Abstract
This article reviews and discusses the thermodynamic properties of dimer-Mott-type molecular superconductive compounds with (BEDT-TTF)2X composition, where BEDT-TTF is bis(ethylenedithio)tetrathiafulvalene and X denotes counter-anions, respectively. We focus mainly on the features occurring in the κ-type structure in which the d-wave superconductive phase appears depending on the Coulomb repulsion U and the bandwidth W, which is tunable by external and chemical pressures. First, we report the high-pressure ac (alternating current) calorimetry technique and experimental system constructed to measure single-crystal samples of molecule-based compounds to derive low-temperature thermodynamic parameters. Using extremely small resistance chips as a heater and a thermometer allows four-terminal detection of an accurate temperature and its oscillation in the sample part with sufficient sensitivity. From the analyses of the temperature dependence of the ac heat capacity of κ-(BEDT-TTF)2Cu(NCS)2 under external pressures, we discuss the changes in the peak shape of the thermal anomaly at the superconductive transition temperature Tc at various external pressures p. The rather sharp peak in CpT−1 at Tc = 9.1 K with a strong coupling character at ambient pressure is gradually reduced to weaker coupling as the pressure increases to 0.45 GPa concomitant with suppression of the transition temperature. This feature is compared with the systematic argument of the chemical–pressure effect on the basis of thermal anomalies around the superconductive transition of κ-(BEDT-TTF)2X compounds and other previously studied typical dimer-Mott 2:1 compounds. Finally, the discussion is extended to the chemical pressure effect on the normal state electronic heat capacity coefficient γ obtained by applying magnetic fields higher than Hc2 and the residual γ*, which remains in the superconductive state due to the induced electron density of states around the node structure. From the overall arguments with respect to both chemical and external pressures, we suggest that a crossover of the electronic state inside the superconductive phase occurs and the coupling strength of electron pairs varies from the electron correlation region near the metal-insulator boundary to the band picture region.
Highlights
Molecule-based superconductors are attracting much attention in condensed matter science because they provide a platform to discuss the physics related to the electron correlations in low-dimensional and relatively soft lattice systems [1,2,3,4]
Among the various superconductive complexes, we have focused mainly on the κ-type dimer-Mott systems of BEDT-TTF and analogous molecules, which are extensively studied as a prototype of effective half-filling compounds
We summarize the thermodynamic features in the superconductive phase of dimer-Mott compounds from heat capacity measurements
Summary
Molecule-based superconductors are attracting much attention in condensed matter science because they provide a platform to discuss the physics related to the electron correlations in low-dimensional and relatively soft lattice systems [1,2,3,4]. Among the various superconductive complexes, we have focused mainly on the κ-type dimer-Mott systems of BEDT-TTF and analogous molecules, which are extensively studied as a prototype of effective half-filling compounds. They sometimes show antiferromagnetic insulating states due to the electron correlation mechanism. By analyzing the features of the thermal anomalies at the transitions and low energy excitations simultaneously, it is possible to grasp systematic changes in the superconductive phase where the quantum mechanical crossover is observed For this purpose, pressure-controlled thermodynamic measurements to tune the U/W ratio and systematic arguments with the parameter of this ratio are required [32,33].
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