Ferroelectric Mott-Hubbard phase in organic conductors

We present key issues of related phenomenons of the Ferroelectricity and the Charge Disproportionation in organic metals. In (TMTTF_2X the dielectric susceptibility demonstrates clear cases of the ferroelectric and anti-ferroelectric phase transitions. Both the susceptibility and the conductivity prove independence and occasional coexistence of "structurless" ferroelectric transitions and usual "anionic" ones. Their sequence gives access to physics of three types of solitons emerging upon cooling via several steps of symmetry breaking. The theory invokes a concept of the Combined Mott-Hubbard State which focuses upon weak processes of electronic Umklapp scattering coming from both the build-in nonequivalence of bonds and the spontaneous one of sites. We propose that the charge ordering in its form of the ferroelectricity exists hiddenly even in the Se subfamily (TMTSF)_2X, giving rise to the unexplained yet low frequency optical peak and the enhanced pseudogap.Comment: Proceedings of the ICSM 200

The ferroelectric Mott-Hubbard phase of organic (TMTTF)2X conductors

We present experimental evidences for a ferro-electric transition in the family of quasi one- dimensional conductors (TMTTF)2X. We interpret this new transition in the frame of the combined Mott-Hubbard state taking into account the double action of the spontaneous charge disproportionation on the TMTTF molecular stacks and of the X anionic potentials

Critical dynamics and domain motion from permittivity of the electronic ferroelectric (TMTTF)2AsF6

The quasi one-dimensional organic conductor (TMTTF)2AsF6 shows the charge ordering transition at Tc101K to a state of the ferroelectric Mott insulator which is still well conducting. We present and interpret the experimental data on the gigantic dielectric response in the vicinity of TCO, concentrating on the frequency dependence of the inverse $1/\epsilon$ of the complex permittivity $\epsilon=\epsilon^\prime+i\epsilon^{\prime\prime}$. Surprisingly for a ferroelectric, we could closely approach the 2nd order phase transition and to deeply reach the critical dynamics of the polarization. We could analyse the critical slowing-down when approaching Tc from both sides and to extract the anomalous power law for the frequency dependence of the order parameter viscosity. Moreover, below Tc we could extract a sharp absorption feature coming from a motion of domain walls which shows up at a frequency well below the relaxation rate.Comment: Proceedings of the international school-workshop on Electronic Crystals: ECRYS-2014, Physica B (2014

Influence of the anion potential on the charge ordering in quasi-one dimensional charge transfer salts

We examine the various instabilities of quarter-filled strongly correlated electronic chains in the presence of a coupling to the underlying lattice. To mimic the physics of the (TMTTF)$_2$X Bechgaard-Fabre salts we also include electrostatic effects of intercalated anions. We show that small displacements of the anion can stabilize new mixed Charged Density Wave-Bond Order Wave phases in which central symmetry centers are suppressed. This finding is discussed in the context of recent experiments. We suggest that the recently observed charge ordering is due to a cooperative effect between the Coulomb interaction and the coupling of the electronic stacks to the anions. On the other hand, the Spin-Peierls instability at lower temperature requires a Peierls-like lattice coupling.Comment: Latex, 4 pages, 4 postscript figure

Dielectric response of charge induced correlated state in the quasi-one-dimensional conductor (TMTTF)2PF6

Conductivity and permittivity of the quasi-one-dimensionsional organic transfer salt (TMTTF)2PF6 have been measured at low frequencies (10^3-10^7 Hz) between room temperature down to below the temperature of transition into the spin-Peierls state. We interpret the huge real part of the dielectric permittivity (up to 10^6) in the localized state as the realization in this compound of a charge ordered state of Wigner crystal type due to long range Coulomb interaction.Comment: 11 pages, 3 .eps figure

Electron-lattice coupling and the broken symmetries of the molecular salt (TMTTF)2_2SbF6_6

(TMTTF)$_2$SbF$_6$ is known to undergo a charge ordering (CO) phase transition at $T_{CO}\approx156K$ and another transition to an antiferromagnetic (AF) state at $T_N\approx 8K$. Applied pressure $P$ causes a decrease in both $T_{CO}$ and $T_N$. When $P>0.5 GPa$, the CO is largely supressed, and there is no remaining signature of AF order. Instead, the ground state is a singlet. In addition to establishing an expanded, general phase diagram for the physics of TMTTF salts, we establish the role of electron-lattice coupling in determining how the system evolves with pressure.Comment: 4 pages, 5 figure

Disproportionation Phenomena on Free and Strained Sn/Ge(111) and Sn/Si(111) Surfaces

Distortions of the $\sqrt3\times\sqrt3$ Sn/Ge(111) and Sn/Si(111) surfaces are shown to reflect a disproportionation of an integer pseudocharge, $Q$, related to the surface band occupancy. A novel understanding of the $(3\times3)$-1U (``1 up, 2 down'') and 2U (``2 up, 1 down'') distortions of Sn/Ge(111) is obtained by a theoretical study of the phase diagram under strain. Positive strain keeps the unstrained value Q=3 but removes distorsions. Negative strain attracts pseudocharge from the valence band causing first a $(3\times3)$-2U distortion (Q=4) on both Sn/Ge and Sn/Si, and eventually a $(\sqrt3\times\sqrt3)$-3U (``all up'') state with Q=6. The possibility of a fluctuating phase in unstrained Sn/Si(111) is discussed.Comment: Revtex, 5 pages, 3 figure

Coexisting orders in the quarter-filled Hubbard chain with elastic deformations

The electronic properties of the quarter-filled extended Peierls-Holstein-Hubbard model that includes lattice distortions and molecular deformations are investigated theoretically using the bosonization approach. We predict the existence of a wide variety of charge-elastic phases depending of the values of the Peierls and Holstein couplings. We include the effect of the Peierls deformation in the nearest-neighbor repulsion V, that may be present in real materials where Coulomb interactions depend strongly on the distance, and we show that the phase diagram changes substantially for large V when this term is taken into account.Comment: 6 pages, 3 figure

Charge Ordering in the One-Dimensional Extended Hubbard Model: Implication to the TMTTF Family of Organic Conductors

We study the charge ordering (CO) in the one-dimensional (1D) extended Hubbard model at quarter filling where the nearest-neighbor Coulomb repulsion and dimerization in the hopping parameters are included. Using the cluster mean-field approximation to take into account the effect of quantum fluctuations, we determine the CO phase boundary of the model in the parameter space at T=0 K. We thus find that the dimerization suppresses the stability of the CO phase strongly, and in consequence, the realistic parameter values for quasi-1D organic materials such as (TMTTF)$_2$PF$_6$ are outside the region of CO. We suggest that the long-range Coulomb interaction between the chains should persist to stabilize the CO phase.Comment: 5 pages, 4 eps figures, to appear in 15 Nov. 2001 issue of PR