Ernst Lueder - Liquid Crystal Displays

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LIQUID CRYSTAL DISPLAYS
THE NEW EDITION OF THE GOLD-STANDARD IN TEACHING AND REFERENCING THE FUNDAMENTALS OF LCD TECHNOLOGIES

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Applications are centred around transmissive and reflective displays and light valves for projectors. Plastic substrates and printing of layers replacing vacuum processes are examples of an emerging new display technology.

2

Liquid Crystal Materials and Liquid Crystal Cells

2.1 Properties of Liquid Crystals

2.1.1 Shape and phases of liquid crystals

Most liquid crystals consist of molecules shaped like the rod in Figure 2.1(a). The direction of the long axis is called the director, given by the vector n, which is an apolar vector as картинка 17and картинка 18are equivalent. Rod-shaped molecules are also termed calamitic. Other shapes of molecules are disc-like or discotic, as in Figure 2.1(b), and lath-like.

We focus on calamitic (Bahadur, 1990; Demus et al., 1998a,b) liquid crystals as they are the most important for applications. Below the melting point T mthey are solid, crystalline and anisotropic, whereas above the clearing point with temperature T c> T mthey are a clear isotropic liquid. In the mesophase in Figure 2.2in between T mand T c, the material has the appearance of a milky liquid, but still exhibits the ordered phases shown in Figure 2.2. These phases are now described in the sequence given by increasing temperature. The first phase above T mis the smectic C phase (smectic is derived from the Greek word for soap). As all smectic phases, it is ordered in two dimensions. The molecules are arranged with random deviations tilted to the plane of the layer. In the smectic A phase the directors of the molecules are again with random deviations perpendicular to the plane of the layer. Next to the clearing point, the nematic phase appears with only a one-dimensional order (nematic in Greek means a thread, indicating the thread-like defects in the material). All members of the mesophase are anisotropic, as is the solid phase.

Some other phases of minor importance for display applications are below the smectic C phase, the smectic B hexphase (hexatic B phase), with the same layers as smectic C but a short-range close-packed hexagonal structure, in Figure 2.3(a)seen against the director картинка 19 ; in this direction, the smectic C phase exhibits the irregular structure in Figure 2.3(b). The phases J, G, E, K and H are located above T m, and are smectic-like soft crystals with a long range order.

Figure 21 a Rodlike or calamitic liquid crystal molecule with director n - фото 20

Figure 2.1 (a) Rod-like or calamitic liquid crystal molecule with director n ; (b) disc-like or discotic liquid crystal molecules

The smectic C* phase (chiral smectic C phase) in Figure 2.4possesses a layered smectic structure in which the parallel directors of the molecules are rotated from layer to layer on the surface of a cone, resulting in a helix.

If chiral compounds such as cholesterol esters are added, the nematic phase changes to the cholesteric phase in Figure 2.5, which exhibits a helical structure in which, again, the director is rotated from layer to layer.

An as yet poorly understood peculiarity are the blue phases, which occur in a small temperature range between the cholesteric and solid anisotropic phase.

More than 20 000 calamitic compounds are known.

Liquid crystals, the phases of which change with temperature, are called thermotropic. Those that change with the concentration of solvents and temperature are called lyotropic. Calamitic and thermotropic liquid crystals are important for LCDs. Their nematic phase is the basis for both the most widely used Twisted Nematic (TN) cell with active matrix addressing, and for the SuperTwist Nematic (STN) cell with passive matrix addressing. Further LCDs based on calamitic and thermotropic nematic phases are Polymer Dispersed Liquid Crystals (PDLCs) and guest-host-LCDs. The smectic A and smectic C* phases provide bistable ferro-electric LCDs with passive matrix addressing. The cholesteric phase gave rise to the Stabilized Cholesteric Texture (SCT) with bistability at zero field. LCDs based on these phases will be discussed later.

Figure 22 Phases of LC materials versus temperature To better understand - фото 21

Figure 2.2 Phases of LC materials versus temperature

To better understand electro-optical effects and electronic addressing, some material properties have to be presented (Bahadur, 1990; Demus et al., 1998a,b).

Figure 23 Top view of a the close packed hexagonal structure of the smectic - фото 22

Figure 2.3 Top view of (a) the close packed hexagonal structure of the smectic B hexphase, and (b) of the smectic C phase

Figure 24 The helix in a layered structure of chiral smectic C liquid crystals - фото 23

Figure 2.4 The helix in a layered structure of chiral smectic C liquid crystals with polarization картинка 24perpendicular to картинка 25

2.1.2 Material properties of anisotropic liquid crystals

The rod-like molecules have a head and a tail, which is, however, not taken into account by the direction of картинка 26 . Molecules in an unordered alignment exhibit an average director.

The individual molecules have an angle Θ to this average director. The order parameter S of a phase is defined by (Tsvetkov, 1942)

(2.1) Liquid Crystal Displays - изображение 27

where the bracket indicates that the average over a large number of molecules with angles Θ is taken. In a perfectly ordered state, Θ = 0, and hence S= 1. A completely unordered phase has S = 0. In typical nematic phases, S lies in the region of 0.4 to 0.7, indicating that the molecules are rather disordered.

The energy needed for a phase transition, e.g., from smectic A to smectic C , is characterized by a transition enthalpy in kJ/mol. Extensive investigations of phase transitions have revealed the temperature dependence of physical parameters such as the helical pitch, the viscosity or the elastic coefficients.

Due to the ordered structure, all phases between Tm and Tc are anisotropic, meaning that all dielectric, optical and mechanical properties depend upon the direction.

The dielectric constant is ε = ε r ε 0, where ε 0= 8.854.10 -12F/m stands for the permittivity in vacuum and ε rfor the relative dielectric constant. This means, as shown in Figure 2.1, εr = ε ||in the direction parallel to the director and perpendicular to the director leading to the dielectric anisotropy Figure - фото 28perpendicular to the director, leading to the dielectric anisotropy

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