arXiv subjects

Andreas Hoser

Publications and source records attributed to Andreas Hoser.

15 recordsLinked to original sources

arXiv2023

Rich Magnetic Phase Diagram of Putative Helimagnet Sr$_3$Fe$_2$O$_7$

The cubic perovskite SrFeO$_3$ was recently reported to host hedgehog- and skyrmion-lattice phases in a highly symmetric crystal structure which does not support the Dzyaloshinskii-Moriya interactions commonly invoked to explain such magnetic order. Hints of a complex magnetic phase diagram have also recently been found in powder samples of the single-layer Ruddlesden-Popper analog Sr$_2$FeO$_4$, so a reinvestigation of the bilayer material Sr$_3$Fe$_2$O$_7$, believed to be a simple helimagnet, is called for. Our magnetization and dilatometry studies reveal a rich magnetic phase diagram with at least 6 distinct magnetically ordered phases and strong similarities to that of SrFeO$_3$. In particular, at least one phase is apparently multiple-$\mathbf{q}$, and the $\mathbf{q}$s are not observed to vary among the phases. Since Sr$_3$Fe$_2$O$_7$ has only two possible orientations for its propagation vector, some of the phases are likely exotic multiple-$\mathbf{q}$ order, and it is possible to fully detwin all phases and more readily access their exotic physics.

cond-mat.str-el↗

arXiv2022

Crystal and magnetic structures of $R_2$Ni$_2$In compounds ($R$ = Tb and Ho)

Crystal and magnetic structures of $R_2$Ni$_2$In ($R$ = Tb and Ho) have been studied by powder neutron diffraction at low temperatures. The compounds crystallize in an orthorhombic crystal structure of the Mn$_2$AlB$_2$-type. At low temperatures, the magnetic moments localized solely on the rare earth atoms form antiferromagnetic structures. The Tb magnetic moments, equal to 8.65(6) $μ_B$ and parallel to the $c$-axis, form a collinear magnetic structure described by the propagation vector $\boldsymbol{k} = [\frac{1}{2}, \frac{1}{2}, \frac{1}{2}]$. This magnetic structure is stable up to the Néel temperature equal to 40 K. For Ho$_2$Ni$_2$In a complex, temperature-dependent magnetic structure is detected. In the temperature range 3.5-8.6 K, an incommensurate magnetic structure, described by the propagation vector $\boldsymbol{k}_1 = [0.76, 0, 0.52]$ is observed, while in the temperature interval 2.2-3.1 K the magnetic order is described by two propagation vectors, namely, $\boldsymbol{k}_2 = [\frac{5}{6}, 0.16, \frac{1}{2}]$ and its third harmonics $3\boldsymbol{k}_2 = [\frac{5}{2}, 0.48, \frac{3}{2}]$. Below 2 K, a coexistence of all magnetic structures detected at higher temperatures is observed. For all magnetic phases, the Ho magnetic moments are parallel to the $c$-axis. The low temperature heat capacity data confirm a first order transition near 3 K.

cond-mat.mtrl-sci↗

arXiv2021

Localized-delocalized crossover of spin-carriers and magnetization reversal in Co$_{2}$VO$_{4}$

Neutron diffraction, magnetization and muon spin relaxation measurements, supplemented by density functional theory (DFT) calculations are employed to unravel temperature-driven magnetization reversal (MR) in inverse spinel Co$_2$VO$_4$. All measurements show a second-order magnetic phase transition at $T_{\rm C} = 168$\,K to a collinear ferrimagnetic phase. The DFT results suggest the moments in the ferrimagnetic phase are delocalized and undergo gradual localization as the temperature is lowered below $T_{\rm C}$. The delocalized-localized crossover gives rise to a maximum magnetization at $T_{\rm NC} = 138$\,K and the continuous decrease in magnetization produces sign-change at $T_{\rm MR} \sim 65$\,K. Muon spectroscopy results support the DFT, as a strong $T_1$-relaxation is observed around $T_{\rm NC}$, indicating highly delocalized spin-carriers gradually tend to localization upon cooling. The magnetization reversal determined at zero field is found to be highly sensitive to the applied magnetic field, such that above $B\sim 0.25$\,T instead of a reversal a broad minimum in the magnetization is apparent at $T_{\rm MR}$. Analysis of the neutron diffraction measurements shows two antiparallel magnetic sub-lattice-structure, each belonging to magnetic ions on two distinct crystal lattice sites. The relative balance of these two structural components in essence determines the magnetization. Indeed, the order parameter of the magnetic phase on one site develops moderately more than that on the other site. Unusual tipping of the magnetic balance, caused by such site-specific magnetic fluctuation, gives rise to a spontaneous flipping of the magnetization as the temperature is lowered.

cond-mat.str-el↗

arXiv2021

Complex interplay of magnetic ordering and spin-lattice coupling in orthochromite Nd$_{0.5}$Dy$_{0.5}$CrO$_{3}$

The mixed rare-earth orthochromite Nd$_{0.5}$Dy$_{0.5}$CrO$_{3}$ has a Néel temperature ($T_\mathrm{N}$) of ${\sim}$ 175\,K, resulting in the G-type antiferromagnetic ordering of Cr$^{3+}$ spins. The inverse susceptibility shows a deviation from Curie-Weiss law at 230\,K, with a large effective paramagnetic moment of 8.8\,$μ_{\mathrm{B}}$. The ZFC-FC magnetization bifurcate just above $T_\mathrm{N}$ and show a distinct signature of spin reorientation near 60\,K. Neutron diffraction show that below $T_\mathrm{N}$, the Cr$^{3+}$ spins align in $Γ_{2}$ representation as ($F_{x}$, $G_{z}$). Below 60\,K, due to spin reorientation, the magnetic structure is in $Γ_{1}$ ($G_{y}$) configuration. The neutron diffraction does not show any signature of rare-earth ordering even at 1.5\,K. First principles density functional theory calculations within GGA+U and GGA+U+SO approximations reveal that the G-type antiferromagnetic order is the ground state magnetic structure of Cr sublattice and the spin-reorientation of Cr$^{3+}$ spins can happen in the absence of 3d-4f interactions unlike in the case of orthoferrites. The specific heat shows a `$λ$' anomaly at $T_\mathrm{N}$, while at low temperature two distinct Schottky anomalies are observed; a Schottky peak at 2\,K and an additional step-like feature above 10\,K. Above $T_\mathrm{N}$, the magnetic transition is preceded by structural anomalies as seen in our x-ray diffraction and Raman measurements. The deviation of structural parameters near Néel temperature is smaller. The phonon frequencies show deviation from the standard anharmonic behaviour: first near 250\,K, due to magneto-volume effects while the second deviation occurs near 200\,K due to spin-phonon coupling.

cond-mat.str-el↗

arXiv2020

Magnetic phase diagram of Cu$_{4-x}$Zn$_x$(OH)$_6$FBr studied by neutron-diffraction and $μ$SR techniques

We have systematically studied the magnetic properties of Cu$_{4-x}$Zn$_x$(OH)$_6$FBr by the neutron diffraction and muon spin rotation and relaxation ($μ$SR) techniques. Neutron-diffraction measurements suggest that the long-range magnetic order and the orthorhombic nuclear structure in the $x$ = 0 sample can persist up to $x$ = 0.23 and 0.43, respectively. The temperature dependence of the zero-field (ZF) $μ$SR spectra provide two characteristic temperatures, $T_{A0}$ and $T_λ$. Comparison between $T_{A0}$ and $T_M$ from previously reported magnetic-susceptibility measurements suggest that the former comes from the short-range interlayer-spin clusters that persist up to $x$ = 0.82. On the other hand, the doping level where $T_λ$ becomes zero is about 0.66, which is much higher than threshold of the long-range order, i.e., $\sim$ 0.4. Our results suggest that the change in the nuclear structure may alter the spin dynamics of the kagome layers and a gapped quantum-spin-liquid state may exist above $x$ = 0.66 with the perfect kagome planes.

cond-mat.str-el↗

arXiv2020

Detection of antiskyrmions by topological Hall effect in Heusler compounds

Heusler compounds having $\textit{D}$${}_{2d}$ crystal symmetry gained much attention recently due to the stabilization of a vortex-like spin texture called antiskyrmions in thin lamellae of Mn${}_{1.4}$Pt${}_{0.9}$Pd${}_{0.1}$Sn as reported in the work of Nayak $\textit{et al.}$ [Nature (London) 548, 561 (2017)]. Here we show that bulk Mn${}_{1.4}$Pt${}_{0.9}$Pd${}_{0.1}$Sn undergoes a spin-reorientation transition from a collinear ferromagnetic to a noncollinear configuration of Mn moments below 135 K, which is accompanied by the emergence of a topological Hall effect. We tune the topological Hall effect in Pd and Rh substituted Mn${}_{1.4}$PtSn Heusler compounds by changing the intrinsic magnetic properties and spin textures. A unique feature of the present system is the observation of a zero-field topological Hall resistivity with a sign change which indicates the robust formation of antiskyrmions.

cond-mat.mtrl-sci↗

arXiv2020

Crystal and magnetic structure of antiferromagnetic Mn$_{2}$PtPd

We have investigated the crystal and magnetic structure of Mn${}_{2}$PtPd alloy using powder x-ray and neutron diffraction experiments. This compound is believed to belong to the Heusler family having crystal symmetry $\mathit{I}$4/$\mathit{mmm}$ (TiAl${}_{3}$-type). However, in this work we found that the Pd and Pt atoms are disordered and thus Mn${}_{2}$PtPd crystallizes in the $\mathit{L}$1${}_{0}$ structure having $\mathit{P}$4/$\mathit{mmm}$ symmetry (CuAu-I type) like MnPt and MnPd binary alloys. The lattice constants are $\mathit{a}$ = 2.86 Å and $\mathit{c}$ = 3.62 Å at room temperature. Mn${}_{2}$PtPd has a collinear antiferromagnetic spin structure below the Néel temperature $\mathit{T}$${}_{N}$ = 866 K, where Mn moments of $\mathrm{\sim}$4 $μ$${}_{B}$ lie in the $\mathit{ab}$-plane. We observed a strong change in the lattice parameters near $\mathit{T}$${}_{N}$. The sample exhibits metallic behaviour, where electrical resistivity and carrier concentration are of the order of 10${}^{-5}$ $Ω$ cm and 10${}^{21}$ cm${}^{-3}$, respectively.

cond-mat.mtrl-sci↗

arXiv2019

Long-range magnetic ordering in rocksalt-type high-entropy oxides

We report the magnetic properties of Mg$_{0.2}$Co$_{0.2}$Ni$_{0.2}$Cu$_{0.2}$Zn$_{0.2}$O, a high-entropy oxide with rocksalt structure, and the influence of substitutions on these properties. From the magnetic susceptibility and neutron diffraction measurements, we found that this compound exhibits long-range magnetic order below 120 K despite the substantial structuraldisorder. The other rocksalt-type high-entropy oxides with various chemical substitutions were found to host either an antiferromagnetic order or spin-glass state depending on the amount of magnetic ions. The presence of magnetic order for such a disordered material potentially provide a route to explore novel magnetic properties and functions.

cond-mat.str-el↗

arXiv2019

Neutron diffraction study of a metallic kagome lattice, Tb3Ru4Al12

We present the results of neutron diffraction studies on polycrystals of a metallic kagome lattice, Tb3Ru4Al12, reported recently to undergo reentrant magnetism, with the onset of long range antiferromagnetic order below (TN=) 22 K and spin-glass features below about 17 K. The present results reveal long-range antiferromagnetic order of an incommensurate type with the moments oriented along c-axis at all temperatures below TN. There are however notable changes in the T dependence of propagation vector along b-axis across 17 K. An observation of interest is that there is no decrease of intensity of magnetic Bragg peaks on entrance into the glassy phase (that is, below 17 K). This finding suggests that the magnetism of this compound is an exotic one and we wonder whether this compound is an example for dynamical spin-glass freezing phenomenon, as a consequence of geometrical frustration.

cond-mat.str-el↗

arXiv2018

Mechanochemical Synthesis of the Lead-Free Double Perovskite Cs2[AgIn]Br6 and its Optical Properties

Hitting hard on the binary halides yields in the formation of Cs2[AgIn]Br6. The lead-free double perovskite marks, although not usable itself, a further step forward in finding sustainable and durable perovskite materials for photovoltaic applications. Cs2[AgIn]Br6 is one of the prominent examples of double perovskites materials that have been suggested to circumvent the use of lead compounds in perovskite solar cells. We herein report the successful synthesis of the material using a mechanochemical approach. It crystallizes in an elpasolite-type structure, an ordered perovskite superstructure, with a cell parameter of a = 11.00 Å. However, the compound exhibits a relatively large optical bandgap of 2.36 eV and is unstable under illumination, which impedes its use as solar absorber material at this early stage. Still, substitution of lead and the potential of this synthesis method are promising as well as the fruitful combination of theoretical considerations with experimental materials discovery.

cond-mat.mtrl-sci↗

arXiv2018

Canted ferrimagnetism and giant coercivity in the non-stoichiometric double perovskite La2Ni1.19Os0.81O6

The non-stoichiometric double perovskite oxide La2Ni1.19Os0.81O6 was synthesized by solid state reaction and its crystal and magnetic structures were investigated by powder x-ray and neutron diffraction. La2Ni1.19Os0.81O6 crystallizes in the monoclinic double perovskite structure (general formula A2BB'O6) with space group P21/n, where the B site is fully occupied by Ni and the B' site by 19 % Ni and 81 % Os atoms. Using x-ray absorption spectroscopy an Os4.5+ oxidation state was established, suggesting presence of about 50 % paramagnetic Os5+ (5d3, S = 3/2) and 50 % non-magnetic Os4+ (5d4, Jeff = 0) ions at the B' sites. Magnetization and neutron diffraction measurements on La2Ni1.19Os0.81O6 provide evidence for a ferrimagnetic transition at 125 K. The analysis of the neutron data suggests a canted ferrimagnetic spin structure with collinear Ni2+ spin chains extending along the c axis but a non-collinear spin alignment within the ab plane. The magnetization curve of La2Ni1.19Os0.81O6 features a hysteresis with a very high coercive field, HC = 41 kOe, at T = 5 K, which is explained in terms of large magnetocrystalline anisotropy due to the presence of Os ions together with atomic disorder. Our results are encouraging to search for rare earth free hard magnets in the class of double perovskite oxides.

cond-mat.str-el↗

arXiv2017

Magnetic structure of NdMn$_{0.8}$Fe$_{0.2}$O$_{3+δ}$; neutron powder diffraction experiment

The magnetic structure of the mixed antiferromagnet NdMn$_{0.8}$Fe$_{0.2}$O$_3$ was resolved. Neutron powder diffraction data definitively resolve the Mn-sublattice with a magnetic propagation vector ${\bf k} = (000)$ and with the magnetic structure (A$_x$, F$_y$, G$_z$) for 1.6~K~$< T < T_N (\approx 59$~K). The Nd-sublattice has a (0, f$_y$, 0) contribution in the same temperature interval. The Mn sublattice undergoes spin-reorientation transition at $T_1 \approx 13$~K while the Nd magnetic moment keep ordered abruptly increases at this temperature. Powder X-ray diffraction shows a strong magnetoelastic effect at $T_N$ but no additional structural phase transitions from 2~K to 300~K. Density functional theory calculations confirm the magnetic structure of the undoped NdMnO$_3$ as part of our analysis. Taken together, these results show the magnetic structure of Mn-sublattice in NdMn$_{0.8}$Fe$_{0.2}$O$_3$ is a combination of the Mn and Fe parent compounds, but the magnetic ordering of Nd sublattice spans over broader temperature interval than in case of NdMnO$_3$ and NdFeO$_3$. This result is a consequence of the fact that the Nd ions do not order independently, but via polarization from Mn/Fe sublattice.

cond-mat.mtrl-sci↗

arXiv2017

Antiferromagnetic structure and electronic properties of BaCr2As2 and BaCrFeAs2

The chromium arsenides BaCr2As2 and BaCrFeAs2 with ThCr2Si2 type structure (space group I4/mmm; also adopted by '122' iron arsenide superconductors) have been suggested as mother compounds for possible new superconductors. DFT-based calculations of the electronic structure evidence metallic antiferromagnetic ground states for both compounds. By powder neutron diffraction we confirm for BaCr2As2 a robust ordering in the antiferromagnetic G-type structure at T_N = 580 K with mu_Cr = 1.9 mu_B at T = 2K. Anomalies in the lattice parameters point to magneto-structural coupling effects. In BaCrFeAs2 the Cr and Fe atoms randomly occupy the transition-metal site and G-type order is found below 265 K with mu_Cr/Fe = 1.1 mu_B. 57Fe Moessbauer spectroscopy demonstrates that only a small ordered moment is associated with the Fe atoms, in agreement with electronic structure calculations with mu_Fe ~ 0. The temperature dependence of the hyperfine field does not follow that of the total moments. Both compounds are metallic but show large enhancements of the linear specific heat coefficient gamma with respect to the band structure values. The metallic state and the electrical transport in BaCrFeAs2 is dominated by the atomic disorder of Cr and Fe and partial magnetic disorder of Fe. Our results indicate that Neel-type order is unfavorable for the Fe moments and thus it is destabilized with increasing iron content.

cond-mat.supr-con↗

arXiv2014

Lattice-site-specific spin-dynamics in double perovskite Sr2CoOsO6

We have studied the magnetic properties and spin-dynamics of the structurally-ordered double perovskite Sr$_2$CoOsO$_6$. Our neutron diffraction, muon spin relaxation and ac-susceptibility measurements reveal two antiferromagnetic (AFM) phases on cooling from room temperature down to 2 K. In the first AFM phase, with transition temperature $T_{\mathrm{N}}=108$ K, cobalt (3$d^7$, $S=3/2$) and osmium (5$d^2$, $S=1$) moments fluctuate dynamically, while their \textit{average} effective moments undergo long-range order. In the second AFM phase with $T_{\mathrm{N}}=67$ K, cobalt moments first become frozen and induce a noncollinear spin-canted AFM state, while dynamically fluctuating osmium moments are later frozen into a randomly canted state at $T\approx 5$ K. Our \textit{ab initio} calculations indicate that the effective exchange coupling between cobalt and osmium sites is rather weak, so that cobalt and osmium sublattices exhibit different ground states and spin-dynamics, making Sr$_2$CoOsO$_6$ distinct from previously reported double-perovskite compounds.

cond-mat.mtrl-sci↗

arXiv2013

Lattice Instability and Competing Spin Structures in the Double Perovskite Insulator Sr2FeOsO6

The semiconductor Sr2FeOsO6, depending on temperature, adopts two types of spin structures that differ in the spin sequence of ferrimagnetic iron - osmium layers along the tetragonal c-axis. Neutron powder diffraction experiments, 57Fe Mössbauer spectra, and density-functional theory calculations suggest that this behavior arises because a lattice instability resulting in alternating iron-osmium distances fine-tunes the balance of competing exchange interactions. Thus, Sr2FeOsO6 is an example for a double perovskite, in which the electronic phases are controlled by the interplay of spin, orbital, and lattice degrees of freedom.

cond-mat.mtrl-sci↗