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For a system of two identical particles, where $r_1$ is the position vector of particle 1 and $r_2$ is the position vec. of particle 2, the wave function should be one of the plus or minus states: \begin{equation} \psi _ \pm (r_1,r_2) = A [\psi _a(r_1) \psi_b (r_2) \pm \psi_b(r_1) \psi_a(r_2)] , \end{equation} where $\psi_a$ and $\psi_b$ are the wave functions of particle 1 and 2 respectively [equation 5.10 of Griffith's Intro to Quantum Mechanics 2nd Ed.].

I see that this equation makes the wave function $\psi_\pm$ treat the two particles identically, but I don't know of any proof that it is actually the only way of writing this wave equation to treat them identically. For example, why not a wave function like: \begin{equation} \psi _ \pm (r_1,r_2) = A \sqrt{\psi^2 _a(r_1) \psi_b^2 (r_2) \pm \psi^2_b(r_1) \psi^2_a(r_2)}~? \end{equation}

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    $\begingroup$ It's a valid wavefunction, but you lose the interpretation of having one particle in state a and the other in state b. You just have two particles in some complicated state. $\endgroup$
    – Javier
    Commented Nov 15, 2018 at 21:08

4 Answers 4

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The requirement is $$ \psi(x_1,x_2) = \begin{cases} \psi(x_2,x_1) & \text{for bosons} \\ -\psi(x_2,x_1) & \text{for fermions}. \end{cases} \tag{1} $$ This property is required by the spin-statistics theorem in relativistic quantum field theory. Since non-relativistic quantum mechanics is supposed to be an approximation to relativistic quantum field theory, we also enforce it in non-relativistic QM. A special case of equation (1) is $$ \psi(x_1,x_2) \approx \begin{cases} f(x_1)g(x_2)+f(x_2)g(x_1) & \text{for bosons} \\ f(x_1)g(x_2)-f(x_2)g(x_1) & \text{for fermions}, \end{cases} \tag{2} $$ but like Lewis Miller's answer said, this is only a special case. The general requirement is equation (1).

The square-root example written in the question does not satisfy the requirement (1).

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  • $\begingroup$ Thanks @Dan Yand for mentioning that theorem. If we take $A=i$, wouldn't condition (1) be satisfied by the square-root wave function? $\endgroup$
    – Mathist
    Commented Nov 16, 2018 at 17:46
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    $\begingroup$ @Mathophile-Mathochist For a complex quantity $z$, the function $z\mapsto \sqrt{z}$ is double-valued, with opposite signs. We can choose the sign for one value of $z$, but then the sign for other values of $z$ should be determined by continuity. So, suppose we start with $z=1$ and apply a continuous rotation in the complex plane to get to $z=-1$, say $z=\exp(i\theta)$ with $0\leq \theta\leq \pi$. If we choose $\sqrt{1}=1$, then $\sqrt{\exp(i\theta)}=\exp(i\theta/2)$. Since $\exp(i\pi/2)\neq -1$, this shows that the square-root example does not satisfy the fermion sign-change requirement. $\endgroup$ Commented Nov 16, 2018 at 18:15
  • $\begingroup$ I see, it makes sense. $\endgroup$
    – Mathist
    Commented Nov 17, 2018 at 22:57
  • $\begingroup$ (+1) The BCS model of a superconductive electron seems to be that $V(r)=ΣnV(r−Rn)$ and $H=\nabla^2+V(r)$. $R_n$ represents the position of the different ions which vibrates (i.e. has small random position change per time step). Ref: youtube.com/watch?v=qC6zPZtz3nk When time is evolved, the phenomena of superconductive electron should be emergent, right? Is it fair/accurate to say that this is the entirety of the argument, and that all the operator algebra analysis that follows aim to prove algebraically that indeed "the phenomena of superconductive electron should be emergent" in this setup? $\endgroup$
    – James
    Commented Jul 18 at 21:48
  • $\begingroup$ $V = V_{Coulomb} + V_{phonon}$ contains a phonon correction term which varies per time step depending on the state of these "phonon energies". Let's suppose that the lattice vibration (and therefore implicitly phonon waves propagation within the lattice too) is simulated directly using mutual ion attraction/repulsion of each lattice point by its surrounding points, then $V_{phonon}$ term can be completely disregarded as it is now completely described by the $V_{Coulomb}$ term which incorporates any phonon wave propagation into its time-varying lattice ion positions, right? $\endgroup$
    – James
    Commented Jul 18 at 22:25
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This product form of two-particle wave function is only correct if the particles are not interacting. Nevertheless, it is often used as a first approximation, and if you take the expectation value of the true Hamiltonian and minimize it (by taking a variational derivative) you get the two-body Hartree-Fock equation which is often used to approximate the ground state energy and wave function for many-body systems of Fermions. This approximation is often called the mean field approximation.

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  • $\begingroup$ Thanks @Lewis Miller. True, this is only for non-interacting particles. I don't know about the two-body Hartree-Fock equation. I'm familiar with variational calculus, so I would appreciate it if you would explain the relation between this equation and OP. $\endgroup$
    – Mathist
    Commented Nov 16, 2018 at 17:43
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If we have two particles, one in state $\psi_a$ and the other in state $\psi_b$, then the state vector would be $|\psi_a\rangle|\psi_b\rangle$.

However, if the particles are indistinguishable, then it is equally likely to have the opposite be true (i.e. the "first" particle in state $\psi_b$ and the "second" particle in state $\psi_a$). Therefore, we would want the entire state to be a linear combination of these two states, each with equal weight. Therefore we end up with

$$|\Psi\rangle=|\psi_a\rangle|\psi_b\rangle\pm|\psi_b\rangle|\psi_a\rangle$$

If we choose to work in the $|r_1\rangle|r_2\rangle$ basis, then we end up with the expression you state.

I think the issue with your state is that it is not a "nice" linear combination of the states where one particle is in state $\psi_a$ and the other in state $\psi_b$. We need this if we want the postulate to hold that when $|\psi\rangle=\sum c_i|\psi_n\rangle$, we know that there is a probability of $|c_i|^2$ to measure the system to be in state $|\psi_i\rangle$

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You’re forgetting that the wave function must also satisfy the TISE. With this condition the combine wavefunctions must be the sum of a permutation of products.

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