Careful
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Vanesch said:Uh![]()
The idea is simply that we have "two electrons, one in the state "left to me and flying off to the left" and one in the state "right to me and flying off to the right".
The problem is that the way we write the (non-relativistic) wavefunction, we have to assign certain degrees of freedom as "belonging to electron 1", and other degrees of freedom as "belonging to electron 2".
But clearly, the physical description:
(A) we have "two electrons, one in the state "left to me and flying off to the left" and one in the state "right to me and flying off to the right"
and
(B) we have "two electrons, one in the state "right to me and flying off to the right" and one in the state "left to me and flying off to the left"
are equivalent physical descriptions ; in other words, they should not correspond to *different* physical states.
Sure, but this is entirely similar in classical mechanics, and there I will call the one flying to the left number one, and the one flying to the right number two. After this, I am never going to say that number one is flying to the right. Here, by definition both particles are distinguishable, since the labelling depends upon their physical properties.
Now, suppose I would color two particles in my box red and green then I have 50 percent chance (given random dynamics within the box) that the green (red) one is flying to the right (left) and 50 percent chance that it flies to the left (right) (in case the red one would always fly to the left for some reason then the following reasoning does not apply). So in this case, I have a statistical mixture which is very different from a superposition. So, now you are left with a dilemma, either you assume your wavefunction to be a description of an ensemble of particles giving rise to independent emissions and then you might proceed as usual (but then the wavefunction is extremely nonlocal in a *spatio-temporal* sense). On the other side, on the individual level, it clearly makes no sense and you are left with the conclusion I draw. In any case, the reason for the single particles building up the correlations of the symmetric/antisymmetric state has to be very different from the reasoning employed previously.
Vanesch said:But the way we write the wavefunction, there are a priori two different wavefunctions corresponding to (A) and to (B), simply because when making a cartesian product of hilbert spaces (for "electron 1" and for "electron 2") there's a difference between H1 x H2 and H2 x H1. So we have a whole lot of states in H1 x H2 which are different from those in H2 x H1, and that shouldn't be.
Why not ?! Imagine the situation of two different nuclei (call them 1 and 2) and two different electrons red and green bound to 1 and 2 respectively. Then, clearly particles red and green are distinguishable since they are bound to different nuclei and swapping them requires work to overcome the potential barriers of both nuclei. In order to get different statistics here, I would have to imagine that although the nuclei are fixed, the electrons were somehow placed there randomly in a previous moment in time or that in a statistical ensemble of two nuclei boxes I have freedom in identifying the nuclei.
Vanesch said:So we have to work "modulo the flip" of H1 and H2, because in H1 x H2, there are different states which correspond to identical physical situations (A) and (B).
Doing this "modulo" thing would give us a lousy space, so another way to do the "modulo" thing is to find in each equivalence class a "preferred representative". This is the state that is "symmetrical" in the equivalence class. It can be the symmetrical, or the anti-symmetrical one.
Like I explained before, this depends upon your notion of distinguishability as well as your notion of what quantum mechanics is supposed to mean. It is not that simple (and was actually much debated upon) as you try to present it.
The whole disagreement boils down to (a) when to work with statistical ensembles (b) when to work with single wave equations (and this is not silly as epicurus tries to tell us) and (c) how to label particles. Classically, I could do the same : suppose I would be studying wave dynamics in which I had two wave types red and green which emerge through one of two opposite holes of the source respectively. Then I could have emissions RG and GR each with chance 1/2. Now, nobody in his right mind would say that actually RG - GR occurs with probability one, but that our detectors only allow for R or G to be observed (in a consistent way). Now in case something strange happens, then a classical physicist would say that something else occurs which is not properly taken into account yet. This is all I wanted to say.
I do not understand, as epicurus suggests, why these considerations can be confusing (actually it is rather worrying that some do not make them).
Cheers,
Careful
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