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added angular momentum operators and hydrogen atom basics
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10
HW
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HW
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Quantum Mechanics Assignments
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Chap 2: 2, 3, 14, 15, 17, 22, 23
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Chap 5: 2, 6, 8, 12, in-class assignment
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Chap 9: 7, 11, 12, 13, 14
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Chap 7: 7, 8, one from last class, 11
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due friday 3-18
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@ -55,7 +55,4 @@ Understanding a System:
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With the eigenvalue equation
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❬r❙E,l,mₗ❭ = E❬r❙E,l,mₗ❭
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❬r❙E,l,mₗ❭ = E❬r❙E,l,mₗ❭
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@ -1,4 +0,0 @@
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[L̂𝓏,p̂𝓏] = ιħp̂𝓎
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[L̂𝓏,p̂𝓍] = -ιħp̂𝓎
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[L̂𝓏,p̂𝓏] = 0
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[L̂𝓏,p̂²] =
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20
lecture_notes/3-16/hydrogen atom
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20
lecture_notes/3-16/hydrogen atom
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V = E͟_͟Z͟ (?)
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r
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❬r❙E,l,mₗ❭ ≝ R(𝐫) ≝ U͟(𝐫͟)
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r
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∂²/∂r² (u/r) + 2/r ∂/∂r U/r
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= ∂/∂r (1/r (∂/∂r u) - u/r²) + 2/r ((1/r ∂/∂r u) - u/r²)
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= 1/r (∂²/∂r² u) - 2/r^2 ∂/∂r u + 2 u/r³ + 2/r² ∂/∂r u - 2u/r³
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= 1/r (∂²/∂r² u)
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So,
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(-ħ/2m ∂²/∂r² + Veff(│r│)) = V(│r│) + l͟(l͟+͟1͟)ħ͟²͟
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2mr²
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| ↓ |
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Centrifugal
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barrier
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lecture_notes/3-18/overview
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lecture_notes/3-18/overview
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Vibrations and rotations of a diatomic molecule
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atoms vibrate about an equilibrium position r₀
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⊙~~~~~~~~~⊙
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|← r₀ →|
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(pic MISSEd) potential, with taylor approximation
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(pic MISSEd) A taylor series solution is appropriate to solve this diffEQ.
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Experiments indicate vibration (E~visible light) has more energy than rotation (E~infrared), so vibrations happen much faster.
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The Rotational eigen-value spectrum
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L²,L̂𝓍,L̂𝓎,L̂𝓏 (Hermition operators)
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Say
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L̂𝓏❙Ψ❭ = mₗħ❙Ψ❭
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(pic) mₗ is bound by λ: m has value from -λ to λ
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Introduced raising and lower operators
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L̂± = L̂𝓍 ± ιL̂𝓎 = (pic) proof = ±ħL±
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L̂𝓏(L̂ ± ❙λ,mₗ❭) => (pic) proof => L̂± ❙λ,mₗ❭ = ❙λ,mₗ±1❭
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Very important point:
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Let m=l be the maximum value of m
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L̂₊❙λ,l❭ = 0 (required because wave function goes to 0 in a forbiddin region)
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This is also true for L̂₋❙λ,l′❭ with l′ the minimum value of m
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(pic) L̂₋L̂₊❙λ,l❭ = ...
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gives λ = l(l+1)
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(pic) L̂₊L̂₋❙λ,l′❭ = ...
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gives λ = l′(l′+1)
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These show that m = -l, -l+1, 0, l
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solutions/chap7/prob7
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88
solutions/chap7/prob7
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Angular momentum system is prepared in the state
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❙Ψ❭ = 1͟ ❙11❭ - 2͟ ❙10❭ + ι͟2͟ ❙22❭ + ι1͟ ❙20❭
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√10 √10 √10 √10
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Possible results of 𝐋² measurement?
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The 𝐋̂² operator was developed in lecture and in the text. The related eigenvalue equation is
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𝐋̂²❙lm❭ = l(l+1) ħ²❙lm❭
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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.
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For lm = 11 & 10, 𝐋̂² = 2ħ²
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For lm = 22 & 20, 𝐋̂² = 6ħ².
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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.
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𝓟(𝐋̂²=2ħ²) = │❬11❙Ψ❭│² + │❬10❙Ψ❭│².
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❬11❙Ψ❭ = ❬11❙⎛ 1͟ ❙11❭ - 2͟ ❙10❭ + ι͟2͟ ❙22❭ + ι1͟ ❙20❭ ⎞
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⎝ √10 √10 √10 √10 ⎠.
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The eigenstates for this system are LaPlace's spherical harmonic functions, which comprise an orthogonal set, I.E.:
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❬lm❙l′m′❭ = δₗₗ′ δₘₘ′.
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│❬11❙Ψ❭│² = │❬11❙ 1͟ ❙11❭│² = ¹/₁₀.
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│ √10 │
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│❬10❙Ψ❭│² = │❬10❙ 2͟ ❙10❭│² = ⁴/₁₀.
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│ √10 │
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(𝐚)
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𝓟(𝐋̂²=2ħ²) = ½.
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No need to calculate the other set: since the vector is normalized, the probability of measuring 𝐋̂²=6ħ² is also
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𝓟(𝐋̂²=6ħ²) = ½.
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For 𝐋̂𝓏 the eigenvalue equation is
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𝐋̂𝓏❙lm❭ = mħ❙lm❭,
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so the expected measurements are,
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for lm = 11 & 21, 𝐋̂𝓏 = ħ.
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for lm = 10 & 20, 𝐋̂𝓏 = 0.
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In this case, the probabilities will be
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𝓟(𝐋̂𝓏=ħ) = │❬11❙Ψ❭│² + │❬21❙Ψ❭│² and
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𝓟(𝐋̂𝓏=0) = │❬10❙Ψ❭│² + │❬20❙Ψ❭│².
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The method has already been demonstrated, so taking the probability components and summing,
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(𝐛)
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𝓟(𝐋̂𝓏=ħ) = ²/₁₀.
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𝓟(𝐋̂𝓏=0) = ⁸/₁₀.
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Histogram of probabilities:
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𝓟 𝓟
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╭─────────────────┬────────────────╮
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1 │ │ │ 1
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│ │ │
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.8 │ │ ▧ │ .8
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│ │ ▧ │
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│ │ ▧ │
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.5 │ ▧ ▧ │ ▧ │ .5
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│ ▧ ▧ │ ▧ │
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│ ▧ ▧ │ ▧ │
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│ ▧ ▧ │ ▧ ▧ │
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.1 │ ▧ ▧ │ ▧ ▧ │ .1
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╰─────────────────┼────────────────╯
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2ħ² 6ħ² │ 0 ħ
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𝐋̂² │ 𝐋̂𝓏
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h
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3322
solutions/chap7/prob7.ps
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3322
solutions/chap7/prob7.ps
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