Coarsening and pearling instabilities in silver nanofractal aggregates.

We investigate the morphological changes of 3D supported fractal aggregates generated through the deposition of silver clusters on graphite. The fractal relaxation, activated after their formation by perturbing them either by thermal annealing or by using a surfactant, as oxide molecules, carried by silver clusters in a subsequent deposition, shows evidence of two distinct fragmentation patterns. The post coarsening, driven by thermal heating, gives a broad asymmetrical distribution of fragments in agreement with a random process, whereas the entire silver fractal pearling fragmentation is driven by chemical adjunction of the surfactant.

Dynamics of polymorphic nanostructures: from growth to collapse.

The deposition of preformed clusters on surfaces offers new possibilities to build complex artificial nanostructures, the shape of which depends on the cluster size. We describe routes for generating unusual polymorphic nanoislands, which constitute unique platforms for exploring instabilities. As coverage increases, the constraints accumulated in such nanostructures induce spectacular flattening collapse processes, which are not observed when the constraints are imposed by the substrate.

Synthesis of silver molybdate clusters driven by laser-annealing.

The synthesis of silver rich molybdate clusters is achieved by laser induced chemical reaction of coadsorbed MoO(3) and O(2) molecules on free silver clusters. The reactants MoO(3) and/or O(2) molecules condensed at low temperature (77 K-175 K) on free silver clusters. Then, the silver clusters together with their adsorbed molecules are flashed either ionized with a discharge or ionized and heated by a laser. Then they are cooled down by evaporation. The synthesized chemical compounds are analyzed by a high-resolution time-of-flight mass spectrometer. If only one type of reactant is adsorbed on the cluster, only one oxide molecule is stabilized on the metallic core after the heating and cooling cycle. On the contrary, the coadsorption of the two types of molecules MoO(3) and O(2) on Ag(n) (+), at 77 K, leads to complex aggregates that transform, after laser heating, into a molybdate rich metal clusters. These synthesized species cool down by evaporating silver atoms showing evidence of a binary oxide that is more stable than the metallic core. Moreover we demonstrate that for small size molybdate clusters, a stoichiometric composition may differ from the bulk one.

Dissipation effects in cluster fission.

The fission of Sr(2+)(n) is studied from time-of-flight (TOF) measurements. The TOF acts both as a mass spectrometer and as a velocity dispersion analyzer. Evidence of the postfission ejection of a fast neutral atom is shown. It is explained assuming a strong deformation of the fissioning system at the transition state. The relaxation of the deformation energy into vibrations promotes the evaporation of the large fragment.

Caloric curves of small fragmenting clusters.

The kinetic energy release distribution of neutral atoms emitted from photoexcited clusters Sr(+)(n) with n=4-15, has been obtained by time-of-flight velocity dispersion. The deduced temperature is plotted as a function of the excitation energy. For small sizes n<7 a general increase is observed. For cluster sizes larger than n=9, the deduced caloric curves first increase, and then show evidence of a plateau regime as excitation energy increases. This limiting temperature in neutral atom ejection is consistent with a bound cluster-vapor phase transition in a microcanonical system.

Charge transfer and dissociation in collisions of metal clusters with atoms.

We present a combined theoretical and experimental study of charge transfer and dissociation in collisions of slow Li31(2+) clusters with Cs atoms. We provide a direct quantitative comparison between theory and experiment and show that good agreement is found only when the exact experimental time of flight and initial cluster temperature are taken into account in the theoretical modeling. We demonstrate the validity of the simple physical image that consists in explaining evaporation as resulting from a collisional energy deposit due to cluster electronic excitation during charge transfer.

Thermal quenching of electronic shells and channel competition in cluster fission.

Experimental and theoretical studies of fission of doubly charged Li, Na, and K clusters in the low-fissility regime reveal the strong influence of electronic shell effects on the fission products. The electronic entropy controls the quenching of the shell effects and the competition between magic-fragment channels, leading to a transition from favored channels of higher mass symmetry to the asymmetric channel involving the trimer cation at elevated temperatures.

Instability driven fragmentation of nanoscale fractal islands.

Formation and evolution of fragmentation instabilities in fractal islands, obtained by deposition of silver clusters on graphite, are studied. The fragmentation dynamics and subsequent relaxation to the equilibrium shapes are controlled by the deposition conditions and cluster composition. Sharing common features with other materials' breakup phenomena, the fragmentation instability is governed by the length-to-width ratio of the fractal arms.