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We report giant anisotropy in thermoelectric power factor ($S^2\sigma$) of marcasite structure-type PtSb$_{1.4}$Sn$_{0.6}$. PtSb$_{1.4}$Sn$_{0.6}$, synthesized using ambient pressure flux growth method upon mixing Sb and Sn on the same atomic site, is a new phase different from both PtSb$_2$ and PtSn$_2$ that crystallize in the cubic $Pa\bar{3}$ pyrite and $Fm\bar{3}m$ fluorite unit cell symmetry, respectively. Giant difference in $S^2\sigma$ for heat flow applied along different principal directions of the orthorhombic unit cell mostly stems from anisotropic Seebeck coefficients.

Connections between crystal chemistry and critical temperature Tc have been in the focus of superconductivity, one of the most widely studied phenomena in physics, chemistry, and materials science alike. In most Fe-based superconductors, materials chemistry and physics conspire so that Tc correlates with the average anion height above the Fe plane, i.e., with the geometry of the FeAs4 or FeCh4 (Ch = Te, Se, or S) tetrahedron. By synthesizing Fe1–ySe1–xSx (0 ≤ x ≤ 1; y ≤ 0.1), we find that in alloyed crystals Tc is not correlated with the anion height like it is for most other Fe superconductors. Instead, changes in Tc(x) and tetragonal-to-orthorhombic (nematic) transition Ts(x) upon cooling are correlated with disorder in Fe vibrations in the direction orthogonal to Fe planes, along the crystallographic c-axis. The disorder stems from the random nature of S substitution, causing deformed Fe(Se,S)4 tetrahedra with different Fe–Se and Fe–S bond distances. Our results provide evidence of Tc and Ts suppression by disorder in anion height. The connection to local crystal chemistry may be exploited in computational prediction of new superconducting materials with FeSe/S building blocks.

We report inelastic neutron scattering measurements of magnetic excitations in YbMnSb2, a low-carrier-density Dirac semimetal in which the antiferromagnetic Mn layers are interleaved with Sb layers that host Dirac fermions. We observe a considerable broadening of spin waves, which is consistent with substantial spin fermion coupling. The spin wave damping, $\gamma$, in YbMnSb2 is roughly twice larger compared to that in a sister material, YbMnBi2, where an indication of a small damping consistent with theoretical analysis of the spin-fermion coupling was reported. The inter-plane interaction between the Mn layers in YbMnSb2 is also much stronger, suggesting that the interaction mechanism is rooted in the same spin-fermion coupling. Our results establish the systematics of spin-fermion interactions in layered magnetic Dirac materials.

International audience; Magnetism in two-dimensional (2D) van der Waals (vdW) materials has recently emerged as one of the most promising areas in condensed matter research, with many exciting emerging properties and significant potential for applications ranging from topological magnonics to low-power spintronics, quantum computing, and optical communications. In the brief time after their discovery, 2D magnets have blossomed into a rich area for investigation, where fundamental concepts in magnetism are challenged by the behavior of spins that can develop at the single layer limit. However, much effort is still needed in multiple fronts before 2D magnets can be routinely used for practical implementations. In this comprehensive review, prominent authors with expertise in complementary fields of 2D magnetism (i.e., synthesis, device engineering, magneto-optics, imaging, transport, mechanics, spin excitations, and theory and simulations) have joined together to provide a genome of current knowledge and a guideline for future developments in 2D magnetic materials research.

A highly tunable band gap of the layered semiconductor Zn3In2S6 under pressure is reported. The change in the band gap is strongly coupled to the variation and transformation of the crystal structure.

Identifying and understanding the mechanisms behind strong phonon–phonon scattering in condensed matter systems is critical to maximizing the efficiency of thermoelectric devices. To date, the leading method to address this has been to meticulously survey the full phonon dispersion of the material in order to isolate modes with anomalously large linewidth and temperature-dependence. Here we combine quantitative MeV ultrafast electron diffraction (UED) analysis with Monte Carlo based dynamic diffraction simulation and first-principles calculations to directly unveil the soft, anharmonic lattice distortions of model thermoelectric material SnSe. A small single-crystal sample is photoexcited with ultrafast optical pulses and the soft, anharmonic lattice distortions are isolated using MeV-UED as those associated with long relaxation time and large displacements. We reveal that these modes have interlayer shear strain character, induced mainly by c-axis atomic displacements, resulting in domain formation in the transient state. These findings provide an innovative approach to identify mechanisms for ultralow and anisotropic thermal conductivity and a promising route to optimizing thermoelectric devices.

Physical review / B 106(21), 214516 (2022). doi:10.1103/PhysRevB.106.214516, Superconductivity in binary ruthenium pnictides occurs proximal to and upon suppression of a nonmagnetic ground state, preceded by a pseudogap phase associated with Fermi surface instability, and its critical temperature, $T_c$, is maximized around the pseudogap quantum critical point. By analogy with isoelectronic iron-based counterparts, antiferromagnetic fluctuations became “usual suspects” as putative mediators of superconducting pairing. Here we report on a high-temperature local symmetry breaking in RuP, the nonsuperconducting parent of the maximum-$T_c$ branch of these novel superconductors, revealed by combined nanostructure-sensitive powder and single-crystal x-ray total scattering analyses. Large local distortions of Ru chains associated with orbital-charge trimerization, further assembled into hexamers, exist above the two-stage electronic transition in RuP. In the pseudogap regime the precursors order with distortions retaining their strength, whereas they acquire spin-singlet characteristics which dramatically enhances the distortion as the nonmagnetic ground state establishes. The precursors enable the nonmagnetic ground state and presumed complex oligomerization, and the relevance of pseudogap fluctuations for superconductivity emerges as a distinct prospect. As a transition metal system in which partial d-manifold filling combined with high crystal symmetry promotes electronic instabilities, this represents a further example of local electronic precursors underpinning the macroscopic collective behavior of quantum materials., Published by Inst., Woodbury, NY

Acta crystallographica / A 77(6), 611 - 636 (2021). doi:10.1107/S2053273321010159, We explore data reduction and correction steps and processed data reproducibility in the emerging single crystal total scattering based technique of three-dimensional differential atomic pair distribution function (3D-$\Delta$PDF) analysis. All steps from sample measurement to data-processing are outlined in detail using a CuIr$_2$S$_4$ example crystal studied in a setup equipped with a high-energy x-ray beam and a flat panel area detector. Computational overhead as it pertains to data-sampling and the associated data processing steps is also discussed. Various aspects of the final 3D-$\Delta$PDF reproducibility are explicitly tested by varying data-processing order and included steps, and by carrying out a crystal-to-crystal data comparison. We identify situations in which the 3D-$\Delta$PDF is robust, and caution against a few particular cases which can lead to inconsistent 3D-$\Delta$PDFs. Although not all the approaches applied here-in will be valid across all systems, and a more in-depth analysis of some of the effects of the data processing steps may still needed, the methods collected here-in represent the start of a more systematic discussion about data processing and corrections in this field., Published by Blackwell, Oxford [u.a.]

We investigate the surface oxidation in a van der Waals ferromagnet Fe3-xGeTe2, a material widely utilized for spintronic applications. While known for its relative air-insensitivity, exposure to air during the handling process (e.g. device or heterostructure fabrication) can lead to reduction or disappearance of its magnetic signal. Comparison of x-ray absorption and x-ray magnetic circular dichroism spectra between pristine and air-exposed Fe3-xGeTe2 confirm a naturally oxidized surface layer on the material. The surface oxide layer has predominantly Fe3+ content. X-ray absorption spectroscopy done on micron-sized exfoliated Fe3-xGeTe2 flakes reveal that the change in the surface chemical properties can be quite significant for thin flakes. The surface modulation of Fe3-xGeTe2 can lead to inaccuracies in characterizing its interfacial magnetic and spin transport properties, and complicate device and heterostructure fabrication processes.

Superconductivity in binary ruthenium pnictides occurs proximal to and upon suppression of a mysterious non-magnetic ground state, preceded by a pseudogap phase associated with Fermi surface instability, and its critical temperature, T$_{c}$, is maximized around the pseudogap quantum critical point. By analogy with isoelectronic iron based counterparts, antiferromagnetic fluctuations became "usual suspects" as putative mediators of superconducting pairing. Here we report on a high temperature local symmetry breaking in RuP, the parent of the maximum-Tc branch of these novel superconductors, revealed by combined nanostructure-sensitive powder and single crystal X-ray total scattering experiments. Large local Ru$_{6}$ hexamer distortions associated with orbital-charge trimerization form above the two-stage electronic transition in RuP. While hexamer ordering enables the nonmagnetic ground state and presumed complex oligomerization, the relevance of pseudogap fluctuations for superconductivity emerges as a distinct prospect. As a transition metal system in which partial d-manifold filling combined with high crystal symmetry promotes electronic instabilities, this represents a further example of local electronic precursors underpinning the macroscopic collective behavior of quantum materials., 10 pages 6 figures

Two-dimensional magnetic materials (2DMMs) are significant not only for studies on the nature of 2D long-range magnetic order but also for future spintronic devices. Of particular interest are 2DMMs where spins can be manipulated by electrical conduction. Whereas Cr

The idea of employing non-Abelian statistics for error-free quantum computing ignited interest in reports of topological surface superconductivity and Majorana zero modes (MZMs) in FeTe0.55Se0.45. However, the topological features and superconducting properties are not observed uniformly across the sample surface. The understanding and practical control of these electronic inhomogeneities present a prominent challenge for potential applications. Here, we combine neutron scattering, scanning angle-resolved photoemission spectroscopy, and microprobe composition and resistivity measurements to characterize the electronic state of Fe1+yTe1-xSex. We establish a phase diagram in which the superconductivity is observed only at sufficiently low Fe concentration, in association with distinct antiferromagnetic correlations, whereas the coexisting topological surface state occurs only at sufficiently high Te concentration. We find that FeTe0.55Se0.45 is located very close to both phase boundaries, which explains the inhomogeneity of superconducting and topological states. Our results demonstrate the compositional control required for use of topological MZMs in practical applications.

Ultrathin crystals including monolayers have been reported for various transition-metal dichalcogenides (TMDCs) with van der Waals bonds in the crystal structure. Herein, we report a detailed synthesis procedure and characterization of ultrathin iron ditelluride crystals. This material crystallizes in an orthorhombic marcasite Pnnm crystal structure whose bonding is dominantly covalent and without loosely connected van der Waals (vdW) bonds, making monolayer FeTe2 synthesis less straightforward than other TMDC monolayer syntheses. The chemical vapor deposition synthesis process described is simple, effective, and results in a range of crystal thicknesses from approximately 400 nm down to the FeTe2 monolayer.

We present a detailed investigation of the crystal structure of VI3, a two-dimensional van der Waals material of interest for studies of low-dimensional magnetism. As opposed to the average crystal structure that features R3 symmetry of the unit cell, our Raman scattering and X-ray atomic pair distribution function analysis supported by density functional theory calculations point to the coexistence of short-range ordered P31c and long-range ordered R3 phases. The highest-intensity peak, A1g3, exhibits a moderate asymmetry that might be traced back to the spin-phonon interactions, as in the case of CrI3.

Visualizing atomic-orbital degrees of freedom is a frontier challenge in scanned microscopy. Some types of orbital order are virtually imperceptible to normal scattering techniques because they do not reduce the overall crystal lattice symmetry. A good example is dxz/dyz ({\pi},{\pi}) orbital order in tetragonal lattices. For enhanced detectability, here we consider the quasiparticle scattering interference (QPI) signature of such ({\pi},{\pi}) orbital order in both normal and superconducting phases. The theory reveals that sublattice-specific QPI signatures generated by the orbital order should emerge strongly in the superconducting phase. Sublattice-resolved QPI visualization in superconducting CeCoIn5 then reveals two orthogonal QPI patterns at lattice-substitutional impurity atoms. We analyze the energy dependence of these two orthogonal QPI patterns and find the intensity peaked near E=0, as predicted when such ({\pi}) orbital order is inte,{\pi}rtwined with d-wave superconductivity. Sublattice-resolved superconductive QPI techniques thus represent a new approach for study of hidden orbital order., Comment: 19 pages, 5 figures

Two-dimensional magnetic materials (2DMM) are significant for studies on the nature of 2D long range magnetic order but also for future spintronic devices. Of particular interest are 2DMM where spins can be manipulated by electrical conduction. Whereas Cr$_2$Si$_2$Te$_6$ exhibits magnetic order in few-layer crystals, its large band gap inhibits electronic conduction. Here we show that the defect-induced short-range crystal order in Cr$_2$Si$_2$Te$_6$ on the length scale below 0.6 nm induces substantially reduced band gap and robust semiconducting behavior down to 2 K that turns to metallic above 10 GPa. Our results will be helpful to design conducting state in 2DMM and call for spin-resolved measurement of the electronic structure in exfoliated ultrathin crystals.

Identifying material parameters affecting properties of ferromagnets is key to optimized materials that are better suited for spintronics. Magnetic anisotropy is of particular importance in van der Waals magnets, since it not only influences magnetic and spin transport properties, but also is essential to stabilizing magnetic order in the two-dimensional limit. Here, we report that hole doping effectively modulates the magnetic anisotropy of a van der Waals ferromagnet and explore the physical origin of this effect. Fe3-xGeTe2 nanoflakes show a significant suppression of the magnetic anisotropy with hole doping. Electronic structure measurements and calculations reveal that the chemical potential shift associated with hole doping is responsible for the reduced magnetic anisotropy by decreasing the energy gain from the spin-orbit induced band splitting. Our findings provide an understanding of the intricate connection between electronic structures and magnetic properties in two-dimensional magnets and propose a method to engineer magnetic properties through doping.

The name of the third author of the article by Koch et al. [Acta Cryst. (2021). A77, 611–636] is corrected.

We report our investigations on the effects of pressure on the electronic and magnetic properties of magnetic Dirac semimetal ${\mathrm{EuMnBi}}_{2}$ by using electrical transport, synchrotron x-ray diffraction, and x-ray absorption spectroscopy. The antiferromagnetic interaction due to the Eu magnetic moment in ${\mathrm{EuMnBi}}_{2}$ is enhanced under pressure up to $\ensuremath{\sim}3.9\phantom{\rule{0.16em}{0ex}}\mathrm{GPa}$. The N\'eel temperature (${T}_{N}$) is found to disappear above 4 GPa and a new transition ${T}_{t}$ at around 29 K emerges above 6 GPa. ${T}_{t}$ remains relatively constant up to 15 GPa, above which it increases with further compression, reaching $\ensuremath{\sim}60\phantom{\rule{0.16em}{0ex}}\mathrm{K}$ at 22 GPa. Eu $L$-edge x-ray absorption spectroscopy revealed a valence change of Eu toward a trivalent state that begins above 6 GPa, which indicates that ${T}_{t}$ is likely related to the valence transition temperature of Eu. Sign reversal of the Hall resistivity above 7 GPa suggests that the valence change of Eu also induces a Fermi surface modification.

Topological fermions have mainly been addressed in the limit of weakly correlated systems, while the realization of Kondo-like physics arising from Dirac-Weyl fermions and implying strong correlations is rare. The noncentrosymmetric Weyl fermion $R\mathrm{AlGe}$ compounds (with $R=\mathrm{La} \mathrm{and} \mathrm{Ce}$) provide a promising playground for revealing the impact of electronic correlations driven by $f$-electron states on Weyl fermions. Here, we tackle their charge dynamics as a function of temperature. Besides spotting typical optical signatures of a type-II Weyl semimetal in both materials, we discover that electronic correlations at low temperatures renormalize the nontrivial bands hosting the Weyl nodes and lead to a reduction of the Fermi velocity as well as an enhancement of the charge carriers effective mass in CeAlGe with respect to LaAlGe, both being a fingerprint of a so-called Weyl-Kondo system.

We present a polarization-resolved, high-resolution Raman scattering study of the three consecutive charge density wave (CDW) regimes in $1T\ensuremath{-}{\mathrm{TaS}}_{2}$ single crystals, supported by ab initio calculations. Our analysis of the spectra within the low-temperature commensurate (C-CDW) regime shows $P\overline{3}$ symmetry of the system, thus excluding the previously proposed triclinic stacking of the ``star-of-David'' structure, and promoting trigonal or hexagonal stacking instead. The spectra of the high-temperature incommensurate (IC-CDW) phase directly project the phonon density of states due to the breaking of the translational invariance, supplemented by sizable electron-phonon coupling. Between 200 and 352 K, our Raman spectra show contributions from both the IC-CDW and the C-CDW phases, indicating their coexistence in the so-called nearly commensurate (NC-CDW) phase. The temperature dependence of the symmetry-resolved Raman conductivity indicates the stepwise reduction of the density of states in the CDW phases, followed by a Mott transition within the C-CDW phase. We determine the size of the Mott gap to be ${\mathrm{\ensuremath{\Omega}}}_{\mathrm{gap}}\ensuremath{\approx}170\text{--}190$ meV, and track its temperature dependence.

We carried out a comprehensive study of the structural, electrical transport, thermal, and thermodynamic properties in ferrimagnetic ${\mathrm{Mn}}_{3}{\mathrm{Si}}_{2}{\mathrm{Te}}_{6}$ single crystals. Mn and Te $K$-edge x-ray absorption spectroscopy and synchrotron powder x-ray diffraction were measured to provide information on the local atomic environment and the average crystal structure. The dc and ac magnetic susceptibility measurements indicate a second-order paramagnetic to ferrimagnetic transition at ${T}_{c}\ensuremath{\sim}74$ K, which is further confirmed by the specific heat measurement. ${\mathrm{Mn}}_{3}{\mathrm{Si}}_{2}{\mathrm{Te}}_{6}$ exhibits semiconducting behavior along with a large negative magnetoresistance of $\ensuremath{-}87%$ at ${T}_{c}$ and a relatively high value of thermopower up to $\ensuremath{\sim}10$ mV/K at 5 K. Besides the rapidly increasing resistivity $\ensuremath{\rho}(T)$ and thermopower $S(T)$ below 20 K, the large discrepancy between the activation energy for resistivity ${E}_{\ensuremath{\rho}}$ and thermopower ${E}_{S}$ above 20 K indicates the polaronic transport mechanism. Furthermore, the thermal conductivity $\ensuremath{\kappa}(T)$ of ${\mathrm{Mn}}_{3}{\mathrm{Si}}_{2}{\mathrm{Te}}_{6}$ is notably rather low, comparable to ${\mathrm{Cr}}_{2}{\mathrm{Si}}_{2}{\mathrm{Te}}_{6}$, and is strongly suppressed in the magnetic field across ${T}_{c}$, indicating the presence of strong spin-lattice coupling, also similar with ${\mathrm{Cr}}_{2}{\mathrm{Si}}_{2}{\mathrm{Te}}_{6}$.

Two-dimensional (2D) materials with intrinsic ferromagnetism provide unique opportunity to engineer new functionalities in nano-spintronics. One such material is CrI3, showing long-range magnetic order in monolayer with the Curie temperature (Tc) of 45 K. Here we study detailed evolution of magnetic transition and magnetic critical properties in response to systematic reduction in crystal thickness down to 50 nm. Bulk Tc of 61 K is gradually suppressed to 57 K, however, the satellite transition at T * = 45 K is observed layer-independent at fixed magnetic field of 1 kOe. The origin of T * is proposed to be a crossover from pinning to depinning of magnetic domain walls. The reduction of thickness facilitates a field-driven metamagnetic transition around 20 kOe with out-of-plane field, in contrast to the continuous changes with in-plane field. The critical analysis around Tc elucidates the mean-field type interactions in microscale-thick CrI3.

We present a comprehensive study on anisotropic magnetocaloric porperties of the van der Waals weak-itinerant ferromagnet Fe3−xGeTe2 that features gate-tunable room-temperature ferromagnetism in few-layer device. Intrinsic magnetocrystalline anisotropy is observed to be temperature-dependent and most likely favors the long-range magnetic order in thin Fe3−xGeTe2 crsytal. The magnetic entropy change ΔSM also reveals an anisotropic characteristic between H//ab and H//c, which could be well scaled into a universal curve. The peak value $$-\Delta {S}_{M}^{{\max }}$$−ΔSMmax of 1.20 J kg−1 K−1 and the corresponding adiabatic temperature change ΔTad of 0.66 K are deduced from heat capacity with out-of-plane field change of 5 T. By fitting of the field-dependent parameters of $$-\Delta {S}_{M}^{{\max }}$$−ΔSMmax and the relative cooling power RCP, it gives $$-{\rm{\triangle }}{S}_{M}^{{\max }}$$−∆SMmax ∝ Hn with n = 0.603(6) and RCP ∝ Hm with m = 1.20(1) when H//c. Given the high and tunable Tc, Fe3−xGeTe2 crystals are of interest for fabricating the heterostructure-based spintronics device.

Fundamental electronic principles underlying all transition metal compounds are the symmetry and filling of the $d$-electron orbitals and the influence of this filling on structural configurations and responses. Here we use a sensitive local structural technique, x-ray atomic pair distribution function analysis, to reveal the presence of fluctuating local-structural distortions at high temperature of one such compound, \cis . We show that this hitherto overlooked fluctuating symmetry lowering is electronic in origin and will significantly modify the energy-level spectrum and electronic and magnetic properties. The explanation is a local, fluctuating, orbital-degeneracy-lifted state. The natural extension of our result would be that this phenomenon is likely to be widespread amongst diverse classes of partially filled nominally degenerate d-electron systems, with potentially broad implications for our understanding of their properties., 10 pages 3 figures

We provide a discussion of our previously collected data (Chinotti et al., Phys. Rev. B 94, 245101 (2016)) on the electrodynamic response in YbMnBi2, a representative Weyl semimetal, and in its gapped semimetal counterpart EuMnBi2, which can be fairly well reproduced within a recent devoted theoretical treatment (S.P. Mukherjee and J.P. Carbotte, J. Phys.: Condens. Matter 29 (2017) 425301). This allows identifying and catching all the essential features of their peculiar electronic structure as imaged by the excitation spectrum.

We report the synthesis and characterization of Fe 0.36(4) Pd 0.64(4) Se 2 with a pyrite-type structure. Fe 0.36(4) Pd 0.64(4) Se 2 was synthesized using ambient pressure flux crystal growth methods even though the space group Pa3 is high-pressure polymorph for both FeSe 2 and PdSe 2 . Combined experimental and theoretical analysis reveal magnetic spin glass state below 23 K in 1000 Oe that stems from random Fe/Pd occupancies on the same atomic site. The frozen-in magnetic randomness contributes significantly to electronic transport. Electronic structure calculations confirm dominant d-electron character of hybridized bands and large density of states near the Fermi level. Flux-grown single crystal alloys in Pd-Fe-Se atomic system therefore open new pathway for exploring different polymorphs in crystal structures and their novel properties. © 2019 American Chemical Society.

Van der Waals (vdW) ferromagnets are an important class of materials for spintronics applications. The recent discovery of atomically vdW magnets ${\mathrm{CrI}}_{3}$ and ${\mathrm{Cr}}_{2}{\mathrm{Ge}}_{2}{\mathrm{Te}}_{6}$ has triggered a renaissance in the area of two-dimensional (2D) magnetism. Herein we systematically studied 2H-${\mathrm{Mn}}_{0.28}{\mathrm{TaS}}_{2}$ single crystal, a 2D vdW ferromagnet with ${T}_{c}\ensuremath{\sim}82.3\phantom{\rule{0.16em}{0ex}}\mathrm{K}$, and a large in-plane magnetic anisotropy. Mn $K$-edge x-ray absorption spectroscopy was measured to provide information on its electronic state and local atomic environment. The detailed magnetic isotherms measured in the vicinity of ${T}_{c}$ indicates that the spin coupling inside 2H-${\mathrm{Mn}}_{0.28}{\mathrm{TaS}}_{2}$ is of a 3D Heisenberg type coupled with the attractive long-range interaction between spins that decay as $J(r)\ensuremath{\approx}{r}^{\ensuremath{-}4.85}$. Both resistivity $\ensuremath{\rho}(T)$ and thermopower $S(T)$ exhibit anomalies near ${T}_{c}$, confirming that the hole-type transport carriers strongly interact with local moments. An unusual angle-dependent magnetoresistance is further observed, suggesting a possible field-induced novel magnetic structure.

Semiconducting CoSbS is well known for its thermoelectric performance at high temperatures but it is also of interest because of its colossal low-temperature thermopower. Here, we address the temperature dependence of its optical response over a broad spectral range, from which we reveal several ingredients determining the thermoelectric properties at cryotemperatures. We discover coherent phonon modes and with the additional support of scanning transmission electron microscopy investigations we provide evidence for in-gap impurity states driving the formation of correlated electrons in the valence band. Their implications, with respect to the high thermoelectric power at low temperatures, are discussed within the framework of the phonon-drag transport of low-mobility heavy quasiparticles.

We examine the magnetic properties of the quasi 2D ferrimagnetic single crystal Mn3Si2Te6 (MST) through critical phenomena and magnetic entropy analysis in the easy axis (H || ab) as a function of proton irradiance. Employing a modified asymptotic analysis method, we find that upon proton irradiation the critical exponents do not fall into any particular universality class but lie close to mean field critical exponents ({\gamma} = 1, \b{eta} = 0.5). The presence of long-range interactions can be safely assumed for the pristine and irradiated cases of MST examined in this work. Further analysis on the effective spatial dimensionality reveal that MST remains at d = 3 under proton irradiation transitioning from an n = 1 spin dimensionality to n = 2 and n=3 for 1 x 10^15 and 5 x 10^15 H+/cm^2, indicating an XY interaction and a Heisenberg interaction, respectively. The pair (spin-spin) correlation function reveals an increase in magnetic correlations at the proton irradiance of 5 x 10^15 H+/cm^2. In conjunction, the maximum change in magnetic entropy obtained from isothermal magnetization at 3 T is the largest for 5 x 10^15 H+/cm^2 with a value of 2.45 J/kgK at T = 73.66 K, in comparison to 1.60 J/kgK for pristine MST at T = 73 K. Magnetic entropy derived from zero-field heat capacity does not show large deviations across the proton irradiated samples. This suggests that the antiferromagnetic coupling between the Mn sites is stable even after proton irradiation. Such result implies that magnetization is enhanced through a strengthening of the super-exchange interaction between Mn atoms mediated through Te rather than a weakening of the AFM component. Overall, our study finds that the magnetic interactions are manipulated the greatest when MST is irradiated at 5 x 10^15 H+/cm^2.

We carried out a comprehensive study of electronic transport, thermal, and thermodynamic properties in $\mathrm{Fe}{\mathrm{Cr}}_{2}{\mathrm{Te}}_{4}$ single crystals. It exhibits bad-metallic behavior and anomalous Hall effect (AHE) below a weak-itinerant paramagnetic-to-ferrimagnetic transition ${T}_{c}\ensuremath{\sim}123$ K. The linear scaling between the anomalous Hall resistivity ${\ensuremath{\rho}}_{xy}$ and the longitudinal resistivity ${\ensuremath{\rho}}_{xx}$ implies that the AHE in $\mathrm{Fe}{\mathrm{Cr}}_{2}{\mathrm{Te}}_{4}$ is most likely dominated by an extrinsic skew-scattering mechanism rather than an intrinsic KL or an extrinsic side-jump mechanism, which is supported by our Berry phase calculations.

The coupling between charge and spin orderings in strongly correlated systems plays a crucial role in fundamental physics and device applications. As a candidate of multiferroic materials, LuFe2O4 with a nominal Fe2.5+ valence state has the potential for strong charge-spin interactions; however, these interactions have not been fully understood until now. Here, combining complementary characterization methods with theoretical calculations, two types of charge orderings with distinct magnetic properties are revealed. The ground states of LuFe2O4 are decided by the parallel/antiparallel coupling of both charge and spin orderings in the adjacent FeO double layers. Whereas the ferroelectric charge ordering remains ferrimagnetic below 230 K, the antiferroelectric ordering undergoes antiferromagnetic-ferrimagnetic-paramagnetic transitions from 2 K to room temperature. This study demonstrates the unique aspects of strong spin-charge coupling within LuFe2O4. Our results shed light on the coexistence and competing nature of orderings in quantum materials.

Spectroscopic Imaging Scanning Tunneling Microscopy (SI-STM) measurements have previously been applied to the study of the heavy-fermion system CeCoIn5 to examine the superconducting gap structure and band dispersions via quasiparticle intereference. Here we directly measure the dispersing electron bands with angle-resolved photoelectron spectroscopy (ARPES) and compare with first-principles electronic structure calculations. By autocorrelating the ARPES-resolved bands with themselves we can measure the potential q vectors and discern exactly which bands the STM is measuring. We find that the STM results are dominated by scattering associated with a cloverleaf shaped band centered at the zone corners. This same band is also a viable candidate to host the superconducting gap. The electronic structure calculations indicate that this region of the Fermi surface involves significant contributions from the Co d electrons, an indication that the superconductivity in these materials is more three dimensional than that found in the related unconventional superconductors, the cuprates and the pnictides. publishedVersion

We present a detailed investigation of the crystal structure of VI