Evolution of Plasmonic Features in Pentagonal Ag Clusters.

In the present work, we apply recently developed real-time descriptors to study the time evolution of plasmonic features of pentagonal Ag clusters. The method is based on the propagation of the time-dependent Schrödinger equation within a singly excited TDDFT ansatz. We use transition contribution maps (TCMs) and induced density to characterize the optical longitudinal and transverse response of such clusters, when interacting with pulses resonant with the low-energy (around 2-3 eV, A1) size-dependent or the high-energy (around 4 eV, E1) size-independent peak. TCMs plots on the analyzed clusters, Ag25+ and Ag43+ show off-diagonal peaks consistent with a plasmonic response when a longitudinal pulse resonant at A1 frequency is applied, and dominant diagonal spots, typical of a molecular transition, when a transverse E1 pulse is employed. Induced densities confirm this behavior, with a dipole-like charge distribution in the first case. The optical features show a time delay with respect to the evolution of the external pulse, consistent with those found in the literature for real-time TDDFT calculations on metal clusters.

Photoluminescence Anisotropy in Eutectic Crystals of Polynuclear Lanthanide Complexes and Silver Clusters

AbstractAnisotropy is an intrinsic property of crystalline materials. However, the photoluminescence anisotropy in eutectic crystals of organometallic complexes has remained unexplored. Herein, the eutectic of polynuclear lanthanide complexes and Ag clusters was prepared, and the crystal shows significant photoluminescence anisotropy. The polarization anisotropy of emission δ and degree of excitation polarization P are 2.62 and 0.53, respectively. The rare excitation polarization properties have been proved to be related to the regular arrangement of electric transition dipole moments of luminescent molecules in the crystal. Our design provides a reference for developing new photoluminescence anisotropy materials and expanding their applications.

Photoluminescence Anisotropy in Eutectic Crystals of Polynuclear Lanthanide Complexes and Silver Clusters.

Anisotropy is an intrinsic property of crystalline materials. However, the photoluminescence anisotropy in eutectic crystals of organometallic complexes has remained unexplored. Herein, the eutectic of polynuclear lanthanide complexes and Ag clusters was prepared, and the crystal shows significant photoluminescence anisotropy. The polarization anisotropy of emission δ and degree of excitation polarization P are 2.62 and 0.53, respectively. The rare excitation polarization properties have been proved to be related to the regular arrangement of electric transition dipole moments of luminescent molecules in the crystal. Our design provides a reference for developing new photoluminescence anisotropy materials and expanding their applications.

Five new luminescent Pb(II) and Ag(I) coordination polymers based on 1-(4-carboxybenzyl)-1H-pyrazole-3,5-dicarboxylic acid and different neutral ligands

Five new coordination polymers (CPs), namely {Pb1.5(L)} (1), {Pb3(L)2(2,2′-bpy)·2·5H2O} (2), {[Pb(HL)(phen)]·H2O} (3), {Ag2(HL)} (4) and {Ag(H2L)(phen)} (5), have been constructed by using 1-(4-carboxybenzyl)-1H-pyrazole-3,5-dicarboxylic acid (H3L) as an organic ligand. Compound 1 reveals a three-dimensional (3D) (4,6,7)-connected framework with the point symbol of {410·65}{46}2{48·613}2. Compound 2 exhibits a novel (3,6)-connected 3D framework based on a trinuclear Pb(II) cluster with point symbol {42.6}2{44.62.88.10}. Compound 3 is a 1D chain that is further assembled into a 3D supramolecular framework by hydrogen-bonds. Compound 4 shows a (3,6)-connected 3D structure based on a tetranuclear Ag(I) cluster with {4·62}2{42·610·83} topology. Compound 5 is a 0D structure, and can be further expanded into a 3D supramolecular network by various weak interactions. The solid-state luminescent spectra have been measured at room temperature. The results show that compounds 1–5 exhibit strong luminescent emission in the visible region, and can be tunable by varying excitation wavelengths.

Silver Vapor Supersonic Jets: Expansion Dynamics, Cluster Formation, and Film Deposition.

Supersonic jets of metal vapors with carrier gas are promising for producing nanostructured metal films at relatively low source temperatures and high deposition rates. However, the effects of the carrier gas on the jet composition and expansion dynamics, as well as on film properties, remain virtually unexplored. In this work, the free-jet expansion of a mixture of silver vapor with helium in a rarefied regime at an initial temperature of 1373 K is investigated through mass spectrometry and direct-simulation Monte Carlo methods. Introducing the carrier gas into the source is found to result in a transition from a collisionless to a collision-dominated expansion regime and dramatic changes in the Ag jet, which becomes denser, faster, and more forward-directed. The changes are shown to be favorable for the formation of small Ag clusters and film deposition. At a fairly high helium flow, silver Ag2 dimers are observed in the jet, both in the experiment and the simulations, with a mole fraction reaching 0.1%. The terminal velocities of silver atoms and dimers are nearly identical, indicating that the clusters are likely formed due to the condensation of silver vapor in the expanding jet. A high potential of supersonic Ag-He jets for the deposition of nanostructured silver films is demonstrated. The deposited jet Ag2 dimers appear to serve as nucleation centers and, thus, allow for controlling the size of the produced surface nanostructures.

Effect of Ag addition on the oxidation behavior of CrAlN coating at elevated temperatures

The effect of oxidation temperature and amount of Ag addition on CrAlN coating was investigated in this study. No Ag and Ag-based CrAlN coatings were deposited on a substrate using a physical vapor deposition (PVD) technique. The coatings then were isothermally heated at 800 °C and 900 °C for the 2 hr. Interestingly it is found that even with a small difference in temperature (100 °C), CrAlNAg coating shows different nature of oxidation, mass gain curve, coating microstructure and surface morphology.Surface morphology revels the Ag clusters formation on the top associated with the high temperature heating. While cross-section morphology gives information about Ag distribution and oxides layer formation. Mass gain curve and EDS (Energy-dispersive X-ray spectroscopy) results revealed that the oxidation resistant behavior of the CrAlN coating was degrade with increasing Ag content and/or increasing oxidation temperature. Overall, the results suggest that the temperature has a significant effect on the microstructure and properties of Ag-based coatings, and optimizing the deposition temperature can improve the performance of these coatings in various applications.

Functionalization of metal-organic frameworks with metallic nanoclusters for ultra-sensitive monitoring of morphine in biological fluids

A reliable, fast, and cost-effective method of monitoring morphine (MO) concentration in biological fluids is highly desired in clinical and modern medicine. Nanotechnology has opened up new possibilities for developing morphine biosensors, but the most advanced electrodes available offer a detection limit (LOD) of ≥10 nM. This work introduces a new, ultrasensitive electrochemical biosensor based on microporous metal-organic frameworks (∼1100 cm2 g−1 surface area) modified by Ag clusters (∼2 nm) and functionalized by Au nanoparticles (∼180 nm). Electrochemical studies show that functionalizing the microporous crystalline particles (620 ± 45 nm) with metal nanoclusters enhances charge transfer kinetics and electrochemical surface area by about 50 and 10 folds, respectively, resulting in high sensitivity (0.127 µA µM−1), broad linear dynamic range (0.05–600 µM), and low LOD (3 ± 0.2 nM). The differential pulse voltammetry confirms the stability (over 6 weeks), repeatability (RSD=3.0%), and reproducibility (RSD=4.0%) of the hybrid biosensor. The decent selectivity and specificity (RSD=7.4%) of the biosensor against various analogs co-existing with MO in urine have also been determined. Therefore, the hybrid metal-inorganic biosensor presents a promising prospect for simple, low-cost, and precise monitoring of biomolecules, including morphine, in biological fluids and clinical medicine.

Concentration dependent SERS profile of p-tolyl 2-acetamido-3-(4-fluorophenyl)propanoate (AFP) in silver colloidal nanohydrosols: Experimental and DFT investigations

Based on Density Functional Theory (DFT) calculations and the Surface Enhanced Raman Scattering (SERS) technique, the adsorption properties of p-tolyl 2-acetamido-3-(4-fluorophenyl)propanoate (AFP) on silver surface were examined. The title compound, AFP showed balanced inhibition of acetyl- and butyrylcholinesterase along with mild cytotoxicity of HepG2 cells according to the previous study. After adsorption on silver surface, the structural properties of AFP exhibit a small modification, indicating an interaction between the AFP and Ag6 cluster. Experimental research on AFP and SERS spectra at various concentrations was conducted. Raman frequencies for AFP and AFP adsorbed on silver were computed. FMOs for AFP and AFP adsorbed on the silver surface were conducted. After AFP was adsorbed on the silver, the energy gap was dramatically lowered. The greater bioactivity of AFP is caused by the lowering energy gap, which denotes the electron delocalization. According to SERS spectrum analysis, AFP was adsorbed on silver with a tilted orientation. As a result, the current study has been used as a model system to comprehend how silver nanoprticles (NP) interact with AFP. Silver nanoparticles are successfully used for the treatment of different diseases alone or in association with other active components and the incorporation of AFP with silver nanocolloids will act as a nanodrug delivery system.

Elucidating the Structures of Intermediate Fragments during Stepwise Dissociation of Monolayer-Protected Silver Clusters.

Fragmentation dynamics of ligated coinage metal clusters reflects their structural and bonding properties. So far methodological challenges limited probing structures of the fragments. Herein, we resolve the geometric structures of the primary fragments of [Ag29 L12 ]3- , i.e. [Ag24 L9 ]2- , [Ag19 L6 ]- and [Ag5 L3 ]- (L is 1,3-benzene dithiolate). For this, we used trapped ion mobility mass spectrometry to determine collision cross sections of the fragments and compared them to structures calculated by density functional theory. We also report that following two sequential [Ag5 L3 ]- elimination steps, further dissociation of [Ag19 L6 ]- also involves a new channel of Ag2 loss and Ag-S and C-S bond cleavages. This reflects a competition between retaining the electronic stability of 8 e- superatom cluster cores and increasing steric strain of ligands and staples. These results are also of potential interest for future soft-landing deposition studies aimed at probing catalytic behavior of Ag clusters on supports.

Elucidating the Structures of Intermediate Fragments during Stepwise Dissociation of Monolayer‐Protected Silver Clusters

AbstractFragmentation dynamics of ligated coinage metal clusters reflects their structural and bonding properties. So far methodological challenges limited probing structures of the fragments. Herein, we resolve the geometric structures of the primary fragments of [Ag29L12]3−, i.e. [Ag24L9]2−, [Ag19L6]− and [Ag5L3]− (L is 1,3‐benzene dithiolate). For this, we used trapped ion mobility mass spectrometry to determine collision cross sections of the fragments and compared them to structures calculated by density functional theory. We also report that following two sequential [Ag5L3]− elimination steps, further dissociation of [Ag19L6]− also involves a new channel of Ag2 loss and Ag−S and C−S bond cleavages. This reflects a competition between retaining the electronic stability of 8 e− superatom cluster cores and increasing steric strain of ligands and staples. These results are also of potential interest for future soft‐landing deposition studies aimed at probing catalytic behavior of Ag clusters on supports.

Highly-Loaded Ag Clusters Prepared by Flame Synthesis

Highly-Loaded Ag Clusters Prepared by Flame Synthesis

Mechanical and Tribological Properties of Ag/TiBx Nanocomposite Thin Films with Strong Antibacterial Effect Prepared by Magnetron Co-Sputtering

The use of silver-based antimicrobial materials has been growing recently. Considering the threat of developing silver-resistant bacteria, it is essential to address the endurance of such materials and the amount of silver released into the environment. Here we report on a durable, antibacterial Ag/TiBx nanocomposite coating prepared by conventional magnetron sputtering. The coating consists of fine Ag clusters embedded in extremely hard, wear-resistant overstoichiometric TiBx, which serves as a protective matrix. The highest E. coli growth inhibition of 97% is observed for the coating containing 24 at.% of Ag. A strong antibacterial effect is also maintained after 45 days of immersion in the Luria–Bertani + 5% HNO3 solution. Despite a marked hardness decrease from 40 GPa for TiBx to 6.4 GPa for Ag/TiBx with 28 at.% of Ag, the coating maintains a good specific wear rate of 6 × 10−5 mm3/Nm. Moreover, the addition of Ag, which acts as a solid lubricant, decreases the coefficient of friction from 0.77 to 0.35, even at room temperature. Thanks to the combination of antibacterial properties and enhanced wear resistance, such material can find application as a protective coating for cutlery, door handles, water taps, and other daily-used objects in public areas.