Ken G
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First you need a classical measurable. Electron energy flux density will suffice (we could use electron number flux, but my point is that we never need to think of these things as particles at all to "understand" diffraction). Now you need a wave theory. Huygen's principle works fine. Let's simplify life and just get a theory that works for electrons of a given energy (which here means a given ratio of energy flux to mass flux). The wave equation with the v of that population of electrons will work fine, where v is found from timing experiments. Now we need a concept of frequency because it's a wave theory, and here we can leave the frequency as a free parameter that the interference experiment will determine. The wave equation describes the speed of signal propagation, Huygen's principle tells us how to handle the sources and the slits, and the frequency parameter gives us the interference we need. Every one of these is a 100% classical concept, remember that we are pretending we don't even know we have particles here. Now we put them together to calculate the energy fluxes everywhere subject to the free frequency parameter, compare to experiments, and poof, both the frequency parameter drops out, and the fact that we have what we would call a correct theory for electron diffraction, and all classical.SpectraCat said:I really don't know what you are talking about, to clarify the situation, please write down the classical formulation of wave mechanics that predicts the diffraction of "large ensembles of electrons".
This will all work fine as long as the electron ensemble is prepared in a uniform way, say by using a fixed potential drop to accelerate the beam (which in our present quantum understanding would say gives "monoenergetic electrons"). If you object that the theory so far only handles one voltage, we can just repeat the whole experience for other values of the voltage, ultimately tracing out the dependence of frequency on voltage. Still purely classical, and now we have the "Green's functions" for a complete classical description of any type of electron diffraction experiment on a large ensemble of electrons, so long as we know how that ensemble was generated. All perfectly mundane classical physics, we can do the whole thing imagining we have an "electron field" and no electrons at all.
That we can always do all this depends on only one thing: the correspondence principle. I'm saying the correspondence principle could be reframed thusly: "If the experiment is done in the classical limit, it will be describably by a classical theory", or "any quantum theory gives birth to a classical theory in the limit of large occupation numbers."
And you trace that to its quantum nature? What in the Schroedinger equation jumps up and says "I'm a quantum"? Nothing.The Schrodinger equation is mathematically similar to a classical wave equation, but it is physically distinct.
Again you seem to be saying there is no correspondence principle. But there is.The important distinction is that the energy of a classical wave is related to its amplitude, whereas the energy of a quantum wave is related to its frequency.
Labelling something a "trick" does not make it untrue. If a procedure spawns a classical theory, then voila, you have a classical theory. I'm sorry if you feel you got tricked in the process. The Schroedinger equation for electrons spawns a nonrelativistic classical theory simply by taking the limit of h-->0 keeping h/m a constant, all it has is a different dispersion relation from the dispersionless wave equation we are most used to seeing.You can rationalize it by using mathematical tricks like taking the limit as h-->0, but those are just tricks.
All of which is irrelevant to anything I've said. Note I never said "there is no such thing as a quantum effect that has no classical analog." What I did say is "many quantum effects do have classical analogs that we take advantage of all the time, especially when testing quantum mechanics, yet many people seem to be unaware of this fact."However, we use devices everyday that rely on h NOT being zero, such as photoelectric detectors, flash memory and LCD monitors.
Again, nothing we are talking about has anything to do with the philosophical interpretation that we commonly give to quantum phenomena. The point I'm making is quite a bit simpler than that: all quantum theories spawn classical theories in the classical limit, and such classical analogs can be very useful for understanding a wide array of what we call quantum phenomena, in stark contrast to what is often said about many kinds of quantum weirdness. Most quantum weirdness is simply the fact that it seems weird to us that a wave theory applies to quanta, but since wave theories are classical, we should not say that it's weird because there's no classical analog, we should say it's weird because there is a classical analog and we didn't expect that.Nope, that is just not correct .. it's not a matter of having the equations, it's a matter of the significance of the terms in those equations.
And that just doesn't make any sense. There is no distinction between "mathematical similarities" and "physical similarities", the mathematical is all we have to understand the physical.As I said above, the mathematical similarity between the classical and quantum mechanical wave equations does not equate to a physical similarity.
Ah, the uncertainty principle-- another 'quantum phenomenon' with a perfectly classical analog. Comes up in Fourier transforms of classical fields all the time, thanks for bringing that up.What you seem to be missing in all of your classically based arguments is the fundamental importance of the uncertainty principle.
[qutoe]That is where the "wave-like" properties of massive particles originate from (in the theoretical treatment anyway), and without it, you can never get from the equations of classical mechanics to the diffraction of electrons.[/QUOTE]Well, I just told you how you could do just exactly that. Remember, we arleady agreed that "classical" does not mean "Newton's laws."

, is rather weak I am afraid. That is one of the reasons I find PF so valuable.