Many modern lattice problems (six-vertex, eight-vertex, Ising, Heisenberg-XYZ) can be solved by obtaining eigenvalues of the transfer matrix or Hamiltonian by the Bethe ansatz. This is a very general method for solving certain classes of very large eigenvalue problems.
We use as an example the quantum -XX model: a spin chain with nearest neighbor dipole-dipole interactions
and if . Bethe developed the technique to solve the model, add a term onto the Hamiltonian above. His method has become a mainstay of many-body and statistical physics.
Let me remind you that what we mean by is
with the Pauli spin matrix in the slot. Denote eigenstates of by
First we work out a few useful identities. Acting on two-particle spin tensors
(1)
The ansatz (the goal of which is to produce all eigenvectors and eigenvalues of ) has several stages.
1. Establish a “vacuum” and “first excited” state spectrum.
Beginning with a lowest eigenvalue state (we refer to this as our Bethe vacuum) , create a “singly excited state” by flipping one spin, for example the
and prove that
Let’s call and rewrite in terms of actual spin operators. Every term in kills so , but
Apply to
take inner products with both sides
We have seen this recursion relation in 711 in our studies of normal modes: the ansatz gives
for which periodic boundary conditions forces , so with wavenumbers labeled by . This is why I present the periodic simple atomic chain in 711, to prepare you for learning the Bethe ansatz first step.
Our first excited state spectrum is , an “optical branch” dispersion relation.
2. Progress to the doubly excited states. This is a critical step in which the “ansatz equation” is obtained. Formulate doubly excited states (two flipped spins)
and propose Hamiltonian eigenfunctions
and prove that the secular equations are
(2)
in which the coefficients are for absurd/forbidden terms which we retain since they are a critical part of the ansatz. These are called “unwanted” terms. The condition that eliminates the unwanted terms is where the magic lies.
Here it goes:
first let so the two flipped spins are not nearest neighbors, there will be four terms in that do not annihilate ; , ,, , so application oh to followed by inner products gives the first of
(3)
We can simply set in the first equation to get the second, but the second is not the correct Hamiltonian action on , that would be since only and do not annihilate .
The secret of the Bethe ansatz is to apply operators to every abstractly, without regard to physical meaning of . Think of as an abstract tensor and as a label permutation and nothing more.
Then we demand that the true equation agree with the naive version gotten from the general which results in an identity (our ansatz equation)
(this identity is usually much more complex than in this example, which is probably the simplest in its category).
3. Don’t just take . Instead propose a form
( ie a sum over permutations of the products of the wavenumbers). Take
where is the identity permutation and here the transposition. This leads to
the latter two are incompatible, forcing to be the solution to the first equation (again, this is usually quite complex), and the solutions to the second must be ( and are independent exponentials)
independent of one another. Usually there is a complicated relation between the wavenumbers . Note that this tells us that coefficients of terms in the proposed wavefunction have opposite signs if the particle labels in the two terms are switched (a wavefunction antisymmetric under particle label transpositions).
4. The final stage of the Bethe ansatz is to assume that higher-order excitations Bethe ansatz wave-functions are
and the ansatz conditions lead to
in which is a permutation of the labels, and is the permutation gotten by switching labels and after permuting by . Can you see where this comes from? This is the crux of the technique, and you might see it more readily if you explicitly write out the details for a triple excitation, but this is rarely done.
This wavefunction describes a system of free fermions ( because the wave-function is antisymmetric under the interchange of any pair of up-spin location labels). If decomposes into successive relative transpositions,
and the Bethe wave-function is the Slater determinant ,
In the spirit of the ansatz we would show that for -fold excitations
and assume that the result carries over to -fold excitations. Note that
(4)
Adding these and substituting into the secular equation for lets you cancel to get
which is a sum of two single excitations but with different wavenumbers. We suspect then that
An English translation of Bethe’s original Zeits f. Physik 71, 205 (1931) paper appears in Daniel C. Mattis {\it The Many-Body Problem}, World Scientific, (1993), p. 689.