The influence of electronic correlations on structural and electronic properties of polyacetylene is studied by adding a Hubbard term (on-site Coulomb coupling U) to the Su-Schrieffer-Heeger Hamiltonian. We use the Gutzwiller wave function as an ansatz for the electronic ground state. For weak electron-phonon coupling (λ≪1) and U/(4$t_0$)≪1 (where 4$t_0$ is the π bandwidth) we obtain analytical results for the ground-state energy, the amplitude of bond alternation, the effective force constant for the bond-stretching mode, and a mean-field gap parameter Δ. For intermediate couplings the energy is minimalized numerically. Our results are applicable for U/(4$t_0$)≲1 where they agree surprisingly well with the Monte Carlo calculations of Hirsch. We find strong indications that everywhere in this region the ground state is dimerized if λ>0. For larger U we expect a smooth crossover to the spin-Peierls phase. For λ<0.37 the Hubbard term initially enhances bond alternation and the dimerization amplitude exhibits a maximum at a finite value of U. For larger values of λ the maximum occurs at U=0 and electronic correlations decrease bond alternation. Using single-particle parameters as deduced from properties of small organic molecules we compare our results with empirical data on polyacetylene. Our analysis consistently reproduces the measured properties if U is chosen between 7 and 9 eV.

• Received 25 September 1984

DOI:https://doi.org/10.1103/PhysRevB.31.6633