Strong electronic correlations in superconducting organic charge transfer salts

We review the role of strong electronic correlations in quasi--two-dimensional organic charge transfer salts such as (BEDT-TTF)$_2X$, (BETS)$_2Y$ and $\beta'$-[Pd(dmit)$_2$]$_2Z$. We begin by defining minimal models for these materials. It is necessary to identify two classes of material: the first class is strongly dimerised and is described by a half-filled Hubbard model; the second class is not strongly dimerised and is described by a quarter filled extended Hubbard model. We argue that these models capture the essential physics of these materials. We explore the phase diagram of the half-filled quasi--two-dimensional organic charge transfer salts, focusing on the metallic and superconducting phases. We review work showing that the metallic phase, which has both Fermi liquid and `bad metal' regimes, is described both quantitatively and qualitatively by dynamical mean field theory (DMFT). The phenomenology of the superconducting state is still a matter of contention. We critically review the experimental situation, focusing on the key experimental results that may distinguish between rival theories of superconductivity, particularly probes of the pairing symmetry and measurements of the superfluid stiffness. We then discuss some strongly correlated theories of superconductivity, in particular, the resonating valence bond (RVB) theory of superconductivity. We conclude by discussing some of the major challenges currently facing the field.Comment: A review: 52 pages; 10 fig

Electrodynamics of quasi-two-dimensional BEDT-TTF charge transfer salts

We consider the millimeter-wave electrodynamics specific to quasi-two-dimensional conductors and superconductors based on the organic donor molecule BEDT-TTF. Using realistic physical parameters, we examine the current polarizations that result for different oscillating (GHz) electric and magnetic field polarizations. We show that, in general, it is possible to discriminate between effects (dissipation and dispersion) due to in-plane and interlayer ac currents. However, we also show that it is not possible to selectively probe any single component of the in-plane conductivity tensor, and that excitation of interlayer currents is strongly influenced by the sample geometry and the electromagnetic field polarization.Comment: 5 pages including 3 figures Minor correction to figure

Ferromagnetism in molecular materials: decamethylferrocenium tetracyanoethanide [DMeFc][TCNE] (invited)

Journal ArticleFerromagnetism has only recently been observed in molecular materials. We present here a summary of the ferromagnetic phenomena observed in the molecular charge transfer salt, decamethylferrocenium tetracyanoethanide (DMeFc) (TCNE), and related compounds. A spontaneous magnetization is observed in this material for T< 4.8 K, with a saturation moment in agreement with alignment of individual spins localized on the DMeFc +' and TCNE (-') ions. A comparison of these results with analogous charge transfer salts is presented. Models for the magnetic interaction in the charge transfer salts and the preparation of other molecular and/or polymeric materials with ferromagnetic exchange are presented

Synthesis of new chiral organosulfur donors with hydrogen bonding functionality and their first charge transfer salts

The syntheses of a range of enantiopure organosulfur donors with hydrogen bonding groups are described including TTF related materials with two, four, six and eight hydroxyl groups and multiple stereogenic centres and a pair of chiral N-substituted BEDT-TTF acetamides. Three charge transfer salts of enantiopure poly-hydroxy-substituted donors are reported, including a 4:1 salt with the meso stereoisomer of the dinuclear [Fe2(oxalate)5 ]4- anion in which both cation and anion have chiral components linked together by hydrogen bonding, and a semiconducting salt with triiodide

Electronic properties of Fabre charge-transfer salts under various temperature and pressure conditions

Using density functional theory, we determine parameters of tight-binding Hamiltonians for a variety of Fabre charge transfer salts, focusing in particular on the effects of temperature and pressure. Besides relying on previously published crystal structures, we experimentally determine two new sets of structures; (TMTTF)$_2$SbF$_6$ at different temperatures and (TMTTF)$_2$PF$_6$ at various pressures. We find that a few trends in the electronic behavior can be connected to the complex phase diagram shown by these materials. Decreasing temperature and increasing pressure cause the systems to become more two-dimensional. We analyze the importance of correlations by considering an extended Hubbard model parameterized using Wannier orbital overlaps and show that while charge order is strongly activated by the inter-site Coulomb interaction, the magnetic order is only weakly enhanced. Both orders are suppressed when the effective pressure is increased.Comment: 12 pages, 16 figure

Chirality in charge-transfer salts of BEDT-TTF of tris(oxalato)chromate(III)

Crystallisation from chiral electrolyte (R)-(−)-carvone has produced three new chiral semiconducting salts of BEDT-TTF from racemic anion tri(oxalato)chromate(III)

Noise in highly correlated commensurate charge transfer salts

Journal ArticleWe present the results of a study of the frequency (f) dependent noise power for commensurate charge transer salts with strong coulomb repulsion. f-1 noise is observed with increasing currents. Excess f-1 noise is measured for samples which were chemically doped to form solitons. Frequency independent shot noise is not observed