Symmetry layer

Compound a b c Angle Symmetry Layer type Approxi- mate match Notes Ref. 

A method has been worked out for eddy current testing of surfaces and surface cracks or corrosion under dielectric or non-magnetic metal layer of up to 10 mm. The method is based on excitation of eddy currents by a coil with U - type core and information reading by a sensitive gradientometric element located on a axis of symmetry of the core (fig. 1). 

The diffraction pattern consists of a small number of spots whose symmetry of arrangement is that of the surface grid of atoms (see Fig. IV-10). The pattern is due primarily to the first layer of atoms because of the small penetrating power of the low-energy electrons (or, in HEED, because of the grazing angle of incidence used) there may, however, be weak indications of scattering from a second or third layer. 

Restructuring of a surface may occur as a phase change with a transition temperature as with the Si(OOl) surface [23]. It may occur on chemisorption, as in the case of oxygen atoms on a stepped Cu surface [24]. The reverse effect may occur The surface layer for a Pt(lOO) face is not that of a terminal (100) plane but is reconstructed to hexagonal symmetry. On CO adsorption, the reconstruction is lifted, as shown in Fig. XVI-8. 

As witli tlie nematic phase, a chiral version of tlie smectic C phase has been observed and is denoted SniC. In tliis phase, tlie director rotates around tlie cone generated by tlie tilt angle [9,32]. This phase is helielectric, i.e. tlie spontaneous polarization induced by dipolar ordering (transverse to tlie molecular long axis) rotates around a helix. However, if tlie helix is unwound by external forces such as surface interactions, or electric fields or by compensating tlie pitch in a mixture, so tliat it becomes infinite, tlie phase becomes ferroelectric. This is tlie basis of ferroelectric liquid crystal displays (section C2.2.4.4). If tliere is an alternation in polarization direction between layers tlie phase can be ferrielectric or antiferroelectric. A smectic A phase foniied by chiral molecules is sometimes denoted SiiiA, altliough, due to the untilted symmetry of tlie phase, it is not itself chiral. This notation is strictly incorrect because tlie asterisk should be used to indicate the chirality of tlie phase and not tliat of tlie constituent molecules. 

As for crystals, tire elasticity of smectic and columnar phases is analysed in tenns of displacements of tire lattice witli respect to the undistorted state, described by tire field u(r). This represents tire distortion of tire layers in a smectic phase and, tluis, u(r) is a one-dimensional vector (conventionally defined along z), whereas tire columnar phase is two dimensional, so tliat u(r) is also. The symmetry of a smectic A phase leads to an elastic free energy density of tire fonn [86]... 

The transition from smectic A to smectic B phase is characterized by tire development of a sixfold modulation of density witliin tire smectic layers ( hexatic ordering), which can be seen from x-ray diffraction experiments where a sixfold symmetry of diffuse scattering appears. This sixfold symmetry reflects tire bond orientational order. An appropriate order parameter to describe tlie SmA-SmB phase transition is tlien [18,19 and 20]... 

Order and dense packing are relative in tire context of tliese systems and depend on tire point of view. Usually tire tenn order is used in connection witli translational symmetry in molecular stmctures, i.e. in a two-dimensional monolayer witli a crystal stmcture. Dense packing in organic layers is connected witli tire density of crystalline polyetliylene. 

Assuming symmetry of vj and V2 with respect to mid-surface at = 0), the velocity components, given by Equation (5.70), are integrated to obtain flow rates in the lateral directions within the limits of the thin layer as... 

In some Hquid crystal phases with the positional order just described, there is additional positional order in the two directions parallel to the planes. A snapshot of the molecules at any one time reveals that the molecular centers have a higher density around points which form a two-dimensional lattice, and that these positions are the same from layer to layer. The symmetry of this lattice can be either triangular or rectangular, and again a positional distribution function, can be defined. This function can be expanded in a two-dimensional Fourier series, with the coefficients in front of the two... 

Mechanical Properties. The hexagonal symmetry of a graphite crystal causes the elastic properties to be transversely isotropic ia the layer plane only five independent constants are necessary to define the complete set. The self-consistent set of elastic constants given ia Table 2 has been measured ia air at room temperature for highly ordered pyrolytic graphite (20). With the exception of these values are expected to be representative of... 

A little later (Bendersky 1985, Chattopadhyay et al. 1985) decagonal (tenfold) symmetry was discovered in other Al-transition metal compounds quasiperiodic layers are stacked periodically in the third dimension. Since then, one or other of these forms of quasicrystal have been identified in many different compositions. A detailed review of the decagonal type is by Ranganathan et al. (1997). 

Of particular importance to carbon nanotube physics are the many possible symmetries or geometries that can be realized on a cylindrical surface in carbon nanotubes without the introduction of strain. For ID systems on a cylindrical surface, translational symmetry with a screw axis could affect the electronic structure and related properties. The exotic electronic properties of ID carbon nanotubes are seen to arise predominately from intralayer interactions, rather than from interlayer interactions between multilayers within a single carbon nanotube or between two different nanotubes. Since the symmetry of a single nanotube is essential for understanding the basic physics of carbon nanotubes, most of this article focuses on the symmetry properties of single layer nanotubes, with a brief discussion also provided for two-layer nanotubes and an ordered array of similar nanotubes. 

In this paper, we review progress in the experimental detection and theoretical modeling of the normal modes of vibration of carbon nanotubes. Insofar as the theoretical calculations are concerned, a carbon nanotube is assumed to be an infinitely long cylinder with a mono-layer of hexagonally ordered carbon atoms in the tube wall. A carbon nanotube is, therefore, a one-dimensional system in which the cyclic boundary condition around the tube wall, as well as the periodic structure along the tube axis, determine the degeneracies and symmetry classes of the one-dimensional vibrational branches [1-3] and the electronic energy bands[4-12]. 

Of the three arrangements of atoms in the second layer shown in Fig. 4, we find the one on the bottom (symmetry I) the most probable. It optimizes the coordination of neighboring atoms within the layer and, as we will see further down, this arrangement can also be well extended to C Q coated with metal. 

It should be pointed out again that these layers would, of course, contain identical numbers of atoms if the triangular faces had not been rotated and, thus, the Ih-symmetry had been preserved[7]. The reason for preferring the arrangement with 1-symmetry (which can still be called icosahedral) is that it leads to higher coordination of the atoms at the borders between the triangular faces. 

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