History of LCD-technique
In 1888, an
Austrian named Friedrich Reinitzer discovered that cholesterol benzoate melted to form a milky
liquid. Upon heating the liquid further, it became transparent. Later, it
was shown that the liquid was birefingent, a property previously known
only to certain crystals, but until then not observed in
liquids.
Normally, the
molecules in these organic materials have rod-like structures that are not
completely randomly orientated above the melting point but form various
structures with some degree of long range ordering within certain
temperature ranges. The possibility of using liquid crystals as optical
shutters has been known for over 50 years. However, the development of
displays did not start until the beginning of the 1960’s. The principle of
the first liquid crystal display was based on light scattering. In 1971, a
description of the twisted nematic (TN) effect was published by Schadt and
Helfrich. A few years later, this initiated a revolution in LCD-watches
and calculators.
The word liquid is often associated with something fluid
and the word crystal something solid; the
expression liquid crystal therefore appears to
be contradictory. The word crystal implies that
there is some degree of long range order in the
structure. A crystal such as quartz has a
regular structure where the molecules are held in an ordered arrangement.
However, glass is an amorphous
material where the molecules are arranged in random positions and
orientations with no order being present.
Phases of matter
Substances normally
occur in three different phases; solid, liquid & gas. The solid phase
can be either crystalline or amorphous (super-cooled liquids). When
crystalline solids are heated, they normally melt to form an amorphous
liquid with an irregular structure. Lowering the temperature of the liquid
causes it to return to the solid phase with a crystalline
structure.
Nematic liquid
crystals are organic materials and the molecules often have rod-like
forms. One example of a liquid crystal molecule is the low molar mass
material p-n pentyl-p’-cyanobiphenyl (5CB).
Phases of liquid crystal (LC) materials
In the solid phase,
the liquid crystal (LC) molecules are arranged in a crystalline
structure. At the melting point, the material transforms between a solid
phase and a liquid crystal (LC) phase. In this phase, there is no short
range stacking order but a long range macro-structure does exist. Unlike
other materials, a liquid crystal material possesses several different
liquid phases depending upon the temperature. Heating the liquid crystal
phase further transforms the material into an amorphous
phase.

Liquid crystal
materials often consist of elongated, rod-shaped molecules that resemble a
liquid in that they are free to flow, but differ from it in that within a
certain temperature range, the molecular shape gives rise to a long range
stacking order. Other molecular shapes that display this phenomenon
include discs and rectangular formed molecules.
Nematic phase of liquid crystal
materials
The long range
stacking sequence displays several different phases depending upon the
temperature and geometry of the liquid crystal molecules. The most
commonly used phase as far as LCD’s are concerned is the nematic phase. Here, the LC molecules possess a
natural tendency for the molecular director axes to align parallel with
each other, whilst their centre of masses remain randomly distributed throughout the
material.

Smectic phases of liquid crystal
materials
A lowering of the
temperature from the nematic phase may produce a further ordering of the
LC structure by causing the molecular centre of masses to align in layers,
although the molecules still remain randomly distributed within each
individual sheet of LC material. This produces both the Smectic A and Smectic C
phases in which the average molecular axes are aligned respectively
perpendicular to and with a small tilt angle away from the planes of these
layers.
Further temperature
reduction beyond this point finally produces the crystalline, solid phase in which the material
also possesses stacking order within the individual layers themselves and
are hence held rigidly in an ordered lattice.

Elastic constants of liquid crystal
materials
We can define an
elastic constant for a liquid crystal material that gives the relative
ease of structure deformation with an externally applied force. However,
the amount of structure deformation depends upon the nature of the
deformation process.
This leads to there being three elastic constants for a liquid
crystal material, one for each of the three deformation mechanisms. In
general, it is relatively easy to induce twist deformation and
consequently k22 < k11 <
k33
Order parameter of liquid crystal
materials
To quantify the
degree of stacking order present in a liquid crystal material, an order
parameter (S) is usually defined where S = ½
<3cos2q – 1>. Here, q is the
angle between the director and the long molecular axis and an average is
taken for all molecules in the sample. The average of the cosine term is
zero for an isotropic liquid, giving the order
parameter as zero. For a perfect crystal, the order parameter
evaluates to one. Typical values for the order parameters of LC
materials lie between 0.3 and 0.9, with the value being a function of
temperature due to kinetic molecular motion.

Most liquid crystal
materials possess a working temperature range of about -20oC to +70oC. This
temperature range covers the majority of both commercial and industrial
applications. In applications where the liquid crystal display will be
out-door or in direct sunlight, a higher temperature range may be
required. The storage temperature is typically -40oC to +90oC.
Structure of a liquid crystal
cell
Twisted nematic (TN)
liquid crystal displays (LCD) are devices used for displaying images and
are found in many different consumer products such as digital clocks,
microwave ovens, CD players and many other modern electronic devices. LCD’s are common because they
offer many advantages over other display technologies; they are thinner
& lighter and require much less power than other display technologies
such as Cathode Ray Tubes (CRTs), etc. LCD’s are also highly cost
effective.

In a liquid crystal
display, the liquid crystal material is enclosed in a cell
consisting of two (2) substrates bonded together by the gasket along
the edges. An opening in the gasket allows the liquid crystal material to
be injected into the cell via the filling-hole. The gap between the
substrates is very thin and typical values lie between 2µm and 20µm. To
maintain the distance between the substrates, spacers are
often used. Spacers are small glass spheres or rods with uniform
diameters.

Surface molecular alignment in liquid crystal
cells
The inner-surfaces of
the liquid crystal cell are usually treated with an alignment
layer. The purpose of the alignment layer is to orientate the surface
liquid crystal molecules in a pre-defined direction. One method of
alignment is to deposit a thin polyimide layer
(100nm) over the inner-surfaces and form a series of microscopic scratches
in a uniform direction by gentle rubbing of a velvet cloth. In such case,
the liquid crystal molecules at the polyimide surface show a tendency to
align parallel to the microscopic groves with a small tilt angle of
between approximately 1.5° and 8°.
Other alignment
techniques also exist such as oblique vacuum deposition procedures. These
orientation methods generate different molecular tilt angles but the cell
still functions in essentially the same physical manner.
The liquid crystal
alignment at both sides of the cell is hence defined during cell
manufacturing. By careful control, any twist-angle can therefore be
induced in the helical structure across the liquid crystal layer. With a
twist-angle of exactly 90°, the standard 90° twisted nematic (TN) cell is
formed. Twist-angles of less than 90° form the low-twist (LT) cell whereas
by definition, super-twist cells are cells that possess twist-angles
exceeding 180°.
Twisted-nematic liquid crystal displays
(TN-LCD)
The twisted nematic
(TN) liquid crystal cell is frequently used in liquid crystal
displays (LCD’s). Here, the liquid crystal material is in the nematic
phase at room temperature. Characteristic for this type of liquid crystal
cell is that the orientation of the rod-like liquid crystal molecules strive to form a
90° twisting helical structure.
Twisted Nematic (TN),
Super Twisted Nematic (STN) and Active Matrix (AM-LCD) displays all use
the nematic liquid crystal phase for their operation. This phase is
selected for its physical properties and the widest temperature range. It
should be noted that the fluids used for display purposes are often
mixtures of several different liquid crystal materials; by mixing several
liquid crystals together, a eutectic mixture will result with the melting
point depressed well below room temperature.
Optical activity of liquid crystal
materials
In the limit of large
cell thickness, a twisting helical structure is capable of rotating the
plane of linearly polarised light with nearly 100% efficiency. Light
rotation occurs due to the inherent anisotropic index of refraction
(birefringence) present in the molecules of the liquid crystal material.
Here, incident radiation experiences two refractive indices depending upon
the oscillation direction; no corresponding
to the ordinary ray with the electric field vector oscillating
perpendicular to the molecular director and ne for the extra-ordinary ray oscillating
parallel to this axis. A phase factor or retardation is therefore
introduced between the two light components upon passage through the
liquid crystal material, inducing a rotation of the
polarisation.
The birefringence or
anisotropic index of refraction, Dn, is defined
as being Dn = (ne -
no). The
majority of liquid crystal materials possess positive anisotropic indices
of refraction, typically lying between +0.05 and +0.30 (i.e ne > no).
The optic-axis of
the liquid crystal material is defined as being in a direction parallel with
the rod-like molecules and along this axis there is no birefringence
(retardation). However, the liquid crystal material exhibits birefringence
in directions perpendicular to the optic axis.
In general, the
refractive index, n, is both wavelength and
temperature dependent, although in practice the variations are relatively
modest, n becoming somewhat smaller both with
increasing wavelength and temperature until the clearing point is reached.
Above the clearing point, rapid molecular rotations average out the
refractive indices for both light components and the anisotropic index of
refraction for the material approaches zero.
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discussing the efficiency of the twisting nematic helical structure to
rotate the plane of polarisation of incident light.
Dielectric anisotropy of liquid crystal
materials
The molecules of a
liquid crystal material also possess a dielectric anisotropy; hence can be
predominantly aligned upon application of an external electric field
across the cell. This destroys the natural helical stacking structure of
the device and forms the homeotropic phase. In
the homeotropic texture, the optical activity of the device is
predominately removed.