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We explore how strain impacts the band structure of metallic-phase VO2 thin films deposited on TiO2(101) substrates. Employing a combination of X-ray absorption linear dichroism and valence band measurements, we demonstrate that strain can alter the intrinsic band structure anisotropy of metallic VO2. Our findings reveal that reducing the thickness of VO2 films leads to a more isotropic band structure. This observation is further supported by an analysis of the electronic population redistribution in the d || − π * bands, which affects the screening length and induces effective mass renormalization. Overall, our results underscore the potential of strain manipulation in tailoring the electronic structure uniformity of thin films, thereby expanding the scope for engineering VO2 functionalities. In this article we studied the evolution of band anisotropy in strained VO2(101) thin films. We found out that strain works as a control agent for the anisotropy and thus controls the features of VO2 bands structure. For this crystal orientation a large strain corresponds to a more homogeneous electronic structure of VO2. This impacts the electrons population redistribution between d|| and π bands, the screening length and the effective mass. By controlling the anisotropy and the band structure properties our results can ease the integration of VO2 into complex electronics. [ABSTRACT FROM AUTHOR]

Electropolymerization is a convenient way to obtain conducting polymers (CPs) directly adhered to an electrode surface. CPs are well-known for their various application fields in photovoltaic cells, chemical sensors, and electronics. By implementing chirality into a CP, the application possibilities will spread further onto chiral sensors or optoelectronics. In this work, we introduce a new inherently chiral polymer based on a macrocyclic 3,4-ethylenedioxythiophene-diketopyrrolopyrrole-3,4-ethylenedioxythiophene triad (EDOT-DPP-EDOT) fused by 1,4-phenylene groups, which was prepared via oxidative electropolymerization directly on the electrode surface. The investigation of the chiroptical properties was performed by circular dichroism spectroscopy in the solid state. The enantiomeric pure polymer films obtained showed dissymmetry factors of up to −2.71 × 10−4, whereby linear dichroism contributions can be widely excluded. [ABSTRACT FROM AUTHOR]

Copper oxide high-temperature superconductors, such as Bi2Sr2CaCu2O8+δ (Bi2212), have garnered extensive research interest due to their high critical temperatures (Tc) surpassing the Bardeen–Cooper–Schrieffer (BCS) limit. The two-dimensional CuO₂ plane is widely regarded as the most crucial element of high-Tc cuprate superconductors. The anisotropy of this CuO₂ layer remains a topic of ongoing interest. Although a few experimental results have reported strong optical anisotropy in both ab and ac-planes of Bi2212 through optical "reflectivity" measurements, there is a lack of studies focusing on the optical anisotropy of these materials using optical "transmittance" measurements by utilizing ultraviolet and visible light. Using a generalized high-accuracy universal polarimeter, we observed significant linear birefringence and linear dichroism peaks in the UV region at room temperature. To investigate the origin of the significant optical anisotropy, single crystals of Bi2−xPbxSr2CaCu2O8+δ with different lead contents (x = 0, 0.4, and 0.6) were grown using the floating zone method, and the wavelength dependencies of linear birefringence and linear dichroism along the c axis were measured. The insights gained into the optical anisotropy of Bi2−xPbxSr2CaCu2O8+δ from this study are significant for discussing its origin of the mechanism of high-Tc superconductivity. [ABSTRACT FROM AUTHOR]

Revealing transient electronic properties in anisotropic 2D materials is a prerequisite for developing ultrafast optoelectronic functional devices. Here, the ultrafast electronic dynamics of polarization anisotropy for the AB‐stacked rhenium disulfide (ReS2) are studied using time‐ and energy‐resolved photoemission electron microscopy. The ultrafast electronic relaxation process exhibits sensitive layer‐dependent polarization anisotropy. The linear dichroism of the ultrafast electronic dynamics is also measured, indicating that the polarization anisotropy is determined by the fast process on the sub‐picosecond scale. With ab initio theory calculations, it is confirmed that the ultra‐sensitive layer dependence of the lifetime of the fast process originates from a stronger interlayer coupling in the K‐Γ direction (along the b‐axis) of ReS2. Further, by analyzing the time‐resolved photoemission energy spectrum, distinct "fast" and "slow" regimes are found in the ultrafast dynamics of excited electrons with different energies. The corresponding energy windows also show substantial polarization anisotropy, which is associated with the linear dichroism of the electron‐phonon coupling in the AB‐stacked ReS2. This work has implications for the design of angle‐sensitive optoelectronic functional devices with the AB‐stacked ReS2. [ABSTRACT FROM AUTHOR]

We present a method of laser frequency stabilization based on the linear dichroism signal in a transverse magnetic field. This method is similar to the DAVLL (Dichroic Atomic Vapor Laser Lock) method. It differs from DAVLL and from its existing modifications primarily by the fact that it uses signals of linearly polarized light caused by alignment, rather than circular refraction caused by orientation, and therefore allows us to obtain error signals at the magnetic field modulation frequency (or its second harmonic) by extremely simple means. The method allows the laser frequency to be stabilized in the vicinity of the low-frequency transition in the D1 line of Cs; it does not require strong magnetic fields or careful shielding of cells containing cesium atoms. Although the absorption line in a gas-filled cell is typically gigahertz wide, the achievable resolution, limited by the signal-to-noise ratio of photon shot noise, can reach units or tens of kilohertz in a one hertz bandwidth. [ABSTRACT FROM AUTHOR]

Ultrathin titanium nitride (TiN) is a novel material platform for constructing active metasurfaces in the near-infrared region (NIR). Here, we realized tunable polarization-selective absorption by gating ultrathin TiN in an Ultrathin TiN Grating Metasurface (UTGM) and a gold resonator/TiN film Hybrid Metasurface (GTHM), respectively. The TM wave absorption (0.96) was much larger than that of the TE wave in the UTGM. When the carrier density decreased by 12%, the near-perfect TM absorption peak blue-shifted by 0.3 μm. Similarly, the linear dichroism (0.96) peak in GTHM blue-shifted by 0.12 μm when gating ultrathin TiN film. Active metasurfaces with tunable polarization-selective absorption have huge potential in dynamic integrated electro-optic devices in NIR. [ABSTRACT FROM AUTHOR]

The ability to freely control the polarization of X‐rays enables measurement techniques relying on circular or linear dichroism, which have become indispensable tools for characterizing the properties of chiral molecules or magnetic structures. Therefore, the demand for polarization control in X‐ray free‐electron lasers is increasing to enable polarization‐sensitive dynamical studies on ultrafast time scales. The soft X‐ray branch Athos of SwissFEL was designed with the aim of providing freely adjustable and arbitrary polarization by building its undulator solely from modules of the novel Apple X type. In this paper, the magnetic model of the linear inclined and circular Apple X polarization schemes are studied. The polarization is characterized by measuring the angular electron emission distributions of helium for various polarizations using cold target recoil ion momentum spectroscopy. The generation of fully linear polarized light of arbitrary angle, as well as elliptical polarizations of varying degree, are demonstrated. [ABSTRACT FROM AUTHOR]

Recently, a technical modification of a Reflectance Anisotropy Spectroscopy (RAS) spectrometer has been proposed to investigate the circular dichroism (CD) of samples instead of the normally studied linear dichroism. CD-RAS measures the anisotropy of the optical properties of a sample under right-handed and left-handed circularly polarized light. Here, we present the application of CD-RAS to measure the circular dichroism of a twisted bilayer of graphene, purposely prepared as a possible substrate for the adsorption of thin molecular layers, in air, in liquid or in a vacuum. This result demonstrates the performance of the apparatus and shows interesting perspectives for the investigation of chiral organic assemblies deposited in solid film. [ABSTRACT FROM AUTHOR]

Conventional imaging techniques can only record the intensity of light while polarization imaging can record the polarization of light, thus obtaining a higher dimension of image information. We use the COMSOL software to numerically propose a circular polarization photodetector composed of the dislocated 2-hole Si chiral metasurfaces controlling the circular polarization lights and the HgCdTe (MCT) photodetector chip to detect the intensity of light signals. The chiral metasurfaces can be equated to a significant radiation source of the Z-type current density under the right circularly polarized incidence conditions, which explains the large circular dichroism (CD) of absorption of 95% in chiral photodetectors. In addition, the linear dichroism (LD) of the linear polarization pixel is 0.62, and the extinction ratio (ER) is 21 dB. The full Stokes pixel using the six-image-element technique can almost measure arbitrary polarization information of light at 4 μm operation wavelength. Our results highlight the potential of circular dichroic metasurfaces as photonic manipulation platforms for miniaturized polarization detectors. [ABSTRACT FROM AUTHOR]

This study proposes a multifunctional terahertz absorber utilizing graphene and vanadium dioxide as functional materials. By utilizing vanadium dioxide in the metallic state, the device achieves linear dichroism, with a maximum value of 0.8 at 1.75 THz, while in the insulating state, the introduction of graphene strips results in a chiral structure that achieves circular dichroism with tunable values ranging from 0 to 0.59 at 1.535 THz by regulating the graphene's Fermi level. The physical mechanism underlying the differential absorption is explained, and the influence of the device's structural parameters and incident angle on the performance is also investigated. This work provides a practical basis for the development of terahertz functional devices in polarization detection and near-field imaging. [ABSTRACT FROM AUTHOR]

Human Rad51 protein (HsRad51)-promoted DNA strand exchange, a crucial step in homologous recombination, is regulated by proteins and calcium ions. Both the activator protein Swi5/Sfr1 and Ca2+ ions stimulate different reaction steps and induce perpendicular DNA base alignment in the presynaptic complex. To investigate the role of base orientation in the strand exchange reaction, we examined the Ca2+ concentration dependence of strand exchange activities and structural changes in the presynaptic complex. Our results show that optimal D-loop formation (strand exchange with closed circular DNA) required Ca2+ concentrations greater than 5 mM, whereas 1 mM Ca2+ was sufficient for strand exchange between two oligonucleotides. Structural changes indicated by increased fluorescence intensity of poly(dεA) (a poly(dA) analog) reached a plateau at 1 mM Ca2+. Ca2+ > 2 mM was required for saturation of linear dichroism signal intensity at 260 nm, associated with rigid perpendicular DNA base orientation, suggesting a correlation with the stimulation of D-loop formation. Therefore, Ca2+ exerts two different effects. Thermal stability measurements suggest that HsRad51 binds two Ca2+ ions with KD values of 0.2 and 2.5 mM, implying that one step is stimulated by one Ca2+ bond and the other by two Ca2+ bonds. Our results indicate parallels between the Mg2+ activation of RecA and the Ca2+ activation of HsRad51. [ABSTRACT FROM AUTHOR]

We propose a chiral metasurface with tunable circular/linear dichroism based on graphene. When a circularly polarized (CP) wave is incident, the metasurface can achieve circular dichroism at two frequencies. Under the incidence of linearly polarized (LP) wave, the metasurface exhibits linear dichroism. At a frequency of 1.89 THz, the designed metasurface has an absorption rate of over 99% for right-handed circularly polarized (RCP) wave, and 11% for left-handed circularly polarized (LCP) wave. The circular dichroism equals 0.88. At 3.0 THz, while the absorptance of the metasurface for LCP and for RCP waves is 97% and 17%, respectively. The circular dichroism is 0.80. At 0.76 THz, and the absorption rate of the metasurface for x-polarized and y-polarized waves is 0.95 and 0.22, respectively. The linear dichroism is 0.73. The near-field imaging is realized by using the differential characteristics of the circular dichroism metasurface. In addition, imaging resolution, linear/Circular dichroism, and single-/dual-frequency terahertz absorption can be effectively adjusted by changing the Fermi level of graphene. This structure has good application prospects in tunable imaging and tunable dichroism. [ABSTRACT FROM AUTHOR]

Motivated by the imperative demand for design integration and miniaturization within the terahertz (THz) spectrum, this study presents an innovative solution to the challenges associated with singular functionality, limited application scope, and intricate structures prevalent in conventional metasurfaces. The proposed multifunctional tunable metasurface leverages a hybridized grapheme–metal structure, addressing critical limitations in existing designs. Comprising three distinct layers, namely a graphene–gold resonance layer, a Topas dielectric layer, and a bottom gold film reflective layer, this terahertz metasurface exhibits multifunctionality that is both polarization and incident-angle independent. The metasurface demonstrates a broadband circular dichroism (CD) function when subjected to incident circularly polarized waves. In contrast, under linear incidence, the proposed design achieves functionalities encompassing linear dichroism (LD) and polarization conversion. Remarkably, graphene's chemical potential and the incident light's state can be manipulated to tune each functional aspect's intensity finely. The proposed tunable multifaceted metasurface showcases significant referential importance within the terahertz spectrum, mainly contributing to advancing CD metamirrors, chiral photodetectors, polarization digital imaging systems, and intelligent switches. [ABSTRACT FROM AUTHOR]

We present a method of laser frequency stabilization based on the linear dichroism signal in a transverse magnetic field. This method is similar to the DAVLL (Dichroic Atomic Vapor Laser Lock) method. It differs from DAVLL and from its existing modifications primarily by the fact that it uses signals of linearly polarized light caused by alignment, rather than circular refraction caused by orientation, and therefore allows us to obtain error signals at the magnetic field modulation frequency (or its second harmonic) by extremely simple means. The method allows the laser frequency to be stabilized in the vicinity of the low-frequency transition in the D1 line of Cs; it does not require strong magnetic fields or careful shielding of cells containing cesium atoms. Although the absorption line in a gas-filled cell is typically gigahertz wide, the achievable resolution, limited by the signal-to-noise ratio of photon shot noise, can reach units or tens of kilohertz in a one hertz bandwidth.

The rich physical properties unveiled in a plethora of transition and rare-earth metal oxides have been attributed to the intricate interplays between the orbital, charge, and spin degrees of freedom. Among them, rare-earth manganites (RMnO3) have been attracting tremendous attention owing to the ionic size-induced lattice distortion dictated by the Goldschmidt tolerance factor and the substantial Jahn–Teller distortion unique to Mn3+ ions, which evidently have resulted in a variety of emergent characteristics in electronic, magnetic, and orbital ordering. In this work, we deliberately engineered the orientation of a series of orthorhombic YMnO3 (o-YMO) films grown on SrTiO3(100) [STO(100)] and SrTiO3(110) [STO(110)] substrates by means of pulsed laser deposition. The x-ray diffraction (XRD) and reciprocal space mapping revealed that o-YMO/STO(100) is c-axis-oriented and o-YMO/STO(110) is a-axis-oriented, respectively. The XRD ϕ-scans further indicate that both films have excellent in-plane crystallinity, allowing the exploration of anisotropies along the respective crystallographic orientations. Indeed, the x-ray absorption linear dichroism spectroscopy taken along the respective crystallographic orientations evidently exhibited substantial anisotropy. Theoretical fitting with configuration interaction cluster calculations suggests that the d 3 z 2 − r 2 orbitals are parallel to YMO[001]/(100), leading to stronger electron scattering along the c-axis. Independent polarization-dependent Δ R/R spectra obtained using the femtosecond pump–probe method exhibited substantial anisotropic behaviors in carrier relaxation dynamics when probing along different crystallographic orientations, presumably due to orbital ordering anisotropies. [ABSTRACT FROM AUTHOR]

We demonstrate both theoretically and experimentally that a linearly polarized optical beam incident on a linearly dichroic nematic liquid crystal cell with a topological defect of the topological strength q and linear dichroism, transforms into a composite vector beam consisting of elementary vector beams with the polarization singularity orders m=2q and m=q. Consequently, it has been proved that due to the linear dichroism a liquid crystal defect of the topological strength q=1 transforms an incident circularly polarized beam into a composite vortex beam consisting of the double-charged vortex beam and vector-vortex beam with polarization order and topological charge that are equal to unity. [ABSTRACT FROM AUTHOR]

Important attention in forensic medical practice is given to the solution of issues that arise during the examination in the case of traumatic brain injury (TBI), as this type of injury leads to high mortality and disability. Conducting an autopsy of the body of the deceased, whose death occurred from a TBI, there are cases when the injury occurs as a result of a fall of a person who previously developed a cerebral infarction, and sometimes vice versa. In this case, it is important to accurately verify the primary cause of death, therefore, timely and objective determination of the time of formation of a hemorrhage in the human brain is necessary. The purpose and tasks of the research. To evaluate the possibility of detecting time of formation of a hemorrhage of traumatic and non-traumatic genesis by the generally accepted histological method and polarization phase microscopy, and to compare their effectiveness. Research materials and methods. For the study, human brain samples were selected from 140 deceased individuals whose deaths occurred between 1 and 3 days after the onset of bleeding, according to medical records. As a control group, human brain samples were selected from 40 individuals who died of coronary heart disease. Light microscopy was performed by preliminary staining of histologic specimens according to the Perls method. Phase polarization tomography of the samples was performed using a Stokes polarimeter. Research Results. Stained human brain preparations of the experimental and control groups were examined and analyzed and it was found that hemosiderin was not present in all experimental samples (only in 31 out of 40 samples were present). It was not possible to establish the corresponding time dependences of the age of the formation of hemorrhages, regardless of the genesis, since the random appearance of the pigment in the experimental samples is noted at different time intervals. Analytical processing of the results of the statistical processing of the topographic structure of tomograms of the anisotropy of linear dichroism of the fibrillar networks of samples of the deceased from the experimental and control groups revealed a wider time range of sensitivity of this method to destructive changes in nervous tissue, in comparison with the polarimetric methods used in previous studies. As a result, there is an accelerated temporal decrease in the absolute values and the range of dispersion of the anisotropy of linear dichroism value with increasing time since the formation of hemorrhage. Conclusions. Polarization-phase microscopy has shown a significant advantage in its use in comparison with the gold standard - the Perls' staining method for determining the time of hemorrhage formation in the human brain. [ABSTRACT FROM AUTHOR]

Linear dichroism (LD) is a differential polarized light absorption spectroscopy used for studying filamentous molecules such as DNA and protein filaments. In this study, we review the applications of LD for the analysis of DNA-protein interactions. LD signals can be measured in a solution by aligning the sample using flow-induced shear force or a strong electric field. The signal generated is related to the local orientation of chromophores, such as DNA bases, relative to the filament axis. LD can thus assess the tilt and roll of DNA bases and distinguish intercalating from groove-binding ligands. The intensity of the LD signal depends upon the degree of macroscopic orientation. Therefore, DNA shortening and bending can be detected by a decrease in LD signal intensity. As examples of LD applications, we present a kinetic study of DNA digestion by restriction enzymes and structural analyses of homologous recombination intermediates, i.e., RecA and Rad51 recombinase complexes with single-stranded DNA. LD shows that the DNA bases in these complexes are preferentially oriented perpendicular to the filament axis only in the presence of activators, suggesting the importance of organized base orientation for the reaction. LD measurements detect DNA bending by the CRP transcription activator protein, as well as by the UvrB DNA repair protein. LD can thus provide information about the structures of protein-DNA complexes under various conditions and in real time. [ABSTRACT FROM AUTHOR]

The phenomena of magneto-optical polarization rotation and circular magnetic dichroism are well known in the Faraday configuration. We present another effect, an odd magneto-optical linear dichroism, arising in nanostructures with polarization-dependent mode Q-factors and magneto-optical components. It reveals itself as the magneto-optical modulation of light intensity for the two opposite magnetization directions in the Faraday configuration. The effect was demonstrated on a magnetophotonic crystal with a cavity mode, the polarization-dependent Q-factor of which is due to oblique incidence. For a polarization angle of 60° (or 120°) and an angle of incidence around 60°, the magneto-optical intensity modulation maximizes and reaches 6%. [ABSTRACT FROM AUTHOR]

Under different conditions, the DNA double helix can take different geometric forms. Of the large number of its conformations, in addition to the "canonical" B form, the A, C, and Z forms are widely known, and the D, Hoogsteen, and X forms are less known. DNA locally takes the A, C, and Z forms in the cell, in complexes with proteins. We compare different methods for detecting non-canonical DNA conformations: X-ray, IR, and Raman spectroscopy, linear and circular dichroism in both the infrared and ultraviolet regions, as well as NMR (measurement of chemical shifts and their anisotropy, scalar and residual dipolar couplings and inter-proton distances from NOESY (nuclear Overhauser effect spectroscopy) data). We discuss the difficulties in applying these methods, the problems of theoretical interpretation of the experimental results, and the prospects for reliable identification of non-canonical DNA conformations. [ABSTRACT FROM AUTHOR]

Linear dichroism is an important tool to characterize the transmission matrix and determine the crystal or orbital orientation in a material. In order to achieve high-resolution mapping of transmission properties, the linear-dichroism scattering model in ptychographic imaging is introduced, and an efficient two-stage reconstruction algorithm is developed. Using the proposed algorithm on a uniaxial material, the dichroic transmission matrix can be recovered without an analyzer by using ptychography measurements with as few as three different polarization angles, with the help of an empty region to remove phase ambiguities.

Isolated magnetic skyrmions are stable, topologically protected spin textures that are at the forefront of research interests today due to their potential applications in information technology. A distinct class of skyrmion hosts are rare earth - transition metal (RE-TM) ferrimagnetic materials. To date, the nature and the control of basic traits of skyrmions in these materials are not fully understood. We show that for an archetypal ferrimagnetic material DyCo3 that exhibits a strong perpendicular anisotropy, the ferrimagnetic skyrmion size can be tuned by an external magnetic field. Moreover, by taking advantage of the high spatial resolution of scanning transmission X-ray microscopy (STXM) and utilizing a large x-ray magnetic linear dichroism (XMLD) contrast that occurs naturally at the RE resonant edges, we resolve the nature of the magnetic domain walls of ferrimagnetic skyrmions. We demonstrate that through this method one can easily discriminate between Bloch and Néel type domain walls for each individual skyrmion. For all isolated ferrimagnetic skyrmions, we observe that the domain walls are of Néel-type. This key information is corroborated with results of micromagnetic simulations and allows us to conclude on the nature of the Dzyaloshinskii-Moriya interaction (DMI) which concurs to the stabilisation of skyrmions in this ferrimagnetic system. Establishing that an intrinsic DMI occurs in RE-TM materials will also be beneficial towards a deeper understanding of chiral spin texture control in ferrimagnetic materials. Magnetic skyrmions are topological spin textures that have potential implications for spintronic devices but greater control over their stability and physical characteristics are first required. Here, the authors study the formation of skyrmions in ferrimagnetic thin films of DyCo3 and using a combination of X-ray measurements determine them to be of the Néel type. [ABSTRACT FROM AUTHOR]

Optically anisotropic materials were produced via colloidal lithography and characterized using scanning electronic microscopy (SEM), confocal microscopy, and polarimetry. A compact hexagonal array mask composed of silica sub-micron particles was fabricated via the Langmuir–Blodgett self-assembly technique. Subsequently, the mask pattern was transferred onto monocrystalline silicon and commercial glass substrates using ion beam etching in a vacuum. Varying the azimuthal angle while etching at oblique incidence carved screw-like shaped pillars into the substrates, resulting in heterochiral structures depending on the azimuthal angle direction. To enhance the material's optical properties through plasmon resonance, gold films were deposited onto the pillars. Polarimetric measurements were realized at normal and oblique incidences, showing that the etching directions have a clear influence on the value of the linear birefringence and linear dichroism. The polarimetric properties, especially the chiroptical responses, increased with the increase in the angle of incidence. [ABSTRACT FROM AUTHOR]

We report the deposition of monolayers and multilayers of {Cr10(OMe)20(O2CCMe3)10} wheels, hereafter {Cr10}, onto Au(111) and Cu(111) single‐crystal substrates, and their characterization combining scanning tunneling microscopy, X‐ray photoelectron spectroscopy, X‐ray absorption spectroscopy, X‐ray natural linear dichroism, and X‐ray magnetic circular dichroism (XMCD). {Cr10} in bulk shows axial magnetic anisotropy and a cluster total spin S = 9 ground state, stemming from an interaction scheme of two semi‐crowns containing four Cr3+ ions interacting ferromagnetically, separated by two Cr3+ antiferromagnetically coupled. The one‐monolayer (1ML) samples of {Cr10} sublimated on Ag(111) and Cu(111) show slightly different applied magnetic field dependence of XMCD signal. The field‐dependence of the magnetization evolves from a lower curve for the 1ML {Cr10} samples to a curve resembling the bulk one as the number of layers is increased, as shown in a 14ML sample. Monte Carlo simulations allow rationalizing the magnetization curves of the 1ML samples in terms of a reduction of the cluster ground‐state total spin, S = 3 or S = 6, as a consequence of variations in the intra‐wheel coupling interactions induced by the on‐surface deposition. The sensitivity of the magnetic configuration of {Cr10} to minor distortions of the intramolecular conformation might be exploited to control magnetism by external stimuli for applications. [ABSTRACT FROM AUTHOR]

The stability, mechanical and electronic properties of a BC2N monolayer and its potential use as an anode material for Li-ion batteries were explored using the density functional theory calculation. The proposed BC2N monolayer shows good thermal and dynamical stabilities, as indicated by the ab initio molecular dynamics simulations and phonon dispersion calculations. The BC2N monolayer exhibits highly anisotropic mechanical properties. The electronic structure calculation based on the hybrid functional suggests that the BC2N monolayer is an indirect bandgap (~1.8 eV) semiconductor. The BC2N monolayer shows linear dichroism and is able to harvest visible and ultraviolet light. To investigate the application of the BC2N monolayer as a potential anode material for Li-ion batteries, the Li adsorption and diffusion on the monolayer were studied. The BC2N monolayer exhibits a high theoretical capacity of 1098 mAh/g for Li-ion batteries. The calculated diffusion barrier of Li ion is 0.45 eV, suggesting a rapid Li-ion charge and discharge rate. The unique mechanical and optical properties of the BC2N monolayer also make it an attractive material for use in advanced nanomechanical and optoelectronic devices. [ABSTRACT FROM AUTHOR]

The article discusses the use of layer-by-layer assembled 2D nanocomposites for extreme polarization optics, showcasing their potential in high-temperature environments. The study by Kotov and colleagues demonstrates the assembly of nano-achiral 2D nanoplatelets into polarization-active nanocomposites with exceptional optical properties. These nanocomposites exhibit intense circular polarization even at 250°C, surpassing the performance of typical nanomaterials by approximately 500 times. The research highlights the simplicity of the manufacturing process and the significant impact of these optically active nanocomposites on extreme polarization optics. [Extracted from the article]

Many unusual and promising properties have been reported recently for the transition metal trichalcogenides of the type MPS3 (M = V, Mn, Fe, Ni...), such as maintaining magnetic order to the atomically thin limit, ultra-sharp many-body excitons, metal-insulator transitions and, especially for Fe2P2S6, giant linear dichroism among others. Here we conduct a detailed investigation of the electronic structure of Fe2P2S6 using angle-resolved photoemission spectroscopy, q-dependent electron energy loss spectroscopy, optical spectroscopies and density functional theory. Fe2P2S6 is a Mott insulator with a gap of Egap ≈ 1.4 eV and zigzag antiferromagnetism below TN = 119 K. The low energy excitations are dominated by Fe 3d states. Large and sign-changing linear dichroism is observed. We provide a microscopic mechanism explaining key properties of the linear dichroism based on the correlated character of the electronic structure, thereby elucidating the nature of the spin-charge coupling in Fe2P2S6 and related materials. [ABSTRACT FROM AUTHOR]

We report on the magnetic properties of antiferromagnetic NiO(001) thin films in epitaxially grown NiO/MgO(dMgO)/Cr/MgO(001) system for different thicknesses of MgO, dMgO. Results of X-ray Magnetic Linear Dichroism show that together with an increase of dMgO, rotation of NiO spins from in-plane towards out-of-plane direction occurs. Furthermore, we investigated how the proximity of Fe modifies the magnetic state of NiO in Fe/NiO/MgO(dMgO)/Cr/MgO(001). We proved the existence of a multidomain state in NiO as a result of competition between the ferromagnet/antiferromagnet exchange coupling and strain exerted on the NiO by the MgO buffer layer. [ABSTRACT FROM AUTHOR]

The presence of the van der Waals gap in layered materials creates a wealth of intriguing phenomena different to their counterparts in conventional materials. For example, pressurization can generate a large anisotropic lattice shrinkage along the stacking orientation and/or a significant interlayer sliding, and many of the exotic pressure-dependent properties derive from these mechanisms. Here we report a giant piezoresistivity in pressurized β′-In2Se3. Upon compression, a six-orders-of-magnitude drop of electrical resistivity is obtained below 1.2 GPa in β′-In2Se3 flakes, yielding a giant piezoresistive gauge πp of −5.33 GPa−1. Simultaneously, the sample undergoes a semiconductor-to-semimetal transition without a structural phase transition. Surprisingly, linear dichroism study and theoretical first principles modelling show that these phenomena arise not due to shrinkage or sliding at the van der Waals gap, but rather are dominated by the layer-dependent atomic motions inside the quintuple layer, mainly from the shifting of middle Se atoms to their high-symmetric location. The atomic motions link to both the band structure modulation and the in-plane ferroelectric dipoles. Our work not only provides a prominent piezoresistive material but also points out the importance of intralayer atomic motions beyond van der Waals gap. Lattice shrinkage is a dominating factor for the strain-induced change of the electronic properties in vdW layered materials. Here, the authors discover a piezoresistivity in pressurized β′-In2Se3, which originates from the intralayer atomic motions. [ABSTRACT FROM AUTHOR]

In this paper, a graphene-based multi-functional anisotropic metamaterial composed of two finite parallel graphene ribbons in each unit cell is designed and proposed in the 0.1–5.5 terahertz (THz) region. Simulations are performed by the finite element method (FEM) in the frequency-domain solver of CST Software. An equivalent circuit modeling (ECM) as a simplified approach has been provided by a MATLAB code to model the performance of the metamaterial. The metastructure is polarization-sensitive because of the geometric non-symmetry. The absorption/reflection spectrum of the metamaterial is dynamically tunable by changing the Fermi energy level of the graphene. The introduced metamaterial can act as a THz switch and inverter at 1.23 and 4.21 THz. It acts as an ON state when the incident electric field is in the x-direction and acts as an OFF state when the incident electric field is in the y-direction. It can also act as a bi-functional mirror: a triple-band mirror for the incident electric field in the x-direction and an ultra-broadband mirror for the incident electric field in the y-direction. The proposed metamaterial has a maximum absorption of 100%, maximum linear dichroism (LD) of 100%, and a maximum switching extinction ratio of 33.01 dB. The metamaterial and its applications could be used as a potential platform in future THz devices and systems. [ABSTRACT FROM AUTHOR]

Cyanine dyes are known to form H- and J-aggregates in aqueous solutions. Here we show that the cyanine dye, S0271, assembles in water into vortex induced chiral J-aggregates. The chirality of the J-aggregates depends on the directionality of the vortex. This study utilised both conventional benchtop CD spectropolarimeters and Mueller matrix polarimetry. It was found that J-aggregates have real chirality alongside linear dichroism and linear and circular birefringence. We identify the factors that are key to the formation of metastable chiral J-aggregates and propose a mechanism for their assembly. [ABSTRACT FROM AUTHOR]

Collagenous tissues exhibit anisotropic optical properties such as birefringence and linear dichroism (LD) as a result of their structurally oriented supraorganization from the nanometer level to the collagen bundle scale. Changes in macromolecular order and in aggregational states can be evaluated in tendon collagen bundles using polarization microscopy. Because there are no reports on the status of the macromolecular organization in tendon explants, the objective of this work was to evaluate the birefringence and LD characteristics of collagen bundles in rat calcaneal tendons cultivated in vitro on substrates that differ in their mechanical stiffness (plastic vs. glass) while accompanying the expected occurrence of cell migration from these structures. Tendon explants from adult male Wistar rats were cultivated for 8 and 12 days on borosilicate glass coverslips (n = 3) and on nonpyrogenic polystyrene plastic dishes (n = 4) and were compared with tendons not cultivated in vitro (n = 3). Birefringence was investigated in unstained tendon sections using high-performance polarization microscopy and image analysis. LD was studied under polarized light in tendon sections stained with the dichroic dyes Ponceau SS and toluidine blue at pH 4.0 to evaluate the orientation of proteins and acid glycosaminoglycans (GAG) macromolecules, respectively. Structural remodeling characterized by the reduction in the macromolecular orientation, aggregation and alignment of collagen bundles, based on decreased average gray values concerned with birefringence intensity, LD and morphological changes, was detected especially in the tendon explants cultivated on the plastic substrate. These changes may have facilitated cell migration from the lateral regions of the explants to the substrates, an event that was observed earlier and more intensely upon tissue cultivation on the plastic substrate. The axial alignment of the migrating cells relative to the explant, which occurred with increased cultivation times, may be due to the mechanosensitive nature of the tenocytes. Collagen fibers possibly played a role as a signal source to cells, a hypothesis that requires further investigation, including studies on the dynamics of cell membrane receptors and cytoskeletal organization, and collagen shearing electrical properties. [ABSTRACT FROM AUTHOR]

The Rh-catalyzed annulation reaction of 2-(ethynylaryl)ethaneamines was used as key step to synthesize two berberine derivatives with hydroxy and phenyl substituents in 11- and 13-position. These compounds showed absorption and emission properties comparable to the parent alkaloid berberine. The fluorescence of the hydroxy-substituted berberine (pKa = 6.3) is efficiently quenched under acidic conditions, whereas a fluorescence light-up effect was observed with increasing pH values. The interactions of the berberine derivatives with duplex DNA and quadruplex DNA were investigated with absorption, circular dichroism (CD), and linear dichroism (LD) spectroscopy. The 13-phenyl-substituted berberine binds to duplex DNA with a binding constant of Kb = 1.2 x 105 M-1 and to quadruplex DNA with Kb = 1.9 x 105 M-1. The CD- and LD-spectroscopic studies showed that the 11-hydroxy-13-phenyl-substituted berberine binds to duplex DNA by intercalation and to quadruplex DNA by terminal π-stacking. [ABSTRACT FROM AUTHOR]

Being able to probe the polarization states of light is crucial for applications from medical diagnostics and intelligent recognition to information encryption and bio-inspired navigation. Current state-of-the-art polarimeters based on anisotropic semiconductors enable direct linear dichroism photodetection without the need for bulky and complex external optics. However, their polarization sensitivity is restricted by the inherent optical anisotropy, leading to low dichroic ratios of typically smaller than ten. Here, we unveil an effective and general strategy to achieve more than 2,000-fold enhanced polarization sensitivity by exploiting an anisotropic charge trapping effect in organic phototransistors. The polarization-dependent trapping of photogenerated charge carriers provides an anisotropic photo-induced gate bias for current amplification, which has resulted in a record-high dichroic ratio of >104, reaching over the extinction ratios of commercial polarizers. These findings further enable the demonstration of an on-chip polarizer-free bionic celestial compass for skylight-based polarization navigation. Our results offer a fundamental design principle and an effective route for the development of next-generation highly polarization-sensitive optoelectronics. The direct linear dichroism photodetection without external optics is crucial for applications. Here, Jie et al. exploit the anisotropic charge trapping in organic phototransistors to achieve the dichroic ratio of 104 and to demonstrate a polarizer-free celestial compass for bio-inspired navigation. [ABSTRACT FROM AUTHOR]

Multi-element layered materials have gained substantial attention in the context of achieving the customized light-matter interactions at subwavelength scale via stoichiometric engineering, which is crucial for the realization of miniaturized polarization-sensitive optoelectronic and nanophotonic devices. Herein, naturally occurring hydrated sodium sulfosalt gerstleyite is introduced as one new multi-element van der Waals (vdW) layered material. The mechanically exfoliated thin gerstleyite flakes are demonstrated to exhibit polarization-sensitive anisotropic linear and nonlinear optical responses including angle-resolved Raman scattering, anomalous wavelength-dependent linear dichroism transition, birefringence effect, and polarization-dependent third-harmonic generation (THG). Furthermore, the third-order nonlinear susceptibility of gerstleyite crystal is estimated by the probed flake thickness-dependent THG response. We envisage that our findings in the context of polarization-sensitive light-matter interactions in the exfoliated hydrated sulfosalt layers will be a valuable addition to the vdW layered material family and will have many implications in compact waveplates, on-chip photodetectors, optical sensors and switches, integrated photonic circuits, and nonlinear signal processing applications. [ABSTRACT FROM AUTHOR]

The design and formation of van der Waals (vdW) heterostructures with different two-dimensional (2D) materials provide an opportunity to create materials with extraordinary physical properties tailored toward specific applications. Mechanical exfoliation of natural vdW materials has been recognized as an effective way for producing high-quality ultrathin vdW heterostructures. Abramovite is one of such naturally occurring vdW materials, where the superlattice is composed of alternating Pb2BiS3 and SnInS4 2D material lattices. The forced commensuration between the two incommensurate constituent 2D material lattices induces in-plane structural anisotropy in the formed vdW heterostructure of abramovite, even though the individual 2D material lattices are isotropic in nature. Here, we show that ultrathin layers of vdW heterostructures of abramovite can be achieved by mechanical exfoliation of the natural mineral. Furthermore, the structural anisotropy induced highly anisotropic vibrational and optical responses of abramovite thin flakes are demonstrated by angle-resolved polarized Raman scattering, linear dichroism, and polarization-dependent third-harmonic generation. Our results not only establish abramovite as a promising natural vdW material with tailored linear and nonlinear optical properties for building future anisotropic integrated photonic devices, but also provide a deeper understanding of the origin of structural, vibrational and optical anisotropy in vdW heterostructures. [ABSTRACT FROM AUTHOR]

Optical metasurfaces with high quality factors (Q-factors) of chiral resonances can boost substantially light-matter interaction for various applications of chiral response in ultrathin, active, and nonlinear metadevices. However, current approaches lack the flexibility to enhance and tune the chirality and Q-factor simultaneously. Here, we suggest a design of chiral metasurface supporting bound state in the continuum (BIC) and demonstrate experimentally chiroptical responses with ultra-high Q-factors and near-perfect circular dichroism (CD = 0.93) at optical frequencies. We employ the symmetry-reduced meta-atoms with high birefringence supporting winding elliptical eigenstate polarizations with opposite helicity. It provides a convenient way for achieving the maximal planar chirality tuned by either breaking in-plane structure symmetry or changing illumination angle. Beyond linear CD, we also achieved strong near-field enhancement CD and near-unitary nonlinear CD in the same planar chiral metasurface design with circular eigen-polarization. Sharply resonant chirality realized in planar metasurfaces promises various practical applications including chiral lasers and chiral nonlinear filters. Here, the authors employ the physics of chiral bound states in the continuum and suggest planar chiral metasurfaces with simultaneous ultrahigh quality factor and near-perfect circular dichroism in both linear regime and nonlinear regime. [ABSTRACT FROM AUTHOR]

Cannizzarite is a naturally occurring mineral formed by van der Waals (vdW) stacking of alternating layers of PbS-like and Bi2S3-like two-dimensional (2D) materials. Although the PbS-type and Bi2S3-type 2D material layers are structurally isotropic individually, the forced commensuration between these two types of layers while forming the heterostructure of cannizzarite induces strong structural anisotropy. Here we demonstrate the mechanical exfoliation of natural cannizzarite mineral to obtain thin vdW heterostructures of PbS-type and Bi2S3-type atomic layers. The structural anisotropy induced anisotropic optical properties of thin cannizzarite flakes are explored through angle-resolved polarized Raman scattering, linear dichroism, and polarization-dependent anisotropic third-harmonic generation. Our study establishes cannizzarite as a new natural vdW heterostructure-based 2D material with highly anisotropic optical properties for realizing polarization-sensitive linear and nonlinear photonic devices for future on-chip optical computing and optical information processing. [ABSTRACT FROM AUTHOR]

Terahertz (THz) spin dynamics and vanishing stray field make antiferromagnetic (AFM) materials the most promising candidate for the next-generation magnetic memory technology with revolutionary storage density and writing speed. However, owing to the extremely large exchange energy barriers, energy-efficient manipulation has been a fundamental challenge in AFM systems. Here, we report an electrical writing of antiferromagnetic orders through a record-low current density on the order of 106 A cm−2 facilitated by the unique AFM-ferromagnetic (FM) phase transition in FeRh. By introducing a transient FM state via current-induced Joule heating, the spin-orbit torque can switch the AFM order parameter by 90° with a reduced writing current density similar to ordinary FM materials. This mechanism is further verified by measuring the temperature and magnetic bias field dependences, where the X-ray magnetic linear dichroism (XMLD) results confirm the AFM switching besides the electrical transport measurement. Our findings demonstrate the exciting possibility of writing operations in AFM-based devices with a lower current density, opening a new pathway towards pure AFM memory applications. Electrical manipulation of antiferromagnetic order is crucial for future memory devices, but existing switching schemes require a large current density. Here, the authors achieve record low current density switching in FeRh by taking advantage of its antiferromagnetic to ferromagnetic phase transition. [ABSTRACT FROM AUTHOR]

Studying the optical properties of photosynthetic pigment–protein complexes (PPCs) in the visible light range, both experimentally and theoretically, is one of the ways of gaining knowledge about the function of the photosynthetic machinery of living species. To simulate the PPC optical response, it is necessary to use semiclassical theories describing the effect of external fields–matter interaction, energy migration in molecular crystals, and electron–phonon coupling. In this paper, we report the results of photosystem II reaction center (PSIIRC) linear optical response simulations. Applying the multimode Brownian oscillator model and the theory of molecular excitons, we have demonstrated that the absorption, circular and linear dichroism, and steady-state fluorescence of PSIIRC can be accurately fitted with the help of differential evolution (DE), the multiparametric evolutionary optimization algorithm. To explore the effectiveness of DE, we used the simulated experimental data as the target functions instead of those actually measured. Only 2 of 10 DE strategies have shown the best performance of the optimization algorithm. With the best tuning parameters of DE/rand-to-best/1/exp strategy determined from the strategy tests, we found the exact solution for the PSIIRC exciton model and fitted the spectra with a reasonable convergence rate. [ABSTRACT FROM AUTHOR]

The mechanical properties of polymeric materials are strongly affected by molecular orientation occurring under processing conditions. Infrared dichroism is particularly well suited for characterizing polymer chain orientation at a molecular level. The usefulness of this technique has been demonstrated through various applications in homopolymers, semi-crystalline polymers, copolymers, polymer blends, as well as in polymer composites. Determination of molecular orientation can be carried out in the mid- and near-infrared ranges and very small dichroic effects can be detected with the use of a photoelastic modulator. Chain orientation in polymer composites is seen to increase with the filler content in the case of a strong interface between the two phases, making possible a quantification of the degree of bonding between the host polymeric matrix and the incorporated inclusions. [ABSTRACT FROM AUTHOR]

α-RuCl3 is a promising candidate material to realize the so far elusive quantum spin liquid ground state. However, at low temperatures, the coexistence of different exchange interactions couple the effective pseudospins into an antiferromagnetically zigzag (ZZ) ordered state. The low-field evolution of spin structure is still a matter of debate and the magnetic anisotropy within the honeycomb planes is an open and challenging question. Here, we investigate the evolution of the ZZ order parameter by second-order magneto-optical effects, the magnetic linear dichroism and magnetic linear birefringence. Our results clarify the presence and nature of metamagnetic transitions in the ZZ phase of α-RuCl3. The experimental observations show the presence of initial magnetic domain repopulation followed by a spin-flop transition for small in-plane applied magnetic fields (≈1.6 T) along specific crystallographic directions. In addition, using a magneto-optical approach, we detected the recently reported emergence of a field-induced intermediate phase before suppressing the ZZ order. The results disclose the details of various angle-dependent in-plane metamagnetic transitions quantifying the bond-anisotropic interactions present in α-RuCl3. [ABSTRACT FROM AUTHOR]

We demonstrate a probe of long-range antiferromagnetic (AF) order in FeRh thin films using non-resonant magnetic x-ray scattering. In particular, x-rays at energies below the Fe K-edge have been used for the observation of magnetic Bragg peaks. Due to the low efficiency of the magnetic scattering, a grazing incidence geometry was used to optimise the diffracted intensity from the thin film samples. Based on Scherrer analysis, we estimate a coherence length similar to previous reports from x-ray magnetic linear dichroism (XMLD) experiments, indicating that domain sizes are limited to 40 nm which is consistent with the grain size. The temperature dependent behaviour of the AF order shows an inverse correlation with the emergence of the ferromagnetic (FM) moment, as expected from the phase diagram. [ABSTRACT FROM AUTHOR]

Breast cancer is a well-known health issue that has been a major focus for healthcare professionals for quite some time. Still, the most common noninvasive diagnostic tool - mammography - results in a high false positive rate along with risks of exposure to radiation. These disadvantages are magnified and become more severe when screenings are done repeatedly. To tackle this problem, we introduce a novel framework for uncomplicated diagnosis of breast cancer. Our method utilizes the analytical technique of Mueller matrix decomposition and Stokes vector polarimetry from a polarized light system consisting of a helium-neon laser (wavelength of 632.5 nm), a quarter-wave plate, polarizers, and a Stokes polarimeter. Thus, this technique introduces no radiation. We extracted nine optical parameters of a breast cancer cell line - BT474 - and determined the relationship and separation power of these parameters to cancerous cells and healthy cells. Specifically, the samples were designed as a two-dimensional cellular model of malignant breast tumours that combined a range of four cell densities - 104, 105, 106, and 107 cells - per an area of 9 cm2. Nine optical parameters - orientation angle of linear birefringence (α), retardance or linear birefringence (β), optical rotation angle or circular birefringence (γ), orientation angle of linear dichroism (θd), linear dichroism (D), circular dichroism (R), degrees of linear depolarization (e1 and e2), and degree of circular depolarization (e3) - were extracted from a total of 40 samples using the polarized light system. The results revealed the positive correlations between three cell densities (104, 105, and 106) and the orientation angle of linear birefringence (R2 = 0.8038), linear birefringence (R2 = 0.8627), and linear dichroism (R2 = 0.9662). Meanwhile, both the orientation angle of linear dichroism and circular dichroism illustrated the negative correlation with that range of cell densities with R2 = 0.9983 and 0.9447, respectively. This proves that the optical parameters measured demonstrate significant association with the cells’ characteristics and thus, the proposed method could pave the way for an accessible diagnosis of breast cancer.

An equivalent circuit model (ECM) using a MATLAB code to analyze a tunable two-layered graphene-based chiral dual-function metamirror, is proposed in this work. The investigated metastructure is composed of complementary U-shaped graphene resonator arrays in the terahertz (THz) region. The ECM analysis could be used for any two-layered chiral metastructure for any frequencies, containing resonators with a thickness less than λ/50. The characteristics of the proposed tunable metamirror were analyzed numerically using the finite element method (FEM) in CST Software to verify the ECM analysis. The proposed metamirror can be used in polarization-sensitive devices in the THz region with simpler biasing without a need for ion gels or similar. It works as a broadband TE and multiband (four bands) TM mirror in the 0.3–4.5 THz bandwidth with a strong linear dichroism (LD) response (up to 96%). The designed mirror is a dynamically tunable, dual-functional structure, requiring only 90° rotation of the incident electromagnetic fields to switch between broadband and multiband spectral behavior making it a promising candidate for future THz intelligent systems. The proposed ECM is in agreement with the FEM results. The ECM analysis provides a simple, fast, and effective way to understand the metamirror's behavior and guides for the design and analysis of graphene-based chiral metastructures in the THz region. [ABSTRACT FROM AUTHOR]

Heusler alloys are theoretically predicted to become half-metals at room temperature (RT). The advantages of using these alloys are good lattice matching with major substrates, high Curie temperature above RT and intermetallic controllability for spin density of states at the Fermi energy level. The alloys are categorised into half- and full-Heusler alloys depending upon the crystalline structures, each being discussed both experimentally and theoretically. Fundamental properties of ferromagnetic Heusler alloys are described. Both structural and magnetic characterisations on an atomic scale are typically carried out in order to prove the half-metallicity at RT. Atomic ordering in the films is directly observed by X-ray diffraction and is also indirectly probed via the temperature dependence of electrical resistivity. Element specific magnetic moments and spin polarisation of the Heusler alloy films are directly measured using X-ray magnetic circular dichroism and Andreev reflection, respectively. By employing these ferromagnetic alloy films in a spintronic device, efficient spin injection into a non-magnetic material and large magnetoresistance are also discussed. Fundamental properties of antiferromagnetic Heusler alloys are then described. Both structural and magnetic characterisations on an atomic scale are shown. Atomic ordering in the Heusler alloy films is indirectly measured by the temperature dependence of electrical resistivity. Antiferromagnetic configurations are directly imaged by X-ray magnetic linear dichroism and polarised neutron reflection. The applications of the antiferromagnetic Heusler alloy films are also explained. The other nonmagnetic Heusler alloys are listed. A brief summary is provided at the end of this review. [ABSTRACT FROM AUTHOR]

Lengenbachite is a naturally occurring layered mineral formed with alternating stacks of two constituent PbS-like and M2S3-like two-dimensional (2D) material layers due to the phase segregation process during the formation. Here, we demonstrate to achieve van der Waals (vdW) heterostructures of lengenbachite down to a few layer-pair thickness by mechanical exfoliation of bulk lengenbachite mineral. The incommensurability between the constituent isotropic 2D material layers makes the formed vdW heterostructure exhibit strong in-plane structural anisotropy, which leads to highly anisotropic optical responses in lengenbachite thin flakes, including anisotropic Raman scattering, linear dichroism, and anisotropic third-harmonic generation. Moreover, we exploit the nonlinear optical anisotropy for polarization-dependent intensity modulation of the converted third-harmonic optical vortices. Our study establishes lengenbachite as a new natural vdW heterostructure-based 2D material with unique optical properties for realizing anisotropic optical devices for photonic integrated circuits and optical information processing. [ABSTRACT FROM AUTHOR]

The momentum-dependent orbital character in crystalline solids, referred to as orbital texture, is of capital importance in the emergence of symmetry-broken collective phases, such as charge density waves as well as superconducting and topological states of matter. By performing extreme ultraviolet multidimensional angle-resolved photoemission spectroscopy for two different crystal orientations linked to each other by mirror symmetry, we isolate and identify the role of orbital texture in photoemission from the transition metal dichalcogenide 1T-TiTe2. By comparing our experimental results with theoretical calculations based on both a quantitative one-step model of photoemission and an intuitive tight-binding model, we unambiguously demonstrate the link between the momentum-dependent orbital orientation and the emergence of strong intrinsic linear dichroism in the photoelectron angular distributions. Our results represent an important step towards going beyond band structure (eigenvalues) mapping and learning about electronic wavefunction and orbital texture of solids by exploiting matrix element effects in photoemission spectroscopy. [ABSTRACT FROM AUTHOR]