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Emergence of superconductivity, valence bond order and Mott insulators in Pd[(dmit)2] based organic salts

Abstract

The \EtMeP and \EtMeSb nearly triangular organic salts are distinguished from most other Pd[(dmit)2_2] based salts, as they display valence bond and no long range order, respectively. Under pressure, a superconducting phase is revealed in EtMe3_3P near the boundary of valence bond order. We use slave-rotor theory with an enlarged unit cell to study competition between uniform and broken translational symmetry states, offering a theoretical framework capturing the superconducting, valence bond order, spin liquid, and metallic phases on an isotropic triangular lattice. Our finite temperature phase diagram manifests a remarkable resemblance to the phase diagram of the EtMe3_3P salt, where the re-entrant transitions of the type insulator-metal-insulator can be explained by an entropy difference between metal and the U(1) spin liquid. We find that the superconducting pairing symmetry is d±idd \pm id, and predict different temperature dependences of the specific heat between the spin liquid and metal.Comment: minor changes, references adde

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