Two co-existing and opposing mechanisms of proton transfer in one-dimensional open-end water chains.

The proton transport in one-dimensional (1D) confined water chains has been extensively studied as a model for ion channels in cell membrane and fuel cell. However, the mechanistic understanding of the proton transfer (PT) process in 1D water chains remains incomplete. In this study, we demonstrate that the two limiting structures of the hydrated excess proton, H5O2+ (Zundel) and H3O+ (linear H7O3+), undergo a change in dominance as the water chain grows, causing two co-existing and opposing PT mechanisms. Specifically, H5O2+ is stable in the middle of the chain, whereas H3O+ serves as a transition state (TS). Except for this region, H3O+ is stabilized while H5O2+ serves as a TS. The interaction analysis shows that the electrostatic interaction plays a crucial role in the difference in PT mechanisms. Our work fills a knowledge gap between the various PT mechanisms reported in bulk water and long 1D water chains, contributing to a deeper understanding of biological ion channels at the atomic level.

High-pressure-induced electronic and structural transition of superatoms.

High pressure has been recognized as an important tool in molecule and materials research, and thus, it is expected to be used to understand the evolution of electronic states and geometric structures in superatoms. In this work, by studying three characteristic axial compressions on a typical endohedral metallofullerene superatom U@C28 with Td symmetry, we find that the triplet ground electronic state is preserved when the compression moves along the direction that reduces the symmetry to D2d, but the electronic state of the structure compressed along the direction of symmetry reduction to C2v or Cs is transformed into a singlet. The transition is attributed to the distinction in the response of electron spin to different axial compressions, which results in a change in the electron occupation mode of the system. Furthermore, we also confirm the gradual evolution from stereo to near-plane superatoms and the connection between their electron structures. This is reflected in the fact that the electron density distributions of the superatomic molecular orbitals (SAMOs) with extension along the restricted degrees of freedom (Dz2, Fz3 SAMOs) gradually contract, and the delocalization destruction of special orbitals is associated with this freedom. In addition, Raman and ultraviolet-visible spectra show a hyperchromic effect and redshift of characteristic peaks during axial compression, which are expected to be used for fingerprinting the superatomic planarization. Therefore, our work provides new insights based on high pressure for future research toward the discovery of physical properties and applications of superatoms.

Self-isomerization of nearly planar superatoms formed by actinide embedded gold clusters.

First-principles calculations show a self-isomerization process of the nearly planar superatom, in which the maximum energy difference between different extreme points is below 0.1 eV and a crossing between singlet and triplet states is also involved. Further UV-Vis spectra reveal a correlation between the spectra and structures caused by self-isomerization.

"Z"-Type Tilted Quasi-One-Dimensional Assembly of Actinide-Embedded Coinage Metal Near-Plane Superatoms and Their Optical Properties.

In this work, a novel discovery that the coinage-metal near-plane superatoms (CM-NPSs) formed by embedding actinide elements into the coinage metal rings can realize the "Z"-type tilted quasi-one-dimensional (1D) direct assembly is reported. This success can be attributed to the strong bonding between the overlapping parts of adjacent superatomic motifs. First-principles calculations reveal that the motifs maintain their geometric and electronic structures robustly during the assembly process. With the accumulation of motifs, the intensity of the absorption peak increases continuously in the ultraviolet-visible (UV-Vis) absorption spectra range of 300-450 nm, resulting in the hyperchromic effect, which is closely related to the degree of the participation of Th atoms. Furthermore, the absorption spectra show a continuously tunable feature in the 450-900 nm range, as the interlayer stacking pattern leads to a pronounced redshift. More importantly, the valence 5f-shells of Th atoms have an increased contribution to the final orbitals of electronic transition, which demonstrates the advantages of the active high angular momentum electrons of actinide elements in spectral properties. These findings provide a valuable reference for the direct artificial assembly of near-plane superatoms and optical properties of superatomic assemblies embedded with rare elements.

Super-Excimer: Anomalous Bonding in a Metastable Excited-State Dimer of Superatomic Dimers.

A new type of excimer formation was reported, which stems from an unexpected discovery of a short-lived excited-state dimer of superatomic dimers. In theoretical investigation of the dimer formation, it was found that the physical adsorption states maintain the closed-shell properties of the dimeric units via van der Waals interaction, while the chemical adsorption excited state is a broken-symmetry (BS) state, having a higher energy of about 0.5 eV. Potential energy surface calculations indicate that the short-lived metastable chemical bonding state can transform into energetically lower physical adsorption states by crossing a shallow energy barrier and eventually disintegrate into two ground-state dimers. Since the basic unit is a superatomic cluster, the chemical adsorption state discovered may be called "super-excimer", which opens up a new avenue for the discovery of tailorable excimer materials.

High-Stability Light-Element Magnetic Superatoms Determined by Hund's Rule.

Achieving stable high-magnetism light-element structures at nanoscale is vital to the field of magnetism, which has traditionally been ruled by transition-metal elements with localized d or f electrons. By first-principles calculations, we show that superatoms made of pure earth-abundant light elements (i.e., boron and nitrogen) exhibit desired magnetic properties that rival those of rare-earth elements, and the magnetism is dictated entirely by Hund's maximum spin rule. Importantly, the chemical and structural stabilities of the superatoms are not jeopardized by its high spins and are in fact better than those of transition-metal-element-embedded clusters. Our work thus establishes the basic principles for designing novel light-element, high-stability, and high-moment magnetic superatoms.

Quantum tunneling of hydrogen atom transfer affects mandrel degradation in inertial confinement fusion target fabrication.

Poly-α-methylstyrene (PAMS) is considered as the preferred mandrel material, whose degradation is crucial for the fabrication of high-quality inertial confinement fusion (ICF) targets. Herein, we reveal that hydrogen atom transfer (HAT) during PAMS degradation, which is usually attributed to the thermal effect, unexpectedly exhibits a strong high-temperature tunneling effect. Specifically, although the energy barrier of the HAT reaction is only 10-2 magnitude different from depolymerization, the tunneling probability of the former can be 14-32 orders of magnitude greater than that of the latter. Furthermore, chain scission following HAT will lead to a variety of products other than monomers. Our work highlights that quantum tunneling may be an important source of uncertainty in PAMS degradation, which will provide a direction for the further development of key technology of target fabricating in ICF research and even the solution of plastic pollution.

Superatomic Rydberg State Excitation.

Superatomic molecular orbitals (SAMOs) have symmetries (angular quantum numbers) similar to those of atoms, and thus, it is possible to realize Rydberg state excitations (RSEs) in superatomic molecules. In this Letter, the feasibility of superatomic Rydberg state excitation (SRSE) is explored using gold superatoms based on first-principles calculations. The results show that the SRSE exists in the high and low excited states of the gold superatoms and their SAMOs make a major contribution to electronic transitions. The radial distribution function of electronic density shows that the main distribution of electrons in the lowest unoccupied molecular orbitals and other unoccupied superatomic molecular orbitals is extremely far from the geometric center, and thus, they can be unambiguously identified as Rydberg orbitals. We found that due to the two-dimensional ductility of the planar SAMOs, superatoms are superior in the RSE regulation. Our findings may provide a new source of superatom-based RSE and will contribute to the regulation and efficient preparation of Rydberg states.

Constructing the bonding interactions between endohedral metallofullerene superatoms by embedded atomic regulation.

We present a possible principle that controls intercluster bonding through embedding different kinds of actinide atoms into the centre of fullerenes, thereby exhibiting different bonding forms. Moreover, these superatoms maintain the robustness of electronic structures.