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      Dimer-Mott and charge-ordered insulating states in the quasi-one-dimensional organic conductors \(\delta'_{P}\)- and \(\delta'_{C}\)-(BPDT-TTF)\(_2\)ICl\(_2\)

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          Abstract

          We investigated the electronic states of the quasi-one-dimensional organic conductors \(\delta'_{P}\)-(BPDT-TTF)\(_2\)ICl\(_2\) and \(\delta'_{C}\)-(BPDT-TTF)\(_2\)ICl\(_2\), both of which are insulating at room temperature owing to strong electron correlations. Through measurements of electrical resistivity, optical conductivity, and magnetic susceptibility, as well as band-structure calculations, we have revealed that the two materials possess completely different ground states, even though they have the same chemical composition and stacking configuration of the donor molecules. We have found that the \(\delta_P'\)-type salt with an effective half-filled band behaves as a dimer-Mott (DM) insulator and exhibits a nonmagnetic transition at 25 K, whereas the \(\delta'_C\)-type salt with a 3/4-filled band shows a charge ordering (CO) transition just above room temperature and becomes nonmagnetic below 20 K. The optical spectra of the \(\delta_P'\)-type salt are composed of two characteristic bands due to intra- and interdimer charge transfers, supporting the DM insulating behavior arising from the strong on-site Coulomb interaction. By contrast, in the \(\delta'_C\)-type salt, a single band characterizing the formation of CO arising from the off-site Coulomb interactions is observed. Upon lowering the temperature, the shape of the optical spectra in the \(\delta_C'\)-type salt becomes asymmetric and shifts to much lower frequencies, suggesting the emergence of domain-wall excitations with fractional charges expected in a one-dimensional CO chain. The temperature dependence of the magnetic susceptibility of the \(\delta_P'\)-type salt is well described by a 2D spin-1/2 Heisenberg AFM model on an anisotropic square lattice in the dimerized picture, while in the \(\delta_C'\)-type salt, it can be explained by a 2D spin-1/2 Heisenberg AFM model on an anisotropic honeycomb lattice formed in the CO state.

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          Most cited references15

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          Classification of Quasi-Two Dimensional Organic Conductors Based on a New Minimal Model

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            Cluster algorithms for general-S quantum spin systems

            We present a general strategy to extend quantum cluster algorithms for S=1/2 spin systems, such as the loop algorithm, to systems with arbitrary size of spins. In general, the partition function of a high-S spin system is represented in terms of the path integral of a S=1/2 model with special boundary conditions. We introduce additional graphs to be assigned to the boundary part and give the labeling probability explicitly, which completes the algorithm together with an existing S=1/2 cluster algorithm. As a demonstration of the algorithm, we simulate the the integer-spin antiferromagnetic Heisenberg chains. The magnitude of the first excitation gap is estimated as to be 0.41048(6), 0.08917(4), and 0.01002(3) for S=1, 2, and 3, respectively.
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              Molecular Dirac Fermion Systems — Theoretical and Experimental Approaches —

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                Author and article information

                Journal
                2017-05-30
                Article
                1705.10936
                f11ade84-29c3-4f8e-8fc0-8ee0363d6e4e

                http://arxiv.org/licenses/nonexclusive-distrib/1.0/

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                Custom metadata
                7 pages, 6 figures
                cond-mat.str-el

                Condensed matter
                Condensed matter

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