By Giovanni Barbero, Luiz Roberto Evangelista

ISBN-10: 0849335841

ISBN-13: 9780849335846

Regardless of the big volume of phenomenological info in regards to the bulk homes of nematic part liquid crystals, little is known in regards to the foundation of the outside power, really the skin, interfacial, and anchoring houses of liquid crystals that impact the functionality of liquid crystal units. Self-contained and certain, Adsorption Phenomena and Anchoring power in Nematic Liquid Crystals presents an account of latest and proven effects spanning 3 many years of study into the issues of anchoring power and adsorption phenomena in liquid crystals. The ebook incorporates a precise dialogue of the beginning and attainable assets of anchoring strength in nematic liquid crystals, emphasizing the dielectric contribution to the anchoring power particularly. starting with basic floor and anchoring houses of liquid crystals and the definition of the nematic section, the authors clarify how selective ion adsorption, dielectric strength density, thickness dependence, and bias voltage dependence impact the uniform alignment of liquid crystals and impact the functionality of liquid crystal units. additionally they speak about primary equations regulating the adsorption phenomenon and the dynamic points of ion adsorption phenomenon in liquid crystalline structures. Adsorption Phenomena and Anchoring power in Nematic Liquid Crystals serves as a superb resource of reference for graduates and researchers operating in liquid crystals, advanced fluids, condensed topic physics, statistical physics, chemical engineering, and digital engineering, in addition to delivering an invaluable common advent to and historical past info at the nematic liquid crystal section.

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**Extra info for Adsorption phenomena and anchoring energy in nematic liquid crystals**

**Example text**

This assumption is equivalent to stating that long range electrostatic contributions in the interaction energy between the molecules of the ﬁlm can be neglected. 45) where |δm| 1. This hypothesis means that m is considered a macroscopic quantity and hence changes over macroscopic distances d ρ. Only in this case it is possible to build an elastic theory for the orienting ﬁlm. 47) δm=0 and g(m, m, r) is the uniform part of the interaction energy. 48) where the expansion coeﬃcient Ca,b,c (r) depends only on the modulus of r.

It is also assumed that the director lies always in the plane (x, z) in such a way that n = sin θ(z)i + cos θ(z)k, where θ(z) is the tilt angle, i and k are the unit vectors parallel to the x and z axes, respectively. In the one-constant approximation, the bulk energy density due to elastic distortion and to the ﬁeld E, applied along the z−direction, apart a constant term, is f= dθ dz 1 K 2 2 + 1 2 a E 2 sin2 θ. 92) In this framework, the total energy of the nematic sample per unit area is given by the functional d/2 F [θ(z)] = −d/2 1 K 2 dθ dz 2 + 1 2 a E 2 sin2 θ dz.

This kind of calculation is relatively simple in the bulk, where the elements of symmetry of the NLC phase reduce to n. Near the surface the situation is more complicated for two diﬀerent reasons. First, the elements of symmetry of the NLC phase are n and the geometrical normal to the bounding surface, k. This implies that usually the number of surface elastic constants is larger than the one in the bulk [17], [36]–[38]. Second, the “elastic constants” are expected to be position dependent. 89) where Kijkl (z) takes into account the incomplete NLC-NLC interaction and δ F for the new elements of symmetry of the phase.

### Adsorption phenomena and anchoring energy in nematic liquid crystals by Giovanni Barbero, Luiz Roberto Evangelista

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