Nanoparticle formation and dynamics in a complex (dusty) plasma: from the plasma ignition to the afterglow.

Complex (dusty) plasmas are a subject of growing interest. They areionized gases containing charged dust particles. In capacitively-coupled RF discharges, dust growth can occur naturally and two methods can be used to grow dust particles: chemically active plasmas or sputtering. The growth of dust particles in argon discharges by RF sputtering and the effect of dust particles on theplasma have been investigated from the plasma ignition to the afterglow. It was shown that plasma and discharge parameters are greatly affected by the dust particles. Furthermore, plasma instabilities can be triggered by the presence of the dust particles. These instabilities can be due to dust particle growth or they can be instabilities of a well established dust cloud filling the interelectrode space. When the discharge is switched off, the dust particles act like a sink for the charge carrier and consequently affect the plasma losses. It was shown that the dust particles do keep residual chargeswhich values are greatly affected by the diffusion of the charge carriers and especially the transition from ambipolar to free diffusion

Temperature-induced structural phase transitions in a two-dimensional self-assembled network

Two-dimensional (2D) supramolecular self-assembly at liquid-solid interfaces is a thermodynamically complex process producing a variety of structures. The formation of multiple network morphologies from the same molecular building blocks is a common occurrence. We use scanning tunnelling microscopy (STM) to investigate a structural phase transition between a densely packed and a porous phase of an alkylated dehydrobenzo[12]annulene (DBA) derivative physisorbed at a solvent-graphite interface. The influence of temperature and concentration are studied and the results combined using a thermodynamic model to measure enthalpy and entropy changes associated with the transition. These experimental results are compared to corresponding values obtained from simulations and theoretical calculations. This comparison highlights the importance of considering the solvent when modeling porous self-assembled networks. The results also demonstrate the power of using structural phase transitions to study the thermodynamics of these systems and will have implications for the development of predictive models for 2D self-assembly. © 2013 American Chemical Society

Role of Substrate in Directing the Self-Assembly of Multicomponent Supramolecular Networks at the Liquid-Solid Interface

The self-assembly of multicomponent networks at the liquid-solid interface between Au(111) or highly oriented pyrolytic graphite (HOPG) and organic solvents was investigated using scanning tunneling microscopy. Alkoxylated dehydrobenzo[12]annulene (DBA) derivatives form hexagonal nanoporous networks, which trap either single molecules of coronene (COR) or small clusters of COR and isophthalic acid to form multicomponent networks. The pattern of interdigitation between alkyl chains from DBA molecules produces hexagonal pores that are either chiral or achiral. On Au(111) substrates multicomponent networks display an ordered superlattice arrangement of chiral and achiral pores. In comparison, similar networks on HOPG display only chiral pores. The unique superlattice structure observed on Au(111) is related to a lower energetic preference for chiral pores than on HOPG and increased diffusion barriers for guest molecules. The increased diffusion barriers for guests allow them to act as nucleation sites for the formation of achiral pores. Following the initial nucleation of an achiral pore, restrictions imposed by the accommodation of guests within the porous network mean that subsequent growth naturally leads to the formation of the superlattice structure