InterferenceReturn to Table of ContentsDiffraction


Polarization

In studying polarization, we can split light into two cases: that of a single electromagnetic wave, and that caused by the superposition of multiple waves. The case of a single electromagnetic wave is fairly straightforward. We have already seen that light is a transverse electromagnetic wave, with the electric field and the magnetic field oscillating at right angles to each other and the direction of propagation. The field define specific planes, and thus a single electromagnetic wave is said to be linearly, or plane, polarized. The plane is defined as that which contains the electric field, E, and the propagation vector, k.

When there are two or more waves superimposed in a region the situation becomes more complicated. For simplicity, we can restrict our attention to two waves. When the electric field vectors are collinear, the resulting field will simply combine to form another linearly polarized wave. However, if the two waves are not collinear, then the second wave can be split into collinear and perpendicular components. The collinear component will form a linearly polarized wave again. The resultant wave formed by the perpendicular components can have various states of polarization.

Linear Polarization

Start with two orthogonal waves

 formula                                       (14.1)

and

 formula                                    (14.2)

where epsilon is the relative phase difference between the waves, both of which are traveling in the z direction. The resulting superposition of these waves is

 formula.                                      (14.3)

If formula the waves are said to be in phase. In this case,

 formula.                                   (14.4)

This wave has a fixed amplitude equal to formula, which shows that this wave is also linearly polarized. Similarly, if formula, the resultant wave is again linearly polarized, but now the original waves are said to be out of phase.

Circular Polarization

Another special case comes about when both of the original waves have equal amplitude and a relative phase difference of formula. In this case
formula

and

formula,

so that the resulting wave is given by

 formula.                               (14.5)

Notice that the scalar amplitude, E0, is a constant, but the direction of the amplitude varies with time. This implies that the amplitude is not restricted to a single plane as before, but instead rotates so that the axis of rotation (as given by the right hand rule) is opposite the direction of motion. The angular frequency of the rotation is omega. This wave is said to be right circularly polarized. In a similar way, if formula, then the resulting wave is

                                formula.                                (14.6)

In this case the wave rotates with the axis of rotation in the same direction as the motion, and the wave is said to be left circularly polarized.

As an interesting aside, a linearly polarized wave can be constructed from two oppositely polarized waves,

 formula       (14.7)

This wave has an amplitude of twice the original wave and is linearly polarized in the x plane.

Elliptical Polarization

The three polarization states that we have found so far are really special cases of elliptically polarized light. To find the magnitude of elliptical polarization, start with (14.3)

 formula.       (14.8)

From (14.1), we have that

formula

so that (14.8) becomes

                            formula               (14.9)

Since EE = Ex + Ey, this can be solved to yield

formula.

Squaring both sides and rearranging yields

 formula.                     (14.10)

This is the equation of an ellipse making an angle alpha with the (Ex,Ey) coordinate system such that

 formula.                                           (14.11)

If we rotate the (Ex,Ey) coordinate system through an angle alpha, this takes on the more familiar form,

 formula.                                           (14.12)

To see that both circularly polarized and plane polarized light are special cases of equation (14.10), consider the following. If formula, and Ex,0 = Ey,0 = E0, then (14.10) becomes

 formula                                                   (14.13)

which is the equation of a circle. Similarly, if formula, equation (14.10) is

 formula                                                  (14.14)

This is the equation of a straight line with a slope of formula.

Using our results so far, we can now describe a particular wave of light in terms of its specific state of polarization. If the light is linearly, or plane, polarized, then we say it is in the P­state. Light that is in right (left) circularly polarized is in the R- (L-) state. Finally, elliptically polarized light is referred to as being in the E-state.

Angular Momentum

According to quantum mechanics, an electromagnetic wave carries energy in quantized packets called photons. The energy of each photon is given by the relation

 formula                                                           (14.15)

and the intrinsic angular momentum, or spin, of a photon is either -h bar or +h bar, where the sign indicates right- or left-handedness, respectively. It is important to note that the angular momentum of a photon is completely independent of its energy. Whenever a charged particle emits or absorbs electromagnetic radiation, along with changes to its energy and linear momentum, it will undergo a change of plus minush bar in its angular momentum.

The energy transferred to a target by an incident monochromatic wave can be viewed as being a stream of identical photons. Thus, a purely left­circularly polarized plane wave will impart angular momentum to the target as if all the constituent photons in the beam had their spins aligned in the direction of propagation. Similarly, right-circularly polarized wave have their spin opposite the direction of propagation.

Malus's Law

An optical device which takes in unpolarized light and which outputs polarized light is known as a polarizer. How do we determine whether or not a device is actually a linear polarizer? Simple deduction tells us that if unpolarized light is incident on a linear polarizer, then P-state polarized light is the result. The orientation of the P-state determines the transmission axis of the polarizer.

Now suppose that a second polarizer is inserted into the light path. This second polarizer is known as the analyzer. If the analyzer is placed at an angle theta with respect to the polarizer, then the amplitude of the electric field that exits the analyzer is E0 costheta. From this, we see that the irradiance behind the analyzer is

 formula.                                              (14.16)

When theta = 0, a maximum amount of irradiance is transmitted, so (14.16) can be rewritten as

 formula,                                                 (14.17)

where formula. Equation (14.17) is known as Malus's law. By using Malus's law, we can determine experimentally if a material is a linear polarizer or not.

Dichroism

Dichroism is the selective absorption of one of the two orthogonal P­state components of an incident light wave. A dichroic polarizer is physically anisotropic; producing a preferential absorption of one field component while being essentially transparent to the other.

The simplest form of a dichroic polarizer is a grid of parallel conducting wires. There are also certain materials which are inherently dichroic due to the anisotropy which exists in their crystal structure. One of the best known naturally occurring examples is the mineral tourmaline. Certainly the most famous dichroic material is the Polaroid sheet. The initial Polaroid was known as the J­sheet. It was made from the mineral herapathite. These crystals were ground into submicroscopic crystals, which we aligned by using magnetic or electric fields. They could also be mechanically aligned using a viscous colloidal suspension. By drawing this suspension through a long, narrow slit, the resulting sheet acts effectively like a large flat dichroic crystal. Unfortunately, the individual submicroscopic crystals still scattered light so that the J-sheet resulted in images which were somewhat hazy. The more common type of Polaroid is the H­sheet. It does not use dichroic crystals, but instead consists of a molecular analogue of the wire grid. Each separate dichroic entity is known as a dichromiphore. In the H­sheet the dichromiphores are molecular sized, so scattering is reduced to minimal levels.

Birefringence

Many crystalline substances are optically anisotropic. This means that their optical properties are not the same in all directions within the sample. The dichroic crystals are one subgroup of this phenomenon. It is convenient to represent optically isotropic substances as a spherically charged shell bound to a positive nucleus by springs of equal strength. For anisotropic substances, we can envision the springs as being pairs of springs with differing stiffness. An electron that is displaced from equilibrium along a direction parallel to one set of "springs" will oscillate with a different characteristic frequency than if it were displaced in some other direction.

The usefulness of this model can be seen by considering how light propagates through a transparent medium in reality. We have seen that the light excites the electrons within the medium. The electrons are driven by the electric field; they re-radiate secondary wavelets, which then recombine and the resultant wave continues on. The speed of the wave, and thus the index of refraction, is determined by the difference between the frequency of the electric field and the natural, or characteristic, frequency of the electrons. An anisotropy in the binding force will therefore be manifest in an anisotropy in the index of refraction. A material of this sort, which displays two different indices of refraction, is said to be birefringent.

Scattering

When an electromagnetic wave encounters an atom or molecule, it interacts with the bound electron cloud, transferring energy to the atom. Using the spring model for the electron cloud, we see that the effect is the same as if the ground state of the atom was set into motion. This motion will oscillate about the nucleus with a frequency equal to the frequency of the harmonic electric field. For most cases, the amplitude of the oscillation will be small; however, if the field frequency, nu, is near the resonant frequency of the atom, then a significant amount of energy can be transferred. In particular, when the field frequency equals the resonance, the atom will transition from the ground state into one of its excited states. In this case, all of the energy in the photon in absorbed by the atom.

An atom in the excited state is not stable, and it will eventually return to its ground state. If the atom is in a dense media, the excess energy will usually be dissipated thermally. On the other hand, when the atom is in a rarefied gas, the atom will usually release the energy through the emission of a new photon. This process is known as resonance radiation. The emitted photon will have no knowledge of its previous direction and will be sent with equal probability in any direction.

When the frequency is away from resonance, the electrons vibrate with respect to the nucleus. The atom can then be viewed as a set of oscillating dipoles. This causes the atom to radiate electromagnetic energy at a frequency equal to that of the incident field. This nonresonant emission propagates out in the standard dipole radiation pattern described earlier. The absorption of energy out of an incident wave by the atom, and the subsequent reemission of some of that energy is known as scattering. It is the underlying physical mechanism responsible for reflection, refraction and diffraction.

In addition to electron oscillations in an atom, which generally result in absorption and emission of ultraviolet light, there are also atomic oscillators. In this case the constituent atoms in a molecule vibrate about the center of mass of the molecule. These oscillations usually have resonances in the infrared region of the spectrum due to the larger masses associated with atoms.

The amplitude of an oscillator, and thus the amount of energy removed from the incident wave, increases as the frequency of the wave approaches one of the natural frequencies of the atom. Assuming that the energy is not lost via thermal interactions, we find that the scattered wave carries of more and more energy as the incident frequency approaches a resonance.

Lord Rayleigh was the first to work out the dependence of the scattered flux density on frequency. He found that the scattered flux density is directly proportional to the fourth power of the incident frequency. This result is in agreement with the radiation pattern associated with an oscillating dipole. The scattering of light by objects that are small in comparison with the wavelength of the incoming wave is known as Rayleigh scattering.

Stokes Parameters

So far, we have described polarization in terms of the electric field component of the incident light wave. In general, this incident field can be described using elliptical polarization, where the period of the orbit of the electric field around the ellipse is equal to that of the original light wave. This period is too short to be detected. Standard measurements are usually averaged over comparatively long time intervals, and the nuances of the polarization are lost. From this perspective, it is advantageous to use an alternate description of polarization; one which is based on observable quantities. The easiest quantity that can be found is the irradiance. It will be seen that this formulation will serve as a link between the classical and quantum mechanical view of radiation.

The modern formulation of polarized light has its origins in the work of G. G. Stokes in 1852. He introduced four quantities which are functions only of observables of the electromagnetic wave. These quantities are now know as the Stokes parameters. In order to understand the parameters, image that we have a set of four filters, each of which, under natural illumination, will transmit half of the incident light, discarding the other half. The choice of filters is not a unique one, and a number of equivalent possibilities exist. For our purposes, suppose that the first filter is an isotropic one, passing all polarization states equally. Let the second and third filters be linear polarizers whose transmission axes are horizontal and at +45degrees, respectively. Choose the last filter so that it is a circular polarizer which only transmits R-states. If each filter is placed singly in the path of the light beam, then we can assume that the transmitted irradiances are measured to be I0, I1, I2, and I3. Then the operational definition of Stokes parameters are

 formula                                                  (14.17)

where S0 is the incident irradiance, and S1, S2 and S3 specify the state of polarization. Physically, we can interpret the last three as follows. S1 is a statement of the amount that the polarization resembles either a horizontal P­state (so that S1 > 0) or a vertical P-state (where S1 < 0). When S1 = 0, the beam is either elliptical at plus minus45degrees, circularly polarized, or unpolarized. In a similar way, S2 represents the likelihood that the light is in a P-state oriented at +45degrees (when S2 > 0), -45degrees, (when S2 < 0), or neither (S2 = 0). Finally, S3 is related to the probability that the beam is in a R-state (S3 > 0), L-state (S3 < 0), or neither (S3 = 0).

We can connect the Stokes parameters with the electromagnetic field directly by using the expressions for quasimonochromatic waves,

      formula                                  (14.18)

and

  formula                                  (14.19)

where E = Ex + Ey. From the definition of irradiance, Stokes parameters become

 formula, (14.20)

where formula and we've dropped the constant formula.

If the beam is unpolarized, then formula. In this case formula, and S1 = S2 = S3 = 0. It is convenient to normalize the Stokes parameters by dividing each one by S0. This implies that the incident light has an irradiance of unity. The set of parameters (S0, S1, S2, S3) for unpolarized light is then (1, 0, 0, 0). If the light is horizontally polarized, the normalized parameters are (1, 1, 0, 0). Similar results can be found for other orientations. Notice that for completely polarized light,

 formula,                                              (14.21)

while for partially polarized light

 formula,                                           (14.22)

where V is defined as the degree of polarization.

Jones Vectors

Another representation of polarized light, which compliments that of the Stokes parameters, was invented in 1941 by R. Clark Jones. His method is more concise, but it should be noted that it is only applicable to polarized waves. If the wave is polarized, we can represent the beam as a column vector consisting of the electric field vector,

 formula.                                                 (14.23)

Such a vector is called a Jones vector. Notice that a knowledge of E allows us to know everything about the polarization state, while the phase information, script phix and script phiy, enables us to also handle coherent waves. The sum of two beams is formed by the sum of the corresponding components. Thus, when E0,x = E0,y = E0 and script phixscript phiyscript phi, E is given by

formula.

Frequently we do not need to know the exact amplitude and phase of the polarized components. In this case we can normalize the irradiance to unity to get

                                                             formula.                                              (14.24)

Notice that Eh and Ev form an orthonormal set. In other words, 

formula

and 

formula.

In a similar manner, EL and ER are orthonormal. Thus, any polarization state can be described as a linear combination of either one of the orthonormal sets. This approach has great importance in quantum mechanics, where we are dealing with orthonormal wave functions. 


InterferenceReturn to Table of ContentsDiffraction

Last updated: July 24, 1997

Comments to: D-Suson@tamuk.edu