The material is modelled as a lattice with atoms in the sites with conduction electrons (or holes) moving between them, like in the Hubbard model. Unlike the Hubbard model, the electrons are strongly-correlated, meaning the electrons are sensitive to reciprocal coulombic repulsion, and so are less likely to occupy lattice sites already occupied by another electron. In the basic Hubbard model, the repulsion, indicated by U, can be small or even zero, and electrons are more free to jump (hopping, parametrized by t as transfer or tunnel) from one site to another. In the t-J model, instead of U, there is the parameter J, function of the ratio t/U.
Like the Hubbard model, it is a prospective microscopic theory of high temperature superconductivity in cuprate superconductors which arise from doped antiferromagnets, particularly in the case where the lattice considered is the two-dimensional lattice.[4][5] Cuprate superconductors are currently (as of 2024) the superconductors with the highest known superconducting transition temperature at ambient pressure, but there is no consensus on the microscopic theory responsible for their superconducting transition.
The t-J Hamiltonian can be derived from the of the Hubbard model using the Schrieffer–Wolff transformation, with the transformation generator depending on t/U and excluding the possibility for electrons to doubly occupy a lattice's site,[6] which results in:[7]
where the term in t corresponds to the kinetic energy and is equal to the one in the Hubbard model. The second one is the potential energy approximated at the second order, because this is an approximation of the Hubbard model in the limit U >> t developed in power of t. Terms at higher order can be added.[1]
If ni = 1, that is when in the ground state, there is just one electron per lattice's site (half-filling), the model reduces to the Heisenberg model and the ground state reproduce a dielectric antiferromagnets (Mott insulator).[8]
The model can be further extended considering also the next-nearest-neighbor sites and the chemical potential to set the ground state in function of the total number of particles:[9][10]
where ⟨...⟩ and ⟨⟨...⟩⟩ denote the nearest and next-nearest neighbors, respectively, with two different values for the hopping integral (t1 and t2) and μ is the chemical potential.
^This is done using a projector quantum operator that project on the subspace where fermionic operators can not add an electron on a site already occupied (see next note)