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Register a new userStrongly correlated superconductivity in a copper-based metal-organic framework with a perfect kagome lattice
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Added by
Kenichiro Hashimoto
Publication date
2021
fields
Physics
and research's language is
English
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Metal-organic frameworks (MOFs), which are self-assemblies of metal ions and organic ligands, provide a tunable platform to search a new state of matter. A two-dimensional (2D) perfect kagome lattice, whose geometrical frustration is a key to realizing quantum spin liquids, has been formed in the ${pi}$-${d}$ conjugated 2D MOF [Cu$_{3}$(C$_{6}$S$_{6}$)]$_{n}$ (Cu-BHT). The recent discovery of its superconductivity with a critical temperature $T_{rm c}$ of 0.25,kelvin raises fundamental questions about the nature of electron pairing. Here, we show that Cu-BHT is a strongly correlated unconventional superconductor with extremely low superfluid density. A nonexponential temperature dependence of superfluid density is observed, indicating the possible presence of superconducting gap nodes. The magnitude of superfluid density is much smaller than those in conventional superconductors, and follows the Uemuras relation of strongly correlated superconductors. These results imply that the unconventional superconductivity in Cu-BHT originates from electron correlations related to spin fluctuations of kagome lattice.
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Recently, the superconductivity in a metal-organic framework (MOF) has been discovered for the first time in copper(II) benzenehexathiolate ([Cu$_3$(C$_6$S$_6$)]$_n$, Cu-BHT). The Cu atoms form a two-dimensional perfect Kagome lattice, which has the potential to host a metallic quantum spin liquid state. Here we present high-precision measurements of in-plane magnetic penetration depth $lambda$ in Cu-BHT films down to 40,mK. The temperature dependence of $lambda$ shows a non-exponential, quasi-linear behavior at low temperatures, suggesting that unconventional superconductivity with low-energy quasiparticle excitations is realized in this system. With the reported non-Fermi liquid behavior, this finding implies that MOFs can provide a flexible platform to investigate the superconducting pairing mechanisms in the presence of spin frustration and strong quantum fluctuations.
Here we present experimental and computational evidences to support that rock-salt cubic VO is a strongly correlated metal with Non-Fermi-Liquid thermodynamics and an unusually strong spin-lattice coupling. An unexpected change of sign of metallic thermopower with composition is tentatively ascribed to the presence of a pseudogap in the density of states. These properties are discussed as signatures of the proximity to a magnetic quantum phase transition. The results are summarized in a new electronic phase diagram for the 3d monoxides, which resembles that of other strongly correlated systems. The structural and electronic simplicity of 3d monoxides make them ideal candidates to progress in the understanding of highly correlated electron systems.
The multielectron LDA+GTB approach has been developed to calculate electronic structure of strongly correlated cuprates. At low energies the effective Hamiltonian of the $t - t - t - {t_ bot } - {J^ * } - {J_ bot }$-model has been derived with parameters coming from the ab initio calculation for LSCO. The electronic structure of LSCO has been calculated self-consistently with the short-range antiferromagnetic order for various doping level. Two Lifshitz-type quantum phase transitions with Fermi surface topology changes have been found at dopings $x_{c1}=0.15$ and $x_{c2}=0.24$. Its effect on normal and superconducting properties has been calculated. The interatomic exchange parameter and its pressure dependence has been calculated within LDA+GTB scheme. The magnetic mechanisms of d-wave pairing induced by static and dynamical spin correlations are discussed. Simultaneous treatment of magnetic and phonon pairing results in the conclusion that both contributions are of the same order. For two layer cuprates like YBCO the interlayer hopping and exchange effects on the electronic structure and doping dependence of $T_c$ is discussed as well as the Coulomb interaction induced mechanism of pairing.
In the dense metal-organic framework Na[Mn(HCOO)$_3$], Mn$^{2+}$ ions ($S=frac{5}{2}$) occupy the nodes of a `trillium hyperkagome net. We show that this material exhibits a variety of behaviour characteristic of geometric frustration: the Neel transition is suppressed well below the characteristic magnetic interaction strength; short-range magnetic order persists far above the Neel temperature; and the magnetic susceptibility exhibits a pseudo-plateau at $frac{1}{3}$-saturation magnetisation. We demonstrate that a simple nearest-neighbour Heisenberg antiferromagnet model accounts quantitatively for each observation, and hence Na[Mn(HCOO)$_3$] is the first experimental realisation of this model on the trillium net. We develop a mapping between this trillium model and that on the two-dimensional Shastry-Sutherland lattice, and demonstrate how both link geometric frustration within the classical spin liquid regime to a strong magnetocaloric response at low fields.
We report a systematic study of electron doping of Sr2RuO4 by non-isovalent substitution of La^(3+) for Sr^(2+). Using a combination of de Haas-van Alphen oscillations, specific heat, and resistivity measurements, we show that electron doping leads to a rigid-band shift of the Fermi level corresponding to one doped electron per La ion, with constant many-body quasiparticle mass enhancement over the band mass. The susceptibility spectrum is substantially altered and enhanced by the doping but this has surprisingly little effect on the strength of the unconventional superconducting pairing.
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