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D. Boldrin

Publications and source records attributed to D. Boldrin.

13 recordsLinked to original sources

Disentangling magnetic and optical contributions in ultrafast dynamics of antiperovskite non-collinear antiferromagnets

Non-collinear antiferromagnets are a class of spin-polarized antiferromagnets in which chiral spin textures give rise to Berry-curvature-driven phenomena, such as the anomalous Hall effect (AHE), without net magnetization. We investigate the properties of thin films of antiperovskite non-collinear antiferromagnetic metals Mn3NiN and Mn3GaN using pump-probe experiments. In both materials, we observe a strong dependence of pump-polarization-independent dynamics, induced by femtosecond laser pulses, on the angle between the sample normal and the direction of probe propagation. In Mn3NiN, where the presence of a sizable AHE indicates the {\Gamma}4g phase, the measured magnetooptical (MO) signals acquire an additional, strong dependence on the external magnetic field when the probe pulses are incident at nonzero angles. In contrast, in Mn3GaN, where the absence of AHE indicates the {\Gamma}5g phase, the measured signals do not depend on the magnetic field. Using probe-polarization-resolved measurements combined with full optical modeling based on Yeh's formalism, we quantitatively separate magnetic and non-magnetic contributions to the measured signals. We show that in Mn3NiN, the observed magnetic field dependence results from field-controlled redistribution of magnetic domain populations, enabled by their piezomagnetic moments and detected by a Kerr-like MO effect, while this effect is absent in Mn3GaN. Temperature-dependent measurements reveal a change from single-step to two-step quenching dynamics with increasing temperature in Mn3NiN. This behavior contrasts with the nearly temperature-independent quenching dynamics reported for the non-collinear antiferromagnetic Heusler compound Mn3Sn, but resembles the crossover from type-I to type-II demagnetization dynamics in metallic ferromagnets.

cond-mat.mtrl-sci

Ultrafast control of spin order by linearly polarized light in noncollinear antiferromagnetic metals

The non-thermal optical control of magnetic order offers a promising route to ultrafast, energy-efficient information technologies. Although optical manipulation of magnetism in metals has been extensively studied, experimentally demonstrated effects have so far been limited to heat-driven dynamics or helicity-dependent mechanisms. Here, we report ultrafast non-thermal control of spin order in noncollinear antiferromagnetic Mn-based antiperovskite nitrides Mn3NiN and Mn3GaN, driven solely by the polarization orientation of linearly polarized femtosecond laser pulses. Using time-resolved magneto-optical pump-probe experiments based on the Voigt effect, we observe sub-picosecond changes in magnetic order followed by picosecond relaxation. The magneto-optical response depends on the relative orientation of the pump and probe polarization planes, with linear-polarization dependence reaching up to 95%, a value unprecedented in metallic magnets. This phenomenon is observed in two different materials and persists over a wide range of excitation wavelengths, fluences, and temperatures, demonstrating its robustness. Symmetry analysis and microscopic modeling indicate that optically induced torques alone cannot fully explain the observed dynamics. We therefore propose laser-induced formation of transient spin-spiral states as a possible excitation mechanism.

cond-mat.mtrl-sci

Fluctuating magnetism in Zn-doped averievite with well-separated kagome layers

Kagome lattice decorated with S=1/2 spins is one of the most discussed ways to realize a quantum spin liquid. However, all previous material realizations of this model have suffered from additional complications, ranging from additional interactions to impurity effects. Recently, a new quantum kagome system has been identified in the form of averievite Cu(5-x)ZnxV2O10(CsCl), featuring a unique double-layer spacing between the kagome planes. Using muon spin spectroscopy we show that only a complete substitution (i.e. $x=2$) of interplanar copper ions leads to a quantum-disordered ground state. In contrast, the parent compound ($x=0$) exhibits long-range magnetic order, with a phase transition around 24 K. Experiments performed on the partially substituted material ($x=1$) show that the transformation proceeds through an intermediate disordered, partially frozen ground state, unaffected by pressures up to 23 kbar. Our study provides a microscopic view of the magnetism of the decoupling of the kagome layers and establishes the averievite as a new material platform for the experimental study of the fully-decoupled kagome layers.

cond-mat.str-el

Magnetic ground states and excitations in Zn-doped averieite -- a family of oxide-based $S=1/2$ kagome antiferromagnets

Spin-1/2 kagome materials have recently attracted a resurgence of interest as they are considered an ideal host of the quantum spin liquid (QSL) state, which can underpin functionality such as superconductivity. Here we report the first synthesis and characterization of a new oxide-based distorted $S=1/2$ kagome antiferromagnet (KAFM) in the Zn$_x$Cu$_{5-x}$(VO$_4$)$_{2}$O$_2$CsCl (termed Zn$\mathbf {_x}$) series, namely Zn$_2$-averievite, Zn$\mathbf {_2}$ ($x=2$). Using magnetometry, synchrotron diffraction and neutron scattering we demonstrate an evolution of ground states with $x$ in Zn$\mathbf {_x}$; from long-range magnetic order in averievite ($x=0$), via a spin-glass-like ground state in Zn$\mathbf {_1}$, to a quantum spin liquid (QSL) in Zn$\mathbf {_2}$ for which inelastic neutron scattering reveals a gapless continuum of excitations. Similar to archetypal $S = 1/2$ KAFMs herbertsmithite and SrCr$_{8.19}$Ga$_{3.81}$O$_{19}$ (SCGO), the dynamic magnetic susceptibility of Zn$\mathbf {_2}$ shows scaling behavior consistent with proximity to a quantum critical point. The results demonstrate that the new Zn$\mathbf {_2}$ material is an excellent test bed for achieving the elusive goal of charge carrier doping in QSL states of $S = 1/2$ KAFMs, in-line with previous theoretical studies.

cond-mat.str-el

Magnetically ordered and kagome quantum spin liquid states in the Zn-doped claringbullite series

Neutron scattering measurements have been performed on deuterated powder samples of claringbullite and Zn-doped claringbullite (Zn$_x$Cu$_{4-x}$(OD)$_{6}$FCl). At low temperatures, claringbullite Cu$_4$(OD)$_{6}$FCl forms a distorted pyrochlore lattice with long-range magnetic order and spin-wave-like magnetic excitations. Partial Zn doping leads to the nominal ZnCu$_3$(OD)$_{6}$FCl compound, a geometrically frustrated spin-1/2 kagome antiferromagnet that shows no transition to magnetic order down to 1.5 K. The magnetic excitations form a gapless continuum, a signature of fractional excitations in a quantum spin liquid.

cond-mat.str-el

Identifying the octupole Antiferromagnetic domain orientation in Mn$_{3}$NiN by scanning Anomalous Nernst Effect microscopy

The intrinsic anomalous Nernst effect in a magnetic material is governed by the Berry curvature at the Fermi energy and can be realized in non-collinear antiferromagnets with vanishing magnetization. Thin films of (001)-oriented Mn$_{3}$NiN have their chiral antiferromagnetic structure located in the (111) plane facilitating the anomalous Nernst effect unusually in two orthogonal in-plane directions. The sign of each component of the anomalous Nernst effect is determined by the local antiferromagnetic domain state. In this work, a temperature gradient is induced in a 50 nm thick Mn$_{3}$NiN two micron-size Hall cross by a focused scanning laser beam, and the spatial distribution of the anomalous Nernst voltage is used to image and identify the octupole macrodomain arrangement. Although the focused laser beam width may span many individual domains, cooling from room temperature through the antiferromagnetic transition temperature in an in-plane magnetic field prepares the domain state producing a checkerboard pattern resulting from the convolution of contributions from each domain. These images together with atomistic and micromagnetic simulations suggest an average macrodomain of the order of $1 {\mu}m^{2}$.

cond-mat.str-el

Room temperature weak collinear ferrimagnet with symmetry driven, large intrinsic magneto-optic signatures

Here we present a magnetic thin film with a weak ferrimagnetic (FIM) phase above the N\'eel temperature ($T_{N}$ = 240 K) and a non-collinear antiferromagnetic (AFM) phase below, exhibiting a small net magnetisation due to strain-associated canting of the magnetic moments. A long-range ordered FIM phase has been predicted in related materials, but without symmetry analysis. We now perform this analysis and use it to calculate the MOKE spectra in AFM and FIM phases. From the good agreement between the form of the measured and predicted MOKE spectra, we propose the AFM and FIM phases share the magnetic space group C2'/m' and that the symmetry driven magneto-optic and magneto-transport properties are maximised at room temperature in the FIM phase due to the non-zero intrinsic Berry phase contribution present in these materials. A room temperature FIM phase with large optical and transport signatures, as well as sensitivity to lattice strain and magnetic field, has useful prospects for high-speed spintronic applications.

cond-mat.str-el

Canted Antiferromagnetic Order in the Kagome Material Sr-Vesignieite

We report $^{51}$V NMR, $\mu$SR and zero applied field $^{63,65}$Cu NMR measurements on powder samples of Sr-vesignieite, SrCu$_3$V$_2$O$_8$(OH)$_2$, a $S = 1/2$ nearly-kagome Heisenberg antiferromagnet. Our results demonstrate that the ground state is a $\mathbf{q} = 0$ magnetic structure with spins canting either in or out of the kagome plane, giving rise to weak ferromagnetism. We determine the size of ordered moments and the angle of canting for different possible $\mathbf{q} = 0$ structures and orbital scenarios, thereby providing insight into the role of the Dzyaloshinskii-Moriya (DM) interaction in this material.

cond-mat.str-el

Vesignieite: a $S = \frac{1}{2}$ kagome antiferromagnet with dominant third-neighbor exchange

The spin-$\frac{1}{2}$ kagome antiferromagnet is an archetypal frustrated system predicted to host a variety of exotic magnetic states. We show using neutron scattering measurements that deuterated vesignieite BaCu$_{3}$V$_{2}$O$_{8}$(OD)$_{2}$, a fully stoichiometric $S=1/2$ kagome magnet with $<$1% lattice distortion, orders magnetically at $T_{\mathrm{N}}=9$K into a multi-k coplanar variant of the predicted triple-k octahedral structure. We find this structure is stabilized by a dominant antiferromagnetic 3$^{\mathrm{rd}}$-neighbor exchange $J_3$ with minor 1$^{\mathrm{st}}$- or 2$^{\mathrm{nd}}$--neighbour exchange. The spin-wave spectrum is well described by a $J_3$-only model including a tiny symmetric exchange anisotropy.

cond-mat.str-el

Orbital frustration in the S = 1/2 kagome magnet vesignieite, BaCu3V2O8(OD)2

Here we report crystallographic and magnetic studies on high quality samples of the magnetically frustrated S = 1/2 kagome antiferromagnet vesignieite, BaCu3V2O8(OD)2. Powder neutron diffraction data collected from samples obtained by a new hydrothermal synthetic route reveal a previously unobserved trigonal P3121 structure, similar to the isoelectronic mineral SrCu3V2O8(OH)2. The refined structure is consistent with orbital frustration of the eg d-orbitals in a sublattice of the Cu2+ kagome network due to a dynamic Jahn-Teller effect, which persists below the magnetic transition at TN = 9K and makes the material an interesting candidate for exploring concomitant spin and orbital frustration. A combination of crystallographic strain analysis and magnetisation measurements indicate strong magnetostructural coupling which may explain the varied magnetic behaviour between samples of vesignieite in the literature. The revised orbital structure is similar to that found in volborthite, rather than the quantum spin liquid herbertsmithite, and provides a convincing argument for the differing magnetic properties found in these frustrated magnets.

cond-mat.mtrl-sci

Haydeeite: a spin-1/2 kagome ferromagnet

The mineral haydeeite, alpha-MgCu3(OD)6Cl2, is a S=1/2 kagome ferromagnet that displays long-range magnetic order below TC=4.2 K with a strongly reduced moment. Our inelastic neutron scattering data show clear spin-wave excitations that are well described by a Heisenberg Hamiltonian with ferromagnetic nearest-neighbor exchange J1=-38 K and antiferromagnetic exchange Jd=+11 K across the hexagons of the kagome lattice. These values place haydeeite very close to the quantum phase transition between ferromagnetic order and non-coplanar twelve-sublattice cuboc2 antiferromagnetic order. Diffuse dynamic short-range ferromagnetic correlations observed above TC persist well into the ferromagnetically ordered phase with a behavior distinct from critical scattering.

cond-mat.str-el

Dzyaloshinsky-Moriya interaction in vesignieite: A route to freezing in a quantum kagome antiferromagnet

We report an electron spin resonance investigation of the geometrically frustrated spin-1/2 kagome antiferromagnet vesignieite, BaCu$_3$V$_2$O$_8$(OH)$_2$. Analysis of the line widths and line shifts indicates the dominance of in-plane Dzyaloshinsky-Moriya anisotropy that is proposed to suppress strongly quantum spin fluctuations and thus to promote long-range ordering rather than a spin-liquid state. We also evidence an enhanced spin-phonon contribution that might originate from a lattice instability and discuss the origin of a low-temperature mismatch between intrinsic and bulk susceptibility in terms of local inhomogeneity.

cond-mat.str-el

Ground State and Intrinsic Susceptibility of the Kagome Antiferromagnet Vesignieite as seen by 51V NMR

The intrinsic magnetic susceptibility and local magnetization of the near-kagome quantum magnet vesignieite, Cu3BaV2O8(OH)2, are presented as measured using 51V NMR. The NMR line shift gives an accurate measurement of the intrinsic susceptibility of the kagome sites which closely resembles that of the quantum spin liquid herbertsmithite [A. Olariu et al. Phys. Rev. Lett. 100, 087202 (2008)]. It is therefore surprising that, at Tc ~ 9 K, a transition to a heterogeneous ground state is observed. A gradual wipeout of half the NMR intensity indicates a slowly fluctuating spin liquid component and a detailed analysis of the linewidth reveals the onset of static magnetism at the remaining half of the sites. It is proposed that this transition and unusual ground state originate from a nearby quantum critical point induced by the Dzyaloshinskii-Moriya interaction.

cond-mat.str-el