arXiv subjects

D. L. Schlagel

Publications and source records attributed to D. L. Schlagel.

At least 19 recordsLinked to original sources

arXiv2026

Chemical tuning of electronic and transport properties of the Bi-Se-Te family of topological insulators

We use laser-based Angle-Resolved Photoemission Spectroscopy (ARPES) to study how chemical substitution modifies the electronic properties of the Bi2(Se{1-x}Tex)3 (BiSeTe) family of topological insulators. We find that increasing the Te content lowers the chemical potential, leading to a decrease in the binding energy of the Dirac point and a reduction in the density of states originating from the bulk band. This reduction leads to a transition from metallic to semiconducting temperature dependence of the resistivity. For the highest Te concentration, the resistivity nearly saturates at the lowest temperatures. The presence of this plateau indicates that metallic topological surface states dominate the conductance, opening the possibility of studying their transport properties.

cond-mat.other↗

arXiv2025

Interplay between aging and rejuvenation in spin glasses

Aging in a single crystal spin glass ($\mathrm{Cu}_{0.92}\mathrm{Mn}_{0.08}$) has been measured using ac susceptibility techniques over a temperature range of $0.3 - 0.8 \, T_g$. In these studies, traditional aging experiments (or ``quench'' aging protocols) are compared to aging curves constructed from finite-cooling-rate curves. By comparing the growth rates of spin glass order between the two types of aging curves, it is determined that quantitative comparisons between protocols which are taken by quenching and protocols using a finite cooling rate are not possible without a deeper understanding of the interplay between aging and rejuvenation. We then demonstrate that the data presented indicate that rejuvenation, rather than cumulative aging, is the cause for the discrepancies between the two growth rates.

cond-mat.dis-nn↗

arXiv2025

Quantifying memory in spin glasses

Rejuvenation and memory, long considered the distinguishing features of spin glasses, have recently been proven to result from the growth of multiple length scales. This insight, enabled by simulations on the Janus~II supercomputer, has opened the door to a quantitative analysis. We combine numerical simulations with comparable experiments to introduce two coefficients that quantify memory. A third coefficient has been recently presented by Freedberg et al. We show that these coefficients are physically equivalent by studying their temperature and waiting-time dependence.

cond-mat.dis-nn↗

arXiv2024

Memory and Rejuvenation in Glassy Systems

The memory effect in a single crystal spin glass ($\mathrm{Cu}_{0.92}\mathrm{Mn}_{0.08}$) has been measured using \freq ac susceptibility techniques over a temperature range of $0.4 - 0.7 \, T_g$ and a model of the memory effect has been developed. A double-waiting-time protocol is carried out where the spin glass is first allowed to age at a temperature below $T_g$, followed by a second aging at a lower temperature, \Tw{2}, after it has fully rejuvenated. The model is based on calculating typical coincident growth of correlated regions at the two temperatures. It accounts for the absolute magnitude of the memory effect as a function of both waiting times and temperatures. The data can be explained by the memory loss being a function of the relative change in the correlated volume at the first waiting temperature because of the growth in the correlations at the second waiting temperature.

cond-mat.dis-nn↗

arXiv2023

On the superposition principle and non-linear response in spin glasses

The extended principle of superposition has been a touchstone of spin glass dynamics for almost thirty years. The Uppsala group has demonstrated its validity for the metallic spin glass, CuMn, for magnetic fields $H$ up to 10 Oe at the reduced temperature $T_\mathrm{r}=T/T_\mathrm{g} = 0.95$, where $T_\mathrm{g}$ is the spin glass condensation temperature. For $H > 10$ Oe, they observe a departure from linear response which they ascribe to the development of non-linear dynamics. The thrust of this paper is to develop a microscopic origin for this behavior by focusing on the time development of the spin glass correlation length, $ξ(t,t_\mathrm{w};H)$. Here, $t$ is the time after $H$ changes, and $t_\mathrm{w}$ is the time from the quench for $T>T_\mathrm{g}$ to the working temperature $T$ until $H$ changes. We connect the growth of $ξ(t,t_\mathrm{w};H)$ to the barrier heights $Δ(t_\mathrm{w})$ that set the dynamics. The effect of $H$ on the magnitude of $Δ(t_\mathrm{w})$ is responsible for affecting differently the two dynamical protocols associated with turning $H$ off (TRM, or thermoremanent magnetization) or on (ZFC, or zero field-cooled magnetization). In this paper, we display the difference between the zero-field cooled $ξ_{\text {ZFC}}(t,t_\mathrm{w};H)$ and the thermoremanent magnetization $ξ_{\text {TRM}}(t,t_\mathrm{w};H)$ correlation lengths as $H$ increases, both experimentally and through numerical simulations, corresponding to the violation of the extended principle of superposition in line with the finding of the Uppsala Group.

cond-mat.dis-nn↗

arXiv2022

Decagonal Sn clathrate on $d$-Al-Ni-Co

Decagonal quasiperiodic ordering of Sn thin film on $d$-Al-Ni-Co, is shown based on scanning tunneling microscopy (STM), low-energy electron diffraction and density functional theory (DFT). Interestingly, the decagonal structural correlations are partially retained up to a large film thickness of 10 nm grown at a 165$\pm$10 K. The nucleation centers called 'Sn white flowers' identified by STM at submonolayer thickness are recognized as valid patches of the decagonal clathrate structure with low adsorption energies. Due to the excellent lattice matching (to within 1%) between columns of Sn dodecahedra in the clathrate structure and pentagonal motifs at the $d$-Al-Ni-Co surface, the interfacial energy favors clathrate over the competing Sn crystalline forms. DFT study of the Sn/Al-Ni-Co composite model shows good mechanical stability, as shown by the work of separation of Sn from Al-Ni-Co slab that is comparable to clathrate self-separation energy. The relaxed surface terminations of the R$_2$T$_4$ clathrate approximant are in self-similarity correspondence with the motifs observed in the STM images from monolayer to thickest Sn film.

cond-mat.mtrl-sci↗

arXiv2021

Scanning tunneling microscopy study of Ni2MnGa(100) surface

Ni2MnGa(100) surface has been investigated in the premartensite and martensite phase by using scanning tunneling microscopy. The presence of twined morphology is observed in the premartensite phase for Mn excess surface which exhibit non-equispaced parallel bands in one side of the twin boundary. Moreover, in the flat region of the surface two domains of non-periodic parallel bands corresponding to the incommensurate CDW is observed. Although, stoichiometric surface also exhibit twining but the parallel bands are equispaced and have equal corrugation. Most interestingly, coexistence of twined morphology and the CDW pattern is observed in the premartensite phase for Ni excess surface which was not reported till date. In the martensite phase for Mn excess surface, incommensurate CDW is transformed to commensurate CDW corresponding to the equispaced parallel bands. In stark contrast, stoichiometric surface exhibit parallel bands that have different periodicity in different regions. Both the voltage dependent STM and STS measurement establishes that this morphology is also related to the CDW.

cond-mat.mtrl-sci↗

arXiv2021

Spin-glass dynamics in the presence of a magnetic field: exploration of microscopic properties

The synergy between experiment, theory, and simulations enables a microscopic analysis of spin-glass dynamics in a magnetic field in the vicinity of and below the spin-glass transition temperature $T_\mathrm{g}$. The spin-glass correlation length, $ξ(t,t_\mathrm{w};T)$, is analysed both in experiments and in simulations in terms of the waiting time $t_\mathrm{w}$ after the spin glass has been cooled down to a stabilised measuring temperature $T<T_\mathrm{g}$ and of the time $t$ after the magnetic field is changed. This correlation length is extracted experimentally for a CuMn 6 at. % single crystal, as well as for simulations on the Janus II special-purpose supercomputer, the latter with time and length scales comparable to experiment. The non-linear magnetic susceptibility is reported from experiment and simulations, using $ξ(t,t_\mathrm{w};T)$ as the scaling variable. Previous experiments are reanalysed, and disagreements about the nature of the Zeeman energy are resolved. The growth of the spin-glass magnetisation in zero-field magnetisation experiments, $M_\mathrm{ZFC}(t,t_\mathrm{w};T)$, is measured from simulations, verifying the scaling relationships in the dynamical or non-equilibrium regime. Our preliminary search for the de Almeida-Thouless line in $D=3$ is discussed.

cond-mat.dis-nn↗

arXiv2020

Scaling law describes the spin-glass response in theory, experiments and simulations

The correlation length $ξ$, a key quantity in glassy dynamics, can now be precisely measured for spin glasses both in experiments and in simulations. However, known analysis methods lead to discrepancies either for large external fields or close to the glass temperature. We solve this problem by introducing a scaling law that takes into account both the magnetic field and the time-dependent spin-glass correlation length. The scaling law is successfully tested against experimental measurements in a CuMn single crystal and against large-scale simulations on the Janus II dedicated computer.

cond-mat.stat-mech↗

arXiv2020

On the Slowing Down of Spin Glass Correlation Length Growth:simulations meet experiments

The growth of the spin-glass correlation length has been measured as a function of the waiting time $t_{\mathrm{w}}$ on a single crystal of CuMn (6 at.\%), reaching values $ξ\sim 150$ nm, larger than any other glassy correlation-length measured to date. We find an aging rate $\mathrm{d}\ln\,t_{\mathrm{w}}/\mathrm{d}\ln\,ξ$ larger than found in previous measurements, which evinces a dynamic slowing-down as $ξ$ grows. Our measured aging rate is compared with simulation results by the Janus collaboration. After critical effects are taken into account, we find excellent agreement with the Janus data.

cond-mat.dis-nn↗

arXiv2017

Reorientations, relaxations, metastabilities and multidomains of skyrmion lattices

Magnetic skyrmions are nano-sized topologically protected spin textures with particle-like properties. They can form lattices perpendicular to the magnetic field and the orientation of these skyrmion lattices with respect to the crystallographic lattice is governed by spin-orbit coupling. By performing small angle neutron scattering measurements, we investigate the coupling between the crystallographic and skyrmion lattices in both Cu$_2$OSeO$_3$ and the archetype chiral magnet MnSi. The results reveal that the orientation of the skyrmion lattice is primarily determined by the magnetic field direction with respect to the crystallographic lattice. In addition, it is also influenced by the magnetic history of the sample which can induce metastable lattices. Kinetic measurements show that these metastable skyrmion lattices may or may not relax to their equilibrium positions under macroscopic relaxation times. Furthermore, multidomain lattices may form when two or more equivalent crystallographic directions are favored by spin-orbit coupling and oriented perpendicular to the magnetic field.

cond-mat.str-el↗

arXiv2017

Magnetic Fluctuations, Precursor Phenomena and Phase Transition in MnSi under Magnetic Field

The reference chiral helimagnet MnSi is the first system where skyrmion lattice correlations have been reported. At zero magnetic field the transition at $T_C$ to the helimagnetic state is of first order. Above $T_C$, in a region dominated by precursor phenomena, neutron scattering shows the build up of strong chiral fluctuating correlations over the surface of a sphere with radius $2π/\ell$, where $\ell$ is the pitch of the helix. It has been suggested that these fluctuating correlations drive the helical transition to first order following a scenario proposed by Brazovskii for liquid crystals. We present a comprehensive neutron scattering study under magnetic fields, which provides evidence that this is not the case. The sharp first order transition persists for magnetic fields up to 0.4 T whereas the fluctuating correlations weaken and start to concentrate along the field direction already above 0.2 T. Our results thus disconnect the first order nature of the transition from the precursor fluctuating correlations. They also show no indication for a tricritical point, where the first order transition crosses over to second order with increasing magnetic field. In this light, the nature of the first order helical transition and the precursor phenomena above $T_C$, both of general relevance to chiral magnetism, remain an open question.

cond-mat.mtrl-sci↗

arXiv2015

Itinerant and localized magnetization dynamics in antiferromagnetic Ho

Using femtosecond time-resolved resonant magnetic x-ray diffraction at the Ho L3 absorption edge, we investigate the demagnetization dynamics in antiferromagnetically ordered metallic Ho after femtosecond optical excitation. Tuning the x-ray energy to the electric dipole (E1, 2p -> 5d) or quadrupole (E2, 2p -> 4f) transition allows us to selectively and independently study the spin dynamics of the itinerant 5d and localized 4f electronic subsystems via the suppression of the magnetic (2 1 3-tau ) satellite peak. We find demagnetization timescales very similar to ferromagnetic 4f systems, suggesting that the loss of magnetic order occurs via a similar spin-flip process in both cases. The simultaneous demagnetization of both subsystems demonstrates strong intra-atomic 4f-5d exchange coupling. In addition, an ultrafast lattice contraction due to the release of magnetostriction leads to a transient shift of the magnetic satellite peak.

cond-mat.str-el↗

arXiv2011

Anisotropic magnetic deflagration in single crystals of Gd5Ge4

Experimental evidence of the anisotropy of the magnetic deflagration associated with the low-temperature first order antiferromagnetic (AFM) --> ferromagnetic (FM) phase-transition in single crystals of Gd5Ge4 is reported. The deflagrations have been induced by controlled pulses of surface acoustic waves (SAW) allowing us to explore both the magnetic field and temperature dependencies on the characteristic times of the phenomenon. The study was done using samples with different geometries and configurations between the SAW pulses and the direction of the applied magnetic field with respect to the three main crystallographic directions of the samples. The effect of temperature is nearly negligible, whereas observed strong magnetic field dependence correlates with the magnetic anisotropy of the sample. Finally, the role of the SAW pulses in both the ignition and formation of the deflagration front was also studied, and we show that the thermal diffusivity of Gd5Ge4 must be anisotropic, following \kappaa>\kappab>\kappac.

cond-mat.mes-hall↗

arXiv2009

Short-range magnetic correlations in Tb5Ge4

We present a single crystal neutron diffraction study of the magnetic short-range correlations in Tb$_5$Ge$_4$ which orders antiferromagnetically below the Neel temperature $T_N$ $\approx$ 92 K. Strong diffuse scattering arising from magnetic short-range correlations was observed in wide temperature ranges both below and above $T_N$. The antiferromagnetic ordering in Tb$_5$Ge$_4$ can be described as strongly coupled ferromagnetic block layers in the $ac$-plane that stack along the b-axis with weak antiferromagnetic inter-layer coupling. Diffuse scattering was observed along both $a^*$ and $b^*$ directions indicating three-dimensional short-range correlations. Moreover, the $q$-dependence of the diffuse scattering is Squared-Lorentzian in form suggesting a strongly clustered magnetic state that may be related to the proposed Griffiths-like phase in Gd$_5$Ge$_4$.

cond-mat.str-el↗

arXiv2009

Lattice dynamics in magnetic superelastic Ni-Mn-In alloys. Neutron scattering and ultrasonic experiments

Neutron scattering and ultrasonic methods have been used to study the lattice dynamics of two single crystals of Ni-Mn-In Heusler alloys close to Ni$_{50}$Mn$_{34}$In$_{16}$ magnetic superelastic composition. The paper reports the experimental determination of the low-lying phonon dispersion curves and the elastic constants for this alloy system. We found that the frequencies of the TA$_{2}$ branch are relatively low and it exhibits a small dip anomaly at a wave number $ξ_{0} \approx 1/3$, which softens with decreasing temperature. Associated with the softening of this phonon, we also observed the softening of the shear elastic constant $C'=(C_{11}-C_{12})/2$. Both temperature softenings are typical for bcc based solids which undergo martensitic transformations and reflect the dynamical instability of the cubic lattice against shearing of $\{110\}$ planes along $<1\bar{1}0>$ directions. Additionally, we measured low-lying phonon dispersion branches and elastic constants in applied magnetic fields aimed to characterize the magnetoelastic coupling.

cond-mat.mtrl-sci↗

arXiv2008

Single Crystal Growth, Crystallography, Magnetic Susceptibility, Heat Capacity, and Thermal Expansion of the Antiferromagnetic S = 1 Chain Compound CaV2O4

The compound CaV2O4 contains V^{+3} cations with spin S = 1 and has an orthorhombic structure at room temperature containing zigzag chains of V atoms running along the c-axis. We have grown single crystals of CaV2O4 and report crystallography, static magnetization, magnetic susceptibility χ, ac magnetic susceptibility, heat capacity Cp, and thermal expansion measurements in the temperature T range of 1.8-350 K on the single crystals and on polycrystalline samples. An orthorhombic to monoclinic structural distortion and a long-range antiferromagnetic (AF) transition were found at sample-dependent temperatures T_S \approx 108-145 K and T_N \approx 51-76 K, respectively. In two annealed single crystals, another transition was found at \approx 200 K. In one of the crystals, this transition is mostly due to V2O3 impurity phase that grows coherently in the crystals during annealing. However, in the other crystal the origin of this transition at 200 K is unknown. The χ(T) shows a broad maximum at \approx 300 K associated with short-range AF ordering and the anisotropy of χabove T_N is small. The anisotropic χ(T \to 0) data below T_N show that the (average) easy axis of the AF magnetic structure is the b-axis. The Cp(T) data indicate strong short-range AF ordering above T_N, consistent with the χ(T) data. We fitted our χ(T) data near room temperature by a J1-J2 S = 1 Heisenberg chain model, where J1(J2) is the (next)-nearest-neighbor exchange interaction. We find J1 \approx 230 K, and surprisingly, J2/J1 \approx 0 (or J1/J2 \approx 0). The interaction J_\perp between these S = 1 chains leading to long-range AF ordering at T_N is estimated to be J_\perp/J_1 \gtrsim 0.04.

cond-mat.str-el↗

arXiv2007

^{17}O and ^{51}V NMR for the zigzag spin-1 chain compound CaV2O4

$^{51}$V NMR studies on CaV2O4 single crystals and $^{17}$O NMR studies on $^{17}$O-enriched powder samples are reported. The temperature dependences of the $^{17}$O NMR line width and nuclear spin-lattice relaxation rate give strong evidence for a long-range antiferromagnetic transition at Tn = 78 K in the powder. Magnetic susceptibility measurements show that Tn = 69 K in the crystals. A zero-field $^{51}$V NMR signal was observed at low temperatures (f $\approx$ 237 MHz at 4.2 K) in the crystals. The field swept spectra with the field in different directions suggest the presence of two antiferromagnetic substructures. Each substructure is collinear, with the easy axes of the two substructures separated by an angle of 19(1) degree, and with their average direction pointing approximately along the b-axis of the crystal structure. The two spin substructures contain equal number of spins. The temperature dependence of the ordered moment, measured up to 45 K, shows the presence of an energy gap Eg in the antiferromagnetic spin wave excitation spectrum. Antiferromagnetic spin wave theory suggests that Eg lies between 64 and 98 K.

cond-mat.str-el↗