Nele Veldeman

Carbon Monoxide Adsorption on Silver Doped Gold Clusters

Well controlled gas phase experiments of the size and dopant dependent reactivity of gold clusters can shed light on the surprising discovery that nanometer sized gold particles are catalytically active. Most studies that investigate the reactivity of gold clusters in the gas phase focused on charged, small sized clusters. Here, reactivity measurements in a low-pressure reaction cell were performed to investigate carbon monoxide adsorption on neutral bare and silver doped gold clusters (Au(n)Ag(m); n = 10-45; m = 0, 1, 2) at 140 K. The size dependence of the reaction probabilities reflects the role of the electronic shells for the carbon monoxide adsorption, with closed electronic shell systems being the most reactive. In addition, the clusters reaction probability is reduced upon substitution of gold atoms for silver. Inclusion of a single silver atom causes significant changes in the reactivity only for a few cluster sizes, whereas there is a more general reduction in the reactivity with two silver atoms in the cluster. The experimental observations are qualitatively explained on the basis of a Blyholder model, which includes dopant induced features such as electron transfer from silver to gold, reduced s-d hybrization, and changes in the cluster geometry.

The Cu7Sc Cluster is a Stable σ‐Aromatic Seven‐Membered Ring

Density functional theory calculations demonstrate that the global minimum of the Cu(7)Sc potential energy surface is a seven-membered ring of copper atoms with scandium in its center, yielding a planar D(7) (h) structure. Nucleus-independent chemical shifts [NICS(1)(zz) and NICS(2)(zz)] show that this cluster has aromatic character, which is consistent with the number of 4s electrons of copper and scandium plus the 3d electrons of scandium satisfying Hückels rule. According to a canonical MO decomposition of NICS(1)(zz) and NICS(2)(zz), the MOs consisting of the 4s atomic orbitals are mainly responsible for the aromatic behavior of the cluster. The electron localizability indicator (ELI-D) and its canonical MO decomposition (partial ELI-D) suggest that a localized basin is formed in Cu(7)Sc by the copper atoms whereas the two circular localized domains are situated below and above the ring. The planar Cu(7)Sc cluster can thus be considered as a sigma-aromatic species. These findings agree with the phenomenological shell model.

Stability and dissociation pathways of doped AunX+ clusters (X = Y, Er, Nb)

Size dependent stabilities, fragmentation pathways and dissociation energies of a series of gas phase cationic doped gold clusters, Au(n)X+ (3 < or = n < or = 20; X = Y, Er and Nb), and pure Au(n)+ clusters were investigated in photofragmentation experiments. Size dependent stability patterns were obtained and the branching between monomer and dimer evaporation was studied. For bare gold, the competing neutral monomer and dimer evaporation channels were found to be in agreement with earlier studies. For doped clusters, monomer evaporation is the most likely fragmentation channel with the exception of Au18Y+ and Au20Y+ for which gold dimer evaporation is also observed. Relations between the evaporative activation energies and both the experimental abundances and the fragment yield were derived based on unimolecular rate constants. The dissociation energies from this analysis show an odd-even staggering and enhanced stabilities for certain cluster sizes, in agreement with simple electronic shell model predictions.

Growth Mechanism and Chemical Bonding in Scandium-Doped Copper Clusters: Experimental and Theoretical Study in Concert

Size matters! The electronic structure and size-dependent stability of neutral and cationic scandium-doped copper clusters have been investigated by mass spectrometric studies (for the cations) and also quantum chemical computations. The proposed reaction paths ultimately lead to the most stable Frank-Kasper-shaped Cu(16)Sc(+) cluster (shown here), which could be the germ of a new crystallization process.Electronic structure and size-dependent stability of scandium-doped copper cluster cations, Cu(n)Sc(+), were investigated by using a dual-target dual-laser vaporization production scheme followed by mass spectrometric studies and also quantum chemical computations in the density functional theory framework. The neutral species also were studied by using computational methods. Enhanced abundances and dissociation energies were measured in the case of Cu(n)Sc(+) for n=4, 6, 8, 10 and 16, the last of these identified as being extraordinary stable. Neutral clusters are stable with n=5, 7, 9 and 15, which are isoelectronic with respect to the number of the valence s electrons with the stable cationic clusters; hence a simple electron count determines cluster properties to a great extent. The Cu(17)Sc cluster was found to be a superatomic molecule, containing Cu(16)Sc(+) and Cu(-) units; however, the charge separation is not as pronounced as in the case of CuLi. Cu(15)Sc was found to be a stable cluster with a large dissociation energy and a closed electronic structure; hence this can be regarded as a superatom, analogous to the noble gases. The main factors determining the growth patterns of these clusters are the central position of the scandium atom and the successive filling of the shell orbitals. For smaller clusters, the reaction paths appear to diverge yielding various products; however all paths ultimately lead to the most stable Frank-Kasper shaped Cu(16)Sc cluster, which in turn can be the germ of the crystallization process.