added angular momentum operators and hydrogen atom basics

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othocaes 2016-03-23 01:17:40 -04:00
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Quantum Mechanics Assignments
Chap 2: 2, 3, 14, 15, 17, 22, 23
Chap 5: 2, 6, 8, 12, in-class assignment
Chap 9: 7, 11, 12, 13, 14
Chap 7: 7, 8, one from last class, 11
due friday 3-18

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With the eigenvalue equation With the eigenvalue equation
❬r❙E,l,mₗ❭ = E❬r❙E,l,mₗ❭ ❬r❙E,l,mₗ❭ = E❬r❙E,l,mₗ❭

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[L̂𝓏,p̂𝓏] = ιħp̂𝓎
[L̂𝓏,p̂𝓍] = -ιħp̂𝓎
[L̂𝓏,p̂𝓏] = 0
[L̂𝓏,p̂²] =

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V = E͟_͟Z͟ (?)
r
❬r❙E,l,mₗ❭ ≝ R(𝐫) ≝ U͟(𝐫͟)
r
∂²/∂r² (u/r) + 2/r ∂/∂r U/r
= ∂/∂r (1/r (∂/∂r u) - u/r²) + 2/r ((1/r ∂/∂r u) - u/r²)
= 1/r (∂²/∂r² u) - 2/r^2 ∂/∂r u + 2 u/r³ + 2/r² ∂/∂r u - 2u/r³
= 1/r (∂²/∂r² u)
So,
(-ħ/2m ∂²/∂r² + Veff(│r│)) = V(│r│) + l͟(l͟+͟1͟)ħ͟²͟
2mr²
| ↓ |
Centrifugal
barrier

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Vibrations and rotations of a diatomic molecule
atoms vibrate about an equilibrium position r₀
⊙~~~~~~~~~⊙
|← r₀ →|
(pic MISSEd) potential, with taylor approximation
(pic MISSEd) A taylor series solution is appropriate to solve this diffEQ.
Experiments indicate vibration (E~visible light) has more energy than rotation (E~infrared), so vibrations happen much faster.
The Rotational eigen-value spectrum
L²,L̂𝓍,L̂𝓎,L̂𝓏 (Hermition operators)
Say
𝓏❙Ψ❭ = mₗħ❙Ψ❭
(pic) mₗ is bound by λ: m has value from -λ to λ
Introduced raising and lower operators
L̂± = L̂𝓍 ± ι𝓎 = (pic) proof = ±ħL±
𝓏(L̂ ± ❙λ,mₗ❭) => (pic) proof => L̂± ❙λ,mₗ❭ = ❙λ,mₗ±1❭
Very important point:
Let m=l be the maximum value of m
L̂₊❙λ,l❭ = 0 (required because wave function goes to 0 in a forbiddin region)
This is also true for L̂₋❙λ,l❭ with l the minimum value of m
(pic) L̂₋L̂₊❙λ,l❭ = ...
gives λ = l(l+1)
(pic) L̂₊L̂₋❙λ,l❭ = ...
gives λ = l(l+1)
These show that m = -l, -l+1, 0, l

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Angular momentum system is prepared in the state
❙Ψ❭ = 1͟ ❙11❭ - 2͟ ❙10❭ + ι͟2͟ ❙22❭ + ι1͟ ❙20❭
√10 √10 √10 √10
Possible results of 𝐋² measurement?
The 𝐋̂² operator was developed in lecture and in the text. The related eigenvalue equation is
𝐋̂²❙lm❭ = l(l+1) ħ²❙lm❭
The possible measurements of 𝐋̂² for this system are those associated with the initial state vector, i.e. the values lm = 11, 10, 22, 20.
For lm = 11 & 10, 𝐋̂² = 2ħ²
For lm = 22 & 20, 𝐋̂² = 6ħ².
Since the same 𝐋̂² is measures for two states, the sum of the probabilities of measuring those states is the probability of measuring that squared angular momentum.
𝓟(𝐋̂²=2ħ²) = │❬11❙Ψ❭│² + │❬10❙Ψ❭│².
❬11❙Ψ❭ = ❬11❙⎛ 1͟ ❙11❭ - 2͟ ❙10❭ + ι͟2͟ ❙22❭ + ι1͟ ❙20❭ ⎞
⎝ √10 √10 √10 √10 ⎠.
The eigenstates for this system are LaPlace's spherical harmonic functions, which comprise an orthogonal set, I.E.:
❬lm❙lm❭ = δₗₗ′ δₘₘ′.
│❬11❙Ψ❭│² = │❬11❙ 1͟ ❙11❭│² = ¹/₁₀.
│ √10 │
│❬10❙Ψ❭│² = │❬10❙ 2͟ ❙10❭│² = ⁴/₁₀.
│ √10 │
(𝐚)
𝓟(𝐋̂²=2ħ²) = ½.
No need to calculate the other set: since the vector is normalized, the probability of measuring 𝐋̂²=6ħ² is also
𝓟(𝐋̂²=6ħ²) = ½.
For 𝐋̂𝓏 the eigenvalue equation is
𝐋̂𝓏❙lm❭ = mħ❙lm❭,
so the expected measurements are,
for lm = 11 & 21, 𝐋̂𝓏 = ħ.
for lm = 10 & 20, 𝐋̂𝓏 = 0.
In this case, the probabilities will be
𝓟(𝐋̂𝓏=ħ) = │❬11❙Ψ❭│² + │❬21❙Ψ❭│² and
𝓟(𝐋̂𝓏=0) = │❬10❙Ψ❭│² + │❬20❙Ψ❭│².
The method has already been demonstrated, so taking the probability components and summing,
(𝐛)
𝓟(𝐋̂𝓏=ħ) = ²/₁₀.
𝓟(𝐋̂𝓏=0) = ⁸/₁₀.
Histogram of probabilities:
𝓟 𝓟
╭─────────────────┬────────────────╮
1 │ │ │ 1
│ │ │
.8 │ │ ▧ │ .8
│ │ ▧ │
│ │ ▧ │
.5 │ ▧        ▧    │           ▧    │ .5
   │   ▧        ▧    │           ▧    │    
   │   ▧        ▧    │           ▧    │    
   │   ▧        ▧    │   ▧       ▧    │    
.1 │   ▧        ▧    │   ▧       ▧    │ .1
   ╰─────────────────┼────────────────╯
2ħ² 6ħ² │ 0 ħ
𝐋̂² │ 𝐋̂𝓏
h

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