The switching behavior of surface stabilized ferroelectric liquid crystals has been studied using a simple uniform switching model in an applied electric field. We measured the response time as a function of pulse voltage for a ferroelectric liquid crystal material with a negative dielectric anisotropy, which shows a minimum in the response time-voltage curve, and found good agreement between the theory and the experimental results. Accordingly, the parameters appearing in the switching model, the initial azimuthal angle, rotational viscosity, and surface anchoring energy can be determined.

Using embedded-atom-method potentials, the lower-energy structures (LESs) of adatom clusters are obtained directly on a series of metal fcc(111) surfaces by the method based on the genetic algorithm. The structural features, energy distributions, number of LESs and their differences on different surfaces are discussed and explained in terms of the nearest-neighbor and next-nearest-neighbor (NN, NNN) adatom-adatom interactions, and the edge-type difference. When the energetic preference for one edge type over another is slight, e.g., on Ag(111), only one type of structure is included, and it does not change with the increment of cluster size. However, when there is a strong energetic preference for one of the edge types, e.g., on Pt (111), an interesting phenomenon of structure replacement is revealed, by which the structures in the LES group deviate more and more from the configuration with the maximum number of NN bonds as the cluster size increases. The structure replacement also finally leads to the shape of the two-dimensional island on Pt(111) being quite distinct from that on Ag(111). Based on these results, the general trend of the variation of lower-energy structures with cluster size is discussed further for other metal fcc(111) surfaces.

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