arXiv subjects

J. A. Schlueter

Publications and source records attributed to J. A. Schlueter.

At least 19 recordsLinked to original sources

arXiv2021

Charge localization in strongly correlated $κ$-(BEDT-TTF)$_2$Cu[N(CN)$_2$]I due to inherent disorder

In order to understand the physical properties of the series of organic conductors $κ$-(BEDT-TTF)$_2$Cu[N(CN)$_2$]$X$ with $X$ = Cl, Br, and I, not only electronic correlations but also the effect of disorder has to be taken into account. While for Cl- and Br-containing salts the influence of both parameters were investigated and a universal phase diagram was proposed, the position of $κ$-(BEDT-TTF)$_2$Cu[N(CN)$_2$]I is still not settled. Here we have conducted transport, infrared, and dielectric measurements on single crystals of the title compound to clarify its electronic state at low temperatures. The correlation strength was determined as $U/W \approx 2.2$; thus this salt is placed deeper in an insulating state compare to the two sister compounds. We found that inherent disorder leads to a Coulomb localized insulating state similar to the moderately x-ray-irradiated $κ$-(BEDT-TTF)$_2$Cu[N(CN)$_2$]Cl.

cond-mat.str-el↗

arXiv2021

A phase diagram for light-induced superconductivity in $κ$-(ET)$_2$-X

Resonant optical excitation of certain molecular vibrations in $κ$-(BEDT-TTF)$_2$Cu[N(CN)$_2$]Br has been shown to induce transient superconducting-like optical properties at temperatures far above equilibrium $T_c$. Here, we report experiments across the bandwidth-tuned phase diagram of this class of materials, and study the Mott insulator $κ$-(BEDT-TTF)$_2$Cu[N(CN)$_2$]Cl and the metallic compound $κ$-(BEDT-TTF)$_2$Cu(NCS)$_2$. We find non-equilibrium photoinduced superconductivity only in $κ$-(BEDT-TTF)$_2$Cu[N(CN)$_2$]Br, indicating that the proximity to the Mott insulating phase and possibly the presence of preexisting superconducting fluctuations are pre-requisites for this effect.

cond-mat.supr-con↗

arXiv2020

Photo-molecular high temperature superconductivity

Superconductivity in organic conductors is often tuned by the application of chemical or external pressure. With this type of tuning, orbital overlaps and electronic bandwidths are manipulated, whilst the properties of the molecular building blocks remain virtually unperturbed.Here, we show that the excitation of local molecular vibrations in the charge-transfer salt $κ-(BEDT-TTF)_2Cu[N(CN)_2]Br$ induces a colossal increase in carrier mobility and the opening of a superconducting-like optical gap. Both features track the density of quasi-particles of the equilibrium metal, and can be achieved up to a characteristic coherence temperature $T^* \approxeq 50 K$, far higher than the equilibrium transition temperature $T_C = 12.5 K$. Notably, the large optical gap achieved by photo-excitation is not observed in the equilibrium superconductor, pointing to a light induced state that is different from that obtained by cooling. First-principle calculations and model Hamiltonian dynamics predict a transient state with long-range pairing correlations, providing a possible physical scenario for photo-molecular superconductivity.

cond-mat.supr-con↗

arXiv2019

Low-Temperature Dielectric Anomalies at the Mott Insulator-Metal Transition

The correlation-driven Mott transition is commonly characterized by a drop in resistivity across the insulator-metal phase boundary; yet, the complex permittivity provides a deeper insight into the microscopic nature. We investigate the frequency- and temperature-dependent dielectric response of the Mott insulator $κ$-(BEDT-TTF)$_{2}$-Cu$_2$(CN)$_3$ when tuning from a quantum spin liquid into the Fermi-liquid state by applying external pressure and chemical substitution of the donor molecules. At low temperatures the coexistence region at the first-order transition leads to a strong enhancement of the quasi-static dielectric constant $ε_1$ when the effective correlations are tuned through the critical value. Several dynamical regimes are identified around the Mott point and vividly mapped through pronounced permittivity crossovers. All experimental trends are captured by dynamical mean-field theory of the single-band Hubbard model supplemented by percolation theory.

cond-mat.str-el↗

arXiv2019

Probing magnetic order and disorder in the one-dimensional molecular spin chains CuF2(pyz) and [Ln(hfac)3(boaDTDA)]n (Ln=Sm, La) using implanted muons

We present the results of muon-spin relaxation ($μ^{+}$SR) measurements on antiferromagnetic and ferromagnetic spin chains. In antiferromagnetic CuF$_{2}$(pyz) we identify a transition to long range magnetic order taking place at $T_{\mathrm{N}} = 0.6(1)$ K, allowing us to estimate a ratio with the intrachain exchange of $T_{\mathrm{N}}/|J| \approx 0.1$ and the ratio of interchain to intrachain exchange coupling as $|J'/J| \approx 0.05$. The ferromagnetic chain [Sm(hfac)$_{3}$(boaDTDA)]$_{n}$ undergoes an ordering transition at $T_{\mathrm{c}}=2.8(1)$ K, seen via a broad freezing of dynamic fluctuations on the muon (microsecond) timescale and implying $T_{\mathrm{c}}/|J| \approx 0.6$. The ordered radical moment continues to fluctuate on this timescale down to 0.3 K, while the Sm moments remain disordered. In contrast, the radical spins in [La(hfac)$_{3}$(boaDTDA)]$_{n}$ remain magnetically disordered down to $T=0.1$ K suggesting $T_{\mathrm{c}}/|J| < 0.17$.

cond-mat.str-el↗

arXiv2017

Quantum Spin Liquids Unveil the Genuine Mott State

The Widom line identifies the locus in the phase diagram where a supercritical gas crosses over from gas-like to a more liquid-like behavior. A similar transition exists in correlated electron liquids, where the interplay of Coulomb repulsion, bandwidth and temperature triggers between the Mott insulating state and an incoherent conduction regime. Here we explore the electrodynamic response of three organic quantum spin liquids with different degrees of effective correlation, where the absence of magnetic order enables unique insight into the nature of the genuine Mott state down to the most relevant low-temperature region. Combining optical spectroscopy with pressure-dependent dc transport and theoretical calculations, we succeeded to construct a phase diagram valid for all Mott insulators on a quantitative scale. In the vicinity of the low-temperature phase boundary, we discover metallic fluctuations within the Mott gap, exhibiting enhanced absorption upon cooling that is not present in antiferromagnetic Mott insulators. Our findings reveal the phase coexistence region and Pomeranchuk-like anomaly of the Mott transition, previously predicted but never observed.

cond-mat.str-el↗

arXiv2016

Control of the third dimension in copper-based square-lattice antiferromagnets

Using a mixed-ligand synthetic scheme, we create a family of quasi-two-dimensional antiferromagnets, namely, [Cu(HF$_2$)(pyz)$_2$]ClO$_4$ [pyz = pyrazine], [Cu$L_2$(pyz)$_2$](ClO$_4$)$_2$ [$L$ = pyO = pyridine-N-oxide and 4-phpyO = 4-phenylpyridine-N-oxide. These materials are shown to possess equivalent two-dimensional [Cu(pyz)$_2$]$^{2+}$ nearly square layers, but exhibit interlayer spacings that vary from 6.5713~Å~to 16.777~Å, as dictated by the axial ligands. We present the structural and magnetic properties of this family as determined via x-ray diffraction, electron-spin resonance, pulsed- and quasistatic-field magnetometry and muon-spin rotation, and compare them to those of the prototypical two-dimensional magnetic polymer Cu(pyz)$_2$(ClO$_4$)$_2$. We find that, within the limits of the experimental error, the two-dimensional, {\it intralayer} exchange coupling in our family of materials remains largely unaffected by the axial ligand substitution, while the observed magnetic ordering temperature decreases slowly with increasing layer separation. Despite the structural motifs common to this family and Cu(pyz)$_2$(ClO$_4$)$_2$, the latter has significantly stronger two-dimensional exchange interactions and hence a higher ordering temperature. We discuss these results, as well as the mechanisms that might drive the long-range order in these materials, in terms of departures from the ideal $S=1/2$ two-dimensional square-lattice Heisenberg antiferromagnet. In particular, we find that both spin exchange anisotropy in the intralayer interaction and interlayer couplings (exchange, dipolar, or both) are needed to account for the observed ordering temperatures, with the intralayer anisotropy becoming more important as the layers are pulled further apart.

cond-mat.str-el↗

arXiv2016

Charge fluctuations and superconductivity in organic conductors: the case of $β"$-(BEDT-TTF)$_2$SF$_5$CH$_2$CF$_2$SO$_3$

A $^{13}$C NMR study of the normal and superconducting states of the all-organic charge-transfer salt $β"$-(BEDT-TTF)$_2$SF$_5$CH$_2$CF$_2$SO$_3$ is presented. We find that the normal state is a charge-ordered metal configured as vertical stripes, produced by a combination of 1/4-filling, correlations, and a polar counterion sublattice. The NMR properties associated with the superconducting state are consistent with gap nodes and singlet pairing, and therefore similar to other organic superconductors. Quite distinct, however, is the absence of evidence for low-energy antiferromagnetic spin fluctuations for $T>T_c=4.5$ K. Both aspects are discussed in the context of a proposal that the pairing in this compound is driven by charge fluctuations.

cond-mat.str-el↗

arXiv2016

Lattice vibrations of the charge-transfer salt $κ$-(BEDT-TTF)$_2$Cu$_2$(CN)$_{3}$: novel interpretation of the electrodynamic response in a spin-liquid compound

The dimer Mott insulator $κ$-(BEDT-TTF)$_2$Cu$_2$(CN)$_3$ exhibits unusual electrodynamic properties. Numerical investigations of the electronic ground state and the molecular and lattice vibrations reveal the importance of the Cu$_2$(CN)$_3^-$ anion network coupled to the BEDT-TTF molecules: The threefold cyanide coordination of copper and linkage isomerism in the anion structure cause a loss of symmetry, frustration, disorder, and domain formation. Our findings consistently explain the temperature and polarization-dependent THz and infrared measurements, reinforce the understanding of dielectric properties and have important implications for the quantum spin-liquid state, which should be treated beyond two-dimensional, purely electronic models.

cond-mat.str-el↗

arXiv2015

Microscopic study of the Fulde-Ferrell-Larkin-Ovchinnikov state in an all-organic superconductor

Quasi-two dimensional superconductors with sufficiently weak interlayer coupling allow magnetic flux to penetrate in the form of Josephson vortices for in-plane applied magnetic fields. A consequence is the dominance of the Zeeman interaction over orbital effects. In the clean limit, the normal state is favored over superconductivity for fields greater than the paramagnetic limiting field, unless an intermediate, inhomogeneous state is stabilized. Presented here are nuclear magnetic resonance (NMR) studies of the inhomogeneous (FFLO) state for $β^{\prime \prime}$-(ET)$_2$SF$_5$CH$_2$CF$_2$SO$_3$. The uniform superconductivity-FFLO transition is identified at an applied field value of 9.3(0.1) T at low temperature ($T=130$ mK), and evidence for a possible second transition between inhomogeneous states at $\sim11$ T is presented. The spin polarization distribution inferred from the NMR absorption spectrum compares favorably to a single-Q modulation of the superconducting order parameter.

cond-mat.str-el↗

arXiv2015

Origin of the glass-like dynamics in molecular metals $\pmbκ$-(BEDT-TTF)$_{\textbf{2}}$X: implications from fluctuation spectroscopy and $\pmb{\textit{ab initio}}$ calculations

We have studied the low-frequency dynamics of the charge carriers in different organic charge-transfer salts $κ$-(BEDT-TTF)$_2$X with polymeric anions X by using resistance noise spectroscopy. Our aim is to investigate the structural, glass-like transition caused by the conformational degrees of freedom of the BEDT-TTF molecules' terminal ethylene groups. Although of fundamental importance for studies of the electronic ground-state properties, the phenomenology of the glassy dynamics is only scarcely investigated and its origin is not understood. Our systematic studies of fluctuation spectroscopy of various different compounds reveal a universal, pronounced maximum in the resistance noise power spectral density related to the glass transition. The energy scale of this precess can be identified with the activation energy of the glass-like ethylene endgroup structural dynamics as determined from thermodynamic and NMR measurements. For the first time for this class of 'plastic crystals', we report a typical glassy property of the relaxation time, namely a Vogel-Fulcher-Tammann law, and are able to determine the degree of fragility of the glassy system. Supporting $\textit{ab initio}$ calculations provide an explanation for the origin and phenomenology of the glassy dynamics in different systems in terms of a simple two-level model, where the relevant energy scales are determined by the coupling of the ethylene endgroups to the anions.

cond-mat.str-el↗

arXiv2014

Low-Energy Excitations in the Quantum Spin-Liquid $κ$-(BEDT-TTF)$_2$Cu$_2$(CN)$_{3}$

The electrodynamic response of the organic spin-liquid candidate $κ$-(BEDT-TTF)$_2$Cu$_2$(CN)$_3$ has been measured in an extremely wide energy range ($10^{-13}$ to 2 eV) as a function of temperature (5 to 300 K). Below the Mott gap, excitations from the un-gapped spinon continuum cause a considerable contribution to the infrared conductivity, as suggested by the U(1) gauge theory. At THz frequencies we can identify a power-law behavior $σ(ω) \propto ω^β$ with two distinct exponents $β$ that change from 0.9 to 1.3 at low temperatures. The corresponding crossover scales with temperature: $\hbarω_c \approx k_B T$. The observed exponents differ by more than a factor of 2 from the theoretically predicted ones. The findings are compared with those obtained on Herbertsmithites.

cond-mat.str-el↗

arXiv2014

Anisotropic charge dynamics in the quantum spin-liquid candidate $κ$-(BEDT-TTF)$_2$Cu$_2$(CN)$_3$

We have in detail characterized the anisotropic charge response of the dimer Mott insulator $κ$-(BEDT-TTF)$_2$\-Cu$_2$(CN)$_3$ by dc conductivity, Hall effect and dielectric spectroscopy. At room temperature the Hall coefficient is positive and close to the value expected from stoichiometry; the temperature behavior follows the dc resistivity $ρ(T)$. 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.

cond-mat.str-el↗

arXiv2014

ESR studies on the spin-liquid candidate $κ$-(BEDT-TTF)$_2$Cu$_2$(CN)$_{3}$: anomalous response below $T=8$ K

The organic conductor $κ$-(BEDT-TTF)$_2$Cu$_2$(CN)$_{3}$ seems to form a quantum spin liquid, although at low temperatures unusual properties are seen in the charge, spin and lattice degrees of freedom. Here we report results of X-band ESR studies of $κ$-(BEDT-TTF)$_2$Cu$_2$(CN)$_{3}$ single crystals as a function of temperature and angle. We find indications of two anisotropic relaxation mechanisms at low temperatures and compare them to the spin-liquid behavior observed in other strongly correlated systems. In addition, we can recognize charge inhomogeneities in the copper ions of the anion layer. This disorder might be linked to the dielectric response measured in this compound.

cond-mat.str-el↗

arXiv2013

Controlling magnetic order and quantum disorder in one- and zero-dimensional molecule-based magnets

We investigate the structural and magnetic properties of two molecule-based magnets synthesized from the same starting components. Their different structural motifs promote contrasting exchange pathways and consequently lead to markedly different magnetic ground states. Through examination of their structural and magnetic properties we show that [Cu(pyz)(H$_{2}$O)(gly)$_{2}$](ClO$_{4}$)$_{2}$ may be considered a quasi-one-dimensional quantum Heisenberg antiferromagnet while the related compound [Cu(pyz)(gly)](ClO$_{4}$), which is formed from dimers of antiferromagnetically interacting Cu$^{2+}$ spins, remains disordered down to at least 0.03 K in zero field, but shows a field-temperature phase diagram reminiscent of that seen in materials showing a Bose-Einstein condensation of magnons.

cond-mat.str-el↗

arXiv2013

Multiferroicity in the Mott Insulating Charge-Transfer Salt κ-(BEDT-TTF)$_2$Cu[N(CN)$_2$]Cl

The recently proposed multiferroic state of the charge-transfer salt κ-(BEDT-TTF)$_2$Cu[N(CN)$_2$]Cl [P. Lunkenheimer et al., Nature Mater., vol. 11, pp. 755-758, Sept. 2012] has been studied by dc-conductivity, magnetic susceptibility and measurements of the dielectric constant on various, differently prepared single crystals. In the majority of crystals we confirm the existence of an order-disorder-type ferroelectric state which coincides with antiferromagnetic order. This phenomenology rules out scenarios which consider an inhomogeneous, short-range-ordered ferroelectric state. Measurements of the dielectric constant and the magnetic susceptibility on the same crystals reveal that both transitions lie very close to each other or even collapse, indicating that both types of order are intimately coupled to each other. We address issues of the frequency dependence of the dielectric constant ε' and the dielectric loss ε'' and discuss sample-to-sample variations.

cond-mat.str-el↗

arXiv2013

Localized states in the Mott insulator κ-(BEDT-TTF)_2Cu[N(CN)_2]Cl as probed by photoluminescence

We compare the photoluminescence spectra of the low-temperature Mott insulator \etcl (T_{MIT}=40 K) with spectra of metallic κ-(BEDT-TTF)_2Cu[N(CN)_2]Br, which is superconducting below T_c=11.8 K, in the temperature range between 300 and 20 K. In the Mott insulating state of κ-(BEDT-TTF)_2Cu[N(CN)_2]Cl we observe a luminescence band at 1.95 eV due to the recombination of an exciton created by a HOMO-LUMO optical excitation. This luminescence is quenched both in the high-temperature bad metal state of κ-(BEDT-TTF)_2Cu[N(CN)_2]Cl and in metallic κ-(BEDT-TTF)_2Cu[N(CN)_2]Br. The observation of the luminescence of an exciton provides evidence for the local character of excitations in the Mott insulating state.

cond-mat.str-el↗

arXiv2013

Evolution of magnetic interactions in a pressure-induced Jahn-Teller driven magnetic dimensionality switch

We present the results of high-field magnetization and muon-spin relaxation measurements on the coordination polymer CuF_2(H_2O)_2(pyrazine) in pressures up to 22.5 kbar. We observe a transition from a quasi-two-dimensional to a quasi-one-dimensional antiferromagnetic phase at 9.1 kbar, driven by a rotation of the Jahn-Teller axis. Long-range antiferromagnetic ordering is seen in both regimes, as well as a phase separation in the critical pressure region. The magnetic dimensionality switching as pressure is increased is accompanied by a halving of the primary magnetic exchange energy J and a fivefold decrease in the ordering temperature T_N. J decreases gradually with pressure in the two-dimensional phase, and then increases in the one-dimensional regime. We relate both effects to the changes in the crystal structure with applied pressure.

cond-mat.str-el↗