arXiv subjects

John A. Schlueter

Publications and source records attributed to John A. Schlueter.

At least 19 recordsLinked to original sources

arXiv2026

Tuning Charge Order in $κ$-(BEDT-TTF)$_2$Hg(SCN)$_2$X (X=Br, Cl) via Uniaxial Strain

In condensed matter physics, experimental control over material properties reflects a deep understanding of the underlying physics. In recent years, meaningful progress has been made towards a description of the physics of correlated electron systems, but examples of control of these systems remain rare. In this work, we confirm a phase diagram theoretically proposed for organic Mott insulators. We use $κ$-(BEDT-TTF)$_2$Hg(SCN)$_2$X (X=Br,Cl) (BEDT-TTF = bis(ethylenedithio)tetrathiafuvalene) materials as experimental realization of the proposed model and demonstrate the ability to tune them both ways across a phase border between a Mott insulator with a uniformly distributed charge and a charge ordered state through the application of uniaxial strain. We induce charge order at 33 K in the quantum dipole liquid material $κ$-(BEDT-TTF)$_2$Hg(SCN)$_2$Br through the application of tensile strain of 0.4% along the c-axis. We suppress charge order down to 10 K in $κ$-(BEDT-TTF)$_2$Hg(SCN)$_2$Cl by applying a tensile strain of 1.6% along the b-axis. We use Raman scattering spectroscopy to probe the charge state through analysis of charge sensitive molecular vibrations and a low frequency mode of collective dipole fluctuations close to the phase border.

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arXiv2024

Gapped magnetic ground state in the spin-liquid candidate $κ$-(BEDT-TTF)$_2$Ag$_2$(CN)$_3$ suggested by magnetic spectroscopy

The nature of the magnetic ground state of highly frustrated systems remained puzzling to this day. Here, we have performed multifrequency electron spin resonance (ESR) measurements on a putative quantum spin liquid compound $κ$-(BEDT-TTF)$_2$Ag$_2$(CN)$_3$, which is a rare example of $S = 1/2$ spins on a triangular lattice. At high temperatures, the spin susceptibility exhibits a weak temperature dependence which can be described by the Heisenberg model with an antiferromagnetic exchange interaction of strength $J/k_B \approx 175$ K. At low temperatures, however, the rapid drop of the static spin susceptibility, together with monotonic decrease of the ESR linewidth indicates that strong singlet correlations develop below a pairing energy scale $T^*$ accompanied by a spin gap. On the other hand, a weak Curie-like spin susceptibility and the angular dependence of the linewidth suggest additional contribution from impurity spins. We propose the gradual formation of spin singlets with an inhomogeneous spin gap at low temperatures.

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arXiv2020

Gapped magnetic ground state in quantum-spin-liquid candidate $κ$-(BEDT-TTF)$_2$-Cu$_2$(CN)$_3$

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. $κ$-(BEDT-TTF)$_2$-Cu$_2$(CN)$_3$ is considered the best approximation 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.

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arXiv2019

A Near-Ideal Molecule-Based Haldane Spin-Chain

The molecular coordination complex NiI$_2$(3,5-lut)$_4$ [where (3,5-lut) $=$ (3,5-lutidine) $=$ (C$_7$H$_9$N)] has been synthesized and characterized by several techniques including synchrotron X-ray diffraction, ESR, SQUID magnetometry, pulsed-field magnetization, inelastic neutron scattering and muon spin relaxation. Templated by the configuration of 3,5-lut ligands the molecules pack in-registry with the Ni--I$\cdots$I--Ni chains aligned along the $c$--axis. This arrangement leads to through-space I$\cdots$I magnetic coupling which is directly measured for the first time in this work. The net result is a near-ideal realization of the $S = 1$ Haldane chain with $J = 17.5~\rm{K}$ and energy gaps of $Δ^{\parallel} = 5.3~{\rm K}$ $Δ^{\perp} =7.7~{\rm K}$, split by the easy-axis single-ion anisotropy $D=-1.2~{\rm K}$. The ratio $D/J = -0.07$ affords one of the most isotropic Haldane systems yet discovered, while the ratio $Δ_0/J = 0.40(1)$ (where $Δ_0$ is the average gap size) is close to its ideal theoretical value, suggesting a very high degree of magnetic isolation of the spin chains in this material. The Haldane gap is closed by orientation-dependent critical fields $μ_0H_{\rm c}^{\parallel} = 5.3~\rm{T}$ and $μ_0H_{\rm c}^{\perp} = 4.3~\rm{T}$, which are readily accessible experimentally and permit investigations across the entirety of the Haldane phase, with the fully polarized state occurring at $μ_0 H_{\rm s}^{\parallel}=46.0~\rm{T}$ and $μ_0 H_{\rm s}^{\perp}=50.7~\rm{T}$. The results are explicable within the so-called fermion model, in contrast to other reported easy-axis Haldane systems. Zero-field magnetic order is absent down to $20~{\rm mK}$ and emergent end-chain effects are observed in the gapped state, as evidenced by detailed low-temperature measurements.

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arXiv2019

Determining the anisotropy and exchange parameters of polycrystalline spin-1 magnets

Although low-dimensional $S = 1$ antiferromagnets remain of great interest, difficulty in obtaining high-quality single crystals of the newest materials hinders experimental research in this area. Polycrystalline samples are more readily produced, but there are inherent problems in extracting the magnetic properties of anisotropic systems from powder data. Following a discussion of the effect of powder-averaging on various measurement techniques, we present a methodology to overcome this issue using thermodynamic measurements. In particular we focus on whether it is possible to characterise the magnetic properties of polycrystalline, anisotropic samples using readily available laboratory equipment. We test the efficacy of our method using the magnets [Ni(H$_{2}$O)$_{2}$(3,5-lutidine)$_{4}$](BF$_{4}$)$_{2}$ and Ni(H$_{2}$O)$_{2}$(acetate)$_{2}$(4-picoline)$_{2}$, which have negligible exchange interactions, as well as the antiferromagnet [Ni(H$_{2}$O)$_{2}$(pyrazine)$_{2}$](BF$_{4}$)$_{2}$, and show that we are able to extract the anisotropy parameters in each case. The results obtained from the thermodynamic measurements are checked against electron-spin resonance and neutron diffraction. We also present a density functional method, which incorporates spin-orbit coupling to estimate the size of the anisotropy in [Ni(H$_{2}$O)$_{2}$(pyrazine)$_{2}$](BF$_{4}$)$_{2}$.

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arXiv2018

Evidence for electronically-driven ferroelectricity in the family of strongly correlated dimerized BEDT-TTF molecular conductors

By applying measurements of the dielectric constants and relative length changes to the dimerized molecular conductor $κ$-(BEDT-TTF)$_2$Hg(SCN)$_2$Cl, we provide evidence for order-disorder type electronic ferroelectricity which is driven by charge order within the (BEDT-TTF)$_2$ dimers and stabilized by a coupling to the anions. According to our density functional theory calculations, this material is characterized by a moderate strength of dimerization. This system thus bridges the gap between strongly dimerized materials, often approximated as dimer-Mott systems at 1/2 filling, and non- or weakly dimerized systems at 1/4 filling exhibiting charge order. Our results indicate that intra-dimer charge degrees of freedom are of particular importance in correlated $κ$-(BEDT-TTF)$_2$X salts and can create novel states, such as electronically-driven multiferroicity or charge-order-induced quasi-1D spin liquids.

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arXiv2018

Insights from experiment and $ab\,initio$ calculations into the glass-like transition in the molecular conductor $κ$-(BEDT-TTF)$_2$Hg(SCN)$_2$Cl

We present high-resolution measurements of the relative length change as a function of temperature of the organic charge-transfer salt $κ$-(BEDT-TTF)$_2$Hg(SCN)$_2$Cl. We identify anomalous features at $T_g \approx\,63$ K which can be assigned to a kinetic glass-like ordering transition. By determining the activation energy $E_A$, this glass-like transition can be related to conformational degrees of freedom of the ethylene endgroups of the organic building block BEDT-TTF. As opposed to other $κ$-(BEDT-TTF)$_2X$ salts, we identify a peculiar ethylene endgroup ordering in the present material in which only one of the two crystallographically inequivalent ethylene endgroups is subject to glass-like ordering. This experimental finding is fully consistent with our predictions from $ab\,initio$ calculations from which we estimate the energy differences $ΔE$ and the activation energies $E_A$ between different conformations. The present results indicate that the specific interaction between the ethylene endgroups and the nearby anion layers leads to different energetics of the inequivalent ethylene endgroups, as evidenced by different ratios $E_A/ΔE$. We infer that the ratio $E_A/ΔE$ is a suitable parameter to identify the tendency of ethylene endgroups towards glass-like freezing.

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arXiv2017

Low-temperature lattice effects in the spin-liquid candidate $κ$-(BEDT-TTF)$_2$Cu$_2$(CN)$_3$

The quasi-two-dimensional organic charge-transfer salt $κ$-(BEDT-TTF)$_2$Cu$_2$(CN)$_3$ is one of the prime candidates for a quantum spin-liquid due the strong spin frustration of its anisotropic triangular lattice in combination with its proximity to the Mott transition. Despite intensive investigations of the material's low-temperature properties, several important questions remain to be answered. Particularly puzzling are the 6\,K anomaly and the enigmatic effects observed in magnetic fields. Here we report on low-temperature measurements of lattice effects which were shown to be particularly strongly pronounced in this material (R. S. Manna \emph{et al.}, Phys. Rev. Lett. \textbf{104}, 016403 (2010)). A special focus of our study lies on sample-to-sample variations of these effects and their implications on the interpretation of experimental data. By investigating overall nine single crystals from two different batches, we can state that there are considerable differences in the size of the second-order phase transition anomaly around 6\,K, varying within a factor of 3. In addition, we find field-induced anomalies giving rise to pronounced features in the sample length for two out of these nine crystals for temperatures $T <$ 9 K. We tentatively assign the latter effects to $B$-induced magnetic clusters suspected to nucleate around crystal imperfections. These $B$-induced effects are absent for the crystals where the 6\,K anomaly is most strongly pronounced. The large lattice effects observed at 6\,K are consistent with proposed pairing instabilities of fermionic excitations breaking the lattice symmetry. The strong sample-to-sample variation in the size of the phase transition anomaly suggests that the conversion of the fermions to bosons at the instability is only partial and to some extent influenced by not yet identified sample-specific parameters.

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arXiv2017

Metal-Insulator Transition in the Dimerized Organic Conductor $κ$-(BEDT-TTF)$_2$Hg(SCN)$_2$Br

The organic charge-transfer salt $κ$-(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 $κ$-(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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arXiv2015

Antiferromagnetic fluctuations in the quasi-two-dimensional organic superconductor detected by Raman spectroscopy

Using Raman scattering, the quasi-two dimensional organic superconductor k-(BEDT-TTF)2Cu[N(CN)2]Br (T_c=11.8 K) and the related antiferromagnet k-(BEDT-TTF)2Cu[N(CN)2]Cl are studied. Raman scattering provides unique spectroscopic information about magnetic degrees of freedom that has been otherwise unavailable on such organic conductors. Below T=200 K a broad band at about 500 cm-1 develops in both compounds. We identify this band with two-magnon excitation. The position and the temperature dependence of the spectral weight are similar in the antiferromagnet and in the metallic Fermi-liquid. We conclude that antiferromagnetic correlations are similarly present in the magnetic insulator and the Fermi-liquid state of the superconductor.

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arXiv2015

Magnetically-Driven Suppression of Nematic Order in an Iron-Based Superconductor

A theory of superconductivity in the iron-based materials requires an understanding of the phase diagram of the normal state. In these compounds, superconductivity emerges when stripe spin density wave (SDW) order is suppressed by doping, pressure or atomic disorder. This magnetic order is often pre-empted by nematic order, whose origin is yet to be resolved. One scenario is that nematic order is driven by orbital ordering of the iron 3d-electrons that triggers stripe SDW order. Another is that magnetic interactions produce a spin-nematic phase, which then induces orbital order. In this article, we report the observation by neutron powder diffraction of an additional four- fold-symmetric phase in Ba1-xNaxFe2As2 close to the suppression of SDW order, which is consistent with the predictions of magnetically-driven models of nematic order.

cond-mat.supr-con↗

arXiv2014

Barlowite as a canted antiferromagnet: theory and experiment

We investigate the structural, electronic and magnetic properties of the newly synthesized mineral barlowite Cu4(OH)6FBr which contains Cu2+ ions in a perfect kagome arrangement. In contrast to the spin-liquid candidate herbertsmithite ZnCu3(OH)6Cl2, kagome layers in barlowite are perfectly aligned due to the different bonding environments adopted by F- and Br- compared to Cl-. We perform density functional theory calculations to obtain the Heisenberg Hamiltonian parameters of Cu4(OH)6FBr which has a Cu2+ site coupling the kagome layers. The 3D network of exchange couplings together with a substantial Dzyaloshinskii-Moriya coupling lead to canted antiferromagnetic ordering of this compound at TN=15 K as observed by magnetic susceptibility measurements on single crystals.

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arXiv2014

Barlowite: A Spin-1/2 Antiferromagnet with a Geometrically Perfect Kagome Motif

We present thermodynamic studies of a new spin-1/2 antiferromagnet containing undistorted kagome lattices---barlowite Cu$_{4}$(OH)$_{6}$FBr. Magnetic susceptibility gives $θ_{CW}$ = $-$136 K, while long-range order does not happen until $T_{N}$ = 15 K with a weak ferromagnetic moment $μ$ $<$ 0.1$μ_{B}$/Cu. A 60 T magnetic field induces a moment less than 0.5$μ_{B}$/Cu at $T$ = 0.6 K. Specific-heat measurements have observed multiple phase transitions at $T \ll$ $\mid$$θ_{CW}$$\mid$. The magnetic entropy of these transitions is merely 18% of $k_{B}$ln2 per Cu spin. These observations suggest that nontrivial spin textures are realized in barlowite with magnetic frustration. Comparing with the leading spin-liquid candidate herbertsmithite, the superior interkagome environment of barlowite sheds light on new spin-liquid compounds with minimum disorder. The robust perfect geometry of the kagome lattice makes charge doping promising.

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arXiv2014

Charge-order fluctuations and superconductivity in two-dimensional organic metals

We report comprehensive Raman and infrared investigations of charge-order (CO) fluctuations in the organic metal $β^{\prime\prime}$-(BEDT-TTF)$_2$SF$_5$CHFSO$_3$ and superconductor $β^{\prime\prime}$-(BEDT-TTF)$_2$SF$_5$CH$_2$CF$_2$SO$_3$. The charge-sensitive vibrational bands have been analyzed through an extension of the well-known Kubo model for the spectral signatures of an equilibrium between two states. At room temperature, both salts exhibit charge fluctuations between two differently charged molecular states with an exchange frequency of about $6\times10^{11} {\rm s}^{-1}$. The exchange rate of the metallic salt remains roughly constant down to 10 K, while in the superconductor the exchange velocity starts to decrease below 200 K, and a "frozen" charge-ordered state emerges, and coexists with the charge-order fluctuation state down to the superconducting temperature. These findings are confronted with other existing spectroscopic experiments, and a tentative phase diagram is proposed for the $β^{\prime\prime}$ BEDT-TTF quarter-filled salts.

cond-mat.supr-con↗

arXiv2013

Structural, Magnetic, and Superconducting Properties of Ba1-xNaxFe2As2

We report the results of a systematic investigation of the phase diagram of the iron-based superconductor system, Ba1-xNaxFe2As2, from x = 0.1 to x = 1.0 using high resolution neutron and x-ray diffraction and magnetization measurements. We find that the coincident structural and magnetic phase transition to an orthorhombic (O) structure with space group Fmmm and a striped antiferromagnet (AF) with space group F(C)mm'm' in Ba1-xNaxFe2As2 is of first order. A complete suppression of the magnetic phase is observed by x = 0.30, and bulk superconductivity occurs at a critical concentration near 0.15. We compare the new findings to the previously reported results of the hole-doped Ba1-xKxFe2As2 solid solution in order to resolve the differing effects of band filling and A-site cation size on the properties of the magnetic and superconducting ground states. The substantial size difference between Na and K causes various changes in the lattice trends, yet the overarching property phase diagram from the Ba1-xKxFe2As2 phase diagram carries over to the Ba1-xNaxFe2As2 solid solution. We note that the composition dependence of the c axis turns over from positive to negative around x = 0.35, unlike the K-substituted materials. We show that this can be understood by invoking steric effects; primarily the Fe2As2 layer shape is dictated mostly by the electronic filling, which secondarily induces an interlayer spacing adjusted to compensate for the given cation volume. This exemplifies the primacy of even subtle features in the Fe2As2 layer in controlling both the structure and properties in the uncollapsed 122 phases.

cond-mat.supr-con↗

arXiv2012

Search for quantum electronic dipoles in the dimerized κ-(BEDT-TTF)2Cu[N(CN)2]Cl salt

The Mott insulator κ-(BEDT-TTF)2Cu[N(CN)2]Cl consists of molecular dimers arranged on an anisotropic triangular lattice and develops a canted antiferromagnetic ground state. It has recently been suggested that this system features purely electronic ferroelectricity which requires an electric dipole moment. Optical spectroscopy clearly rules out charge imbalance in this system, which excludes the existence of quantum electric dipoles on the dimers and subsequently a dipolar spin coupling. We suggest that the prominent in-plane dielectric response in κ-(BEDT-TTF)2Cu[N(CN)2]Cl is due to short-range discommensurations of the antiferromagnetic phase in the temperature range 30 < T < 50 K, and domain wall relaxations at lower temperatures.

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arXiv2012

Absence of charge order in the dimerized κ-phase BEDT-TTF salts

Utilizing infrared vibrational spectroscopy we have investigated dimerized two-dimensional organic salts in order to search for possible charge redistribution that might cause electronic dipoles and ferroelectricity: the quantum spin liquid κ-(BEDT-TTF)2Cu2(CN)3, the antiferromagnetic Mott insulator κ-(BEDT-TTF)2$Cu[N(CN)2]Cl, and the superconductor κ-(BEDT-TTF)2$Cu[N(CN)2]Br. None of them exhibit any indication of charge disproportionation upon cooling down to low temperatures. No modification in the charge distribution is observed around T = 6 K where a low-temperature anomaly has been reported for the spin-liquid κ-(BEDT-TTF)2$Cu2(CN)3. In this compound the in-plane optical response and vibrational coupling are rather anisotropic, indicating that the tilt of the BEDT-TTF molecules in c-direction and their coupling to the anion layers has to be considered in the explanation of the electromagnetic properties.

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arXiv2012

Power-law dependence of the optical conductivity observed in the quantum spin-liquid compound κ-(BEDT-TTF)2Cu2(CN)3

The Mott-insulator κ-(BEDT-TTF)_2Cu_2(CN)_3 is the prime candidate of a quantum spin liquid with puzzling magnetic properties. Our THz and infrared investigations reveal that also the charge dynamics does not follow the expectations for a Mott insulator. The frequency-dependent conductivity exhibits a power-law behavior $σ_1(ω)\propto ω^n$ that grows stronger as the temperature decreases and extends all the way through the far-infrared. With $n\approx 0.8$ to 1.5 we obtain a significantly smaller exponent than predicted by Ng and Lee [Phys. Rev. Lett. {\bf 99}, 156402 (2007)]. We suggest fluctuations becomes important in the spin-liquid state and couple to the electrodynamic properties differently compared to the antiferromagnetic Mott insulator κ-(BEDT-TTF)_2Cu[N(CN)_2]Cl. We discuss the various possibilities of how charge fluctuations are influenced by the presence or absence of magnetic order.

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