Superposition of two electrons

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Discussion Overview

The discussion revolves around the concept of superposition in quantum mechanics, specifically regarding the possibility of superposing multiple electrons and the implications for their wave functions. Participants explore theoretical frameworks, mathematical representations, and the nature of many-body systems in quantum mechanics.

Discussion Character

  • Exploratory
  • Technical explanation
  • Conceptual clarification
  • Debate/contested
  • Mathematical reasoning

Main Points Raised

  • Some participants question whether two electrons can be represented in superposition as distinct states, raising concerns about probability conservation and the emergence of a new particle.
  • Others argue that in a multi-electron system, indistinguishability leads to Fermi-Dirac statistics, requiring an asymmetric total wavefunction and complicating the superposition principle.
  • One participant notes that superposition can occur when there is no interaction between particles, suggesting that the Hamiltonian must not contain mixed variables for this to hold.
  • Several participants discuss the representation of wave functions for two electrons, debating whether a single wave function can encapsulate the system or if it must be described with multiple variables.
  • There is mention of the Slater determinant as a relevant concept for constructing wave functions in multi-particle systems, particularly for fermions.
  • Some participants assert that the wave function must account for all spatial coordinates of the particles involved, emphasizing the necessity of using six coordinates for two electrons.
  • There is a discussion on the conditions under which wave functions can be expressed as products of single-particle wave functions, noting that this is generally not possible unless the particles are non-interacting.

Areas of Agreement / Disagreement

Participants express differing views on the nature of superposition for multiple electrons, with no consensus reached on whether a single wave function can adequately describe the system or the implications of indistinguishability and interaction. The discussion remains unresolved regarding the specifics of wave function representation in multi-electron systems.

Contextual Notes

Limitations include the dependence on definitions of distinguishability and interaction, as well as the complexity introduced by considering spin in the total state space.

Kruger
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I have a simple question. In quantum mechanics the superposition principle is given:

psi=c1*psi1+c2*psi2+...

Now, is it possible that psi1 is an electron A and psi2 is an electron B? I mean can we bring several electrons in superposition? Couldn't this violate the probability conservation? And can we say psi is a new particle created out of the two other electrons?
 
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Kruger said:
I have a simple question. In quantum mechanics the superposition principle is given:

psi=c1*psi1+c2*psi2+...

Now, is it possible that psi1 is an electron A and psi2 is an electron B? I mean can we bring several electrons in superposition? Couldn't this violate the probability conservation? And can we say psi is a new particle created out of the two other electrons?

First of all, it would be very strange if your psi's represents different electrons IF the system contains only one. Where would the 2nd electron come from if you have, let's say, a hydrogen atom?

Secondly, in multi-electron system, you can have the indistinguishibility phenomena kicking in, giving you the Fermi-Dirac statistics. In that case, a whole set of new rules comes into play and your total wavefunction must be asymmetric. Look further in your QM text for quantum statistics. You will see that the wavefunction can be in a superpostion, but it isn't the simple linear series the way you have written. In fact, you will see the beginning of 'entangled' states there.

Zz.
 
Superposition principle can occur when there is not interaction between particles. I mean, if in the hamiltonian there are not mixed variables, so you can make the state space as the tensor product of the spaces of individual particles, then you can apply the superposition principle. But if you have some like [tex]\hat S_1 \cdot \hat x_2^2[/tex] (something very strange) then you can´t.
 
As I recognised we can't really take a linear combination, as you said ZapperZ. But what is then meant by the different psi's of:

psi = c1*psi1 + c2*psi2 + ...

And another question:

I saw in my textbook that we can describe a many body system like the helium atom with a wave function psi(electron1, electron2). But isn't there a way to make a wave function like psi(WholeState). I mean, my psi(e1, e2)=psi(x1,y1,z1;x2,y2,z2) isn't really the same thing as psi(WS)=(x,y,z).
 
Kruger said:
As I recognised we can't really take a linear combination, as you said ZapperZ. But what is then meant by the different psi's of:

psi = c1*psi1 + c2*psi2 + ...

It means that a system has a probability to be in state psi1, another probability to be in a state psi2, etc... This is true even for a single particle. This is what Schrödinger was trying to illustrate with his cat.

And another question:

I saw in my textbook that we can describe a many body system like the helium atom with a wave function psi(electron1, electron2). But isn't there a way to make a wave function like psi(WholeState). I mean, my psi(e1, e2)=psi(x1,y1,z1;x2,y2,z2) isn't really the same thing as psi(WS)=(x,y,z).

Eh?

Zz.
 
Ok, the state psi can be represented as a linear combination of several possible states psi1, psi2. If I understand this correctly.

With the second question I mean this: let's say we have two free electrons described by the wavefunctions psiE1 and psiE2. Now what happens in nonrelativistic quantum mechanics (not quantum field theory) if the two electron wave functions "come" together? Do we then have an effetive state described by a wave function of the form psi(E1, E2)=psi(x1,y1,z1; x2,y2,z2) or can we build a wave function of the form psi(WholeSystem)=psi(x,y,z). Do you see the difference? I ask, if we can represent the system of the two electrons with a single wave function containing only the position variables x,y,z or can't we do that and have to describe the effective wave function with six position variables (three for each electron).
 
Kruger said:
Ok, the state psi can be represented as a linear combination of several possible states psi1, psi2. If I understand this correctly.

With the second question I mean this: let's say we have two free electrons described by the wavefunctions psiE1 and psiE2. Now what happens in nonrelativistic quantum mechanics (not quantum field theory) if the two electron wave functions "come" together? Do we then have an effetive state described by a wave function of the form psi(E1, E2)=psi(x1,y1,z1; x2,y2,z2) or can we build a wave function of the form psi(WholeSystem)=psi(x,y,z). Do you see the difference? I ask, if we can represent the system of the two electrons with a single wave function containing only the position variables x,y,z or can't we do that and have to describe the effective wave function with six position variables (three for each electron).

You construct something resembling the Slater determinant, and in the case of a 2-particle system, you end with either a single state, or a triplet state, i.e. the system can have two possible configuration depending on how the spins are alligned.

Zz.
 
Ah, thanks, I saw something in my textbook called the Slater determinant. Didn't know, that is has something to do with all that. Thanks
 
Kruger said:
Ok, the state psi can be represented as a linear combination of several possible states psi1, psi2. If I understand this correctly.

With the second question I mean this: let's say we have two free electrons described by the wavefunctions psiE1 and psiE2. Now what happens in nonrelativistic quantum mechanics (not quantum field theory) if the two electron wave functions "come" together? Do we then have an effetive state described by a wave function of the form psi(E1, E2)=psi(x1,y1,z1; x2,y2,z2) or can we build a wave function of the form psi(WholeSystem)=psi(x,y,z). Do you see the difference? I ask, if we can represent the system of the two electrons with a single wave function containing only the position variables x,y,z or can't we do that and have to describe the effective wave function with six position variables (three for each electron).

You *must* have a wavefunction of the form Psi(x1,y1,z1;x2,y2,z2). The meaning of this wavefunction is the following: the square of its magnitude, Psi Psi* represents the probability of finding one of the two particles in a small volume element located at x1, y1,z1 and the other particle located at x2,y2,z2. Since there are two particles, there *must* be be 6 cooordinates. That's the answer to your question.

Now, going a bit further...The question obviously becomes whether it's possible to write this wavefunction in terms of products of wavefunctions of one particle. In general, no. But if the two particles are not interacting, it is possible, although not in a trivial way. The answer depends on whether the two particles are distinguishable or undistinguishable, and if they are undistinguishable, it depends on whether they are fermions or bosons.

Patrick
 
  • #10
nrqed said:
You *must* have a wavefunction of the form Psi(x1,y1,z1;x2,y2,z2). The meaning of this wavefunction is the following: the square of its magnitude, Psi Psi* represents the probability of finding one of the two particles in a small volume element located at x1, y1,z1 and the other particle located at x2,y2,z2. Since there are two particles, there *must* be be 6 cooordinates. That's the answer to your question.

If system's hamiltonian only contains spatial coordinates (such as {x,y,z} or else) you only need one wavefunction to describe the system. But, if you consider spin, since the total state space is built as [tex]\mathcal E = \mathcal{E}_{spatial} \otimes \mathcal{E}_{spin}[/tex] then, a base may be the tensor product of the basis, so the dimension of the whole space state will be higher.

In fact, the spin degeneracy is '2s + 1' (for example, the degeneracy for electrons is 2 so we use +/- to distinguish that two different states with the same energy).

For electrons, (s = 1/2) including the spin makes that we need two wavefunctions to describe the whole system. [tex]\Psi_+[/tex] and [tex]\Psi_-[/tex] or as an spinor [tex]\binom{\Psi_+}{\Psi_-}[/tex].

This is only for a one-particle system and I didn't say yet nothing about Pauli, but its important to say that not all of the mathematical states are allowed, for fermions we must have antisymmetrical states and for bosons symmetrical states (linear symmetric/antisymmetric combinations of the basis vectors since the eigenfunctions of the whole hamiltonian don't have to have symmetry well defined).

Being more general, the number of wavefunctions needed is the dimension of the space state, but considering the symmetry we may need less functions
 

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