Single-Phase L10-Ordered High Entropy Thin Films with High Magnetic Anisotropy.

The vast high entropy alloy (HEA) composition space is promising for discovery of new material phases with unique properties. This study explores the potential to achieve rare-earth-free high magnetic anisotropy materials in single-phase HEA thin films. Thin films of FeCoNiMnCu sputtered on thermally oxidized Si/SiO2 substrates at room temperature are magnetically soft, with a coercivity on the order of 10 Oe. After post-deposition rapid thermal annealing (RTA), the films exhibit a single face-centered-cubic phase, with an almost 40-fold increase in coercivity. Inclusion of 50 at.% Pt in the film leads to ordering of a single L10 high entropy intermetallic phase after RTA, along with high magnetic anisotropy and 3 orders of magnitude coercivity increase. These results demonstrate a promising HEA approach to achieve high magnetic anisotropy materials using RTA.

Magic Numbers in Octahedral Ligated Metal-Chalcogenide Superatoms.

The attainment of the superatomic state offers a unifying framework for the periodic classification of atomic clusters. Metallic clusters attain the superatomic state via the confined nearly free electron gas model that leads to groupings of quantum states marked by radial and angular momentum quantum numbers. We examine ligated octahedral metal-chalcogenide clusters where the nearly free electron gas model is invalid; however, the high symmetry can also lead to the bunching of electronic states. For octahedral TM6E8L6 clusters (TM = transition metal; E = chalcogen; L = ligand), the electronic shells are filled for valence electron counts of 96, 100, and 114 electrons. These magic electron counts are marked by large highest occupied molecular orbital-lowest unoccupied molecular orbital (HOMO-LUMO) gaps, high ionization energies, and low electron affinity─all classic signatures of the superatomic state. We also find that clusters with electron counts differing from the magic counts show periodic patterns reminiscent of those observed in the periodic table of elements.

High-Spin Superatom Stabilized by Dual Subshell Filling.

Quantum confinement in small symmetric clusters leads to the bunching of electronic states into closely packed shells, enabling the classification of clusters with well-defined valences as superatoms. Like atoms, superatomic clusters with filled shells exhibit enhanced electronic stability. Here, we show that octahedral transition-metal chalcogenide clusters can achieve filled shell electronic configurations when they have 100 valence electrons in 50 orbitals or 114 valence electrons in 57 orbitals. While these stable clusters are intrinsically diamagnetic, we use our understanding of their electronic structures to theoretically predict that a cluster with 107 valence electrons would uniquely combine high stability and high-spin magnetic moment, attained by filling a majority subshell of 57 electrons and a minority subshell of 50 electrons. We experimentally demonstrate this predicted stability, high-spin magnetic moment (S = 7/2), and fully delocalized electronic structure in a new cluster, [NEt4]5[Fe6S8(CN)6]. This work presents the first computational and experimental demonstration of the importance of dual subshell filling in transition-metal chalcogenide clusters.

The superatomic state beyond conventional magic numbers: Ligated metal chalcogenide superatoms.

The field of cluster science is drawing increasing attention due to the strong size and composition-dependent properties of clusters and the exciting prospect of clusters serving as the building blocks for materials with tailored properties. However, identifying a unifying central paradigm that provides a framework for classifying and understanding the diverse behaviors is an outstanding challenge. One such central paradigm is the superatom concept that was developed for metallic and ligand-protected metallic clusters. The periodic electronic and geometric closed shells in clusters result in their properties being based on the stability they gain when they achieve closed shells. This stabilization results in the clusters having a well-defined valence, allowing them to be classified as superatoms-thus extending the Periodic Table to a third dimension. This Perspective focuses on extending the superatomic concept to ligated metal-chalcogen clusters that have recently been synthesized in solutions and form assemblies with counterions that have wide-ranging applications. Here, we illustrate that the periodic patterns emerge in the electronic structure of ligated metal-chalcogenide clusters. The stabilization gained by the closing of their electronic shells allows for the prediction of their redox properties. Further investigations reveal how the selection of ligands may control the redox properties of the superatoms. These ligated clusters may serve as chemical dopants for two-dimensional semiconductors to control their transport characteristics. Superatomic molecules of multiple metal-chalcogen superatoms allow for the formation of nano-p-n junctions ideal for directed transport and photon harvesting. This Perspective outlines future developments, including the synthesis of magnetic superatoms.

Massive dipoles across the metal-semiconductor cluster interface: towards chemically controlled rectification.

An interface between a metallic cluster (MgAl12) and a semiconducting cluster (Re6Se8(PMe3)5) is shown to be marked by a massive dipole reminiscent of a dipolar layer leading to a Schottky barrier at metal-semiconductor interfaces. The metallic cluster MgAl12 with a valence electron count of 38 electrons is two electrons short of 40 electrons needed to complete its electronic shells in a superatomic model and is marked by a significant electron affinity of 2.99 eV. On the other hand, the metal-chalcogenide semiconducting cluster Re6Se8(PMe3)5, consisting of a Re6Se8 core ligated with five trimethylphosphine ligands, is highly stable in the +2 charge-state owing to its electronic shell closure, and has a low ionization energy of 3.3 eV. The composite cluster Re6Se8(PMe3)5-MgAl12 formed by combining the MgAl12 cluster through the unligated site of Re6Se8(PMe3)5 exhibits a massive dipole moment of 28.38 D resulting from a charge flow from Re6Se8(PMe3)5 to the MgAl12 cluster. The highest occupied molecular orbital (HOMO) of the composite cluster is on the MgAl12 side, which is 0.53 eV below the lowest unoccupied molecular orbital (LUMO) localized on the Re6Se8(PMe3)5 cluster, reminiscent of a Schottky barrier at metal-semiconductor interfaces. Therefore, the combination can act as a rectifier, and an application of a voltage of approximately 4.1 V via a homogeneous external electric field is needed to overcome the barrier aligning the two states: the HOMO in MgAl12 with the LUMO in Re6Se8(PMe3)5. Apart from the bias voltage, the barrier can also be reduced by attaching ligands to the metallic cluster, which provides chemical control over rectification. Finally, the fused cluster is shown to be capable of separating electron-hole pairs with minimal recombination, offering the potential for photovoltaic applications.

Interfacial magnetism in a fused superatomic cluster [Co6Se8(PEt3)5]2.

An isolated Co6Se8(PEt3)6 cluster is non-magnetic; however, we find that a magnetic unit can be formed by fusing two Co6Se8(PEt3)5 superatoms into a [Co6Se8(PEt3)5]2 dimer. Theoretical studies indicate that the dumbbell-shaped [Co6Se8(PEt3)5]2 dimer has a spin moment of 2µB, and the spin density is primarily localized at the interfacial Co-sites where two clusters are fused into a dimer. The dimer has a low ionization energy of 4.17 eV, allowing the dimer to donate charge to C70 during the formation of a cluster assembled material, as seen in recent experiments by Nuckolls and co-workers. The donation of charge causes the dimer's magnetic moment to drop from 2µB to 1µB. We hypothesize that adding electrons to the dimer, such as doping impurities to the crystal lattice, may enhance the magnetic moment by neutralizing the charged cluster. This reveals a strategy for stabilizing magnetic moments in ligated cluster assemblies.

One-Dimensional Silver-Thiolate Cluster-Assembly: Effect of Argentophilic Interactions on Excited-State Dynamics.

We report the synthesis, crystal structure, and electronic structure calculations of a one-dimensional silver-thiolate cluster-assembled and its ultrafast spectroscopic investigation. Experiments and theory find the material to have a significant gap as the HOMO-LUMO absorption corresponds to 2.69 eV, and the defect-free structure is calculated to have a gap of 2.82 eV. Cluster models demonstrate that the gap energy is length-dependent. Theoretical studies identify a nonbonding metallophilic interaction that exists between two Ag atoms in adjacent strings that helps to stabilize the chain structure. Transient absorption spectroscopy reveals that the electron dynamics is a mixture of the behavior of cluster and nanoparticle, with the material having a 346 fs ground-state relaxation like a cluster, and the electron dynamics is dominated by electron-phonon coupling with a decay time of 1.5 ps, unlike the isolated cluster whose decay is mostly radiative.

A Magnetic Superatomic Dimer with an Intense Internal Electric Dipole Moment.

The electronic and magnetic properties of the ligand-decorated Fe6S8 cluster and fused superatomic dimer are investigated using first-principles density functional theory. It is shown that the redox properties of the Fe6S8 cluster can be effectively controlled by altering the nature of the attached ligands. Donor ligands such as phosphines reduce the ionization energy of the Fe6S8 cluster, whereas the acceptor ligands such as CO increase the electron affinity. Such variation in the redox properties of the Fe6S8 cluster is the result of the ligand-induced shift in the cluster's electronic levels, so the occupation number remains mostly unaffected, leading to a marginal change in the spin magnetic moment of the cluster. A combination of two identical Fe6S8 clusters decorated by unbalanced ligands results in a superatomic dimer with a massive dipole moment and a large spin magnetic moment. Donor ligands on one side of the superatomic dimer with acceptor ligands on the other cause significant intercluster charge transfer. The resulting superatomic dimer offers an interesting motif for spintronics-related applications.

Electron transport properties of PAl12-based cluster complexes.

The electronic transport properties of PAl12-based cluster complexes are investigated by density functional theory (DFT) in combination with the non-equilibrium Green's function (NEGF) method. Joining two PAl12 clusters via a germanium linker creates a stable semiconducting complex with a large HOMO-LUMO gap. Sequential attachment of an electron-donating ligand, N-ethyl-2-pyrrolidone, to one of the two linked clusters results in the shifting of the electronic spectrum of the ligated cluster while the energy levels of the unligated cluster are mostly unchanged. Using this approach, one can eventually align the HOMO of the ligated cluster to the LUMO of the non-ligated cluster, thereby significantly reducing the HOMO-LUMO gap of the complex. As a result, the transport properties of the complex are highly dependent on the number of attached ligands. Although a single ligand is observed to generally decrease the current, the inclusion of two or more ligands shows a significant increase in the amount of current at most voltages. The resulting increase of the current can be attributed to two factors, first the reduction in the HOMO-LUMO gap due to ligand attachment which has moved the transmission orbitals into the bias window. Secondly, when two or more ligands are attached to the complex, the HOMOs become delocalized across the scattering region, and this significantly enhances the currents.

A ligand-induced homojunction between aluminum-based superatomic clusters.

A superatomic molecule formed by joining two metallic clusters linked by an organometallic bridge can behave like a semiconductor and the addition of ligands can induce a significant energy level shift across an inter-cluster homojunction. This shift is induced by the N-ethyl-2-pyrrolidone ligands, and the placement of the ligands strongly affects the direction of the dipole moment, including the case where the dipole moment is parallel to the cluster interface. This computational study provides an alternative strategy for constructing nanometer-scale electronic interfaces between clusters mimicking semiconductor motifs. The semiconducting features in the PAl12 clusters emerge from the grouping of the quantum states in a confined nearly free electron gas that creates a substantial energy gap. An organometallic Ge(CH3)2(CH2)2 bridge links the clusters while maintaining the cluster's electronic shell structure. The amount of level shifting between the bridged clusters can be changed by controlling the number of ligands. Attaching multiple ligands can result in a broken gap energy alignment in which the HOMO level of one cluster is aligned with the LUMO level of the other bridged cluster. Furthermore, the singly ligated bridged superatomic molecule is found to exhibit promising features to separate the electron-hole pairs for photovoltaic applications.

Superatomic molecules with internal electric fields for light harvesting.

Traditional p-n junctions used for photovoltaics require an interface where a light induced electron-hole pair is separated by an electric field. Developing alternative strategies for forming strong internal electric fields for electron-hole pair separation offers the possibility for better performance. We demonstrate that fusing two superatomic clusters with donor/acceptor ligands on opposite sides of the cluster leads to such a strong internal electric field. In two fused metal-chalcogenide Re6S8Cl2(L)4 clusters with donor PMe3 ligands and acceptor CO ligands on the opposite sides of the fused clusters, the electronic levels undergo shifts analogous to band bending in traditional p-n junctions. The fused cluster has a large dipole moment, and an optical spectrum that strongly absorbs excitation above the HOMO-LUMO gap of the fused clusters, but is optically very weak for the lowest energy excitation that can lead to electron-hole pair recombination. This is because the electron is localized on the CO portion of the fused cluster, while the electron-hole pair is localized on the PMe3 side of the cluster. It is shown that the electronic states localized on each side of the cluster can be aligned/misaligned by applying a voltage in different directions, offering diode like characteristics.