Vous êtes sur la page 1sur 10

# 5.

## What is your picture? Quantum mechanical?

BEFORE AFTER
hν (No more photon)
Molecule in Molecule in
ground state excited state

This quantum mechanical picture may satisfy conservation of energy (when you
quantize light and molecular energies), but it has lots of problems and doesn’t tell
you much.

## (1) Light: An oscillating electric (and magnetic) field

(2) Matter: Treat as a harmonic oscillator
(3) Interactions: Oscillating external force field driving harmonic oscillator

1) Light

## An oscillating electromagnetic field, which oscillates in time and space.

( ) () (
E r, t = εˆ r E o cos ωt − k ⋅ r − φ )
Polarization vector Wavevector defines
direction of propagation

Amplitude
2π ω
λ c
c = 2.998 × 108 m / s
To simplify:
(1) Propagate along x̂ ; (2) φ = 0 (for the time being we will drop the polarization)

E ( x, t ) = E o cos ( ωt − kx )

λ= oscillations in space
k
E
E0

x
propagating at c
2π 1
time : = oscillations in time
ω ν

Now, we will drop wave vector ( k → 0 , since λ>>x and we consider molecules at x=0)

c
E ( t ) = E o cos ωt
2
I= Eo

(2) Molecules

## → treat as harmonic oscillator

Why should we be able to call molecules harmonic oscillators? i.e., a mass on a spring?

## 5.33 Lecture Notes: A Classical Model for Spectroscopy Page 2

The covalent bond can be thought of as a spring.

## The equilibrium length is a balance between attractive and repulsive forces. If we

push/pull on this bond, there is a restoring force that pushes the system back to
equilibrium.

## → Electronic states—think of pushing electron clouds away from equilibrium

distribution. (for instance, benzene pi orbitals)

## → Magnetic resonance—In a magnetic field, magnetic spin moments—nuclear

spins—align with field.

## V(q) • For molecules, we expect

anharmonic curves that
reflect attractive and
repulsive forces.
• A finite amount of energy
pulls the molecule apart.
1  ∂ 2 V 
V(q ) = (q − q 0 )2
2  ∂q 
2

1 2
= kQ
2

q0 q

Q=0
(Set Q = q − q0)

## 5.33 Lecture Notes: A Classical Model for Spectroscopy Page 3

k is force constant

∂V
Linear restoring force: Fres = − = − kQ
∂Q

∂ 2Q
Equation of Motion from Newton F = ma m
∂t 2

∂ 2Q
m 2 = Fres + Fdamp + Fext driving force
∂t
∂Q
= − kQ − b + Fext
∂t

∂ 2Q b ∂Q kQ Fext
+ + =
∂t 2 m ∂t m m
with light field
Fext (t ) = Fo cos ωt

Solutions:

## a) Harmonic oscillator with no damping/no external force

∂ 2Q
m 2 + kQ = 0
∂t
Solution:
Q ( t ) = A sin ( ωo t ) + B cos ( ωo t )
drop for now

k
resonance frequency: ωo =
m

## 5.33 Lecture Notes: A Classical Model for Spectroscopy Page 4

Oscillations at ω0 continue forever.

Q
A

ω0

b) Now we add damping—H.O. may feel friction that reduces the amplitude of
oscillation

∂ 2Q ∂Q
m 2 = Fres + Fdamp = − kQ − b
∂t ∂t

∂ 2Q b ∂Q kQ
+ + =0
∂t 2
m ∂t m

## Q ( t ) = A e − γt sin Ω o t Now oscillation decays away exponentially

2
γ = b / 2m Ω o = ωo − γ 2 ≈ ωo

## Q reduced for weak

frequency damping
A e − γt

Ω0
5.33 Lecture Notes: A Classical Model for Spectroscopy Page 5
Rewrite equation of motion:
for F (t ) = 0
∂ 2Q ∂Q Fext ( t ) Q(t ) = e −γt sin Ωot
+ 2 γ + ω2
0 Q =
∂t 2 ∂t m

## You know what to expect:

The effect depends on the frequency of the driving field . . . like pushing someone on
a swing.

## • The most efficient way to push someone higher is to push at a frequency

corresponding to their swinging frequency
• This leads to a big displacement.
• If you push with arbitrary frequency, nothing will happen.

## So you know that we should have a “resonance”:

• When you drive the system with frequency ω ≈ ω o there will be an efficient
transfer of power and the displacement of the H.O. will increase

Indeed, that is what an absorption spectrum is! Measure the power absorbed by the
system from the field.

## Now let’s solve the equation:

Set: F0 ∝ E0
Fext ( t ) = Fo cos ωt

Fo m
Q ( t ) = A sin ( ωt + β ) = sin ( ωt + β )
( ( ω − ω ) + 4γ ω )
1
2 2
2
2 2 2
o

ω2o − ω2
tan β =
2 γω

## 5.33 Lecture Notes: A Classical Model for Spectroscopy Page 6

Notice that it oscillates 90° out of phase with field when driven on resonance. →
absorbing power from field.

## If γ << ω o and near resonance ω o ≈ ω

(ω − ω2 ) = ( ωo − ω) ( ωo + ω) ≈ 4ωo2 ( ωo − ω)
2 2 2 2 2
o

Fo m
Q(t) = 1 sin ( ωt + β )
2ωo ( ωo − ω) + γ 2 
2 2

 

## power = force × velocity

∂Q
Pavg = F (t )⋅
∂t avg

Fo2 γ

4 m (ω − ω o )2 + γ 2

## Let’s plot the power absorbed as a function of frequency:

LORENTZIAN LINESHAPE
peak is at ω = ωo

At what frequency
shift relative to
Pav(ω) γ maximum is the
absorbed power
reduced by ½?

ω − ω o = ±γ
ω0 ω
The full-width at half-maximum intensity (FWHM) is 2γ .

peak → ω o width → γ

## 5.33 Lecture Notes: A Classical Model for Spectroscopy Page 7

So what are we learning about molecules?

Well, you can see from the spectrum that we have been able to determine ω o and γ.

## Take HCl. We take an IR absorption spectrum in solution, and we see:

A

ω0 ω

ω0
≅ 3000cm−1 γ ≅ 15cm −1
2π c

## ω o : We know the frequency of oscillation of the H-Cl bond:

2π −14
= τ = 1 × 10 s 10 fs
ω0

## How do we know that’s what we are seeing? We predict an isotope effect!

k
ω0 =
m

Now for the mass m we want to use the reduced mass µ or mR. (This is the
effective mass: we need this for 2 masses on a spring with a fixed center of mass.)

mAmB
µ = mR = for a diatomic molecule A-B.
mA + mB

µ ( H 35Cl ) = 0.97 ( ω0 ) A ( mR )B
=
µ ( D35Cl ) = 1.89 ( ω0 ) B ( mR )A

Therefore, we predict:
ω0 ( DCl ) → 2150cm −1

What is a?

## • An electric field interacts with charges on molecules.

• A neutral body should feel no force, but molecules are made of many charges
species and have positive and negative charges.

Dipole moment:
µ H

µ=Σql δ+

Cl
distance
δ-
charge
In an electric field, this dipole will feel a force.

V = −µ ⋅ E
∂V  ∂µ 
F=− = ⋅E
∂Q  ∂Q 

## • The E field oscillates along the polarization direction.

• If the bond is aligned with the electric field, then the oscillating field can act to
stretch or compress the bond through attractive and repulsive electrostatic
interactions with the charges.
• The ability of the field to act on Q depends on the alignment of the dipole moment
with the field. If there is an angle θ between µ and E, then

∂µ
F0 = E 0 cos θ (…for a single molecule)
∂Q

## 5.33 Lecture Notes: A Classical Model for Spectroscopy Page 9

So we have also been able to predict:

µ: The strength of the absorption peak is related to how much charge is moved when
you displace a coordinate:

## µ ⋅ E : Absorption will tell you about alignment of molecules:

You can study a crystal where all molecules have the same orientation, and how
by rotating the light polarization, you can tell how different vibrations are
oriented.

## These principles can be applied to electronic spectroscopy — higher frequency → for

instance, me << mw .