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Advanced Quantum Mechanics, Notes Based On Online Course Given by Leonard Susskind - Lecture 1
Advanced Quantum Mechanics, Notes Based On Online Course Given by Leonard Susskind - Lecture 1
Advanced Quantum Mechanics, Notes Based On Online Course Given by Leonard Susskind - Lecture 1
Measurables/observables represented by linear Hermitian operators; he will give them Latin letters
ie A,B etc
◼ if A acts on the state vector and returns the same state vector multiplied by a number then the
state vector is an eigenvector
◼ α outside the ket is eigenvalue; set of eigenvalues are the possible results of measurement
◼ the eigenvectors are the state vectors which give a definite answer, ie the associated
eigenvalue
◼ inner product of two states is a number (can be complex), can represent as < Ψ | Φ >
◼ if two states are uniquely distinguishable by measuring some quantity < Ψ | Φ >=0 ie are
orthogonal, physically identifiably different
x0
There are states that label position eg x0 > with the property that if you measure the position you
will definitely find it at x0
State vectors for different positions are distinguishable so < x | x’> = 0
Take any state of the particle and call it Ψ then <x|Ψ> = ψ(x) called the wave function
Probability density for particle at x, P(x)= ψ * (x)ψ(x) (the chance to find a particle at exactly x is
always zero, except when it is 1, in which case x is defined without any uncertainty; in this case the
momentum is completely undefined.)
Momentum
Next most important observable is momentum
∂ψ(x)
Pψ(x) = -i ℏ
∂x
ip0 x
∂ψ(x)
-i ℏ =p0ψ(x) Solution of type ψ(x) = e ℏ where ψ(x) is amplitude of position
∂x
Given the momentum is known and is p0 what is the probability for measuring position x?
-ip0 x ip0 x
e ℏ e ℏ =1 (just means that it is the same everywhere on the line and that we haven’t nor-
malised)
So the probability distribution is smeared out over the whole line whereas the wave function for a
definite position was a highly concentrated, infinitely narrow Dirac function.
If you know the momentum of a particle, its position is completely uncertain and likewise if you know
the position of a particle, its momentum is completely uncertain.
There is also a momentum representation ψ(p) that is connected to Fourier Transforms for ψ(x) but
we wont go into details here.
Generally the time evolution operation depends on the elapsed time, call it U(t). U stands for unitary
U(t)|Ψ(0)> = |Ψ(t)>
Postulate: Information is conserved. If two states are orthogonal they will evolve into states that are
still orthogonal.
This postulate also means that the inner product is preserved during time evolution.
Postulate gives: < Φ | Ψ > = < Φ |U † U| Ψ> so U † U = I (this is definition of unitary operator)
Unitary operators have eigenvalues that are a phase. A phase can be represented by a point on
the unit circle in the complex plane.
Consider the expansion of eϵh = 1 + ϵh where ϵ is small and h is some just a number
Now consider making ϵ twice as big then
rearranging:
1:03:20 Symmetry
Examples of symmetry:
If you take a system that satisfies a certain set of equations and transform it and the equations and
properties of the system don’t change then that transformation is called a symmetry.
Translation; if move an object and its properties are unchanged. But the presence of an object
might break the symmetry eg if translate eg into a furnace, then the symmetry is broken. If move
everything including the furnace then the symmetry is restored.
Hydrogen atoms have rotational symmetry ie if you rotate your co-ordinates the hydrogen atom isn’t
changed. Or if rotate hydrogen atom the hyrdrogen atom can’t tell it has been rotated. Assuming
nothing present to make direction distinguishable.
Squeezing something generally changes its properties and so is generally not a symmetry.
Assume V is unitary because if I have a symmetry and I have 2 states that are different from each
other and I apply the symmetry operation to each I expect them to stay different. Unitary operators
maintain the difference. V † V = I
We aren’t using U as we are saving that for special case of time evolution.
If there really is a symmetry then |Ψ1 ’> will evolve to the rotated version of |Ψ2 > ie |Ψ2 ’>
So, for a symmetry operation, the operation must commute with the time evolution operator.
To find symmetries need to look for operators that commute with the time-evolution operator.
A symmetry operation is a unitary operation on the space of states which commutes with the Hamilto-
nian.
Symmetry: [H,V]=0 this is the time derivative
2. Interchange a pair of similar particles. eg exchange two electrons. The particles are of exactly
the same kind so can’t tell they have been exchanged.
Time translation is a continuous thing made up of accumulting small changes so we can use the
same technique as we used earlier in the lecture for any continuous symmetry.
The same argument that told us H is Hermitian tells us that G is Hermitian in V = I - iϵG
Also: [H,I - iϵG] = 0 Note: everything commutes with the Identity I, iϵ factors out so [H,G] = 0
Remember: in earlier course we found that items that commute with Hamiltonian are conserved
∂ψ
ψ(x - ϵ) = ψ(x) - ϵ
∂x
∂
V=I -ϵ
∂x
∂ i ∂
Remember P = - i ℏ or P=
∂x ℏ ∂x
∂ i P
Since V = I - iϵG this gives iG = = P or G =
∂x ℏ ℏ
Px
So Generator of x translation is or without Planck’s constant P x
ℏ
1 px2
H = mvx2 =
2 2m
px2
[ , px ] = 0 as every function commutes with itself
2m
What if there are more directions in space? Then there are also symmetries along y and z.
That was an example of the connection between symmetries and conservation laws.
Next Lecture: Rotations and Group Theory and collections of Symmetries that don’t commute with
each other.