Coinage Metal Clusters Research Articles

Gas Phase Reactions of Pristine and Single-Atom-Doped Copper and Silver Clusters: Probing Size-Dependent Stability and Novel Superatoms.

Gas phase reactions have been a subject of research interest, enabling reliable strategies to explore the stability and reactivity of metal clusters as well as to probe novel superatoms that form the building blocks to assemble new materials with tailored properties. Coinage metal clusters have attracted great research attention due to their simple electronic shell structures and rich photochemical and catalytic properties at relatively low cost. This perspective focuses on the recent progress made in studying the gas phase reactions of undamaged and single-atom-doped Cun±,0 and Agn±,0 clusters with O2, CO, and NO molecules. It covers various aspects, such as reaction mechanisms, relationships between structure and activity, control of reactivity by changing cluster size and composition, and the identification of novel superatoms (Cu18-, Ag13-, Ag17-, and Ag15O+). Lastly, we provide a detailed account of the obstacles and prospective avenues for future research in order to establish a connection between these findings and nanocluster systems that have practical applications.

Optical spectra of silver clusters and nanoparticles from 4 to 923 atoms from the TDDFT+U method

The localized surface-plasmon resonances of coinage-metal clusters and nanoparticles enable many applications, the conception and necessary optimization of which require precise theoretical description and understanding. However, for the size range from few-atom clusters through nanoparticles of a few nanometers, where quantum effects and atomistic structure play a significant role, none of the methods employed previously has been able to provide high-quality spectra for all sizes. The main problem is the description of the filled shells of d electrons which influence the optical response decisively. We show that the DFT+U method, employed with real-time time-dependent density-functional theory calculations (RT-TDDFT), provides spectra in good agreement with experiment for silver clusters ranging from 4 to 923 atoms, the latter representing a nanoparticle of 3 nm. Both the electron-hole-type discrete spectra of the smallest clusters and the broad plasmon resonances of the larger sizes are obtained. All calculations use the value of the effective U parameter that provides good results in bulk silver. The agreement with experiment for all sizes shows that the U parameter is surprisingly transferable. Our results open the pathway for calculations of many practically relevant systems including clusters coupled to bio-molecules or to other nano-objects.

LnIII/CuI Bimetallic Nanoclusters with Enhanced NIR-II Luminescence.

Coinage-metal clusters with excellent luminescence properties have attracted considerable interest due to their intriguing structures and potential applications. However, achieving strong near-infrared (NIR) luminescence in these clusters is highly challenging. Here, we have successfully synthesized the first LnIII/CuI bimetallic clusters, formulated as [LnCu54O6Cl3(2-MeO-PhC≡C)36] (ClO4)6 (Ln = Yb for YbCu54, Er for ErCu54, and Gd for GdCu54). Single crystal X-ray diffraction showed that the LnCu54 clusters have a three-layered core-shell structure, consisting of (LnO6)@Cu18Cl3@Cu36 units protected by 36 2-MeO-PhC≡C- ligands. Notably, the YbCu54 cluster exhibits significant NIR-II luminescence at 986 nm with the solid quantum efficiency of 33.3%, the highest among Cu clusters with NIR-II emission. This work not only reports the first category of LnIII/CuI clusters but also presents a method to enhance NIR luminescence in coinage-metal clusters through the incorporation of LnIII ions.

Structure search for transition metal clusters. Towards a rational understanding of their size-dependent properties

Prediction of the lowest energy structure for transition metal clusters and related systems is fundamental in cluster science. Advances in the structure search methods have reduced the computer time for structure prediction, standing on the performance of density functional theory (DFT) calculations. This perspective summarizes recent advances in the employed strategies to tackle geometrical determination of small and large metallic clusters via structure identification and rationalization of the resulting properties. Particularly, we pay attention to coinage metal clusters and noble metals due to their potential technological applications. The basics and recent achievements in structure search methods and related challenges are summarized, towards determining structural evolution accounting contributing to further development on efficient catalytic materials among other applications of technological interest.

Accelerating Relativistic Exact-Two-Component Density Functional Theory Calculations with Graphical Processing Units.

Numerical integration of the exchange-correlation potential is an inherently parallel problem that can be significantly accelerated by graphical processing units (GPUs). In this Letter, we present the first implementation of GPU-accelerated exchange-correlation potential in the GauXC library for relativistic, 2-component density functional theory. By benchmarking against copper, silver, and gold coinage metal clusters, we demonstrate the speed and efficiency of our implementation, achieving significant speedup compared to CPU-based calculations. One GPU card provides computational power equivalent to roughly 400 CPU cores in the context of this work. The speedup further increases for larger systems, highlighting the potential of our approach for future, more computationally demanding simulations. Our implementation supports arbitrary angular momentum basis functions, enabling the simulation of systems with heavy elements and providing substantial speedup to relativistic electronic structure calculations. This advancement paves the way for more efficient and extensive computational studies in the field of density functional theory.

Atomically Precise Ternary Cluster: Polyoxometalate Cluster Sandwiched by Gold Clusters Protected by N-Heterocyclic Carbenes.

Coinage metal (Au, Ag, Cu) cluster and polyoxometalate (POM) cluster represent two types of subnanometer "artificial atoms" with significant potential in catalysis, sensing, and nanomedicine. While composite clusters combining Ag/Cu clusters with POM have achieved considerable success, the assembly of gold clusters with POM is still lagging. Herein, we first designedly synthesized two cluster structural units: an Au3O cluster stabilized by diverse N-heterocyclic carbene (NHC) ligands and an amine-terminated POM linker. The subsequent reaction involved amine substitution in the POM linker for the central O atom in the Au3O cluster, resulting in the first ternary composite cluster - a POM cluster sandwiched by two Au clusters protected by NHCs. Single-crystal X-ray diffraction and other characteristic methods characterized their atomically precise structures. Furthermore, altering the NHC ligands decreased the number of gold atoms in the sandwich structures, accompanying the different protonated degrees of amine ligand in the terminal end of the POM linker. These composite clusters showed excellent performances in catalytic H2O2 conversion through the synergistic effect between gold clusters and POM clusters. This work opens a new avenue to functional composite metal clusters and would promote their enhanced catalysis applications through intercluster synergistic interactions within composite systems.

Advancing Single-Particle Analysis in Synthetic Chemical Systems: A Forward-Looking Discussion.

Single-particle analysis (SPA) is a fundamental method of cryo-electron microscopy developed to resolve the structures of biological macromolecules. This method has seen significant success in structural biology, yet its potential applications in synthetic chemical systems remain underexplored. In this perspective article, SPA and associated electron microscopy techniques are first briefly introduced. It is then proposed that SPA is well-suited for structural analysis of chemical systems where discrete, identical macromolecules can be readily obtained. Applicable systems include various clusters such as coinage metal clusters, metal-oxo/sulfur clusters, metal-organic clusters, and supramolecular compounds like coordination cages and metallo-supramolecular cages. When high-quality large single crystals are unattainable, SPA provides an alternative method for determining their structures. Beyond these end products, it is suggested that SPA can be instrumental in studying synthetic intermediates of materials with specific building units, such as metal-organic frameworks and zeolites. Given that various intermediates coexist in the reaction system, a purification step is necessary before conducting SPA, which can be facilitated by soft-landing electrospray ionization mass spectrometry.

Chemical Flexibility of Atomically Precise Metal Clusters.

Ligand-protected metal clusters possess hybrid properties that seamlessly combine an inorganic core with an organic ligand shell, imparting them exceptional chemical flexibility and unlocking remarkable application potential in diverse fields. Leveraging chemical flexibility to expand the library of available materials and stimulate the development of new functionalities is becoming an increasingly pressing requirement. This Review focuses on the origin of chemical flexibility from the structural analysis, including intra-cluster bonding, inter-cluster interactions, cluster-environments interactions, metal-to-ligand ratios, and thermodynamic effects. In the introduction, we briefly outline the development of metal clusters and explain the differences and commonalities of M(I)/M(I/0) coinage metal clusters. Additionally, we distinguish the bonding characteristics of metal atoms in the inorganic core, which give rise to their distinct chemical flexibility. Section 2 delves into the structural analysis, bonding categories, and thermodynamic theories related to metal clusters. In the following sections 3 to 7, we primarily elucidate the mechanisms that trigger chemical flexibility, the dynamic processes in transformation, the resultant alterations in structure, and the ensuing modifications in physical-chemical properties. Section 8 presents the notable applications that have emerged from utilizing metal clusters and their assemblies. Finally, in section 9, we discuss future challenges and opportunities within this area.

Oxygen locations and electronic structures of oxygenated coinage-metal clusters

The structure features and stability of MnO (M = Cu, Ag and Au; n = 2–9) clusters are investigated using the genetic algorithm combined with the density functional theory (DFT). It is found that CunO and AgnO are more inclined to 3-dimension compact structures, while the transition of AunO from 2 to 3-dimensions occurs at n = 7, in which O atoms prefer to be located on the vertexes regardless of different sizes and configurations of metal Mn cores. Due to the relativistic effect, the stability of AunO is maximum, while the AgnO are less stable, and that of CunO is in between them. The molecular dynamics simulations show that the structures of M4O can maintain integrity with only slight disturbances of individual atoms at a temperature of 300 K. But only the Au4O is stable at 500K, and the Ag4O and Cu4O have severely structural deformation. In most cases, the density of states of larger-sized MnO can be regarded as the superposition of small clusters, and distributions of the curves are in good agreement on the whole. The molecular orbitals reveal that the HOMO/LUMO orbitals are mainly distributed around the M atoms. The natural population analysis charges show that the charge-transferring direction is from M to O atoms, where the charge of O atoms exhibits odd–even oscillation behaviors, with different intensity peaks at the same n.

Thermally Activated Delayed Fluorescence (TADF)-active Coinage-metal Sulfide Clusters for High-resolution X-ray Imaging.

The study of facile-synthesis and low-cost X-ray scintillators with high light yield, low detection limit and high X-ray imaging resolution plays a vital role in medical and industrial imaging fields. However, the optimal balance between X-ray absorption, decay lifetime and excitonic utilization efficiency of scintillators to achieve high-resolution imaging is extremely difficult due to the inherent contradiction. Here two thermally activated delayed fluorescence (TADF)-actived coinage-metal clusters M6 S6 L6 (M=Ag or Cu) were synthesized by simple solvothermal reaction, where the cooperation of heavy atom-rich character and TADF mechanism supports strong X-ray absorption and rapid luminescent collection of excitons. Excitingly, Ag6 S6 L6 (SC-Ag) displays a high photoluminescence quantum yield of 91.6 % and scintillating light yield of 17420 photons MeV-1 , as well as a low detection limit of 208.65 nGy s-1 that is 26 times lower than the medical standard (5.5 μGy s-1 ). More importantly, a high X-ray imaging resolution of 16 lp/mm based on SC-Ag screen is demonstrated. Besides, rigid core skeleton reinforced by metallophilicity endows clusters M6 S6 L6 strong resistance to humidity and radiation. This work provides a new view for the design of efficient scintillators and opens the research door for silver clusters in scintillation application.

Coinage metal(I) clusters supported by a 1,10-phenanthroline-phosphine: orange-to-NIR phosphorescence, metallophilic interactions and enhanced cytotoxicity.

A series of small coinage metal(I) clusters has been selectively synthesized using 2-(diphenylphosphino)-1,10-phenanthroline (L), a new promising dimetal-binding P,N,N'-ligand (L). Its reaction with CuI yields the complex [Cu2L2(μ2-I)]2[Cu2I4], while the treatment of L with Au(tht)Cl/Ag+ or Au(tht)Cl/Cu+ systems leads to the assembly of [Au2AgL2Cl2]+, [Au2CuL2Cl2]+, [CuAuL2]2+ and [AgAuL2]2+ clusters. Theoretical analysis revealed pronounced intermetallic close shell interactions in these di- and trinuclear ensembles. At 298 K, the title compounds exhibit an orange and near-infrared (NIR) phosphorescence with lifetimes of 0.344-38 μs and quantum efficiencies of 1-21%. Theoretical considerations suggest a 3(M+L)LCT type for the observed phosphorescence. In addition, the above clusters exhibit a strong dose-dependent cytotoxic effect on A549, HepG2, Hep2 and MRC5 human cells with IC50 values ranging from 1.26 to 11.1 μM.

Hydride-doped coinage metal superatoms and their catalytic applications.

Superatomic constructs have been identified as a critical component of future technologies. The isolation of coinage metal superatoms relies on partially reducing metallic frameworks to accommodate the mixed valent state required to generate a superatom. Controlling this reduction requires careful consideration in reducing the agent, temperature, and the ligand that directs the self-assembly process. Hydride-based reducing agents dominate the synthetic wet chemical routes to coinage metal clusters. However, within this category, a unique subset of superatoms that retain a hydride/s within the nanocluster post-reduction have emerged. These stable constructs have only recently been characterized in the solid state and have highly unique structural features and properties. The difficulty in identifying the position of hydrides in electron-rich metallic constructs requires the combination and correlation of several analytical methods, including ESI-MS, NMR, SCXRD, and DFT. This text highlights the importance of NMR in detecting hydride environments in these superatomic systems. Added to the complexity of these systems is the dual nature of the hydride, which can act as metallic hydrogen in some cases, resulting in entirely different physical properties. This review includes all hydride-doped superatomic nanoclusters emphasizing synthesis, structure, and catalytic potential.

Ligand-free supermolecules: [Pd2@Ge18]4- and [Pd2@Sn18]4- as multiple-bonded Zintl-ion clusters based on Pd@Ge9 and Pd@Sn9 assembled units.

Understanding intercluster bonding interactions is important in the rational synthesis of building blocks for molecular materials. Such characteristics have been developed for coinage metal clusters resembling single-, double-, and triple-bonded species, coined as supermolecules. Herein, we extend such an approach for understanding main-group clusters, thus evaluating [Pd2@E18]4- clusters (E = Ge, Sn) involving the fusion of parent spherical aromatic [Pd@E12]2- building units. Our results indicate intercluster bonding provided by contribution from 2P and 1G shells centered at each building motif, leading to an overall bond order of 2.70 and 2.31 for [Pd2@Ge18]4- and [Pd2@Sn18]4-, respectively. In addition, 119Sn-NMR patterns were evaluated to complement the experimental characterization of a single peak owing to the insolution fluxional behavior of [Pd2@Sn18]4- as three peaks owing to the three sets of unique Sn atoms within the structure. Magnetic response properties revealed that spherical aromatic characteristics from parent [Pd@E12]2- building units are retained in the overall [Pd2@E18]4- oblate cluster as two spherical aromatic units. Hence, the notion of superatomic molecules is extended to Zintl-ion clusters, favoring further rationalization for the fabrication of cluster-assembled solids.

Tailoring Vacancy Defects in Isolated Atomically Precise Silver Clusters through Mercury-Doped Intermediates.

Vacancy defects are known to have significant effects on the physical and chemical properties of nanomaterials. However, the formation and structural dynamics of vacancy defects in atomically precise coinage metal clusters have hardly been explored due to the challenges associated with isolation of such defected clusters. Herein, we isolate [Ag28(BDT)12]2- (BDT is 1,3-benzenedithiol), a cluster with a "missing atom" site compared to [Ag29(BDT)12]3-, whose precise structure is known from X-ray diffraction. [Ag28(BDT)12]2- was formed in the gas-phase by collisional heating of [Ag28Hg(BDT)12]2-, a Hg-doped analogue of the parent cluster. The structural changes resulting from the loss of the Hg heteroatom were investigated by trapped ion mobility mass spectrometry. Density functional theory calculations were performed to provide further insights into the defect structures, and molecular dynamics simulations revealed defect site-dependent structural relaxation processes.

Isolation of (Aryl)-(Imino) Phosphide and (Aryl)-(Phosphaalkene) Amide Complexes of Alkali Metals from Carbene-Phosphinidenes under Reductive-Thermal Rearrangements.

Invited for the cover of this issue are Sudipta Roy and co-workers at the Indian Institute of Science Education and Research (IISER) Tirupati. The image depicts the rearrangement of cyclic alkyl(amino) carbene (cAAC)-supported chloro-phosphinidenes affording two ligands, of which one was used for the solid-state isolation of three cyclic alkyl(amino-boryl) phosphaalkenes and two coinage metal clusters. Read the full text of the article at 10.1002/chem.202302120.

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.

Carbene-stabilized enantiopure heterometallic clusters featuring EQE of 20.8% in circularly-polarized OLED

Bright and efficient chiral coinage metal clusters show promise for use in emerging circularly polarized light-emitting materials and diodes. To date, highly efficient circularly polarized organic light-emitting diodes (CP-OLEDs) with enantiopure metal clusters have not been reported. Herein, through rational design of a multidentate chiral N-heterocyclic carbene (NHC) ligand and a modular building strategy, we synthesize a series of enantiopure Au(I)-Cu(I) clusters with exceptional stability. Modulation of the ligands stabilize the chiral excited states of clusters to allow thermally activated delayed fluorescence, resulting in the highest orange-red photoluminescence quantum yields over 93.0% in the solid state, which is accompanied by circularly polarized luminescence. Based on the solution process, a prototypical orange-red CP-OLED with a considerably high external quantum efficiency of 20.8% is prepared. These results demonstrate the extensive designability of chiral NHC ligands to stabilize polymetallic clusters for high performance in chiroptical applications.

On the structures and bonding of copper boride nanoclusters, Cu2Bx– (x = 5–7)

Borophenes, a new class of synthetic 2D nanomaterials, are usually grown on coinage metal surfaces because of the weak boron-metal bonding. Coinage metal and boron binary clusters provide ideal systems to examine the bonding and interactions between coinage metals and boron, which are important to understand and control the growth of borophenes. Here we report a photoelectron spectroscopy and quantum chemical investigation on a series of di-copper boride clusters, Cu2Bx− (x = 5–7). Vibrationally resolved photoelectron spectra are measured for the binary cupper-boron clusters and are combined with quantum calculations to probe their structures and bonding. We find that all three clusters exhibit elongated ribbon-like structures consisting of a double-chain Bx motif and two terminal Cu–B covalent bonds, similar to the corresponding di-hydride (H2Bx−) and di-auride (Au2Bx−) clusters. The surprising covalent bonds between Cu and boron in these clusters are shown to be dictated by the high stability of the double-chain Bx motifs in this size range, whereas ionic bonding between Cu and boron is expected to take place in larger boron motifs.

Thermally Activated Delayed Fluorescence Coinage Metal Cluster Scintillator.

X-ray scintillators are widely used in medical imaging, industrial flaw detection, security inspection, and space exploration. However, traditional commercial scintillators are usually associated with a high use cost because of their substantial toxicity and easy deliquescence. In this work, an atomically precise Au-Cu cluster scintillator (1) with a thermally activated delayed fluorescence (TADF) property was facilely synthesized, which is environmentally friendly and highly stable to water and oxygen. The TADF property of 1 endows it with an ultrahigh exciton utilization rate. Combined with the effective absorption of X-ray caused by the heavy-atom effect and a limited nonradiative transition caused by close packing in the crystal state, 1 exhibits an excellent radioluminescence property. Moreover, 1 has good processability for fabricating a large, flexible thin-film device (10 cm × 10 cm) for high-resolution X-ray imaging, which can reach 40 μm (12.5 LP mm-1). The properties mentioned earlier make the coinage metal cluster promising for use as a substitute for traditional commercial scintillators.

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.