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We show from many-body quantum mechanical calculations that there occur structurally distinct triplet-pair eigenstates in the intramolecular singlet fission (iSF) compound pentacene-tetracene-pentacene. Triplet excitons occupy neigboring pentacene and tetracene monomers in the higher energy doubly degenerate triplet-triplet multiexcitons, and terminal pentacene chromophores in the lower energy multiexciton. The lowest energy multiexciton is reached by ultrafast triplet migration within the triplet-triplet manifold, a result with profound implication for the design of superior iSF compounds.

In the most studied family of organic superconductors kappa-(BEDT-TTF)_2X, the BEDT-TTF molecules that make up the conducting planes are coupled as dimers. For some anions X, an antiferromagnetic insulator is found at low temperatures adjacent to superconductivity. With an average of one hole carrier per dimer, the BEDT-TTF band is effectively 1/2-filled. Numerous theories have suggested that fluctuations of the magnetic order can drive superconducting pairing in these models, even as direct calculations of superconducting pairing in monomer 1/2-filled band models find no superconductivity. Here we present accurate zero-temperature Density Matrix Renormalization Group (DMRG) calculations of a dimerized lattice with one hole per dimer. While we do find an antiferromagnetic state in our results, we find no evidence for superconducting pairing. This further demonstrates that magnetic fluctuations in the effective 1/2-filled band approach do not drive superconductivity in these and related materials., Comment: 9 pages, 6 figures

We study the Hardy identities and inequalities on Cartan-Hadamard manifolds using the notion of a Bessel pair. These Hardy identities offer significantly more information on the existence/nonexistence of the extremal functions of the Hardy inequalities. These Hardy inequalities are in the spirit of Brezis-V\'{a}zquez in the Euclidean spaces. As direct consequences, we establish several Hardy type inequalities that provide substantial improvements as well as simple understandings to many known Hardy inequalities and Hardy-Poincar\'{e}-Sobolev type inequalities on hyperbolic spaces in the literature., Comment: 27 pages

Recent investigations of the magnetic properties and the discovery of superconductivity in quasi-one-dimensional triangular lattice organic charge-transfer solids have indicated the severe limitations of the effective 1/2-filled band Hubbard model for these and related systems. Our computational studies of these materials within a 1/4-filled band Hubbard model in which the organic monomer molecules, and not their dimers, constitute the sites of the Hamiltonian are able to reproduce the experimental results. We ascribe the spin gap transition in kappa-(BEDT-TTF)_2B(CN)_4 to the formation of a two-dimensional paired-electron crystal and make the testable prediction that the spin gap will be accompanied by charge-ordering and period doubling in two directions. We find enhancement of the long-range component of superconducting pairing correlations by the Hubbard repulsive interaction for band parameters corresponding to kappa-(BEDT-TTF)_2CF_3SO_3. The overall results strongly support a valence bond theory of superconductivity we have proposed recently., Comment: 8 pages, 7 figures

We review recent progress in understanding the different spatial broken symmetries that occur in the normal states of the family of charge-transfer solids (CTS) that exhibit superconductivity (SC), and discuss how this knowledge gives insight to the mechanism of the unconventional SC in these systems. We show that a unified theory of the diverse broken symmetry states necessarily requires explicit incorporation of strong electron-electron interactions and lattice discreteness, and most importantly, the correct bandfilling of one-quarter. Uniquely in the quarter-filled band, there is a very strong tendency to form nearest neighbor spin-singlets, in both one and two dimensions. The tendency to spin-singlets, a quantum effect, drives a commensurate charge-order in the correlated quarter-filled band. This charge-ordered spin-singlet, which we label as a paired-electron crystal (PEC), is different from and competes with both the antiferromagnetic state and the Wigner crystal of single electrons. Further, unlike these classical broken symmetries, the PEC is characterized by a spin gap. The tendency to the PEC in two dimensions is enhanced by lattice frustration. Following this characterization of the spatial broken symmetries, we critically reexamine spin-fluctuation and resonating valence bond theories of frustration-driven SC within half-filled band Hubbard and Hubbard-Heisenberg Hamiltonians for the superconducting CTS. We develop a valence-bond theory of SC within which the superconducting state is reached by the destabilization of the PEC by additional pressure-induced lattice frustration that makes the spin-singlets mobile. Our proposed mechanism for SC is the same for CTS in which the proximate semiconducting state is antiferromagnetic instead of charge-ordered, with the only difference that SC in the former is generated via a fluctuating spin-singlet state as opposed to static PEC., Comment: 106 pages, 64 figures

Metal-insulator transition accompanied by charge-ordering has been widely investigated in quasi-one-dimensional conductors, including in particular organic charge-transfer solids. Among such materials the 1/4-filled band charge-transfer solids are of strong interest, because of the commensurate nature of the charge-ordering in these systems. The period-four charge-order pattern ...1100... here is accompanied by two distinct bond distortion patterns, giving rise to bond-charge-density waves (BCDW) of types 1 and 2. Using quantum Monte Carlo methods, we determine the phase diagram within the extended Hubbard Hamiltonian that gives both types 1 and 2 BCDW in the thermodynamic limit. We further investigate the effect of electron-electron and electron-phonon interactions on the amount of charge disproportionation. Our results show that between these two bond patterns, one (BCDW2) in general coexists with a large magnitude charge order, which is highly sensitive to electron-phonon interactions, while the other (BCDW1) is characterized by weak charge order. We discuss the relevance of our work to experiments on several 1/4-filled conductors, focusing in particular on the materials (EDO-TTF)_2X and (DMEDO-TTF)_2X with large amplitude charge-order., Comment: 7 pages, 8 figures

We present the results of precise correlated-electron calculations on the monomer lattices of the organic charge-transfer solids $\kappa$-(BEDT-TTF)$_2$X for 32 and 64 molecular sites. Our calculations are for band parameters corresponding to X = Cu[N(CN)$_2$]Cl and Cu$_2$(CN)$_3$, which are semiconducting antiferromagnetic and quantum spin liquid, respectively, at ambient pressure. We have performed our calculations for variable electron densities $\rho$ per BEDT-TTF molecule, with $\rho$ ranging from 1 to 2. We find that $d$-wave superconducting pair-pair correlations are enhanced by electron-electron interactions only for a narrow carrier concentration about $\rho=1.5$, which is precisely the carrier concentration where superconductivity in the charge-transfer solids occurs. Our results indicate that the enhancement in pair-pair correlations is not related to antiferromagnetic order, but to a proximate hidden spin-singlet state that manifests itself as a charge-ordered state in other charge-transfer solids. Long-range superconducting order does not appear to be present in the purely electronic model, suggesting that electron-phonon interactions also must play a role in a complete theory of superconductivity., Comment: 10 pages, 6 figures; supplemental material contains additional data plots

Attempts to explain correlated-electron superconductivity have largely focused on the proximity of the superconducting state to antiferromagnetism. Yet, there exist many correlated-electron systems that exhibit insulator-superconducting transitions where the insulating state exhibits spatial broken symmetry different from antiferromagnetism. Here we focus on a subset of such compounds which are seemingly very different in which specific chemical stoichiometries play a distinct role, and small deviations from stoichiometry can destroy superconductivity. These superconducting materials share a unique carrier concentration, at which we show there is a stronger than usual tendency to form local spin-singlets. We posit that superconductivity is a consequence of these pseudomolecules becoming mobile as was suggested by Schafroth a few years prior to the advent of the BCS theory., Comment: 19 pages, 6 figures; to appear in Int. J. Quantum Chem

Yoshimi et al. [arXiv:1110.3573] have attempted to explain the pressure(P)-dependent behavior of Fabre salts which exhibit charge order (CO), antiferromagnetic (AFM), and spin-Peierls (SP) phases. Experiments find two AFM phases, AFM1 at large P and AFM2 at small P. Yoshimi et al. suggest that there also exist two distinct zero-temperature SP phases, SP1 and SP2. Here we point out that the occurrence of two distinct SP phases contradicts experiments, and is found because of unrealistic model parameters., Comment: 1 page, 1 figure; Comment on Phys. Rev. Lett. 108, 096402 (2012), arXiv:1110.3573

Strong electron correlation effects in the photophysics of quasi-one-dimensional $\pi$-conjugated organic systems such as polyenes, polyacetylenes, polydiacetylenes, etc., have been extensively studied. Far less is known on correlation effects in two-dimensional $\pi$-conjugated systems. Here we present theoretical and experimental evidence for moderate repulsive electron-electron interactions in a number of finite polycyclic aromatic hydrocarbon molecules with $D_{6h}$ symmetry. We show that the excited state orderings in these molecules are reversed relative to that expected within one-electron and mean-field theories. Our results reflect similarities as well as differences in the role and magnitude of electron correlation effects in these two-dimensional molecules compared to those in polyenes., Comment: 11 pages, 5 figures, 2 tables

We present numerical studies of one- and two-photon excited states ordering in a number of polycyclic aromatic hydrocarbon molecules: coronene, hexa-peri-hexabenzocoronene and circumcoronene, all possessing $D_{6h}$ point group symmetry versus ovalene with $D_{2h}$ symmetry, within the Pariser-Parr-Pople model of interacting $\pi$-electrons. The calculated energies of the two-photon states as well as their relative two-photon absorption cross-sections within the interacting model are qualitatively different from single-particle descriptions. More remarkably, a peculiar role of molecular geometry is found. The consequence of electron correlations is far stronger for ovalene, where the lowest spin-singlet two-photon state is a quantum superposition of pairs of lowest spin triplet states, as in the linear polyenes. The same is not true for $D_{6h}$ group hydrocarbons. Our work indicates significant covalent character, in valence bond language, of the ground state, the lowest spin triplet state and a few of the lowest two-photon states in $D_{2h}$ ovalene but not in those with $D_{6h}$ symmetry., Comment: 11 pages, 3 figures, 3 tables

A frustrated, effective 1/2-filled band Hubbard-Heisenberg model has been proposed to describe the strongly dimerized charge-transfer solid families kappa-(ET)_2X and Z[Pd(dmit)_2]_2. In addition to unconventional superconductivity these materials also exhibit antiferromagnetism, candidate spin-liquid phases, and in the case of Z=EtMe_3P, a so-called valence-bond solid phase. We show that neither superconductivity nor the valence-bond solid phase occurs within the Hubbard-Heisenberg model, indicating that the effective 1/2-filled band model is unsuitable for these materials., Comment: 5 pages, 5 figures

Singlet fission, in which the optical spin-singlet exciton dissociates into two low energy triplet excitons, has been proposed as a viable approach to enhance the quantum efficiency of organic solar cells. We show that even when singlet fission is occurring in the donor molecule, the electronic structure at the donor$-$acceptor interface must satisfy specific requirements for the solar cell performance to be enhanced by this process. We focus on the pentacene$-$C$_{60}$ solar cell, and on the basis of our calculations and available experimental data, we conclude that there is not enough evidence that these requirements are met by the donor$-$acceptor interface here. We propose experiments that can determine whether the minimal requirement for enhanced performance driven by singlet fission is met in this and other solar cells., Comment: 12 pages, 5 figures (including the Table of Contents)

We present many-body calculations of superconducting pair-pair correlations in the ground state of the half-filled band Hubbard model on large anisotropic triangular lattices. Our calculations cover nearly the complete range of anisotropies between the square and isotropic triangular lattice limits. We find that the superconducting pair-pair correlations decrease monotonically with increasing onsite Hubbard interaction U for inter-pair distances greater than nearest neighbor. For the large lattices of interest here the distance dependence of the correlations approaches that for noninteracting electrons. Both these results are consistent with the absence of superconductivity in this model in the thermodynamic limit. We conclude that the effective 1/2-filled band Hubbard model, suggested by many authors to be appropriate for the kappa-(BEDT-TTF)-based organic charge-transfer solids, does not explain the superconducting transition in these materials., Comment: 9 pages, 7 figures. Revised version to appear in Phys. Rev. B

The occurrence of antiferromagnetism in kappa-(ET)_2X can be understood within an effective 1/2-filled band with dimers of ET molecules containing one hole each. We argue that while this effective model can describe the presence of antiferromagnetism, a complete description for these materials requires the correct carrier density of one-half per molecule. For dimerized and strongly frustrated 1/4-filled lattices we show that a singlet-paired state coexisting with charge ordering occurs that we have termed the Paired Electron Crystal (PEC). Here we investigate the 1/4-filled model on a dimerized lattice, showing regions where AFM, PEC, and the Wigner-crystal occur. We point out the need to go beyond quantum spin liquid concepts for highly frustrated materials such as kappa-(ET)_2Cu_2(CN)_3 and beta'-EtMe_3Sb[Pd(dmit)_2]_2 which we believe are PECs at low temperatures., Comment: 4 pages, 4 figures, proceedings of ISCOM 2011

We consider the simplest example of lattice frustration in the 1/4-filled band, a one-dimensional chain with next-nearest neighbor interactions. For this zigzag ladder with electron-electron as well as electron-phonon interactions we present numerical results for ground state as well as thermodynamic properties. In this system the ground state bond distortion pattern is independent of electron-electron interaction strength. The spin gap in the ground state of the zigzag ladder increases with the degree of frustration. Unlike in one-dimension, where the spin-gap and charge ordering transitions can be distinct, we show that in the ladder they occur simultaneously. We discuss spin gap and charge ordering transitions in 1/4-filled materials with one, two, or three dimensional crystal structures. We show empirically that regardless of dimensionality the occurrence of simultaneous or distinct charge and magnetic transitions can be correlated with the ground state bond distortion pattern., Comment: 12 pages, 8 eps figures

We present a study of the effects of simultaneous charge- and spin-frustration on the two-dimensional strongly correlated quarter-filled band on an anisotropic triangular lattice. The broken-symmetry states that dominate in the weakly frustrated region near the rectangular lattice limit are the well known antiferromagnetic state with in-phase lattice dimerization along one direction, and the Wigner crystal state with the checkerboard charge order. For moderate to strong frustration, however, the dominant phase is a novel spin-singlet paired-electron crystal (PEC), consisting of pairs of charge-rich sites separated by pairs of charge-poor sites. The PEC, with coexisting charge-order and spin-gap in two dimension, is the quarter-filled band equivalent of the valence bond solid (VBS) that can appear in the frustrated half-filled band within antiferromagnetic spin Hamiltonians. We discuss the phase diagram as a function of on-site and intersite Coulomb interactions as well as electron-phonon coupling strength. We speculate that the spin-bonded pairs of the PEC can become mobile for even stronger frustration, giving rise to a paired-electron liquid. We discuss the implications of the PEC concept for understanding several classes of quarter-filled band materials that display unconventional superconductivity, focusing in particular on organic charge transfer solids. Our work points out the need to go beyond quantum spin liquid (QSL) concepts for highly frustrated organic charge-transfer solids such as kappa-(BEDT-TTF)_2Cu_2(CN)_3 and EtMe_3Sb[Pd(dmit)_2]_2, which we believe show frustration-induced charge disproportionation at low temperatures. We discuss possible application to layered cobaltates and 1/4-filled band spinels., Comment: 12 pages, 7 figures

A natural explanation for the carrier concentration-dependent electronic behavior in the layered cobaltates emerges within correlated-electron Hamiltonians with finite on-site and significant nearest neighbor hole-hole Coulomb repulsions. The nearest neighbor repulsion decreases hole double-occupancy below hole density 1/3, but increases the same at higher hole densities. Our conclusion is valid for both single-band and three-band extended Hubbard Hamiltonians, and sheds light on concentration-dependent $e_g^\prime$ hole occupancy within the latter., Comment: 4 pages, 4 figures

We report pressure-dependent transient picosecond and continuous-wave photomodulation studies of disordered and ordered films of 2-methoxy-5-(2-ethylhexyloxy) poly(para-phenylenevinylene). Photoinduced absorption (PA) bands in the disordered film exhibit very weak pressure dependence and are assigned to intrachain excitons and polarons. In contrast, the ordered film exhibits two additional transient PA bands in the midinfrared that blueshift dramatically with pressure. Based on high-order configuration interaction calculations we ascribe the PA bands in the ordered film to excimers. Our work brings insight to the exciton binding energy in ordered films versus disordered films and solutions. The reduced exciton binding energy in ordered films is due to new energy states appearing below the continuum band threshold of the single strand., Comment: 5.5 pages, 5 figures

It has been suggested that the metal-insulator transitions in a number of spinel materials with partially-filled t_2g d-orbitals can be explained as orbitally-driven Peierls instabilities. Motivated by these suggestions, we examine theoretically the possibility of formation of such orbitally-driven states within a simplified theoretical model, a two-dimensional checkerboard lattice with two directional metal orbitals per atomic site. We include orbital ordering and inter-atom electron-phonon interactions self-consistently within a semi-classical approximation, and onsite intra- and inter-orbital electron-electron interactions at the Hartree-Fock level. We find a stable, orbitally-induced Peierls bond-dimerized state for carrier concentration of one electron per atom. The Peierls bond distortion pattern continues to be period 2 bond-dimerization even when the charge density in the orbitals forming the one-dimensional band is significantly smaller than 1. In contrast, for carrier density of half an electron per atom the Peierls instability is absent within one-electron theory as well as mean-field theory of electron-electron interactions, even for nearly complete orbital ordering. We discuss the implications of our results in relation to complex charge, bond, and orbital-ordering found in spinels., Comment: 8 pages, 5 figures; revised version

We describe the Paired Electron Crystal (PEC) which occurs in the interacting frustrated two-dimensional 1/4-filled band. The PEC is a charge-ordered state with nearest-neighbor spin singlets separated by pairs of vacant sites, and can be thought of as a bipolaron density wave. The PEC has been experimentally observed in the insulating state proximate to superconductivity in the organic charge-transfer solids. Increased frustration drives a PEC-to-superconductor transition in these systems., Comment: submitted to Physica B special issue for ISCOM 2009

The competition between antiferromagnetic and spin-singlet ground states within quantum spin models and the 1/2-filled band Hubbard model has received intense scrutiny. Here we demonstrate a frustration-induced transition from N\'{e}el antiferromagnetism to spin-singlet in the interacting 1/4-filled band on an anisotropic triangular lattice. While the antiferromagnetic state has equal charge densities 0.5 on all sites, the spin-singlet state is a paired-electron crystal, with pairs of charge-rich sites separated by pairs of charge-poor sites. The paired-electron crystal provides a natural description of the spin-gapped state proximate to superconductivity in many organic charge-transfer solids. Pressure-induced superconductivity in these correlated-electron systems is likely a transition from the 1/4-filled band valence bond solid to a valence bond liquid., Comment: 13 pages, 4 figures. Revised version to appear in J. Phys.: Condens. Matter

We present a theory of the electronic structure and photophysics of 1:1 blends of derivatives of polyparaphenylenevinylene and fullerenes. Within the same Coulomb-correlated Hamiltonian applied previously to interacting chains of single-component $\pi$-conjugated polymers, we find an exciplex state that occurs below the polymer's optical exciton. Weak absorption from the ground state occurs to the exciplex. We explain transient photoinduced absorptions in the blend, observed for both above-gap and below-gap photoexcitations, within our theory. Photoinduced absorptions for above-gap photoexcitation are from the optical exciton as well as the exciplex, while for below-gap photoexcitation induced absorptions are from the exciplex alone. In neither case are free polarons generated in the time scale of the experiment. Importantly, the photophysics of films of single-component $\pi$-conjugated polymers and blends can both be understood by extending Mulliken's theory of ground-state charge transfer to the case of excited-state charge transfer., Comment: 9 pages, 8 figures

We extend Mulliken's theory of ground state charge transfer in a donor-acceptor complex to excited state charge transfer between pairs of identical $\pi$-conjugated oligomers, one of which is in the optically excited state and the other in the ground state, leading to the formation of a charge-transfer exciton. Within our theory, optical absorptions from the charge-transfer exciton should include a low energy intermolecular charge-transfer excitation, as well as distinct intramolecular excitations from both the neutral delocalized exciton component and the Coulombically bound polaron-pair component of the charge-transfer exciton. We report high order configuration-interaction calculations for pairs of oligomers of poly-paraphenylenevinylene (PPV) that go beyond our previous single configuration-interaction calculation and find all five excited state absorptions predicted using heuristic arguments based on the Mulliken concept. Our calculated excited state absorption spectrum exhibits strong qualitative agreement with the complete wavelength-dependent ultrafast photoinduced absorption in films of PPV derivatives, suggesting that a significant fraction of the photoinduced absorption here is from the charge-transfer exciton. We make detailed comparisons to experiments, and a testable experimental prediction.

We suggest that superconductivity (SC) in the organic charge transfer solids (CTS) is reached from a Bond-Charge Density Wave (BCDW). We discuss an effective model for the BCDW to SC transition, an attractive U extended Hubbard Hamiltonian with repulsive nearest neighbor interaction V. We discuss experimental consequences of the theory for different classes of CTS superconductors as well as related inorganic materials., Comment: 4 pages, 2 figures, ECRYS 2008

We show that superconductivity is absent within the 1/2-filled band triangular lattice repulsive Hubbard model that has been proposed for organic charge-transfer solids. We posit that organic superconductivity is rather reached from a Bond-Charge Density Wave that either constitutes the insulating state proximate to superconductivity, or is extremely close in energy to the antiferromagnetic state, and replaces the latter under pressure. The Bond-Charge Density Wave can be described within an effective attractive $U$ extended Hubbard Hamiltonian with repulsive nearest neighbor interaction $V$. A first-order transition from the insulating to the superconducting state occurs within the model with increasing frustration., Comment: 4 pages, 4 figures, submitted to Synthetic Metals

We report exact calculations of magnetic and superconducting pair-pair correlations for the half-filled band Hubbard model on an anisotropic triangular lattice. Our results for the magnetic phases are similar to those obtained with other techniques. The superconducting pair-pair correlations at distances beyond nearest neighbor decrease monotonically with increasing Hubbard interaction U for all anisotropy, indicating the absence of frustration-driven superconductivity within the model., Comment: 4 pages, 4 EPS figures

We demonstrate a robust frustration-driven charge-order to superconductivity transition in the half-filled negative-U extended Hubbard model. Superconductivity extends over a broad region of the parameter space. We argue that the model provides the correct insight to understanding unconventional superconductivity in the organic charge-transfer solids and other quarter-filled systems., Comment: 4 pages, 6 EPS fig files

We measured the variable temperature infrared response of the spin ladder candidate (DTTTF)2Cu(mnt)2 in order to distinguish between two competing ladder models, rectangular versus zigzag, proposed for this family of materials. The distortion along the stack direction below 235 K is consistent with a doubling along b through the metal-insulator transition. While this would agree with either of the ladder models, the concomitant transverse distortion rules out the rectangular ladder model and supports the zigzag scenario. Intramolecular distortions within the DTTTF building block molecule also give rise to on-site charge asymmetry., Comment: 4 pages, 4 figures, submitted to Solid State Sciences

We measured the optical properties of mixed valent vanadium oxide nanoscrolls and their metal exchanged derivatives in order to investigate the charge dynamics in these compounds. In contrast to the prediction of a metallic state for the metal exchanged derivatives within a rigid band model, we find that the injected charges in Mn$^{2+}$ exchanged vanadium oxide nanoscrolls are pinned. A low-energy electronic excitation associated with the pinned carriers appears in the far infrared and persists at low temperature, suggesting that the nanoscrolls are weak metals in their bulk form, dominated by inhomogeneous charge disproportionation and Madelung energy effects., Comment: 4 figures

It is known that within the interacting electron model Hamiltonian for the one-dimensional 1/4-filled band, the singlet ground state is a Wigner crystal only if the nearest neighbor electron-electron repulsion is larger than a critical value. We show that this critical nearest neighbor Coulomb interaction is different for each spin subspace, with the critical value decreasing with increasing spin. As a consequence, with the lowering of temperature, there can occur a transition from a Wigner crystal charge-ordered state to a spin-Peierls state that is a Bond-Charge-Density Wave with charge occupancies different from the Wigner crystal. This transition is possible because spin excitations from the spin-Peierls state in the 1/4-filled band are necessarily accompanied by changes in site charge densities. We apply our theory to the 1/4-filled band quasi-one-dimensional organic charge-transfer solids in general and to 2:1 tetramethyltetrathiafulvalene (TMTTF) and tetramethyltetraselenafulvalene (TMTSF) cationic salts in particular. We believe that many recent experiments strongly indicate the Wigner crystal to Bond-Charge-Density Wave transition in several members of the TMTTF family. We explain the occurrence of two different antiferromagnetic phases but a single spin-Peierls state in the generic phase diagram for the 2:1 cationic solids. The antiferromagnetic phases can have either the Wigner crystal or the Bond-Charge-Spin-Density Wave charge occupancies. The spin-Peierls state is always a Bond-Charge-Density Wave., Comment: 12 pages, 8 EPS figures. Longer version of previous manuscript. Contains new numerical data as well as greatly expanded discussion

We report density-matrix renormalization group calculations of spin gaps in the quarter-filled correlated two-leg rectangular ladder with bond-dimerization along the legs of the ladder. In the small rung-coupling region, dimerization along the leg bonds can lead to large enhancement of the spin gap. Electron-electron interactions further enhance the spin gap, which is nonzero for all values of the rung electron hopping and for arbitrarily small bond-dimerization. Very large spin gaps, as are found experimentally in quarter-filled band organic charge-transfer solids with coupled pairs of quasi-one-dimensional stacks, however, occur within the model only for large dimerization and rung electron hopping that are nearly equal to the hopping along the legs. Coexistence of charge order and spin gap is also possible within the model for not too large intersite Coulomb interaction.

We report accurate numerical studies of excited state orderings in long hypothetical pi-conjugated oligomers in which the hydrogen atoms of trans-polyacetylene are replaced with conjugated sidegroups, within modified Hubbard models. There exists a range of the bare Coulomb repulsion for which the excited state ordering is conducive to photoluminescence in the substituted systems, even as this ordering is opposite in the unsubstituted polyenes of the same lengths. Our work provides motivation to study real pi-conjugated polymers with transverse conjugation and small optical gaps., Comment: 5 pages, 4 figs

We investigate multi-terminal quantum transport through single monocyclic aromatic annulene molecules, and their derivatives, using the nonequilibrium Green function approach in the self-consistent Hartree-Fock approximation. A new device concept, the Quantum Interference Effect Transistor (QuIET) is proposed, exploiting perfect destructive interference stemming from molecular symmetry, and controlling current flow by introducing decoherence and/or elastic scattering that break the symmetry. This approach overcomes the fundamental problems of power dissipation and environmental sensitivity that beset many nanoscale device proposals., Comment: 4 pages, 5 figures

The nature of the primary photoexcitations in semiconducting single-walled carbon nanotubes (S-SWCNTs) is of strong current interest. We have studied the emission spectra of S-SWCNTs and two different $\pi$-conjugated polymers in solutions and films, and have also performed ultrafast pump-probe spectroscopy on these systems. The emission spectra relative to the absorption bands are very similar in S-SWCNTs and polymers, with redshifted photoluminescence in films showing exciton migration. The transient photoinduced absorptions (PAs) in SWCNTs and $\pi$-conjugated polymers are also remarkably similar, with a low energy PA$_1$ and a higher energy PA$_2$ in all cases. Theoretical calculations of excited state absorptions within a correlated $\pi$-electron Hamiltonian find the same excitonic energy spectrum for S-SWCNTs and $\pi$-conjugated polymers, illustrating the universal features of quasi-one-dimensional excitons in carbon-based $\pi$-conjugated systems. In both cases PA$_1$ is an excited state absorption from the optically allowed exciton to a two-photon exciton that occurs below the continuum band threshold. PA$_1$ therefore gives the lower limit of the binding energy of the lowest optical exciton. The binding energy of lowest exciton belonging to the widest S-SWCNTs with diameters $\geq$ 1 nm in films is 0.3--0.4 eV, as determined by both experimental and theoretical methods., Comment: 22 pages, 6 figures, 1 table

We have measured the electric field modulated absorption of a sample of single-walled nanotubes (SWNT) suspended in a solid polyvinyl alcohol matrix. The electroabsorption (EA) spectrum roughly follows the first derivative of the absorption with respect to photon energy, scales quadratically with the electric field strength, and shows a pronounced anisotropy of light polarization with respect to the applied electric field direction. These findings indicate a quadratic Stark effect caused by a change in the polarizability of the excited states, which is common to quasi-one dimensional (1D) excitons in organic semiconductors. The EA spectrum is well described by calculations involving electron-electron interaction in the model Hamiltonian of both zigzag and chiral nanotubes. We have calculated the EA spectra for both zigzag and chiral nanotubes within a model Hamiltonian that includes electron-electron interactions. The calculations reproduce the observed quadratic Stark shift of the lowest optical exciton, as well as the more complicated behavior of the EA spectrum in the energy region that corresponds to the next higher exciton. Our findings show that the low-lying absorption bands in semiconducting SWNT are excitonic in origin, in agreement with transient optical measurements that identify the primary photoexcitations in SWNT as quasi-1D excitons with a substantial binding energy., Comment: 16 pages, 6 figures, PDF format

We propose a new type of molecular transistor, the Quantum Interference Effect Transistor (QuIET), based on tunable current suppression due to quantum interference. We show that any aromatic hydrocarbon ring has two-lead configurations for which current at small voltages is suppressed by destructive interference. A transistor can be created by providing phase relaxation or decoherence at a site on the ring. We propose several molecules which could tunably introduce the necessary dephasing or decoherence, as well as a proof of principle using a scanning tunneling microscope tip. Within the self-consistent Hartree-Fock approximation, the QuIET is shown to have characteristics strikingly similar to those of conventional field effect and bipolar junction transistors., Comment: A provisional patent application has been filed for this invention

We extend our theory of electron--hole recombination in organic light emitting diodes to investigate the possibility that high energy singlet and triplet excited states with large electron--hole separations are generated in such processes, over and above the lowest singlet and triplet excitons. Our approach involves a time-dependent calculation of the interchain / intermolecular charge--transfer within model Hamiltonians that explicitly include electron-electron interactions between the $\pi$-electrons. We show that the electron--hole recombination reaction can be viewed as a tunneling process whose cross section depends on both the matrix element of the interchain part of Hamiltonian and the energy difference between the initial polaron--pair state and the final neutral states. There occurs a bifurcation of the electron--hole recombination path in each of the two spin channels that leads to the generation of both the lowest energy exciton and a specific high energy charge-transfer state, with the matrix elements favoring the lowest energy exciton and the energy difference factor favoring the higher energy state. The overall effect of the electron--electron interactions is to enhance the singlet:triplet yield ratio over the value of 0.25 predicted from statistical considerations that are valid only within noninteracting models., Comment: 29 pages, 10 figures. To appear in 'Organic Light Emitting Diodes' Ed. J. Shinar, JohnWiley

Strong commensurate antiferromagnetism proximate to superconductivity is found in some members of the kappa-(ET) family, while a spin gap (SG) is found in the theta-(ET). Both kappa- and theta-(ET) materials have frustrated triangular lattice structures. We show from calculations of spin-spin correlations within the effective half-filled band triangular lattice proposed for the kappa-ET, as well as for the real lattice, that long range AFM order is not obtained as a consequence of this frustration. We argue that some other mechanism reduces the magnetic frustration in these systems. We show that the low temperature magnetic states in these materials can only be understood if the effects of the {\it cooperative} charge and bond ordering transitions occurring at higher temperatures in these systems are taken into account. In the kappa-ET, this co-operative transition leads to unequal hole populations on the ET dimers that form the triangular lattice., Comment: 4 pages, 4 eps figures, uses synmet.cls and elsart.cls (included). To appear in Synthetic Metals

Strong co-operative interactions occur between four different broken symmetries involving charge-ordering and bond distortions in the quarter-filled correlated zigzag electron ladder. The ground state is singlet, with spin gap several times larger than in the spin-Peierls state of the one-dimensional quarter-filled chain with the same parameters. We propose the quarter-filled zigzag electron ladder model for several different organic charge-transfer solids with coupled pairs of quasi-one-dimensional stacks, the spin-gap transition temperatures in which are unusually high., Comment: 4 pages, 4 EPS figures. accepted in Physical Review Letters

The low-lying singlet and triplet spectrum in conjugated polymers clearly show that the mechanism proposed by Lin et al. to explain their electric field dependence of singlet to triplet yield ratios is wrong. This comment, from theoretical spectrum obtained for long polyenes, shows that the phonon bottleneck proposed by Lin et al. for triplets in polyenes cannot exist., Comment: Revtex, 2 pages, 1 eps figure

We show that the proposed zig--zag charge--ordering model for alpha'--NaV2O5 is incompatible with a single transition that induces both charge--ordering and spin gap. We introduce a two--band model for alpha'--NaV2O5 within which the simultaneous charge--spin order transition is driven principally by electron-phonon interactions. The spin gap is due to the formation of local dimers, thus explaining the weak magnetic effect on this transition., Comment: 5 pages, 3 EPS figures

There is currently a great need for solid state lasers that emit in the infrared. Whether or not conjugated polymers that emit in the IR can be synthesized is an interesting theoretical challenge. We show that emission in the IR can be achieved in designer polymers in which the effective Coulomb correlation is smaller than that in existing systems. We also show that the structural requirement for having small effective Coulomb correlations is that there exist transverse $\pi$--conjugation over a few bonds in addition to longitudinal conjugation with large conjugation lengths.

Within a rigid-band correlated electron model for oligomers of poly-(paraphenylene) (PPP) and poly-(paraphenylenevinylene) (PPV), we show that there exist two fundamentally different classes of two-photon A$_g$ states in these systems to which photoinduced absorption (PA) can occur. At relatively lower energies there occur A$_g$ states which are superpositions of one electron - one hole (1e--1h) and two electron -- two hole (2e--2h) excitations, that are both comprised of the highest delocalized valence band and the lowest delocalized conduction band states only. The dominant PA is to one specific member of this class of states (the mA$_g$). In addition to the above class of A$_g$ states, PA can also occur to a higher energy kA$_g$ state whose 2e--2h component is {\em different} and has significant contributions from excitations involving both delocalized and localized bands. Our calculated scaled energies of the mA$_g$ and the kA$_g$ agree reasonably well to the experimentally observed low and high energy PAs in PPV. The calculated relative intensities of the two PAs are also in qualitative agreement with experiment. In the case of ladder-type PPP and its oligomers, we predict from our theoretical work a new intense PA at an energy considerably lower than the region where PA have been observed currently. Based on earlier work that showed that efficient charge--carrier generation occurs upon excitation to odd--parity states that involve both delocalized and localized bands, we speculate that it is the characteristic electronic nature of the kA$_g$ that leads to charge generation subsequent to excitation to this state, as found experimentally., Comment: Revtex4 style, 2 figures inserted in the text, three tables, 10 pages

There is currently a great need for solid state lasers that emit in the infrared, as this is the operating wavelength regime for applications in telecommunications. Existing $\pi$--conjugated polymers all emit in the visible or ultraviolet, and whether or not $\pi$--conjugated polymers that emit in the infrared can be designed is an interesting challenge. On the one hand, the excited state ordering in trans-polyacetylene, the $\pi$--conjugated polymer with relatively small optical gap, is not conducive to light emission because of electron-electron interaction effects. On the other hand, excited state ordering opposite to that in trans-polyacetylene is usually obtained by chemical modification that increases the effective bond-alternation, which in turn increases the optical gap. We develop a theory of electron correlation effects in a model $\pi$-conjugated polymer that is obtained by replacing the hydrogen atoms of trans-polyacetylene with transverse conjugated groups, and show that the effective on-site correlation in this system is smaller than the bare correlation in the unsubstituted system. An optical gap in the infrared as well as excited state ordering conducive to light emission is thereby predicted upon similar structural modifications., Comment: 15 pages, 15 figures, 1 table