Observation of halogen-like behavior of gold in fluorinated bimetallic CoAuF1-2- and CuAuF1-2- clusters: Anion photoelectron spectroscopy and density functional theory.

Using size-selected anion photoelectron spectroscopy and density functional theory, we investigated the structures and properties of fluorinated bimetallic clusters CoAuF1-2- and CuAuF1-2- and their neutrals. Both experimental and theoretical results show that in these cluster anions, Au behaves like a halogen atom. For example, the measured vertical detachment energies (VDEs) of CoAuF- (2.00 ± 0.08 eV) and CuAuF- (3.8 ± 0.1 eV) are close to those of CoF2- (2.12 ± 0.08 eV) and CuF2- (3.58 ± 0.08 eV), respectively. The theoretical results show that the geometries and electronic structures of CoAuF- and CuAuF- are similar to those of CoF2- and CuF2-. The natural population analysis and natural electron configuration analyses further confirm that the electronic properties of Au in MAuF- (M = Co, Cu) mimic those of MF2-. In addition, the electron localization function analyses show that the M-Au chemical bonds are similar to the corresponding M-F chemical bonds, providing evidence for the ionic nature of the interactions. When a second F atom is attached to the CoAuF- and CuAuF- clusters, the VDEs of the resulting CoAuF2- and CuAuF2- are 4.38 ± 0.08 eV and 3.71 ± 0.08 eV, respectively, indicating their superhalogen character as these values are higher than those of halogen anions. The results may be useful for understanding the properties of gold at the nanoscale that play an important role in catalysis and nanotechnology.

Anion photoelectron spectroscopy and quantum chemical calculations of bimetallic niobium-aluminum clusters NbAln-/0 (n = 3-12): identification of a half-encapsulated symmetric structure for NbAl12.

Bimetallic niobium-doped aluminum clusters, NbAln-/0 (n = 3-12), are investigated through a synergetic combination of size-selected anion photoelectron spectroscopy and theoretical calculations. It is found that the dominant structures of NbAln- anions with n = 3-8 can be described by gradually adding Al atoms to the NbAl3- core. Starting from n = 9, the lowest-energy geometric structures of NbAl9-12- transform into bilayer structures. In particular, NbAl12- has a C3v symmetric structure, which can be viewed as a NbAl6 regular hexagon over a bowl-shaped Al6 structure. More detailed analyses indicate that NbAl9 and NbAl12- possess unusual stability, which may be attributed to their closed-shell electron configurations with superatomic features.

Structures and bonding properties of lithium polysulfide clusters LiSn-/0 (n = 3-5) and Li2S4-/0: size-selected anion photoelectron spectroscopy and theoretical calculations.

The structures and bonding properties of several lithium polysulfide clusters LiSn-/0 (n = 3-5) and Li2S4-/0 were investigated by size-selected anion photoelectron spectroscopy coupled with quantum chemistry calculations. The vertical detachment energies of LiS3-, LiS4-, and LiS5- were estimated to be 2.17 ± 0.08, 3.30 ± 0.08 and 3.66 ± 0.08 eV, respectively, and that of Li2S4- was estimated to be 3.21 ± 0.08 eV. It is found that LiS3- and LiS3 have planar quadrilateral structures, and LiS4- and LiS4 have distorted five-membered ring structures. LiS5- has a distorted six-membered ring structure while neutral LiS5 has a book-shaped structure. The lowest-lying structure of Li2S4- can be viewed as a S2 unit connecting to the Li-Li edge of a Li2S2 tetrahedron. The lowest-lying structure of neutral Li2S4 can be viewed as a S2 unit connecting to the S atoms of a Li2S2 quadrilateral. The natural population analysis (NPA) and electron localization function (ELF) analyses show that the excess electron of LiSn- is mainly localized over the sulfur chains, especially on the S atoms interacting with Li, thus, the most stable structures of LiSn- can be regarded as a Li+ cation interacting with a Sn2- dianion. The results may be useful for understanding the formation of lithium polysulfides in lithium sulfur batteries.

Signature of Au as a Halogen.

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.