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      Real-time density matrix renormalization group dynamics of spin and charge transport in push-pull polyenes and related systems

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          Abstract

          In this paper we investigate the effect of terminal substituents on the dynamics of spin and charge transport in donor-acceptor substituted polyenes (\(D-(CH)_{x}-A\)) chains, also known as push-pull polyenes. We employ long-range correlated model Hamiltonian for the \(D-(CH)_{x}-A\) system, and time-dependent density matrix renormalization group technique for time propagating the wave packet obtained by injecting a hole at a terminal site, in the ground state of the system. Our studies reveal that the end groups do not affect spin and charge velocities in any significant way, but change the amount of charge transported. We have compared these push-pull systems with donor-acceptor substituted polymethine imine (PMI), \(D-(CHN)_{x}-A\), systems in which besides electron affinities, the nature of \(p_{z}\) orbitals in conjugation also alternate from site to site. We note that spin and charge dynamics in the PMIs are very different from that observed in the case of push-pull polyenes, and within the time scale of our studies, transport of spin and charge leads to the formation of a "quasi-static" state.

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          Valence-bond theory of linear Hubbard and Pariser-Parr-Pople models

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            Optical conductivity of the half-filled Hubbard chain

            We combine well-controlled analytical and numerical methods to determine the optical conductivity of the one-dimensional Mott-Hubbard insulator at zero temperature. A dynamical density-matrix renormalization group method provides the entire absorption spectrum for all but very small coupling strengths. In this limit we calculate the conductivity analytically using exact field-theoretical methods. Above the Lieb-Wu gap the conductivity exhibits a characteristic square-root increase. For small to moderate interactions, a sharp maximum occurs just above the gap. For larger interactions, another weak feature becomes visible around the middle of the absorption band.
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              Electron-electron interactions in polyacetylene

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                Author and article information

                Journal
                01 February 2011
                2012-01-26
                Article
                10.1103/PhysRevB.85.035122
                1102.0130
                b4fe21ea-1560-4256-89b6-deccd9b45a10

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

                History
                Custom metadata
                Phys. Rev. B 85, 035122 (2012)
                7 pages, 2 tables, 8 figures; published version
                cond-mat.str-el cond-mat.mtrl-sci physics.chem-ph

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