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Reports that the dissociation energies of singly charged silver cluster cations are determined by multiple-collision induced dissociation in a Penning trap. Analysis of the fragment yield in terms of a linearized impulsive collision theory; Model for energy transfer; Delay in the decay of a cluster; Data analysis; Correction for isotopomers.

Single charged gold clusters Au-n, 12 < n < 28, are stored in a Penning trap, size selected and transformed into dianions, Au2-n by the application of an electron beam. At the onset of dianion production, that is that range of cluster sizes n where the smallest doubly charged clusters are observed, the measured intensity ratio of the dianions to their precursors is not a continuous function of cluster size. Instead, there is a strong odd-even effect and a comparatively intense signal of Au2-18. The observed structures are very reminiscent of similar phenomena in the abundance spectra of metal clusters as observed by Knight et al. (1984, Phys. Rev. Lett., 52, 2141), which gave rise to the electronic shell structure interpretation and the further development of the jellium model as applied to metal clusters. [ABSTRACT FROM AUTHOR]

We report an investigation of (CsI)(n)Cs (+) cluster structures (n = 30-39) studied using the recently developed technique of trapped ion electron diffraction. Contributions to diffraction from both rock salt (NaCl) and cesium chloride lattice (CsCl) derived isomeric structures are observed at size n = 32. This size can form a closed shell rhombic dodecahedron corresponding to the CsI bulk structure. All other sizes, n not equal32, are dominated by the NaCl structure. Density functional calculations and molecular dynamic simulations identify the presence of a stable CsCl lattice derived structure isomer which is consistent with these results.