General Flashcards
What factors influence light-solid interaction
Light matter interactions are fundamentally a function of the material and the light source where the optical properties are described through the refractive index
Light (light-matter interactions)
This is a transverse electromagnetic wave with an electric and magnetic field which oscilate perpindicular to the direction of propogation at an optical frequency of 1013-1017 hz which includes UV, visible, and IR.
Fundamentally light is EMR governed by Maxwell’s equations and produced by the acceleration of electric charges.
Solids (light-matter interactions)
These are considered to be materials of positive and negative charged particles with inducible dipoles
Interaction (light-matter)
The fundamental interaction of light and matter is that light polarizes the atoms by nature of its transverse electromagnetism to produce oscillating dipole moments. The interaction produces either reflection, transmission, absorption, or scattering.
Dipole moments
This is defined as qx where q is the partial charge and x is the distance of the partial charge from equilibrium
Electronic oscillations
This is the concept of electrons surrounding the nucleas behaving like springs where they oscillate about the positively charged protons. In this model there are several electrons attached to springs surrounding the nucleas that oscillates like a hula hoop.
Because mass of electrons is so much less than that of the nucleas the shifting electronic field of EMR makes the electrons shift with respect to the nucleas and not vice versa
Resonant frequency
This describes the frequency of light that coincides with the frequency of oscillations in order to create constructive interference.
Resonant frequency of electronic oscillations
ω is proportional to (1/me + 1/mn).5 = (1/μ).5 where m=mass and μ = reduced mass. Because me<
Resonant frequency of electronic oscillations speed
These are the easiest to induce and therefore and the fastest and have frequencies in the UV and visible spectra. They are a function of collisions, electronegativity, and orbital arrangements
Vibrational oscillators
This is a type of dipole based on charged atoms that are bonded to one another vibrating from their equilibrium position. It is dependent on the rigidity of the bond and the degree of covalent nature.
Because the speed of this type of action is slower the resonant frequency is in the IR range. The oscillating atoms create phonons.
Quantum Theory version of vibrational oscillators
Quantum theory says that electrons do not vibrate in a bond but are elevated from the inner orbitals into the conductance bands at the resonant frequency where they emit photons when returning to the ground state
Free electron oscillator’s
These are electrons that are within the outer orbits of large atoms (like metals) that can oscillate from light interactions without any true restoring force. These oscillations have a resonant frequency of 0.
In metals these are known as the conductance electrons and are responsible for the reflective nature of metals.
Polarization of a Medium Equation
P = εo χ E where
P=Polarizability of the medium (dependent variable)
εo = permittivity of a vacuum =
χ = Dialectric susceptibility of the medium
E = electric field that the material is within
This is the basic way of describing how a material behaves but is best applied to net effects
Diaeletric
A dielectric is an insulator that can be polarized in an electric field not because of electron flow but electron drift. The negative charges in atoms align with the negative end of the electric field and the positive charges to the positive side of the field.
These are effectively capacitors
Electric Susceptibility
χ represents the electric susceptibility of a dielectric material. It is a property of the material that represents the ease at which is polarizes in response to an electric field.
It directly influences the electric permittivity of the material.
Vaccum permittivity
This represents the ability for an electric field to exist in a vacuum. It is given in terms of F/m which represents the capacitance per meter of space.
εo = 8.854 * 10-12
Polarizability of a medium meaning
This represents the density of moment dipoles in the medium. Thus, it is given in C/m2 It represents how easily a material accumulates charge at a point that is not equilibrium.
Moment dipole = qx
3 levels of polarizability with EMR
At low frequency (radio/microwave) χ (magnetic susceptibility) is highest because the wavelength is long enough for materials to reorient to constructively interfere with the EMR. It is a rotational shift.
In the IR/Vis there is vibrational and electronic dipoles. It slowly decreases with frequency in this space. In the lower frequencies (IR) the vibrational dipoles create heat through distortion of the bonds. This is phonons
In the visible and higher frequencies only, electronic vibrations occur because these are the fastest so they can occur rapidly. They resonate with electronic vibrations to create photons.
polarizability with consideration of induced dipoles
P = εo ( χ *E + χ2*EE + χ3*EEE+…)
This equation fundamentally says that the various oscillations of the atoms and charged particles induce impacts onto the polarizability of a material
In most optics (except lasers nothing above the second order term matters.
This represents that the polarizability of the material in electronic oscillations is influenced by the induced electric fields produced within oscillations.
The Dipole Oscillator Model
This says that within electronic vibrations we consider the electron to fluctuate with their natural resonant frequency (ωo) with dampening. Their position is given by
me ( d2x/dt2 + γ (dx/dt) + (ωo)2x) =qE
where γ = dampening constant and x is given by the motion of the electron from the equilibrium point along the vector of E
This fundamentally says that F = ma where a = d2x/dt2
Dipole moment of a Lorentz oscillator (e with springs)
For N = #of charges/volume
P = Σ qx = E*N [q2/m /(ωo2 - ω2 + iγω)] where ω = the frequency of light and ωo =natural frequency of the oscillator
This is found by using E = Eo eiωt as an induced oscillation created by the EMR with the dipole oscillator equation. It represents how polarizable a material is within an EMR interaction
Real Refractive index of a material with 1+ oscillator
n2 = 1 + (q2/εom) (Σin Ni/(ωi2 -ω + iγi ω)
where n = refractive index
εo = permittivity of an electric field in a vacuum
Ni = number of i atoms
ωi = resonant frequency of atom i
γi = dampening of the atom i
ω = frequency of light
The Complex Refractive index
n = n + ik
n = real refractive index = c/v
k = extinction coefficient which is proportional to the absorption coefficient (α) which is related to the dissapation/attenuation of light
How does n vary with ω
IF ω i then n is ~constant and low
IF ω = ωi then n is increases rapidly because iγi ω is ~0. This produces a resonance line.
IF ω > ωi then n is ~ 1
How does n vary with frequency in visible light?
n is proportional to c* ω so at higher ω n increases which changes the angle of refraction and creates dispersion
When are materials transparent?
This occurs between resonant frequencies where n ~n and thus almost no dampening occurs because dampening is given by the term iγi ω
Electric field for a light wave
E = Eo ei(kz - ωt) where
k = the wave vector = nω/c if transparent = (n + iK)(ω/c) with absorption
Plugging this in
E = Eo e-(ωKz)/c ei(ωnz/c - ωt)
Where Eo e-(ωKz)/c is the amplitude and ei(ωnz/c - ωt) represents the real refractive index of a wave
The important part about this function is that it exponentially decays with z
Absorption coefficient
α = 2Kω/c where K = extinction coefficient ω = angular frequency of light
Claussis Masetti equation for isotropic media
n2 - 1 / n2 + 2 = χ/3 This says that for sufficiently dense media that the dipoles of nearby atoms influence the polarization of each dipole. χ is the electric susceptibility which is directly related to P
Four Measurable Optical Parameters
You can measure reflection, absorption, scattering, and transmission
Reflection
R = IR/Io = [(n-1)2 + k2]/ [(n+1)2 + k2]
where: I = beam intensity (lumens)
* n*=real refractive index of the material
k = extinction coefficient ~0 for transparent materials
Absorption
This occurs when the angular frequency of light = resonant frequency and vibrational oscillations lead to changes in kinetic energy due to attenuation of the wave (friction)
α = attenuation efficiency
Absorption Equation
This is given by Beer’s law which says
I(z) = Io e-αz so it decays exponentially with α being the absorption efficiency coefficient.
Scattering
This is the idea that certain light is not attenuated in a solid but the waves are split and change direction which lowers E
Scattering Equation
I(z) = Io e-Sz Where: S = scattering coefficient
S is proportional to 1/λ4
Scattering and attenuation
Because we cannot measure the difference between S and α we say αT = S + α but S is ~0
Conservation of Energy when measuring light
For light with an intensity of Io upon entering a material
1 = (IR/Io) + (I<span>T</span>/Io) + (IA/Io) = R + T + A
Where R = reflection, T = transmission, and A = absorption
Transmission equation
T = (1-R)2 e-αl
Where: R = reflection coefficient
α = attenuation efficienvy
l = thickness of the material
T = proportion of light transmitted