5. The Harmonic Oscillator Flashcards

1
Q

What is good about the Harmonic Oscillator and the TISE?

A

It is exactly solvable for potential

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2
Q

Describe u(x) and V(x) for the harmonic oscillator

A

u(x) - wave funciton

v(x) - 1/2 k’ x^2

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3
Q

Describe the difference between the classical potential and the harmonic oscillator (V(x))

A
  • Classically, V(x) is the spring constant

- Now it is the curvature of the potential well

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4
Q

State the solutions for the wave functions for the harmonic well

A

u_n(x) = c_n sin( (n+1) pi*x/L)

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5
Q

What is the solution called when n = 0 for the harmonic well?

A

The ground state

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6
Q

State the ground state solution for the wave functions for the harmonic well

A

u_0(x) = c_0 sin(pi*x/L)

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7
Q

What should the ground state solution for the harmonic oscillator look like?

A
  • Symmetrical
  • Peak at 0
  • Tend to 0 for x -> ± infinity
    Page 3 on document
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8
Q

What form does the harmonic oscillator shape have for the ground state?

A

A Gaussian

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9
Q

State the Gaussian solution for the harmonic oscillator ground state

A

u_0 = c_0 exp(-α x^2)

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10
Q

Which SE do you use to solve the Gaussian shape for the ground state of the harmonic oscillator?

A

TISE and equate the squared and non squared terms

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11
Q

What solution is obtained for the ground state energy by solving the TISE with the Gaussian

A

E_0 = 1/2 h_bar w

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12
Q

How can you find c_0 from the Gaussian?

A

By integrating the modulus squared of u_0 over all space and setting it equal to 1

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13
Q

Describe u_0 and u_1 for the harmonic oscillator for 0 < x < L

A

u_0 - even function about L/2. 1 Maxmimum
u_1 - odd function about L/2. 2 Maxima
Page 3 on document, but shift the curve from -L/2 < x < L/2 to 0 < x < L

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14
Q

State the trial solution for u_1(x) for the harmonic oscillator

A

u_1(x) = c_1 (x)xexp(-α x^2)

Multiply by a pre factor of x (odd) to generate the shape on page 3 of document

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15
Q

What solution is obtained when solving for the n=1 state of the harmonic oscillator?

A

E_1 = 3/2 h_bar w

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16
Q

State the general energy solution for the harmonic oscillator

A

E_n = (n + 1/2) h_bar w

17
Q

State the eigenvalue spectrum for the harmonic oscillator

A

H_hat u_n(x) = E_n u_n(x)
u_n(x) - eigen function
H_hat - Hamiltonian (energy operator)
E_n - eigenvalue

18
Q

What is the classical assumption about the ground state?

A

That it has 0 KE and minimum (0) PE

19
Q

What does the classical assumption about the ground state violate?

A

The H.U.P

20
Q

Why is the ground state energy non-0?

A

Because of the “fuzziness” in x and p_x

21
Q

What conditions must be met if we want to approximate any potential well?

A
  • Must be sensible

- Use a parabolic potential provided we stay close to the minimum (small oscillation)

22
Q

Describe the peak and trough of a potential graph

A

Peak - unstable equilibrium

Trough - stable equilibrium

23
Q

What assumption can we make about diatomic molecules?

A

They are two masses connected by a spring

24
Q

How do we model the separation of the two masses of a diatomic molecule?

A

x_0 - the “nuclear” separation

25
Q

How are the longitudinal oscillations described for a diatomic molecule?

A

By the TISE solution - A “ladder” of quantum states and wave functions

26
Q

Describe how the energy eigenvalue spectrum changes for the diatomic molecule

A

E_n = (n+1/2) h_bar w
but now w = sqrt(k’/μ)
here k’ - spring constant
μ - reduced mass = m1m2/m1+m2

27
Q

What is μ for the diatomic molecule?

A

The reduced mass = m1m2/m1+m2

28
Q

What is k’ for the diatomic molecule and what does it reflect?

A

The spring constant - reflects the strength of the chemical bond

29
Q

Describe how we can “see” the molecular vibrations

A

The gap between states E_n and E_n+1 is the vibrational energy level.
A photon of energy h_bar w is absorbed and the molecule “jumps” to the next energy level

30
Q

Describe how isotopes would change the components of the diatomic molecule energy eigenvalue spectrum

A

One of the masses change, so the reduced mass μ changes. The chemical bonding is NOT changed, hence k’ is the same.