A spin- Hilbert space has dimension . Its Holstein–Primakoff transformation therefore uses only bosonic occupation numbers . The square root annihilates the upper endpoint. A truncated linear spin-wave approximation formally enlarges this space; it is self-consistent only when boson depletion is small compared with .
The Holstein–Primakoff transformation represents a spin- operator algebra with a bosonic creation operator and annihilation operator:
The order of the square root and oscillator operator matters. On the physical Fock states , , the raising and lowering matrix elements are and . Their squared difference gives , proving the spin commutation relations. Expanding the square root yields the linear spin-wave approximation and its interaction corrections.
The linear spin-wave approximation expands a Holstein–Primakoff transformation about a classical ordered state and retains the quadratic oscillator Hamiltonian. It gives the leading order- excitation energies above the order- classical energy. In a Heisenberg antiferromagnet, first make a bipartite spin rotation. The approximation also predicts a zero-point reduction of the order parameter; infrared-divergent quantum depletion of Néel order signals that the assumed ordered state is not a valid thermodynamic starting point.
The linear spin-wave approximation expands about the rotated all-up state, with :
In the longitudinal product, . Each site belongs to two bonds, so the resulting quadratic Hamiltonian is
The omitted terms are of order at fixed small occupation number. The pair terms describe the quantum fluctuations that were missing from the classical Néel state.
For a linear spin-wave approximation, the ground state is empty of the diagonal quasiparticles but contains the original spin bosons. If , their occupation number is . The staggered magnetization is reduced from to . For the one-dimensional nearest-neighbor Heisenberg antiferromagnet, and the integral diverges logarithmically. This invalidates finite ordered magnetization within the approximation; it is not itself a determination of the exact spectral gap.