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Dr. Umber Kalsoom
2023
_____________________________________
Department of Physics
University of Engineering and Technology Lahore
KERR EFFECT
History
The Kerr effect, named after the Scottish physicist John Kerr, is a phenomenon observed in
applied electric field. In 1875 Kerr discovered that a glass plate to which a strong electric field
was applied became birefractive. His first publication on what came to be known as the Kerr
Background
The Kerr effect occurs in materials that lack inversion symmetry, meaning that their crystal
a material, the electric field induces a polarization in the material, causing its refractive index
to change. The nonlinear Kerr effect is characterized by a nonlinear relationship between the
refractive index change and the applied electric field. The induced polarization is proportional
to the square of the electric field strength. This effect is much stronger and is observed in
Introduction
Monochromatic, vertically polarized light impinges on a PLZT element (lead-lanthanum-
zirconium-titanium compound) which is set in its holder at 45° to the vertical. An electric field
is applied to the PLZT element and causes it to become birefractive. The phase-shift between
the normal and the extraordinary light beam behind the PLZT element is recorded as a function
of the applied voltage and it is shown that the phase-shift is proportional to the square of the
electric field strength respectively of the voltage applied. From the constant of the
The process where the change in refractive index is proportional to the square of the electric
field is called the Kerr effect. (An analogous process where the change is proportional to the
electric field is called Pockel's effect and only occurs in anisotropic media.) The Kerr effect,
Two special cases of the Kerr effect are normally considered, these being the Kerr electro-optic
effect, or DC Kerr effect, and the optical Kerr effect, or AC Kerr effect [2].
polar liquids, such as nitrotoluene (C7 H7 NO2 ) and nitrobenzene (C6 H5 NO2 ) exhibit very large
Kerr constants [3], [4]. Higher values of the Kerr constant allow complete transmission to be
achieved with a smaller applied electric field. A glass cell filled with one of these liquids is
called a Kerr cell. These are frequently used to modulate light, since the Kerr effect responds
very quickly to changes in electric field. Light can be modulated with these devices at
frequencies as high as 10 GHz. Because the Kerr effect is relatively weak, a typical Kerr cell
Pockels cells, which can operate at much lower voltages. Another disadvantage of Kerr cells
is that the best available material, nitrobenzene, is poisonous. Some transparent crystals have
also been used for Kerr modulation, although they have smaller Kerr constants [5].
Problem
1. The phase-shift between the normal and the extra-ordinary light beam is to be recorded for
different voltages applied to the PLZT-element respectively for different electric field
2. By plotting the square of the applied voltage versus the phase shift between normal and
extraordinary beam it is to be shown that the relation between the two quantities is
approximately linear. From the slope of the straight line the Kerr constant is to be calculated.
Experimentation
Equipment:
Apparatus Quantity
Measuring amplifier 1
Digital multimeter 2
The experiment for the demonstration of the Kerr effect is set up as shown in Fig. 1. The PLZT
element is connected directly to the HV power supply whose voltage can be altered between 0
and 1000 Volt with a sufficiently high precision by using a digital voltmeter branched in
parallel to the HV power supply. Do not exceed 1000 V; this will damage the PLZT element.
The light source is He/Ne laser, the power of which is 1 mW. Caution: Never look directly into
Important: Before performing any measurement of luminous intensity the He/Ne laser has to
4. Take down the I0 value. (When both polarizer and analyzer are at 0°.
6. Adjust the voltage to 300 V. (a) count for 5 sec and record the output voltage from the
voltmeter. (b) reduce the voltage to zero and wait for 1 minute.
7. Increase the voltage in steps of 25V, from 300V until 1000V, and tabulate your
As can be seen from Fig. 1, the light from the He/Ne laser which is vertically polarized on
passing through the polarizer, impinges on the PLZT element which is set in its holder at 45°
to the vertical. The incident linearly polarized wave can be regarded as the superimposition of
two “in phase” oscillating waves which are polarized, one perpendicularly and the other
parallel, to the PLZT element and to the electric field that is applied to the PLZT element.
The two light waves pass through the PLZT element at different speeds. The light wave which
oscillates parallel to the electric field of the PLZT element is delayed relative to the light wave
which oscillates perpendicularly to the applied electric field of the PLZT element. This
produces a phase difference between the two waves and the light which has passed through the
Kerr cell (PLZT element) will be elliptically polarized. This results in the analyzer, which is
located behind the Kerr cell at 90° to the polarizer, no longer being able to extinguish the
polarized light.
For a phase difference between the two waves of λ/2 a linear polarized wave results from the
superimposition of the two waves after they have passed through the PLZT element.
This linearly polarized wave is turned by 90° with respect to the direction of incidence, e.g.
with respect to the vertical. The applied voltage is therefore called the “half-wave voltage”. In
this case the light intensity behind the analyzer which is at an angle of 90° to the polarizer will
show a maximum.
A silicon photodiode with amplifier is used as the detector for the luminous intensity behind
the analyzer.
The PLZT element used in this experiment has the advantage that the birefraction, represented
by the Kerr constant, is more than two orders of magnitude larger than for nitrobenzene and
voltages of a few hundred volts are sufficient in order to study the electro-optical effects of the
ceramic element. This one is transparent for wavelengths from 0.4 to 5.6 µm. Its chemical
compositions here described by the formula Pb 0.9125 La 0.0875 Zr 0.65 Ti 0.3503. With
regard to the transmission of light the PLZT element behaves like a transparent polycrystal.
For λ = 633 nm its transition ratio is more than 60%. With respect to an applied electric field,
it behaves like a ferromagnetic substance which is submitted to a magnetic field. Within the
PLZT element there are already prepolarized domains which grow or which are reoriented by
the applied electric field. In this way, the element becomes optically anisotropic respectively
out that the element can deal with modulation frequencies of up to 100 kHz.
Fig. 2 shows a cross-section of the PLZT element. The active element 1 of the modulator is a
parallelpiped of height = 8 mm, length = 1.5 mm and width = 1.4 mm. The width represents
the distance between the electrodes. The electric field strength is given by the ratio of voltage
applied over the distance between the electrodes. The path of the light beam within the element
is equal to the length of the element. Active element (1) is encapsulated using silicon hermetics
(2) an isolating ring (3) and glued between two glass plates (4). As optical glue (5) Canadian
balsam was used. Wire (6) are fixed on the electrode faces of the element and connected with
Method of analysis
The light wave, whose field vector oscillates parallel to the electric field, is called the
extraordinary beam whereas the wave oscillating perpendicular to the field is known as the
normal beam. If the corresponding refractive indices are designated by 𝑛𝑎𝑜 and 𝑛𝑜 and l is the
distance in the PLZT element covered by the light, then there is a difference in optical paths
𝑙(𝑛𝑎𝑜 − 𝑛𝑜 )
polarization P. If we anticipate that the polarization is a linear function of the electric field
strength E and the proportionality factor is designated by 2πk, then the following relation is
obtained:
∆= 2πKlE 2 (2)
K is kerr constant.
E can be expressed by the applied voltage V and the inter-electrode distance d
V
E= (3)
d
The luminous intensity I behind the analyzer is obtained for the given experimental apparatus
(polarizer and analyzer crossed and at 45° to the electric field on the PLZT element) from the
relationship (1):
Δ
I = Io sin2 (4)
2
𝐼𝑜 is the luminous behind the analyser when the polarizer and the analyser are aligned in the
same direction and the electric field on the PLZT element is zero. After substituting (2) in (4)
πKlV 2
I = Io sin2 (5)
d2
Solving the equation for V 2 gives:
d2 I
V2 = sin−1 √ (6)
πKl Io
From eq (2)
I
Δ = 2 sin−1 √ (7)
Io
be derived from its slope, because the geometrical dimensions l and d for the Kerr cell (PLZT
1. The relative luminous intensity behind the analyser is measured as a function of the
Tab1e 1 shows the experimentally measured values. The corresponding graphic is shown
in Fig. 3. The phase shift is clearly indicated as well as the voltages for which maxima and
minima of luminous intensity are observed. At a voltage of 615 Volt the luminous intensity
reaches a maximum for the first time. In this case the normal and extraordinary beam are
phase-shifted by 180°. 615 Volt is therefore the “half-wave voltage”. It is a function of the
2. In Fig. 4 the square of the voltage applied to the PLZT element is represented as a
𝑣𝑜𝑙𝑡 2
regression a straight line was found whose slope is 1.9 × 103 . Using Equ. (6)
𝑑𝑒𝑔𝑟𝑒𝑒
m
we find with I = 1.5 mm and d = 1.4 mm a value of 2.0 × 10−9 volt2 for the Kerr
Table 1: Voltage V across the PLZT-element, light intensity I behind the analyzer and phase
shift ∆ between normal and extraordinary beam. Measured maximum current Io =0.881 µA.
Voltage Square Intensity Relative Phase shift (∆) Phase shift Phase shift
(V) Voltage (I) luminous (∆) (∆)
𝑰
(V2) intensity ∆= 𝟐 𝐬𝐢𝐧−𝟏 √ measured Actual
𝐈 𝑰𝒐
(𝐈)
𝐨
Volts [Volts]2 [µA] [Degree] [Degree] [Degree]
300 90000 0.042 0.047673099 25.225 25.225 25.225
350 122500 0.044 0.049943246 25.829 25.829 25.829
400 160000 0.055 0.062429058 28.940 28.940 28.940
450 202500 0.088 0.099886493 36.851 36.851 36.851
500 250000 0.148 0.167990919 48.396 48.396 48.396
550 302500 0.256 0.290578888 65.243 65.243 65.243
600 360000 0.387 0.439273553 83.030 83.030 83.030
650 422500 0.590 0.66969353 109.848 109.848 109.848
700 490000 0.694 0.787741203 125.143 125.143 125.143
750 562500 0.740 0.839954597 132.846 132.846 132.846
800 640000 0.697 0.791146425 125.621 125.621 234.379(360-∆)
850 722500 0.465 0.527809308 93.195 93.195 266.805(360-∆)
900 810000 0.199 0.225879682 56.758 56.758 303.242(360-∆)
950 902500 0.180 0.20431328 53.749 53.749 306.250(360-∆)
1000 1000000 0.441 0.500567537 90.072 90.072 450.072(360+∆)
1050 1102500 0.640 0.726447219 116.938 116.938 476.938(360+∆)
1100 1210000 0.568 0.6447219 106.832 106.832 613.167(720-∆)
𝑰
Phase Shift [D] Calculated Phase shift using: 𝚫 = 𝟐 𝐬𝐢𝐧−𝟏
𝑰𝒐
25 26 29 37 48 65 83 110 125 133 234 267 303 306 450 477 613
1.0 1.0
0.9 0.9
Relative Intensity Strength [I/Io]
0.7 0.7
0.6 0.6
0.5 0.5
0.4 0.4
0.3 0.3
0.2 0.2
0.1 0.1
0.0 0.0
HWV 754.05884 volts HWV 1050 volts
200 300 400 500 600 700 800 900 1000 1100 1200
Voltage [V]
Figure 3: Relative luminous intensity I/I0 behind the analyzer as a function of the voltage U
applied to the PLZT element and the phase-shift ∆ between normal and extraordinary beam.
I
Plot the graph of vs V (volt) in Fig. 3 indicate clearly the phase shift as well as the voltages
Io
for which maxima and minima of luminous intensity are observed. Determine the voltage at
which the luminous intensity reaches a maximum for the first time. At this voltage the normal
and extraordinary beam are phase-shifted by 180°. It is therefore the ″half wave voltage″
(HWV). The experimentally determined value of HWV is 754 volts. It is a function of the
PLZT element composition and of the temperature. As applied voltage greater than half wave
voltage, horizontally wave again start turning to vertical orientation. Hence intensity of light
When Polarizer at 0°, V=0 (At PLZT), Analyser at 0°, Then Intensity of light is maximum
(Io = 0.881 µA) detected on detector and corresponding measurement of current (µA) on
multi-meter.
When Polarizer at 0°, V=0 (At PLZT), Analyser at 90° (Condition is called cross condition),
When Polarizer at 0°, V=300 volts (At PLZT), Analyser at 90° (Condition is called cross
At 0° phase shift there is linearly (vertically) polarized light. At 90° phase shift we get circular
polarized light. At 180° phase shift there is linearly (horizontally) polarized light. At phase
Equation y = a + b*x
Intercept 173803.84012 ± 30525.44219
1000000 Slope 1919.24976 ± 115.85142 1000000
Square voltage [V2]
Figure 4: Square of the voltage applied to the PLZT-element as a function of the phase-shift
Note Kerr constant value may vary for different histories and different elements. Higher the
value of Kerr constant indicates that the cut-off voltage is less (means voltage require to
Applications
Kerr Electro-optic Effect: The Kerr effect is also used in Kerr electro-optic devices, where
an applied electric field induces a change in the refractive index of a material, allowing the
modulation and control of light. Kerr electro-optic devices, such as modulators and switches,
All-optical switching: All-optical switches based on the Kerr effect can operate at ultrafast
speeds, as the response of the Kerr effect is typically on the order of picoseconds or
femtoseconds. This makes them highly suitable for high-speed optical communication systems,
Optical Kerr Effect Microscopy: The optical Kerr effect can be utilized in microscopy
techniques to study the properties of materials. Optical Kerr effect microscopy measures the
change in the polarization state of light as it passes through a sample under an applied electric
field. This technique provides valuable information about the molecular orientation and
dynamics of the sample, making it useful in materials science, chemical analysis, and biological
imaging [8].
Viva voice
Question 1
experimentally (Switching means, when the phase shift becomes 180 degree or its integral
multiple the light on the detector becomes on/off) means phase shift still takes place, but not
so effectively perhaps and the half wave voltage will be increased perhaps. Because in that case
we will not be able to take effective advantage of anisotropy associated to PLZT crystal.
Question 2
Answer
Kerr constant also known as the electro-optic coefficient indicates the strength of the Kerr
effect in a material. Higher values of the Kerr constant allow complete transmission to be
achieved with a smaller applied electric field. Subsequently, high kerr constant means
relatively low voltage are enough to pass the light from Kerrcell.
Question 3
What are the limitations of using nitrobenzene as Kerr cell?
Answer
Nitrobenzene, is poisonous and injurious to health. It classified as a toxic compound and should
References
[4] J Philip and T A Prasada Rao, “A high-voltage pulse measuring system based on the Kerr
effect,” Meas Sci Technol, vol. 2, no. 6, p. 565, 1991, doi: 10.1088/0957-0233/2/6/014.
[7] P. Weinberger, “John Kerr and his effects found in 1877 and 1878,” Philos Mag Lett, vol. 88,
no. 12, pp. 897–907, Dec. 2008, doi: 10.1080/09500830802526604.
[8] D G Tyson and B R Jennings, “Measurement of the ‘optical’ Kerr effect induced by
nanosecond laser pulses,” J Phys D Appl Phys, vol. 24, no. 5, p. 645, 1991, doi: 10.1088/0022-
3727/24/5/001.