We study the competition between magnetic and spin-liquid phases in the Hubbard model on the anisotropic triangular lattice, which is described by two hopping parameters t and t' in different spatial directions and is relevant for layered organic charge-transfer salts. By using a variational approach that includes spiral magnetic order, we provide solid evidence that a spin-liquid phase is stabilized in the strongly correlated regime and close to the isotropic limit t'/t = 1. Otherwise, amagnetically ordered spiral state is found, connecting the (collinear) Neel and the (coplanar) 120 degrees phases. The pitch vector of the spiral phase obtained from the unrestricted Hartree-Fock approximation is substantially renormalized in the presence of electronic correlations, and the Neel phase is stabilized in a wide regime of the phase diagram, i.e., for t'/t < 0.75. We discuss these results in the context of organic charge-transfer salts. DOI: 10.1103/PhysRevB.87.035143
Spin-liquid versus spiral-order phases in the anisotropic triangular lattice
Tocchio, Luca Fausto;Becca, Federico;
2013-01-01
Abstract
We study the competition between magnetic and spin-liquid phases in the Hubbard model on the anisotropic triangular lattice, which is described by two hopping parameters t and t' in different spatial directions and is relevant for layered organic charge-transfer salts. By using a variational approach that includes spiral magnetic order, we provide solid evidence that a spin-liquid phase is stabilized in the strongly correlated regime and close to the isotropic limit t'/t = 1. Otherwise, amagnetically ordered spiral state is found, connecting the (collinear) Neel and the (coplanar) 120 degrees phases. The pitch vector of the spiral phase obtained from the unrestricted Hartree-Fock approximation is substantially renormalized in the presence of electronic correlations, and the Neel phase is stabilized in a wide regime of the phase diagram, i.e., for t'/t < 0.75. We discuss these results in the context of organic charge-transfer salts. DOI: 10.1103/PhysRevB.87.035143I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.