RESUMO
This study explores the structures and chemical bonding properties of TaSi17Ì and TaSi18Ì clusters by employing anion photoelectron spectroscopy and theoretical computations. Utilizing CALYPSO and ABCluster programs for initial structure prediction, B3LYP hybrid functional for optimization, and CCSD(T)/def2-TZVPPD level for energy calculations, the research identifies the most stable isomers of these clusters. Key findings include the identification of two coexisting low-energy isomers for TaSi17Ì , exhibiting Ta-endohedral fullerene-like cage structures, and the lowest-energy structures of TaSi17Ì and TaSi18Ì anions can be considered as derived from the TaSi16Ì superatom cluster. The study enhances the understanding of group 14 element chemistry and guides the design of novel inorganic metallic compounds, potentially impacting materials science.
RESUMO
This study presents a collaborative experimental and theoretical investigation into the structures and electronic properties of niobium-doped germanium clusters. Anion photoelectron spectra for Nb1-2Gen- (n = 3-7) clusters were acquired using 266 nm photon energies, enabling the determination of adiabatic detachment energies and vertical detachment energies. In conjunction with these experimental measurements, density functional theory (DFT) calculations were conducted to validate the experimentally obtained electron detachment energies and elucidate the geometric and electronic structures of each anionic cluster. The agreement between DFT calculations and experimental data establishes a solid foundation for assessing the structural evolution and electronic properties of niobium-doped germanium clusters. It is noted that both neutral and anionic clusters exhibit predominantly similar overall structural characteristics, with the exception of Nb2Ge6- and Nb2Ge6. Furthermore, this investigation emphasizes the exceptional chemical stability of the D3d symmetric chair-shaped structure in Nb2Ge6-, providing insights into its bonding characteristics.
RESUMO
The structures and bonding characteristics of Ta2Si2Ì /0 clusters are investigated using anion photoelectron spectroscopy and quantum chemical calculations. The vertical detachment energy of the Ta2Si2Ì anion is measured to be 2.00 ± 0.08 eV using the 266 nm photon. It is found that the Ta2Si2Ì anion has three low-energy isomers with a C2v symmetric Ta-Ta dibridged structural framework, all of which contribute to the experimental photoelectron spectrum, while the Ta2Si2 neutral also has a C2v symmetric Ta-Ta dibridged structural framework. The charge-transfer from Ta atoms to Si atoms is discovered using atomic dipole moment corrected Hirshfeld analysis for the Ta2Si2Ì anion and Ta2Si2 neutral. Chemical bonding investigations show that both the Ta2Si2Ì anion and Ta2Si2 neutral have a strong covalent Ta-Ta bond, as well as σ and π double bonding patterns. Furthermore, the Ta atoms are linked together by a single 2c-2e Ta2 σ bond, whereas the Si atoms are linked together with the Ta atoms via four 2c-2e TaSi σ bonds, two 3c-2e TaSi2 σ bonds, one 4c-2e Ta2Si2 σ bond, and one 4c-2e Ta2Si2 π bond.
RESUMO
Gold, although chemically inert in its bulk state, is reactive at the nanoscale and, in small clusters, even behaves like a hydrogen atom. Using a photoelectron spectroscopy experiment and first-principles theory, we show that Au also behaves like a halogen in small clusters. This is evident not only in strong resemblance between the photoelectron spectra of Au2F- and AuF2- but also in Au exhibiting one of the signature properties of halogens, its ability to form superhalogens with electron affinities higher than that of any halogen atom. For example, the electron affinity (EA) of Au2F- is 4.17 eV, while AuF2-, a known superhalogen, has an EA of 4.47 eV. Of particular interest is Au2F2, which, in spite of being a closed-shell system, is a pseudohalogen with an EA of 3.3 ± 0.1 eV. Here, one of the Au atoms behaves like a halogen, making Au2F2 mimic the property of AuF3.