Why Does a 2π Rotation Change the Sign of a Wavefunction in Quantum Mechanics?

neelakash
Messages
491
Reaction score
1
The following is NOT a homework problem.I have difficulty in understanding something is a book quoted below:

After developing the concept of quantum mechanical angular momentum
[ I mean the relation L_z=m (h') where h' means h/2π
http://hyperphysics.phy-astr.gsu.edu/hbase/quantum/qangm.html]

a book says:

"The quantum mechanical origin of these strange restrictions lies in the require-
ment that if either the particle or the laboratory is turned through a complete
rotation around any axis,the observed situation will be the same as before the
rotation.Because observables are related to the square of the wavefunction,the
wavefunction must turn into either plus or minus itself under a rotation by 2π
radians.Its sign remains unchanged if the angular momentum around the rotation
axis is an integer multiple of h(i.e.,forbosons)but changes if the angular momen-
tum around the rotation axis is a half-integer multiple of h (i.e.,forfermions).
Because of this difference in sign under 2π rotations,bosons and fermions each
obey a different type of quantum statistics"

I cannot exactly follow the book here.How can exp[i 2π] result in - of the same wave function?

can anyone please explain?
 
Last edited by a moderator:
Physics news on Phys.org
neelakash said:
I cannot exactly follow the book here.How can exp[i 2π] result in - of the same wave function?

can anyone please explain?

If |\psi\rangle is the state before a rotation, then you can show that after a rotation by an angle \vec{\theta} the state is given by

e^\frac{-i\vec{J}\cdot\vec{\theta}}{\hbar}|\psi\rangle

If you perform a rotation by 2*pi, then by single-valuedness of the wavefunction, you must get back the same state UP TO A PHASE. In three dimensions you can show that this phase must be an overall sign (+ or -).

Now for a spin-1/2 particle

\vec{J}=\frac{\hbar}{2}\vec{\sigma}

so due to the 1/2, a rotation of 2*pi (in the z-direction, say) will give an overall phase of e^{i\pi\sigma_3}|\psi\rangle=-|\psi\rangle. Of course, there was nothing special about the z-direction, so this argument holds regardless of the choice of axis.
 
neelakash said:
I cannot exactly follow the book here.How can exp[i 2π] result in - of the same wave function?

can anyone please explain?

It does... In any way you rotate it, after 360 degrees it is in a state
which negatively interferes with parts of the wave function which
didn't (Say in a two split experiment) If you turn the laboratory
instead of the electron then the electron does not change, contrary
to what your book says, however, all other electrons in the laboratory
do change.

In principle, any object with spin angular moment senses rotations
of its spin axis, while an object with spin precession senses rotations
it makes about any arbitrary axis. So, presumably, there is a mechanism
at work which changes the state of the electron (fermion) during rotation
until the state is inverted after a rotation of 360 degrees.

The spin of an electron should be understood as a continuous spin
density distribution spread out over its wave function. Each point
represents an infinitesimal small point spin and magnetic moment.
Molecular modeling software uses this to calculate the total magnetic
field for instance to determine the magnetic properties of a material.

------------------

Compare spin 1/2 particles with the spin 1 electromagnetic field:

Polarized Light:
Polarized light has two independent components: Horizontal and
Vertical under an angle of 90 degrees. Horizontal polarized light
does not interfere with vertical polarized light. Light which is rotated
180 degrees interferes negatively with parts of the wave which are
not rotated.

Fermions
An electron has two independent components: Spin up and spin
down which are under an angle of 180 degrees. Spin up electrons
do not interfere with spin down electrons. An electron wave
function which is rotated 360 degrees interferes negatively with
parts of the wave which are not rotated.Regards, Hans
 
Last edited:
If you perform a rotation by 2*pi, then by single-valuedness of the wavefunction, you must get back the same state UP TO A PHASE. In three dimensions you can show that this phase must be an overall sign (+ or -).

I suppose this requires that "Because observables are related to the square of the wavefunction",right?

Hans de Vries, I fear I could not follow you.However,I have to read a couple of more times...

thanks to both of you.

regards.
 
neelakash said:
I suppose this requires that "Because observables are related to the square of the wavefunction",right?

yeah, that's the idea.
 
OK,thank you...
 
Not an expert in QM. AFAIK, Schrödinger's equation is quite different from the classical wave equation. The former is an equation for the dynamics of the state of a (quantum?) system, the latter is an equation for the dynamics of a (classical) degree of freedom. As a matter of fact, Schrödinger's equation is first order in time derivatives, while the classical wave equation is second order. But, AFAIK, Schrödinger's equation is a wave equation; only its interpretation makes it non-classical...
Insights auto threads is broken atm, so I'm manually creating these for new Insight articles. Towards the end of the first lecture for the Qiskit Global Summer School 2025, Foundations of Quantum Mechanics, Olivia Lanes (Global Lead, Content and Education IBM) stated... Source: https://www.physicsforums.com/insights/quantum-entanglement-is-a-kinematic-fact-not-a-dynamical-effect/ by @RUTA
Is it possible, and fruitful, to use certain conceptual and technical tools from effective field theory (coarse-graining/integrating-out, power-counting, matching, RG) to think about the relationship between the fundamental (quantum) and the emergent (classical), both to account for the quasi-autonomy of the classical level and to quantify residual quantum corrections? By “emergent,” I mean the following: after integrating out fast/irrelevant quantum degrees of freedom (high-energy modes...
Back
Top