Spin Polarization Research Articles

Tunneling Barrier Thickness Dependence of Spin Polarization of Ferromagnet in Magnetic Tunnel Junctions

Abstract For designing low-impedance magnetic tunnel junctions (MTJs), it has been found that tunneling magnetoresistance strongly correlates with the insulating barrier thickness, imposing a fundamental problem about the relationship between spin polarization of ferromagnet and the insulating barrier thickness in MTJs. Here, we investigate the influence of alumina barrier thickness on tunneling spin polarization (TSP) through a combination of theoretical calculations and experimental verification. Our simulating results reveal a significant impact of barrier thickness on TSP, exhibiting an oscillating decay of TSP with the barrier layer thinning. Experimental verification is realized on FeNi/AlO x /Al superconducting tunnel junctions to directly probe the spin polarization of FeNi ferromagnet using Zeeman-split tunneling spectroscopy technique. These findings provide valuable insights for designs of high-performance spintronic devices, particularly in applications such as magnetic random access memories, where precise control over the insulating barrier layer is crucial.

Flexible focal array engineering with a binary array vector optical field

In recent years, the vector optical field (VOF) with space-variant polarization distribution has attracted great attention due to its unexpected effects and applications in a wide range of areas. The focal engineering plays the most important role, as the focused VOF provides various interesting properties. Here, we propose a kind of binary array VOF (BA-VOF), which can be applied in focal array engineering. The BA-VOF comprises an array of the first base field of radially polarized VOF and an array of the second base field of superposed subfields with phase modulations. We theoretically design and experimentally generate the BA-VOF. Based on the BA-VOF, we present a flexible method to manipulate the amount of the focal spots in the focal array. Moreover, the polarization state and spin angular momentum of each focal spot in the focal spot array can also be flexibly manipulated. The BA-VOF and the flexibly manipulated focal array are inspirable in the area of structured light, which can be applied in regions needing focal engineering, such as optical tweezers, optical fabrication, optical imaging, and so on.

An unusual triplet population pathway in the Reaction Centre of the Chlorophyll-d binding Photosystem I of A. marina, as revealed by a combination of TR-EPR and ODMR spectroscopies

Photo-induced Chlorophyll (Chl) triplet states in the isolated Photosystem I (PSI) of Acaryochloris marina, that harbours Chl d as its main pigment, were investigated by Optically Detected Magnetic Resonance (ODMR) and Time-Resolved Electron Paramagnetic Resonance (TR-EPR), and as a function of pre-illumination of the sample under reducing redox poising. Fluorescence Detected Magnetic Resonance (FDMR) allowed resolving four Chl d triplet (3Chl d) populations (T1-T4) both in untreated and illuminated samples in the presence of ascorbate and N,N,N′,N′-tetramethyl-p-phenylenediamine (TMPD). The FDMR signals increased following the pre-illumination treatment, particularly for the T3 and T4 populations, which are therefore sensitive to the redox state of PSI cofactors. Microwave-induced Triplet minus Singlet (TmS) spectra were detected in the |D|-|E| resonance window of the T3 and T4 triplets. These showed a broad singlet bleaching centred at 740 nm and also displayed complex spectral structure with several derivative-like features, indicating that both the T3 and T43Chl d populations are associated with the PSI reaction centre (RC) triplet, P3740. Parallel measurements by TR-EPR demonstrated that triplet signals observed under all conditions investigated are dominated by an electron spin polarisation (esp), which is typical of intersystem crossing, differently from what expected for recombination triplet states formed from a radical pair precursor. Moreover, stronger reductant conditions obtained by pre-illumination of the samples in the presence of dithionite and 5-methylphenazinium methyl sulfate (PMS) did not lead to a recombination triplet state esp, but rather to a decrease of the whole signal intensity. The energetics of A. marina PSI and the possible occurrence of distributions of cofactors redox properties are discussed in order to address the unexpected P3740 esp.

Single and double quantum transitions in spin-mixed states under photo-excitation

Electronic spins associated with the Nitrogen-Vacancy (NV) center in diamond offer an opportunity to study spin-related phenomena with extremely high sensitivity owing to their high degree of optical polarization. Here, we study both single- and double-quantum transitions (SQT and DQT) in NV centers between spin-mixed states, which arise from magnetic fields that are non-collinear to the NV axis. We demonstrate the amplification of the ESR signal from both these types of transition under laser illumination. We obtain hyperfine-resolved X-band ESR signal as a function of both excitation laser power and misalignment of static magnetic field with the NV axis. This, combined with our analysis using a seven-level model that incorporates thermal polarization and double quantum relaxation, allows us to comprehensively analyze the polarization of NV spins under off-axis fields. Such detailed understanding of spin-mixed states in NV centers under photo-excitation can help greatly in realizing NV-diamond platform’s potential in sensing correlated magnets and biological samples, as well as other emerging applications, such as masing and nuclear hyperpolarization.

Designing Electronic Structures of Multiscale Helical Converters for Tailored Ultrabroad Electromagnetic Absorption

HighlightsThe energy conversion mechanism is thoroughly analyzed, with a detailed quantitative characterization of the dissipation capacities of polarization, conduction, and magnetic loss.Inspired by DNA transcription, atom and geometry configurations co-modulating multi-scale helical converters achieve the RLmin of −63.13 dB at 1.29 mm, and the maximum RCS reduction value reach 36.4 dB m2.Orbital coupling, spin and cross polarization synergize to realize a 6.08 GHz EAB, further expanding to ultrabroad electromagnetic wave absorption of 12.16 GHz through metamaterial design.

Analysis of the electronic nature and transport properties of Co2CrGe, Co2FeGe, and Co2NiGa by computational electronic structure calculations

AbstractElectronic and thermoelectric properties of the full‐Heusler materials Co2CrGe, Co2FeGe, and Co2NiGa are studied, using first‐principles full potential linearized augmented plane waves method. To treat the exchange correlation, Generalized Gradient Approximation parameterized by PBE‐sol with the inclusion of spin polarization is used. The frequency fluctuation order is continual at 300 K after heating to 3 ps with very small distraction in the atomic structure conforming the structure stability of the studied structures. Also inclusion of spin‐orbit coupling effect on density of states undermines significant change in peaks specially d‐states in the materials and caused a degeneracy. Band structure analysis clarified that states crossing the Fermi level have the importance for enhancing the thermoelectric properties of the materials. The topology of the states indicates a gap at the bulk level, which is the unique character of the heavy elements in the materials Co2CrGe, Co2FeGe, and Co2NiGa. Thermoelectric properties are calculated for a temperature of 300 K using semi‐classical Boltzmann's theory implemented in BoltzTraP code. In these calculations, it is found that these materials favor electron doping with having maximum values of ZT in the n‐type region.

An Ultrasensitive Molecular Detector for Direct Sensing of Spin Currents at Room Temperature.

The experimental analysis of pure spin currents at interfaces is one major goal in the field of magnonics and spintronics. Complementary to the established Spin-Hall effect using the spin-to-charge conversion in heavy metals for information processing, we present a novel approach based on spin pumping detection by an interfacial, resonantly excited molecular paramagnet adsorbed to the surface of the spin current generating magnet. Here, we show that the sensitivity of this electron paramagnetic resonance (EPR) detector can be enhanced by orders of magnitude through intramolecular transfer of spin polarization at room temperature. Our proof-of-principle sample consists of octahedral-shaped ferrimagnetic Fe3O4 nanoparticles covered by oleic acid (OA) which has two paramagnetic centers, S1 and S2. S1 arises from the chemisorption of OA and is located directly at the interface to Fe3O4. S2 originates from radical formation at the center of the molecule close to the double bond of oleic acid and is not influenced by chemisorption. Using ferromagnetic resonance (FMR) excitation of the Fe3O4 nanoparticles to pump spins into S1, a population inversion of the spin-split levels of S2 is formed, vastly enhancing the detection sensitivity on the atomic scale.

Quantifying spin-torque efficiency and magnetoresistance coefficient by microwave photoresistance in spin-torque ferromagnetic resonance

During the spin-torque ferromagnetic resonance (ST-FMR) measurement, the magnetization precession driven by the microwave field yields the radio frequency (rf) oscillating magnetoresistance and its time-averaged change (photoresistance). Here, we find that the strength of photoresistance can be directly determined by using dc bias current Idc modulating the symmetric component VS of the ST-FMR voltage spectrum. By measuring the angular dependence of photoresistance, we can quantify the in-plane and out-of-plane precession angles of ST-FMR, the actual rf current distribution in the magnetic and non-magnetic sublayers, and the magnitude of spin-torque and various magnetoresistance coefficients. These experimentally obtained values and analysis methods can more accurately quantify the spin-torque efficiency of both in-plane and out-of-plane spin polarizations by self-consistent calculation of the precession angle without harsh assumptions. And, we further confirm this universal method in three spintronic systems: the prototypical Pt/Py bilayer with anisotropic magnetoresistance (AMR), Py/Cu/Co20Tb80 spin valve trilayer with AMR and giant magnetoresistance, and [Co/Ni]3/Co/Pt multilayer with AMR and anisotropic interface magnetoresistance. This method eliminates potential deviation in calculating spin-torque efficiency by previously reported line shape analyzation and linewidth modulation methods of the ST-FMR technique and significantly extends its application range in characterizing spintronic materials and nanodevices.

Efficiency improvement of spin-resolved ARPES experiments using Gaussian process regression

The experimental efficiency has been a central concern for time-consuming experiments. Spin- and angle-resolved photoemission spectroscopy (spin-resolved ARPES) is renowned for its inefficiency in spin-detection, despite its outstanding capability to directly determine the spin-polarized electronic properties of materials. Here, we investigate the potential enhancement of the efficiency of spin-resolved ARPES experiments through the integration of measurement informatics. We focus on a representative topological insulator Bi2\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\ ext {Bi}_{2}$$\\end{document}Te3\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\ ext {Te}_{3}$$\\end{document}, which has well-understood spin-polarized electronic states. We employ Gaussian process regression (GPR) to assess the accumulation of spin polarization information using an indicator known as the GPR score. Our analyses based on the GPR model suggest that the GPR score can serve as a stopping criterion for spin-resolved ARPES experiments. This criterion enables us to conduct efficient spin-resolved ARPES experiments, significantly reducing the time costs by 5-10 times, compared to empirical stopping criteria.

Many-Body Models for Chirality-Induced Spin Selectivity in Electron Transfer.

We present the first microscopic model for the chirality-induced spin selectivity effect in electron-transfer, in which the internal degrees of freedom of the chiral bridge are explicitly included. By exactly solving this model on short chiral chains we demonstrate that a sizable spin polarization on the acceptor arises from the interplay of coherent and incoherent dynamics, with strong electron-electron correlations yielding many-body states on the bridge as crucial ingredients. Moreover, we include the coherent and incoherent dynamics induced by interactions with vibrational modes and show that they can play an important role in determining the long-time polarized state probed in experiments.

Chiral spin selectivity and chiroptical activity in helical molecules.

Chiral structures, breaking spatial inversion symmetry, exhibit non-zero chiroptical activity (COA) due to the coupling between their electric and magnetic responses under external electromagnetic fields, an effect absent in achiral systems. Non-magnetic chiral structures also exhibit Chiral-Induced Spin Selectivity (CISS), primarily detected in two terminal measurements in the linear regime, where spin selection emerges without external magnetic influence. Despite the different origins of these physical phenomena, our model captures the relevant physics required to address CISS as an intrinsic molecular effect with the basic ingredients: (i) chirality/inversion asymmetry, (ii) meV atomic spin-orbit coupling, and (iii) decoherence as a source of reciprocity breaking. In this work, we derived how the electronic system couples with polarized electromagnetic radiation to yield a spin-dependent polarization rotation power, quantified through the Rosenfeld tensor, predicting characteristic spin signatures in the COA. The model also predicts that a net spin polarization manifests in the molecular terminations that have been surmised as an explanation for chiral species separation of racemic mixtures and interactions with surface magnetic domains. A recent sensitive spectroscopic measurement of electron transfer in donor-acceptor complexes is consistent with the standalone CISS effect.

Exploring spin polarization of heavy quarks in magnetic fields and hot medium

Exploring spin polarization of heavy quarks in magnetic fields and hot medium

Spin/valley dependent dwell time in an 8-Pmmn borophene junction

Spin/valley dependent dwell time in 8-Pmmn borophene junction under Rashba spin–orbit interaction (RSOI) is studied. The dwell time as well as transmission probability for incident electrons with spin-up show a different behavior than the incident electrons with spin-down, and these quantities can be controlled effectively by the junction direction, incident angle, the RSOI strength and the barrier width. Also, the dwell time is dependent on the degree of freedom of the valley and shows oscillating behavior with the increase of the barrier width. The spin polarization and spin filtering in 8-Pmmn borophene junction under RSOI can be obtained in the time domain.

A DFT theoretical prediction of new half-metallic ferromagnetism, mechanical stability, optoelectronic and thermoelectric properties of ZnCrO3 perovskites for spintronic applications

ZnCrO3 perovskites structural stability, optoelectronic, mechanical, along with thermoelectric properties, have all been to be described by calculations based on density functional theory (DFT). To determine the exchange correlation potential, the well-known generalized gradient approximation (GGA) and integration of the mBJ potential were used. The perovskite shows that this is in a cubic structure with Fm3m symmetry. Additionally, to check the stability, cohesive energy, structural optimization, and mechanical stability were requirements. This perovskite was found to be brittle, and their mechanical stability enhanced by the elastic constants. The perovskite has a half-metallic character, as evidenced by the spin-polarized electronic band profile, the behavior of the dielectric constant, and absorption coefficient in the spin-up and down channels. In this article, we also looked at magnetism and the origin of the half-metallic gap. The unpaired electrons in the split d-orbitals of the M-sited elements in the crystal field are responsible for the half-metallic as well as magnetic characteristics. Excellent spin polarization at the Fermi level encourages perovskite's possible use in spintronic technologies. Lastly, we computed the thermoelectric parameters within a chemical potential at various temperatures (300 K, 600, 900 K) to explore the potential application in spin electronic devices. Our finding shows that the ZnCrO3 alloy is exceptionally promising for the next generation of spintronics and thermoelectric devices at room and high temperatures.

Alkali-based half metals as sustainable materials for spin electronics and energy harvesting application — Materials computation

The structural, mechanical, electronic, magnetic, and thermoelectric properties of alkali-based half-Heusler alloys (LiCrGe, LiCrSn, and LiCrPb) are investigated using the Wien2k code. These alloys exhibit half-metallic behavior in both ferromagnetic and antiferromagnetic phases. A phase transition from a stable ferromagnetic phase to a more stable antiferromagnetic phase indicates ductility. In the antiferromagnetic phase, using GGA exchange–correlation functional with 10,000 K-points, a band gap is observed in the spin-up state, with band gap energies of 0.9367 eV, 0.7762 eV, and 0.7913 eV, respectively. The alloys have a spin magnetic moment of −3μB, consistent with the Slater–Pauling rule. They also exhibit high Curie temperatures and 100% spin polarization in the spin-down state. The alloys LiCrZ (Z = Ge, Sn, Pb) shows promising thermoelectric behavior. Using the BolzTrap package, we observed, high Seebeck coefficient, electrical conductivity, low thermal conductivity, and enhanced power factor. The p-type LiCrZ (Z = Ge, Sn, Pb) compounds show thermoelectric figure of merit of 0.52, 0.76, and 0.84 at 1200 K, while n-type compounds have figure of merit of 0.56, 0.65, and 0.80 at the same temperature. These properties make these materials promising for spintronic and thermoelectric applications.

Influence of Pumping Laser Intensity Uniformity on Hybrid Optically Pumped Comagnetometer in the SERF Regime

AbstractThe effect of pumping laser intensity uniformity (PLIU) on the operation of a hybrid optically pumped comagnetometer operating in the spin‐exchange relaxation‐free regime (SERF) regime is investigated in this paper. First, an analytical steady‐state output model for the comagnetometer with two alkali‐metal atoms and one noble‐gas atom is presented. By varying the diameter of the pumping laser beam to control the PLIU, 3D distribution models of the electron spin and nuclear spin polarization under different PLIU conditions are obtained. In the experiment, the effects of PLIU on multi‐parameter, low‐frequency magnetic‐noise suppression capability, and long‐term stability of the SERF comagnetometer are studied. The results indicate that within a certain range, increasing the diameter of the pumping laser beam improves the polarization uniformity of the atomic ensemble and reduces the light shift of the comagnetometer. As a result, both the low‐frequency magnetic noise suppression capability and the long‐term stability of the system increase. However, further reduction of the pumping laser diameter leads to a reversal of the system performance metrics, suggesting the presence of a tipping point. The research presented in this article is critical for advancing the efficient polarization study and hyperpolarization of SERF comagnetometers.

Confrontation of Capitalism and Socialism in Wikipedia Networks

We introduce the Ising Network Opinion Formation (INOF) model and apply it to the analysis of networks of six Wikipedia language editions. In the model, Ising spins are placed at network nodes/articles and the steady-state opinion polarization of spins is determined from the Monte Carlo iterations in which a given spin orientation is determined by in-going links from other spins. The main consideration was the opinion confrontation between capitalism, imperialism (blue opinion) and socialism, communism (red opinion). These nodes have fixed spin/opinion orientation while other nodes achieve their steady-state opinions in the process of Monte Carlo iterations. We found that the global network opinion favors socialism, communism for all six editions. The model also determined the opinion preferences for world countries and political leaders, showing good agreement with heuristic expectations. We also present results for opinion competition between Christianity and Islam, and USA Democratic and Republican parties. We argue that the INOF approach can find numerous applications for directed complex networks.

Rigidly Axial O Coordination-Induced Spin Polarization on Single Ni-N4-C Site by MXene Coupling for Boosting Electrochemical CO2 Reduction to CO.

Regulating the spin states in transition-metal (TM)-based single-atom catalysts (SACs), such as the TM-Nx-C configurations, is crucial for improving the catalytic activity. However, the role of spin in single Ni atoms facilitating the electrochemical CO2 reduction reaction (CO2RR) has been largely overlooked. Using first-principles simulations, we investigated the electrocatalytic performance of Ni-N4-C SACs vertically stacked on the O-terminated MXene nanosheets for the CO2RR. The terminated O atoms on MXene axially interact with the Ni atom due to significant charge transfer between them. Unlike the pure Ni-N4 site, which lacks spin polarization, the newly formed Ni-N4O configuration breaks the spin degeneracy of Ni d orbitals, dramatically lifting the energy level of spin-down d orbitals relative to that of spin-up d orbitals. As a result, the d electrons of Ni in the two spin channels are rearranged, leading to large net spin moments of 1.4 μB. Compared to the Ni-N4 site, the partially filled minority-spin dz2 orbitals of Ni on Ni-N4O weaken the occupied d-π* orbitals between Ni and *COOH, significantly stabilizing the key intermediate. The detailed reaction mechanisms and energetics show that four MXenes, namely, Hf3C2, Zr3C2, Hf2C, and Zr2C, can induce a large spin on the Ni site, thereby improving catalytic activity for CO2 reduction to CO, with a lower onset potential of about -0.75 V vs SHE compared to pure Ni SACs (-1.17 V) according to the potential-constant model with an explicit solvent environment.

Regulating Spin Polarization via Axial Nitrogen Traction at Fe−N5 Sites Enhanced Electrocatalytic CO2 Reduction for Zn−CO2 Batteries

AbstractSingle Fe sites have been explored as promising catalysts for the CO2 reduction reaction to value‐added CO. Herein, we introduce a novel molten salt synthesis strategy for developing axial nitrogen‐coordinated Fe‐N5 sites on ultrathin defect‐rich carbon nanosheets, aiming to modulate the reaction pathway precisely. This distinctive architecture weakens the spin polarization at the Fe sites, promoting a dynamic equilibrium of activated intermediates and facilitating the balance between *COOH formation and *CO desorption at the active Fe site. Notably, the synthesized FeN5, supported on defect‐rich in nitrogen‐doped carbon (FeN5@DNC), exhibits superior performance in CO2RR, achieving a Faraday efficiency of 99 % for CO production (−0.4 V vs. RHE) in an H‐cell, and maintaining a Faraday efficiency of 98 % at a current density of 270 mA cm−2 (−1.0 V vs. RHE) in the flow cell. Furthermore, the FeN5@DNC catalyst is assembled as a reversible Zn−CO2 battery with a cycle durability of 24 hours. In situ IR spectroscopy and density functional theory (DFT) calculations reveal that the axial N coordination traction induces a transformation in the crystal field and local symmetry, therefore weakening the spin polarization of the central Fe atom and lowering the energy barrier for *CO desorption.

Regulating Spin Polarization via Axial Nitrogen Traction at Fe-N5 Sites Enhanced Electrocatalytic CO2 Reduction for Zn-CO2 Batteries.

Single Fe sites have been explored as promising catalysts for the CO2 reduction reaction to value-added CO. Herein, we introduce a novel molten salt synthesis strategy for developing axial nitrogen-coordinated Fe-N5 sites on ultrathin defect-rich carbon nanosheets, aiming to modulate the reaction pathway precisely. This distinctive architecture weakens the spin polarization at the Fe sites, promoting a dynamic equilibrium of activated intermediates and facilitating the balance between *COOH formation and *CO desorption at the active Fe site. Notably, the synthesized FeN5, supported on defect-rich in nitrogen-doped carbon (FeN5@DNC), exhibits superior performance in CO2RR, achieving a Faraday efficiency of 99 % for CO production (-0.4 V vs. RHE) in an H-cell, and maintaining a Faraday efficiency of 98 % at a current density of 270 mA cm-2 (-1.0 V vs. RHE) in the flow cell. Furthermore, the FeN5@DNC catalyst is assembled as a reversible Zn-CO2 battery with a cycle durability of 24 hours. In situ IR spectroscopy and density functional theory (DFT) calculations reveal that the axial N coordination traction induces a transformation in the crystal field and local symmetry, therefore weakening the spin polarization of the central Fe atom and lowering the energy barrier for *CO desorption.