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تسجيل مستخدم جديدSite-specific $^{13}$C NMR study on locally distorted triangular lattice of organic conductor $kappa$-(BEDT-TTF)$_2$Cu$_2$(CN)$_3$
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To verify the effect of geometrical frustration, we artificially distort the triangular lattice of quasi-two-dimensional organic conductor $kappa$-(BEDT-TTF)$_2$Cu$_2$(CN)$_3$ [BEDT-TTF: bis(ethylenedithio)terathiofulvalene] by analogous-molecular substitution and apply $^{13}$C NMR of bulk and substituted sites, electric conductivity, and static magnetic susceptibility measurements. The results indicate that the magnetic characteristics of the substituted sample are quantitatively similar to those of the pure sample. Moreover the magnetic characteristics at the substituted sites are also the same as in the bulk. These results suggest that the observed magnetic properties may not be due to the geometrical frustration but the importance of disorder.
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The ground state of $lambda$-(BEDT-TTF)$_2$GaCl$_4$, which has the same structure as the organic superconductor $lambda$-(BETS)$_2$GaCl$_4$, was investigated by magnetic susceptibility and $^{13}$C NMR measurements. The temperature dependence of the
magnetic susceptibility revealed an antiferromagnetic (AF) correlation with $J/k_{rm B} simeq$ 98 K. NMR spectrum splitting and the divergence of $1/T_1$ were observed at approximately 13 K, which is associated with the AF transition. We found that the AF structure is commensurate according to discrete NMR peak splitting, suggesting that the ground state of $lambda$-(BEDT-TTF)$_2$GaCl$_4$ is an AF dimer-Mott insulating state. Our results suggest that the superconducting phase of $lambda$-type salts would be located near the AF insulating phase.
We have in detail characterized the anisotropic charge response of the dimer Mott insulator $kappa$-(BEDT-TTF)$_2$-Cu$_2$(CN)$_3$ by dc conductivity, Hall effect and dielectric spectroscopy. At room temperature the Hall coefficient is positive and cl
ose to the value expected from stoichiometry; the temperature behavior follows the dc resistivity $rho(T)$. Within the planes the dc conductivity is well described by variable-range hopping in two dimensions; this model, however, fails for the out-of-plane direction. An unusually broad in-plane dielectric relaxation is detected below about 60 K; it slows down much faster than the dc conductivity following an Arrhenius law. At around 17 K we can identify a pronounced dielectric anomaly concomitantly with anomalous features in the mean relaxation time and spectral broadening. The out-of-plane relaxation, on the other hand, shows a much weaker dielectric anomaly; it closely follows the temperature behavior of the respective dc resistivity. At lower temperatures, the dielectric constant becomes smaller both within and perpendicular to the planes; also the relaxation levels off. The observed behavior bears features of relaxor-like ferroelectricity. Because heterogeneities impede its long-range development, only a weak tunneling-like dynamics persists at low temperatures. We suggest that the random potential and domain structure gradually emerge due to the coupling to the anion network.
Geometrical frustration, quantum entanglement and disorder may prevent long-range order of localized spins with strong exchange interactions, resulting in a novel state of matter. $kappa$-(BEDT-TTF)$_2$-Cu$_2$(CN)$_3$ is considered the best approxima
tion of this elusive quantum-spin-liquid state, but its ground-state properties remain puzzling. Here we present a multi-frequency electron-spin resonance study down to millikelvin temperatures, revealing a rapid drop of the spin susceptibility at $T^*=6,mathrm{K}$. This opening of a spin gap, accompanied by structural modifications, suggests the enigmatic `$6,mathrm{K}$-anomaly as the transition to a valence-bond-solid ground state. We identify an impurity contribution that becomes dominant when the intrinsic spins form singlets. Only probing the electrons directly manifests the pivotal role of defects for the low-energy properties of quantum-spin systems without magnetic order.
Low temperature scanning tunneling spectroscopy reveals the local density of states of the organic superconductor $kappa$-(BEDT-TTF)$_2$Cu[N(CN)$_2$]Br, that was cut in-situ in ultra-high vacuum perpendicular to the superconducting BEDT-TTF layers. T
he spectra confirm that superconductivity is confined to the conducting BEDT-TTF layers, while the Cu[N(CN)$_2$]Br anion layers are insulating. The density of states comprises a twofold superconducting gap, which is attributed to the two separated bands crossing the Fermi surface.
The organic charge-transfer salt $kappa$-(BEDT-TTF)$_{2}$Hg(SCN)$_{2}$Br is a quasi two-dimensional metal with a half-filled conduction band at ambient conditions. When cooled below $T=80$ K it undergoes a pronounced transition to an insulating phase
where the resistivity increases many orders of magnitude. In order to elucidate the nature of this metal-insulator transition we have performed comprehensive transport, dielectric and optical investigations. The findings are compared with other dimerized $kappa$-(BEDT-TTF) salts, in particular the Cl-analogue, where a charge-order transition takes place at $T_{rm CO}=30$ K.
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