Dc Magnetometry Research Articles

Charge-Ordering and Magnetic Transitions in Nanocrystalline Half-Doped Rare Earth Manganite Ho0.5Ca0.5MnO3

This work investigates nanostructured Ho0.5Ca0.5MnO3, considered a model system of the Ln0.5Ca0.5MnO3 series of manganites with perovskite structures featuring small lanthanide (Ln) ions half-substituted by Ca ions. Here, we propose a modified hybrid sol–gel–solid-state approach to produce multiple samples with a single batch, obtaining very high crystalline quality and ensuring the same chemical composition, with an average particle size in the range 39–135 nm modulated on-demand by a controlled calcination process. Our findings evidence that, provided the crystalline structure is preserved, the charge-ordering transition can be observed even at the nanoscale. Additionally, this research explores the presence of glassy phenomena, which are commonly seen in this class of materials, to enhance our understanding beyond simplistic qualitative observations. Comprehensive characterization using DC and AC magnetometry, along with relaxation and aging measurements, reveals that the complex dynamics typical of glassy phenomena emerge only at the nanoscale and are not visible in the bulk counterpart. Nevertheless, the analysis confirms that even the sample with the smallest nanoparticles cannot be intrinsically classified as canonical spin glass.

NiFe‐NO3 Layered Double Hydroxide as a Novel Anode for Sodium Ion Batteries

2D materials are emerging materials for energy storage and among these layered double hydroxides (LDHs) seem particularly promising due to their structure, easily adjustable composition, and cheapness. This study marks the first reported application of an LDH, specifically NiFe‐NO3, as anode material in a sodium half‐cell, to the best of our knowledge. Despite an initial loss in capacity, the material demonstrates notable stability, retains a high specific capacity even after 50 discharge/charge cycles (~ 500 mAh/g). The intricate reaction mechanism was explored using various ex‐situ techniques such as DC magnetometry and FTIR, as well as in‐operando X‐ray Absorption Spectroscopy (XAS). The proposed Na‐storage mechanism in NiFe‐NO3 involves an initial irreversible "activation" during the first sodiation, characterized by a phase change reaction that leads to the formation of NiOx and Fe3O4, followed by a reversible mechanism involving both intercalation and conversion in subsequent cycles.

Sensitive ac and dc magnetometry with nitrogen-vacancy-center ensembles in diamond

Sensitive ac and dc magnetometry with nitrogen-vacancy-center ensembles in diamond

Reducing inhomogeneous broadening of spin and optical transitions of nitrogen-vacancy centers in high-pressure, high-temperature diamond

With their optical addressability of individual spins and long coherence time, nitrogen-vacancy (NV) centers in diamond are often called “atom-like solid spin-defects”. As observed with trapped atomic ions, quantum interference mediated by indistinguishable photons was demonstrated between remote NV centers. In high sensitivity DC magnetometry at room temperature, NV ensembles are potentially rivaling with alkali-atom vapor cells. However, local strain induces center-to-center variation of both optical and spin transitions of NV centers. Therefore, advanced engineering of diamond growth toward crystalline perfection is demanded. Here, we report on the synthesis of high-quality HPHT (high-pressure, high-temperature) crystals, demonstrating a small inhomogeneous broadening of the spin transitions, of T2* = 1.28 μs, approaching the limit for crystals with natural 13C abundance, that we determine as T2* = 1.48 μs. The contribution from strain and local charges to the inhomogeneous broadening is lowered to ~17 kHz full width at half maximum for NV ensemble within a > 10 mm3 volume. Looking at optical transitions in low nitrogen crystals, we examine the variation of zero-phonon-line optical transition frequencies at low temperatures, showing a strain contribution below 2 GHz for a large fraction of single NV centers.

Mitigating errors in dc magnetometry via zero-noise extrapolation

Mitigating errors in dc magnetometry via zero-noise extrapolation

Investigation of Gamma-Induced Changes to Screening Currents and AC Losses in Mono- Versus Multi-filamentary REBCO Coated Conductors Using DC and AC Magnetometry

REBCO (rare-earth barium copper oxide) coated conductor tapes are a highly attractive option for magnet materials in future tokamak fusion power plants. However, the threat of intense neutron and gamma radiation, together with AC losses during magnet coil ramping, has raised concerns around magnet coil lifetimes. Irradiation-induced changes to flux creep rate has been identified as a key performance-limiting factor in REBCO tapes at low temperatures and high fields post-irradiation with gamma rays; spontaneous flux creep contributes to hysteretic AC loss in REBCO cables under applied AC fields. Knowing that multi-filamentary tapes are under consideration for tokamaks as an AC loss mitigation, magnetic measurements and gamma irradiation experiments are presented here on striated and mono-filamentary YBCO tapes to investigate the differences in post-irradiation screening currents and AC losses. Reduction in AC losses improved magnetisation critical current density (Jc) retention after 1 MGy in the multi- relative to the mono-filamentary samples. After the 5 MGy dose, striations then made the multi-filamentary tape more susceptible to Jc degradation because of the thinner individual filament width. Scanning transmission electron microscopy analysis on an analogous GdYBCO mono-filamentary tape did not indicate the introduction of nm-scale amorphisation to the active GdYBCO layer after gamma irradiation. A potential theoretical explanation for the underlying mechanism altering the flux-pinning landscape across the REBCO layer surface in gamma-irradiated tapes is discussed. This work concluded that gamma effects on screening current capability should be considered in future tokamak REBCO tape qualification studies.

Quantum vector DC magnetometry via selective phase accumulation

Quantum vector DC magnetometry via selective phase accumulation

Spin canting and slow magnetic relaxation in mononuclear cobalt(II) sulfadiazine ternary complexes.

Monomeric [Co(SDZ)2phen] (1) and [Co(SDZ)(bq)Cl] (2) complexes (SDZ = sulfadiazine, phen = 1,10-phenanthroline, and bq = 2,2'-biquinoline) have been synthesized and characterized. X-ray diffraction studies indicate that SDZ acts as a bidentate ligand coordinating through the sulfonamide and the pyrimidine N atoms in both compounds. In complex 1, the coordination sphere consists of two SDZ ligands and a bis-chelating phen ligand, giving rise to a CoN6 coordination sphere. On the other hand, 2 has a CoN4Cl core, with two N-atoms from SDZ and two from the bq ligand. Both compounds have been studied by dc and ac magnetometry and shown to display slow magnetic relaxation under an optimum external dc field (1 kOe) at low temperatures. Moreover, compound 2 displays long range magnetic ordering provided by spin-canted antiferromagnetism, which has been characterized by further field-dependent magnetic susceptibility measurements, FC/ZFC curves, hysteresis loops and frequency-independent ac curves. The signs of the calculated D parameters, positive in 1 and negative in 2, have been rationalized according to the two lowest-lying transitions in the orbital energy diagrams derived from ab initio ligand field theory (AILFT). In a subsequent attempt to reveal the possible hidden zero-field SMM behaviour, Ni(II)-based 3 and Co(II)-doped Ni(II)-based (with a Ni : Co ratio of 0.9 : 0.1) heterometallic compound 2Ni were synthesized.

Probing Evolution of the Flux-Pinning Landscape in REBCO Coated Conductors Caused by Gamma Irradiation Using DC and AC Magnetometry: A Novel Approach to Tokamak Magnet Material Development

Optimisation of REBCO coated conductor tapes specifically for use in nuclear fusion will help improve the magnet component lifetimes in future tokamak reactor power plants. The focus of this work was exploration of a novel approach to irradiation studies on REBCO tapes, utilising multiple magnetic measurements to probe evolution of the REBCO flux-pinning landscape more deeply than reported in other studies, for the purpose of identifying primary limiting factors affecting performance. Gamma irradiation experiments were conducted, and pre-/post-irradiation results from DC and AC magnetic measurements using a Physical Property Measurement System (PPMS) are discussed. Magnetisation critical current density (Jc) decreased in all samples with increasing dose, except for the silver overlayer-only samples which did not contain artificial pinning centres (APCs), where Jc increased with dose. Removal of the copper stabiliser coupled with the presence of APCs allowed gamma irradiation to induce pinning force maximum peak shifts, from above 14 T before irradiation to below 9 T afterwards. Flux creep rate varied with the evolving pinning landscape, and the degree of Jc degradation directly correlated with creep rate fluctuations post-irradiation. Changes in critical temperature and diamagnetic saturation also corresponded with changes in Jc and flux creep rate. The major conclusion from this study was that minimisation of flux creep rate is the key to maintenance of performance under fusion-relevant operating conditions. Flux creep manifests as problematic AC losses in all high-temperature superconducting machines; therefore, future work will focus on reduction/prevention of the phenomenon to enhance longevity of performance in any application.

Comparing continuous and pulsed nitrogen-vacancy DC magnetometry in the optical-power-limited regime

Ensembles of nitrogen-vacancy (NV) center spins in diamond offer a robust, precise, and accurate magnetic sensor. As their applications move beyond the laboratory, practical considerations including size, complexity, and power consumption become important. Here, we compare two commonly employed NV magnetometry techniques—continuous-wave (CW) versus pulsed magnetic resonance—in a scenario limited by the total available optical power. We develop a consistent theoretical model for the magnetic sensitivity of each protocol that incorporates NV photophysics—in particular, including the incomplete spin polarization associated with limited optical power; after comparing the models’ behavior to experiments, we use them to predict the relative DC sensitivity of CW versus pulsed operation for an optical-power-limited, shot-noise-limited NV ensemble magnetometer. We find a ∼2−3× gain in sensitivity for pulsed operation, which is significantly smaller than seen in power-unlimited, single-NV experiments [Phys. Rev. B 84, 195204 (2011)PRBMDO0163-182910.1103/PhysRevB.84.195204]. Our results provide a resource for practical sensor development, informing protocol choice and identifying optimal operation regimes when optical power is constrained.

Variance properties of the microwave absorption spectrum of an ensemble of nitrogen vacancy centers in diamond

This work presents an original method based on the variance properties of the microwave absorption spectrum of an ensemble of nitrogen vacancy centers in diamond. The spectrum is measured optically. A compact and simple device is designed to optimize the photon collection. We conduct a quantitative comparison of the ensemble's optical signal in both the visible and near infrared range. Using the enhanced signal-to-noise ratio achieved through the device geometry we perform real-time DC magnetometry at moderate light and microwave powers. Under these conditions, the amplitude of a DC magnetic field can be extracted from the variance of the microwave absorption spectrum in a fast and reproducible manner, without the burden of complex fitting techniques.

Synthesis and Structural and Magnetic Properties of Polycrystalline GaMo4Se8

GaMo4Se8, is a lacunar spinel where skyrmions have been recently reported. This compound belongs to the GaM4X8 family, where M is a transition metal (V or Mo) and X is a chalcogenide (S or Se). In this work, we have obtained pure GaMo4Se8 in polycrystalline form through an innovative two-step synthetic route. Phase purity and chemical composition were confirmed through the Rietveld refinement of the powder XRD pattern, the sample characterisation having been complemented with SEM analysis. The magnetic phase diagram was investigated using DC (VSM) and AC magnetometry, which disclosed the presence of cycloidal, skyrmionic and ferromagnetic phases in polycrystalline GaMo4Se8.

Hard-Soft Core-Shell Architecture Formation from Cubic Cobalt Ferrite Nanoparticles.

Cubic bi-magnetic hard-soft core-shell nanoarchitectures were prepared starting from cobalt ferrite nanoparticles, prevalently with cubic shape, as seeds to grow a manganese ferrite shell. The combined use of direct (nanoscale chemical mapping via STEM-EDX) and indirect (DC magnetometry) tools was adopted to verify the formation of the heterostructures at the nanoscale and bulk level, respectively. The results showed the obtainment of core-shell NPs (CoFe2O4@MnFe2O4) with a thin shell (heterogenous nucleation). In addition, manganese ferrite was found to homogeneously nucleate to form a secondary nanoparticle population (homogenous nucleation). This study shed light on the competitive formation mechanism of homogenous and heterogenous nucleation, suggesting the existence of a critical size, beyond which, phase separation occurs and seeds are no longer available in the reaction medium for heterogenous nucleation. These findings may allow one to tailor the synthesis process in order to achieve better control of the materials' features affecting the magnetic behaviour, and consequently, the performances as heat mediators or components for data storage devices.

Transition from AFM Spin Canting to Spin Glass-AFM Exchange as Particle Size Decreases in LaFeO3.

In this work, we have studied structural and magnetic properties of LaFeO3 as a function of the particle size d, from bulk (d >> 1 µm) to nanoscale (d ≈ 30 nm). A large number of twins were observed for large particles that disappear for small particle sizes. This could be related to the softening of the FeO6 distortion as particle size decreases. It was observed that the bulk sample showed spin canting that disappeared for d ~ 125 nm and can be associated with the smoothening of the orthorhombic distortion. On the other hand, for d < 60 nm, the surface/volume ratio became high and, despite the high crystallinity of the nanoparticle, a notable exchange effect bias appeared, originated by two magnetic interactions: spin glass and antiferromagnetism. This exchange bias interaction was originated by the formation of a "magnetic core-shell": the broken bonds at the surface atoms give place to a spin glass behavior, whereas the inner atoms maintain the antiferromagnetic G-type order. The LaFeO3 bulk material was synthesized by the ceramic method, whereas the LaFeO3 nanoparticles were synthesized by the sol-gel method; the particle size was varied by annealing the samples at different temperatures. The physical properties of the materials have been investigated by XRD, HRTEM, TGA, and AC and DC magnetometry.

VdW Mediated Strong Magnetic Exchange Interactions in Chains of Hydrogen-Free Sublimable Molecular Qubits.

Sulfur-rich molecular complexes of dithiolene-like ligands are appealing candidates as molecular spin qubits because spin coherence properties are enhanced in hydrogen-free environments. Herein, we employ the hydrogen-free mononegative 1,3,2-dithiazole-4-thione-5-thiolate (dttt-) ligand as an alternative to common dinegative dithiolate ligands. We report the first synthesis and structural characterization of its Cu2+, Ni2+, and Pt2+ neutral complexes. The XPS analysis of thermal deposition of [Cu(dttt)2] in UHV conditions indicates that films of intact molecules can be deposited on surfaces by sublimation. Thanks to a combined approach employing DC magnetometry and DFT calculations, we highlighted AF exchange interactions of 108 cm-1 and 36 cm-1 attributed to the two different polymorph phases. These couplings are exclusively mediated by S···S VdW interactions, which are facilitated by the absence of counterions and made particularly efficient by the diffuse electron density on S atoms. Furthermore, the spin dynamics of solid-state magnetically diluted samples was investigated. The longest observed T m is 2.3 μs at 30 K, which significantly diverges from the predicted T m > 100 μs. These results point to the diluting matrix severely affecting the coherence lifetime of Cu2+ species via different factors, such as the contributions of neighboring 14N nuclei and the formation of radical impurities in a non-completely controllable way. However, the ease of processing [Cu(dttt)2] via thermal sublimation can allow dispersion in matrices better suited for coherent spin manipulation of isolated molecules and the realization of AF-coupled VdW structures on surfaces.

Application of Magnetic Adaptive Testing for Nondestructive Investigation of 2507 Duplex Stainless Steel

Duplex stainless steels are two-phase alloys, which contain ferritic and austenitic phases in their microstructure. Their duplex structure provides exceptional resistance to pitting and chloride stress corrosion cracking, and their strength is about twice that of austenitic stainless steels. Due to their good properties, they are widely used in chemical and petrochemical industries as a base material in pressure vessels, pipelines and containers. Duplex stainless steel samples were nondestructively investigated by measuring sets of magnetic minor hysteresis loops using the method called magnetic adaptive testing (MAT). Several series of heat-treated and cold-rolled 2507 duplex stainless steels were measured, and the magnetic parameters were compared with the results of the DC magnetometry of the samples. It was found that the changes in the material properties that were generated by heat treatment and mechanical deformation could easily be followed by magnetic measurements. In contrast to DC magnetic measurements, good correlation was found with the magnetic parameters determined by MAT method and Vickers hardness. Based on our experiments, MAT seems to be a powerful tool for the nondestructive characterization of duplex stainless steels.

Spectroscopic and Magnetic Studies of Co(II) Scorpionate Complexes: Is There a Halide Effect on Magnetic Anisotropy?

The observation of single-molecule magnetism in transition-metal complexes relies on the phenomenon of zero-field splitting (ZFS), which arises from the interplay of spin-orbit coupling (SOC) with ligand-field-induced symmetry lowering. Previous studies have demonstrated that the magnitude of ZFS in complexes with 3d metal ions is sometimes enhanced through coordination with heavy halide ligands (Br and I) that possess large free-atom SOC constants. In this study, we systematically probe this "heavy-atom effect" in high-spin cobalt(II)-halide complexes supported by substituted hydrotris(pyrazol-1-yl)borate ligands (TptBu,Me and TpPh,Me). Two series of complexes were prepared: [CoIIX(TptBu,Me)] (1-X; X = F, Cl, Br, and I) and [CoIIX(TpPh,Me)(HpzPh,Me)] (2-X; X = Cl, Br, and I), where HpzPh,Me is a monodentate pyrazole ligand. Examination with dc magnetometry, high-frequency and -field electron paramagnetic resonance, and far-infrared magnetic spectroscopy yielded axial (D) and rhombic (E) ZFS parameters for each complex. With the exception of 1-F, complexes in the four-coordinate 1-X series exhibit positive D-values between 10 and 13 cm-1, with no dependence on halide size. The five-coordinate 2-X series exhibit large and negative D-values between -60 and -90 cm-1. Interpretation of the magnetic parameters with the aid of ligand-field theory and ab initio calculations elucidated the roles of molecular geometry, ligand-field effects, and metal-ligand covalency in controlling the magnitude of ZFS in cobalt-halide complexes.

Static and Dynamic Magnetic Properties of a Co(II)‐Complex with N2O2Donor Set – A Theoretical and Experimental Study

AbstractA representative Co(II) based single ion magnet (SIM) with N2O2donor set and distorted pseudo‐tetrahedral geometry has been synthesized and characterized to study the atomic and electronic structure. DC magnetometry results have been evaluated by means of a phenomenological Hamiltonian approach regarding zero field splitting (ZFS) parameters and compared with results from ab‐initio multi‐reference CASSCF (complete active space self‐consistent field) calculations and qualitative ligand field theory (AILFT). Profound investigation of spin‐lattice relaxation with the variation of temperature (from 1.8 to about 8 K) and magnetic field (at 14 different fields from zero up to 1 T) have been performed based on AC magnetometry. Under an applied dc magnetic field, spin‐lattice relaxation occurs via a direct process withT2temperature dependence due to limited heat transfer at very low temperature and above 5 K relaxation by an Orbach process with an energy barrier of≈80 K dominates.

Magnetic phase diagram and possible Kitaev-like behavior of the honeycomb-lattice antimonate Na3Co2SbO6

Recent theoretical studies have suggested that Kitaev physics and such effects as formation of a mysterious spin-liquid state can be expected not only in RuCl3 and iridates, but also in conventional $3d$ transition metal compounds. Using DC and AC magnetometry, thermodynamic and $^{23}$Na nuclear magnetic resonance measurements (NMR) we studied such a candidate material Na3Co2SbO6. A full phase diagram of Na3Co2SbO6 in a wide range of magnetic fields and temperatures is presented. The results demonstrate transformation of the antiferromagnetic structure under the external magnetic field, gradual development of the saturation phase, as well as evidence of gapped behavior in certain parts of the phase diagram

Tetracoordinate Co(II) complexes with semi-coordination as stable single-ion magnets for deposition on graphene.

We present a theoretical and experimental study of two tetracoordinate Co(II)-based complexes with semi-coordination interactions, i.e., non-covalent interactions involving the central atom. We argue that such interactions enhance the thermal and structural stability of the compounds, making them appropriate for deposition on substrates, as demonstrated by their successful deposition on graphene. DC magnetometry and high-frequency electron spin resonance (HF-ESR) experiments revealed an axial magnetic anisotropy and weak intermolecular antiferromagnetic coupling in both compounds, supported by theoretical predictions from complete active space self-consistent field calculations complemented by N-electron valence state second-order perturbation theory (CASSCF-NEVPT2), and broken-symmetry density functional theory (BS-DFT). AC magnetometry demonstrated that the compounds are field-induced single-ion magnets (SIMs) at applied static magnetic fields, with slow relaxation of magnetization governed by a combination of quantum tunneling, Orbach, and direct relaxation mechanisms. The structural stability under ambient conditions and after deposition was confirmed by X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy. Theoretical modeling by DFT of different configurations of these systems on graphene revealed n-type doping of graphene originating from electron transfer from the deposited molecules, confirmed by electrical transport measurements and Raman spectroscopy.