Optical Birefringence Research Articles

Resonantly Enhanced Optical Birefringence in Ultrathin High‐Index WS2 Metasurfaces

AbstractOptical birefringence plays an important role in the manipulation of polarization states of light. However, the weak birefringence in common birefringent materials restricts the device thickness to tens of microns for desired phase retardation. Although recent advances in dielectric metasurfaces have enabled remarkable birefringence using structurally anisotropic nanostructures, the refractive index contrast between the dielectric and the air cladding fundamentally limits the thickness of metasurfaces to a fraction of a micron to obtain the required phase retardation. Here, birefringent resonances in high‐index tungsten disulfide (WS2) metasurfaces are utilized to push the thickness limit down to the deep subwavelength scale. The inherent high‐index property of WS2 enables birefringent resonances in WS2 metasurfaces which consist of anisotropic nanostructures with a thickness of only 50 nm. Such birefringent resonances enhance the light‐matter interaction and produce an unprecedented birefringence (Δneff) about 4. As a result, it is experimentally realized that circular‐to‐linear polarization conversion with a normalized efficiency of ≈90% within an incident angle range up to ±10°. The results break the fundamental limit of birefringent devices and provide strategies for creating ultimate thin polarization optical devices.

Characterization of single-crystal phenothiazine synthesized using the vertical Bridgman method

Abstract A bulk organic single crystal of phenothiazine measuring 65 mm in length and 10 mm in width was grown using the single zone vertical Bridgman technique (VBT), which was visible to the naked eye. Powder X-ray diffraction, also known as XRD, was used in order to perform crystal structural verification on the manufactured crystal. The Fourier transform infrared spectroscopy (FT-IR) approach was used in order to ascertain the crystals’ respective vibrational frequencies. In order to evaluate the single crystal’s crystalline perfection and optical quality, high-resolution X-ray diffraction rocking curve measurement (HRXRD) and UV transmittance spectrum analysis were used. So as to investigate the nonlinear optical (NLO) activity of the generated single crystals, a Q-switched and pulsed Nd: YAG laser was used in the research. This led to the discovery of the SHG efficiency. The single crystal’s mechanical strength was evaluated using Vicker’s microhardness measurement, which provided an approximation of the true value. Furthermore, the single crystal was examined and reported for its optical birefringence, photoluminescence, and refractive index.

Synthesis, chiral separation and physical properties of the cinnamic acid derivatives exhibiting short-pitch cholesteric and TGB phases

ABSTRACT Two new photosensitive chiral liquid crystalline materials derived from cinnamic acid were synthesised in (R) and (S) enantiomer forms. The materials were characterised by NMR spectroscopy, purified by preparative liquid chromatography, and the chemical purity of the final products was determined by high performance liquid chromatography (HPLC). High optical purity was reached for all enantiomers. The enantiomer elution order was confirmed by the analysis of non-racemic (R) and (S) mixed samples. The cinnamic acid derivatives are capable of undergoing photoisomerisation. Sample irradiation was performed to realise E-Z isomerisation and investigate its effect on the enantioseparation. The conditions of the enantioselective HPLC method were optimised to achieve a baseline separation for all studied materials both before and after irradiation by the UV light. The mesogenic properties of the studied enantiomers and their racemic mixtures were obtained from differential scanning calorimetry measurements, optical textures observed under the polarising light microscope and X-ray diffraction measurements. Cholesteric and TGB phases have been found for the enantiomers and, analogously, nematic and smectic phases have been confirmed for their racemates. The temperature dependence of the optical birefringence has been studied for the racemates in the temperature range of the mesophases.

Tunable and responsive photonic bio‐inspired materials and their applications

AbstractBio‐enabled and bio‐mimetic nanomaterials represent functional materials, which use bio‐derived materials and synthetic components to bring the better of two, natural and synthetic, worlds. Prospective broad applications are flexibility and mechanical strength of lightweight structures, adaptive photonic functions and chiroptical activity, ambient processing and sustainability, and potential scalability along with broad sensing/communication abilities. Here, we summarize recent results on relevant functional photonic materials with responsive behavior under mechanical stresses, magnetic field, and changing chemical environment. We focus on recent achievements and trends in tuning optical materials' properties such as light scattering, absorption and reflection, light emission, structural colors, optical birefringence, linear and circular polarization for prospective applications in biosensing, optical communication, optical encoding, fast actuation, biomedical fields, and tunable optical appearance.

Orientational Order Parameter Undecyloxy-Cyanobiphenyl (11OCB) and DodecyloxyCyanobiphenyl (12OCB) by using Optical Birefringence Method

High resolution optical birefringence studies throughout the nematic and smectic A phases of undecyloxy-cyanobiphenyl (11OCB) and dodecyloxy-cyanobiphenyl (12OCB) have been performed to evaluate orientational order parameter (<P2>) as a function of temperature at wavelength λ=632.8 nm. The temperature dependence of the birefringence (n) data have been exploited to assess <P2> using a well-known Haller’s extrapolation method. Effectively, in the nematic and smectic A phases the values of <P2> have been fitted with the estimated values from Maier-Saupe mean field theory for nematic liquid crystals and McMillan mean field theory for smectic liquid crystals. Experimentally obtained <P2> values have been compared with those achieved from Maier-Saupe mean field theory and McMillan mean field theory. The agreement between experimental and calculated <P2> values at nematic-isotropic (N-I) is much higher than experimental <P2> values.

Chiral amino acid-templated tin fluorides tailoring nonlinear optical properties, birefringence, and photoluminescence.

In this study, we successfully synthesized two types of new chiral amino acid-templated tin fluoride crystals: (R)-[(C8H10NO3)2]Sn(IV)F6, (S)-[(C8H10NO3)2]Sn(IV)F6, (R)-[C8H10NO3]Sn(II)F3, and (S)-[C8H10NO3]Sn(II)F3, employing a slow evaporation method. The crystal structures of Sn(IV)-compounds were determined to belong to the noncentrosymmetric (NCS) nonpolar space group, P21212. Conversely, the structures of Sn(II)-compounds were found to crystallize in the NCS polar space group, P21, as revealed by single-crystal X-ray diffraction analysis. Remarkably, Sn(IV)-compounds exhibited a larger birefringence (0.328@546.1 nm), attributed to the well-stacked arrangement of planar π-conjugated benzene rings along the b-axis. The ability of tin(IV) fluorides to form more hydrogen bonds with ligands increased the probability of π-π interactions between benzene rings, enabling the growth of centimeter-sized crystals in Sn(IV)-compounds. In contrast, Sn(II)-compounds displayed a stronger second-harmonic generation (SHG) response (0.85 × KDP) than Sn(IV)-compounds (0.46 × KDP). This enhanced SHG response in Sn(II)-compounds was attributed to the increased dipole moments resulting from the presence of lone pairs. Additionally, Sn(II)-compounds exhibited photoluminescent properties due to the transition from the metal-to-ligand charge transfer state, facilitated by the presence of the lone pairs.

Plasmonically-boosted exciton-photon coupling strength in a near-infrared LED based on a ZnO:Ga microwire/GaAs heterojunction with surface-coated Au&Ag alloy nanorods.

The development of electrically-driven low-dimensional coherent light sources via highly-polarized polariton emission behavior has been extensively researched, but suffers from limited modulation of the exciton-photon coupling strengths. Herein, an electrically-biased near-infrared exciton-polariton light-emitting diode (LED), which includes a Ga-doped ZnO microwire (ZnO:Ga MW) and p-type GaAs substrate, is demonstrated. The well-designed LED structure is conducive to producing strong coupling between excitons and cavity photons, thus yielding highly-polarized light-emissions due to the optical birefringence in the ZnO:Ga MW microcavity. In particular, when the LED device is modified using Au&Ag alloy nanorods (AuAgNRs) with desired plasmonic properties, the electroluminescence (EL) performance is significantly boosted, especially the Rabi-splitting energy, which increases from 96 to 285 meV. The current-injection exciton-polariton emission from the LED undergoing a strong coupling regime is confirmed through angle-resolved EL measurements. This study exhibits a performance-boosted near-infrared exciton-polariton LED at room temperature, which provides a new scheme toward the realization of highly energy-efficient polariton coherent light sources. Further, the significantly lower density of polariton states induced by the incorporated metal nanostructures highlights a bright future of realizing ultralow-threshold polariton lasers much more feasibly, in comparison to conventional lasers based on narrow bandgap semiconductors.

Structural polymorphism, electronic, and optical properties of NaSbS2: A computational approach toward eco-friendly and emerging semiconductor

In this work, the structural polymorphism and electro-optical characteristics of NaSbS2 ternary chalcogenide are realized using density functional theory (DFT). All of the NaSbS2 polymorphs are energetically stable based on the formation energy. The optimized lattice parameters of the monoclinic and triclinic structures and direct electronic bandgap (1.695 eV) of monoclinic structure are consistent with previous studies. Besides, the trigonal and triclinic structures are indirect bandgap (0.916 and 2.015 eV) semiconductors observed from electronic band structure. The higher degree of ionicity between Na and S atoms while strong covalency in the Sb-S bonds are confirmed from the charge and bond analysis. The lower value of electron-hole effective masses indicates higher carrier mobility leading to outstanding electrical conductivity. It was suggested that the polymorphs would be extremely desired to design Bragg reflectors and waveguides based on the reported high value of the real part of the dielectric constant and refractive index. These polymorphs will contribute significantly to being used as absorbers, as evidenced by their high absorption coefficient and photoconductivity and lower transmittance. All the polymorphs reflect significant optical anisotropy and birefringence, rendering them excellent for usage in the fabrication of waveguides, polarizers, and photonic devices. Thus, the projected good features of NaSbS2 polymorphs would play an essential role in the development of lead-free photovoltaic devices, including solar cells and other optoelectronic devices, and would be able to provide practical information for future theoretical and experimental studies.

Multiscale label-free imaging of myelin in human brain tissue with polarization-sensitive optical coherence tomography and birefringence microscopy.

The combination of polarization-sensitive optical coherence tomography (PS-OCT) and birefringence microscopy (BRM) enables multiscale assessment of myelinated axons in postmortem brain tissue, and these tools are promising for the study of brain connectivity and organization. We demonstrate label-free imaging of myelin structure across the mesoscopic and microscopic spatial scales by performing serial-sectioning PS-OCT of a block of human brain tissue and periodically sampling thin sections for high-resolution imaging with BRM. In co-registered birefringence parameter maps, we observe good correspondence and demonstrate that BRM enables detailed validation of myelin (hence, axonal) organization, thus complementing the volumetric information content of PS-OCT.

Tailored Synthesis of Two Metal Borates KSrM3B2O9 (M = Al and Ga) Exhibiting Wide Ultraviolet Transparency.

Borate materials continue to command considerable attention due to their remarkable capacity for applications in deep ultraviolet (UV) wavelengths. Herein, two new metal borates KSrM3B2O9 (M = Al and Ga) were extracted via the application of flux techniques. These two crystals adopt a centrosymmetric space group P21/c (no. 14), showcasing a layered structural configuration composed of isolated [BO3] plane triangles and [AlO4]/[GaO4] tetrahedra. Thermal analysis revealed that KSrM3B2O9 (M = Al and Ga) exhibits an incongruent nature and possesses good thermal stability up to 1083 and 983 °C, respectively. Notably, these compounds display a short UV-transmission cutoff edge, approximately around 194 and 200 nm, accompanied by band gaps of 5.47 and 4.83 eV, respectively. Furthermore, KSrM3B2O9 (M = Al and Ga) demonstrates a moderate optical birefringence of 0.026 and 0.025, respectively. Additionally, first-principles calculations were employed to shed light on the intricate interplay between the structure and properties of these compounds.

Emission characteristics, crystalline phase and composition of Er3+/Yb3+ doped LiNbO3 thin films deposited by e-beam evaporation

Er3+/Yb3+ doped LiNbO3 (LN) single crystal films with varying Yb3+ doping level were grown on z-cut LiTaO3 bulk single crystals via using e-beam evaporation method. The crystallographic orientation, elemental distribution, fluorescence properties, ionic valence states, Er3+ concentration, Yb3+ concentration and Li2O content of films were carefully studied. Results from XRD, SEM and Raman scattering conclude that the predominant phase of these films is LN and they are oriented along (006). The results of energy dispersive spectroscopy indicate that constituent elements are uniformly distributed over the entirety of the films. The visible and near-infrared luminescence intensities rise with increasing Yb3+-doping concentration. The Li2O content of films remains constant at 48.8 mol% with growing Yb3+-doping level based on the optical birefringence method, which is consistent with the Raman results. XPS results suggest that the Er3+ and Yb3+ concentrations in the films are lower than that in the polycrystalline powder since e-beam evaporation has a low efficiency of heavy Er3+ and Yb3+ ions.

Theoretical and experimental investigations in thermo-mechanical properties of fused silica with pulsed CO2 laser ablation.

Laser ablation is widely used as a flexible and non-contact processing technology for the fabrication of fused silica. However, the introduction of thermal stress inevitably leads to crack growth and reduces the lifetime of fused silica. Due to the complicated coupling interaction and properties of fused silica, the unclear thermal stress formation is the bottleneck restricting further development of laser ablation. In this article, a three-dimensional multi-physics thermo-mechanical model was developed to reveal the evolution mechanism, and experiments were performed to validate the simulated results. The surface morphology evolution was elaborated during process cycles, with recoil pressure identified as the key factor in determining surface morphology. Moreover, thermal stress was quantified utilizing optical retardance and stress birefringence, effectively distinguishing between non-thermal and thermal stress induced by laser ablation. The theoretical simulations fit well with experimental measurements. Meanwhile, stress distribution and evolution behaviors were revealed under different processing parameters by this model. This work not only contributes to a profound understanding of the laser ablation process but also establishes a theoretical foundation for achieving high surface quality and non-thermal stress laser ablation.

On the critical behaviour of the N-SmA phase transition in an induced system: an exploration from high-resolution calorimetric and optical studies

ABSTRACT A systematic study of a binary system composed of 4-n-pentyl 4′-cyanobiphenyl (5CB) and 4-n-pentyl phenyl 4-n′-hexyloxy benzoate (ME6O.5) mesogens showing an induced smectic A at different molar concentrations has been done. Heat capacity and optical birefringence measurements have been performed around the N-SmA phase transition region. The heat capacity peaks could be fitted well below the N-SmA transition by means of an extended Landau mean-field model. The first-order nature of the transition throughout the composition range can be inferred. This transition is rather close to the tricritical point when the nematic range is sufficiently increased. The latent heat decreases with the increase in the nematic range. For large nematic range, the latent heat drops to zero and the heat capacity peak associated with N-SmA phase transition disappear, contrary to previously reported most of the usual N-SmA phase transition. Precision birefringence measurements also agree well with the heat capacity data.

A new nonlinear optical crystal Li0.81Ag0.19InSe2 with balanced properties for efficient nonlinear conversion in the mid-IR region

The achievement of balanced properties among nonlinear optical (NLO) effect, laser induced damage threshold (LIDT) and optical birefringence is the key to obtain the excellent NLO crystals for harmonic mid-IR coherent radiation generation. In this work, we successfully synthesize and grow a new NLO chalcogenide crystal Li0.81Ag0.19InSe2 by utilizing a molecular design strategy with rational replacement between Li and Ag. This crystal not only enlarges the very low birefringence in AgInSe2 from ∼ 0.017 to ∼ 0.047, but also improves the rather small NLO effect in LiInSe2 from 11.8 pm/V to ∼26 pm/V while maintaining the LIDT almost unchanged. Based on the large size Li0.81Ag0.19InSe2 single crystals of optical quality, the spectroscopic properties are measured and the main parameters important for NLO output are determined. All these results demonstrate that Li0.81Ag0.19InSe2 is a promising mid-IR NLO crystal with balanced properties.

Multimodal fluorescence microscope with fast adaptive polarimetry

Polarized light microscopy is a widely used technique to observe specimens that are optically anisotropic, or birefringent. It has a broad applicability in the study of minerals, soft materials such as polymers, complex fluids or liquid crystals, and organic tissues in biology and medicine. Most of these observations are qualitative in nature, as it is not obvious to quantify the spatial distribution of optical anisotropy of specimens. Moreover, existing commercial implementations for quantitative polarimetry are costly and slow in nature, precluding real time observation of dynamical processes. Here, we present a custom-made implementation of an optical microscope for quantitative polarimetry at the cost of a standard scientific polarizing microscope. The instrument allows to extract the local optical axis and birefringence of transparent materials with a frequency of several Hz. The instrument is built using off-the-shelf optomechanical components, which optimizes cost, availability, and modularity. An example of the latter is the fact that we combine the polarimetry measurements with simultaneous fluorescence microscopy, which results in a powerful multimodal instrument with broad potential applications.

Effect of CdSe/ZnS quantum dot dispersion on phase transitional behavior of 8OCB liquid crystal.

We report the effect on the phase transitional behavior of 8OCB liquid crystal (LC) doped with functionalized CdSe/ZnS quantum dots (QDs) in different concentrations. The temperature-dependent data of high-resolution optical birefringence and dielectric anisotropy are utilized to characterize the critical anomaly for both the isotropic-to-nematic (I-N) and nematic-to-smectic-A (N-SmA) phase transitions. The obtained results reveal that the order parameter exponent (β) for the pure LC is found to be β=0.249 and does not vary upon the inclusion of QDs in the pure matrix. It describes the weakly first-order characteristic of the I-N phase transition for all the studied samples, which falls within the limit of the tricritical hypothesis. Conversely, depending on the range of the N phase, we observed a nonuniversal nature of the specific heat capacity critical exponent (α^{'}) linked with the N-SmA phase transition for all the studied samples. A relative comparison was made amongst the α^{'} values extracted from both the anisotropy data, and further, a theoretical relationship is established with these exponent values. The coupling strength among the N and SmA order parameters is determined using the optical birefringence data and discussed from the perspective of mutual interaction between the LC-QDs ligands. The results signify that a strong ligand-ligand interaction between neighboring QDs effectively reduces the N range and slightly influences the N-SmA phase transition.

Arising of magnetically induced optical birefringence in ionic liquid/dielectric systems: The case of diphenyl phosphate / bis(2-ethyl hexyl) amine

Addition of diphenyl phosphate (DPP) to bis(2-ethylhexyl) amine (BEEA) causes the proton transfer from the acidic DPP to the basic BEEA with formation of ionic liquid DPP/BEEA domains. Such mixtures show significant optical birefringence if subjected to a magnetic field. When DPP amount is increased, as highlighted by molar refraction and viscosity measurements, a structural change occurs, most probably due to the percolation of the DPP/BEEA domains. Despite of this, the intensity of the magnetically-induced birefringence monotonically depends on the amount of DPP, with no peak at any specific composition. In addition, the birefringence appears immediately after the magnetic field is switched on and immediately disappears after the magnetic field is switched off, with a reversible and reproducible on/off switching. All this suggests that this property needs to be intended as deriving from a local anisotropy, not implying big supra-molecular rearrangements. Although there is effective modelling of the induced birefringence in well-defined molecular aggregates, there is not yet a theoretical description of the phenomenon shown by the nanoheterogeneities of surfactant-based liquid mixtures. So, our findings open new ways for the comprehension of the dynamics in these liquids.

Elastocaloric signatures of symmetric and antisymmetric strain-tuning of quadrupolar and magnetic phases in DyB2C2

The adiabatic elastocaloric effect measures the temperature change of a given system with strain and provides a thermodynamic probe of the entropic landscape in the temperature-strain space. Here, we demonstrate that the DC bias strain-dependence of AC elastocaloric effect allows decomposition of the latter into symmetric (rotation-symmetry-preserving) and antisymmetric (rotation-symmetry-breaking) strain channels, using a tetragonal [Formula: see text]-electron intermetallic DyB[Formula: see text]C[Formula: see text]-whose antiferroquadrupolar order breaks local fourfold rotational symmetries while globally remaining tetragonal-as a showcase example. We capture the strain evolution of its quadrupolar and magnetic phase transitions using both singularities in the elastocaloric coefficient and its jumps at the transitions, and the latter we show follows a modified Ehrenfest relation. We find that antisymmetric strain couples to the underlying order parameter in a biquadratic (linear-quadratic) manner in the antiferroquadrupolar (canted antiferromagnetic) phase, which are attributed to a preserved (broken) global tetragonal symmetry, respectively. The broken tetragonal symmetry in the magnetic phase is further evidenced by elastocaloric strain-hysteresis and optical birefringence. Additionally, within the staggered quadrupolar order, the observed elastocaloric response reflects a quadratic increase of entropy with antisymmetric strain, analogous to the role magnetic field plays for Ising antiferromagnetic orders by promoting pseudospin flips. Our results demonstrate AC elastocaloric effect as a compact and incisive thermodynamic probe into the coupling between electronic degrees of freedom and strain in free energy, which holds the potential for investigating and understanding the symmetry of a wide variety of ordered phases in broader classes of quantum materials.

Identification of subject-specific fibrillar disposition in healthy rabbit cornea through birefringence analysis

The cornea is an essential component in ocular biomechanics. The modifications in the collagen microstructure of the cornea affect its biomechanical behavior in various ocular conditions. Birefringence is an indicator of the microstructural changes in the cornea. The characterization of birefringence can benefit the patient-specific assessment of disease and surgically driven effects. According to the existing literature, optical birefringence of the cornea is best described as of biaxial nature. However, the biaxial model does not concur with the varying degree of birefringence observed amongst individuals. Using digital photoelasticity, the present study explores the applicability of birefringence of the healthy rabbit cornea as a benchmark model for human cornea. Eight freshly excised healthy rabbit corneas are imaged using the polariscope in the transmission mode. A fringe analysis is performed for each configuration of the polariscope to discern the collagen fiber distribution in the cornea. The birefringence of the rabbit corneas showed inter-corneal variability with varying degrees of biaxiality like the human corneas. Based on the fringe analysis, the fiber families in the cornea were identified in the form of geometric patterns distributed over the corneal surface and incorporated in the finite element model of the cornea. The present study envisages the utilization of birefringence-derived structural information to develop a reliable treatment design based on microstructural features of the cornea.

Optical birefringence measurements of antiferromagnets with Ising spin chains

Optical birefringence measurements were performed on Ising-spin antiferromagnets with the chemical formula ACo[Formula: see text]. The temperature dependences of the birefringences of CsCoCl3 and CsCoBr3 reflect the thermal shrinkage of the crystal lattice and the development of magnetic short-range correlation in Ising spin chains. Moreover, the temperature dependences of the birefringences of RbCoBr3 and TlCoCl3 show marked anomalies at structural phase transition points. We demonstrate a method of numerically analyzing the birefringence in magnetic compounds that undergo structural phase transitions.