Polarization Orientation Research Articles

First Sagittarius A* Event Horizon Telescope Results. VII. Polarization of the Ring

The Event Horizon Telescope observed the horizon-scale synchrotron emission region around the Galactic center supermassive black hole, Sagittarius A* (Sgr A*), in 2017. These observations revealed a bright, thick ring morphology with a diameter of 51.8 ± 2.3 μas and modest azimuthal brightness asymmetry, consistent with the expected appearance of a black hole with mass M ≈ 4 × 106 M ⊙. From these observations, we present the first resolved linear and circular polarimetric images of Sgr A*. The linear polarization images demonstrate that the emission ring is highly polarized, exhibiting a prominent spiral electric vector polarization angle pattern with a peak fractional polarization of ∼40% in the western portion of the ring. The circular polarization images feature a modestly (∼5%–10%) polarized dipole structure along the emission ring, with negative circular polarization in the western region and positive circular polarization in the eastern region, although our methods exhibit stronger disagreement than for linear polarization. We analyze the data using multiple independent imaging and modeling methods, each of which is validated using a standardized suite of synthetic data sets. While the detailed spatial distribution of the linear polarization along the ring remains uncertain owing to the intrinsic variability of the source, the spiraling polarization structure is robust to methodological choices. The degree and orientation of the linear polarization provide stringent constraints for the black hole and its surrounding magnetic fields, which we discuss in an accompanying publication.

An Improved Bio-Orientation Method Based on Direct Sunlight Compensation for Imaging Polarization Sensor.

Direct sunlight in complex environmental conditions severely interferes with the light intensity response for imaging Polarization Sensor (PS), leading to a reduction in polarization orientation accuracy. Addressing this issue, this article analyzes the impact mechanism of direct sunlight on polarization sensor detection in a complex environment. The direct sunlight interference factor is introduced into the intensity response model of imaging polarization detection, enhancing the accuracy of the polarization detection model. Furthermore, a polarization state information analytical solution model based on direct sunlight compensation is constructed to improve the accuracy and real-time performance of the polarization state information solution. On this basis, an improved bio-orientation method based on direct sunlight compensation for imaging polarization sensor is proposed. The outdoor dynamic reorientation experiment platform is established to validate the effectiveness of the proposed method. Compared with the traditional methods, the experimental results demonstrate a 23% to 47% improvement in the polarization orientation accuracy under various solar zenith angles.

Constructing Dynamic Anode/Electrolyte Interfaces Coupled with Regulated Solvation Structures for Long-Term and Highly Reversible Zinc Metal Anodes.

Aqueous zinc ion batteries (AZIBs) show a great potential for next-generation energy storage due to their high safety and high energy density. However, the severe side reactions of zinc negative electrode largely hinder the further application of AZIBs. Herein, trace tris(hydroxymethyl)aminomethane (Tris) additive with rich lone-pair-electrons and zincophilic sites is firstly introduced to achieve long-term and highly reversible Zn plating/stripping. Specifically, Tris not only regulates the solvation structure of Zn2+, but is also adsorbed vertically on the Zn anode surface with a changed coordination intensity during the plating/stripping process of Zn to generate an in situ dynamic adsorption layer for the first time. The dynamic adsorption layer could successively attract the solvated Zn2+ and then promote the de-solvation of the solvated Zn2+ owing to the orientation polarization with regularly-changed applied electric field, the volume rejection effect, and strong intermolecular force towards H2O of the vertically-adsorbed Tris. Therefore, an improved Zn2+-transport kinetics as well as the inhibition of side reactions of Zn anode are successfully realized. Accordingly, the Zn||Zn symmetric cell provides an ultra-long cycle life of 2600 h. Furthermore, the Zn||MnO2 full cell with Tris could demonstrate a high capacity and structural stability for practical applications.

Longitudinal attenuation in political polarization: Evidence from COVID-19 vaccination adherence in Brazil

BackgroundWhile political polarization in policy opinions, preferences, and observance is well established, little is known about whether and how such divisions evolve, and possibly attenuate, over time. Using the COVID-19 pandemic in Brazil as the backdrop, we examine the longitudinal evolution of a highly relevant and polarizing policy: adherence to the COVID-19 vaccination. MethodsStudies 1 (N = 3346) and 2 (N = 10,214) use nationwide surveys to document initial differences and subsequent changes in vaccination adherence between conservatives ("Bolsonaristas") and non-conservatives ("non-Bolsonaristas"). Study 3 (N = 742) uses an original dataset to investigate belief changes among conservatives and their association with asymmetric changes in vaccination adherence. ResultsDespite substantial differences at the early stages of rollout, the gap in vaccination adherence between conservatives and non-conservatives significantly decreased with the passage of time, driven essentially by a much faster uptake among the initially most skeptic—the conservatives. Study 3 demonstrates that the asymmetric changes in vaccination adherence were associated with meaningful belief changes among the conservatives, especially about the perceived effectiveness of the COVID-19 vaccines and the expected adherence of peers to the vaccination campaign. ConclusionsTogether, these studies show that, in a context where the superiority of the promoted policy becomes clear over time and individuals have the opportunity to revisit prior beliefs, even intense political polarization can be attenuated.

Terahertz sum-frequency excitation of coherent optical phonons in the two-dimensional semiconductor WSe2

Driving fundamental excitations via strong light fields is one of the most important issues in solid state physics, which opens up new avenues to control material properties. Two-dimensional materials are fruitful platforms for future semiconductor applications, including opto-electronic and phononic devices, yet the phonon dynamics and nonlinear phonon–phonon coupling remain under-explored. Here, we demonstrate coherent phonon excitation in thin films of the layered two-dimensional semiconductor WSe2 induced by intense and broadband ultrafast terahertz (THz) pulses. We performed THz Kerr effect spectroscopy and observed coherent phonon oscillations assigned to the E2g optical phonon mode. The phonon amplitude displays a quadratic THz field strength dependence, indicating a sum-frequency THz excitation process. Furthermore, pump–probe polarization and crystal orientation relationships, supported by symmetry analysis of the nonlinear susceptibility and Raman tensors, provide helpful insight into nonlinear phonon–phonon interactions and potential coherent control schemes for the manipulation of phonon polarization and material properties in WSe2.

Dual-shot approach for polarization retrieval through a scattering medium

A dual-shot technique based on the field basis addition of two statistically independent speckle patterns is developed to recover an input polarization through a scattering layer. It is proposed theoretically, and demonstrated both numerically and experimentally that by tuning the linear polarization orientation of the reference speckle pattern to 0° and 45° w.r.t. the x-axis, polarization retrieval of an object beam through a scattering layer can be achieved by measuring the degree of polarization of the superposed speckle pattern. The proposed technique can have a wide range of applications in polarization sensing and biomedical imaging.

PVDF/PI/BT nanocomposites with excellent charge/discharge efficiency obtained by inserting linear polymer to adjust the ferroelectricity

The problem of low charge/discharge efficiency of ceramic/polymer composites is still one of the hot topics in current research on dielectric materials. Here, we demonstrate that the ferroelectric property of ceramic/PVDF-based composites can be modulated by the introduction of linear polymer PI and the use of a spin-coating process. PI inhibits some polarization and partial dipole orientation by interacting with the molecular chains of the amorphous phase of PVDF and BT nanoparticles. As a result, the decrease in crystallinity and loss led to improved dielectric properties and charge/discharge efficiency. The findings demonstrate that the microstructure of PVDF-PI/BT nanocomposite is uniform and dense, with outstanding dielectric characteristics and high charge/discharge efficiency. The permittivities were stabilized in the range of 12.87–17.86 at 100 Hz, and the dielectric losses were all less than 0.27. Compared with the previously reported binary ceramic/polymer composites, the PVDF-PI/BT nanocomposites possessed a high charge/discharge efficiency with a small variation (63%-84%). This work offers an easy and efficient scheme to obtain nanocomposites with outstanding dielectric characteristics and charge/discharge efficiency. It may be a potential candidate for flexible dielectric substrates for advanced flexible capacitive energy storage devices.

Influence of interface on the domain polarization orientation in ferroelectric Hf0.5Zr0·5O2 thin films

Ferroelectric HfO2-based materials have attracted extensive attention in the research of next-generation nonvolatile memories and logic devices due to their superior scaling properties and compatibility with the CMOS process. However, forming the ferroelectric metastable phase in the thin films of a few nanometers requires clamping of the top and bottom electrodes. As a result, the interface can significantly impact domain structure and polarization, leading to imprinting effects and non-uniform space charge distribution. Here, we have demonstrated how the interface affects the ferroelectric polarization in Hf0.5Zr0·5O2 (HZO) thin films produced by ALD and the physical mechanisms behind it. We found that by regulating the quantity of oxygen vacancy content at the top and bottom interfaces of TiN/HZO/TiN ferroelectric capacitors, it is possible to achieve inversion of polarization orientation. By using a spherical aberration-corrected transmission electron microscope and first-principles calculation, we identified that the internal electric field generated by the accumulation of oxygen vacancies at an interface and the asymmetrical electrostatic energy of the interfacial T-phase layer jointly play a role in the ferroelectric polarization orientation. Our results will significantly help the interface engineering of HfO2-based ferroelectric thin films and devices.

Particle motion polarization of offshore fish vocalizations, boat noise, and ambient soundscapes

Acoustic particle motion is an important acoustic cue for fish and aquatic invertebrate hearing. When reported for bioacoustics applications, it is often described as a magnitude only. However, particle motion is a vector quantity with polarization information (including directionality) relevant to detection and localization of sound cues by fishes and invertebrates. This study applied established metrics of particle motion polarization including ellipse amplitude, angle, orientation, and degree of polarization, to compare sounds of fish vocalizations with that of boat and ambient sounds at a 900 m-deep site (in the Atlantic Deepwater Ecosystem Observatory Network) offshore of Florida. Polarization metrics were computed for bivariate signals in the plane formed by the horizontal source-receiver and vertical axes. Boat sound polarization was quantified at multiple distances from the closest point of approach. Fish and boat sounds had narrower particle motion ellipses and larger amplitudes in the horizontal compared to ambient sounds that were more circular with larger relative vertical amplitudes. Fish and boat sounds were often strongly polarized, which may allow spatial release from masking given sufficient angular separation of sounds. This analysis framework has promising applications for monitoring in situ directionality of fish and other animal vocalizations and for modelling directional masking.

Dust Polarization of Prestellar and Protostellar Sources in OMC-3

We present the Atacama Large Millimeter/submillimeter Array observations of linearly polarized 1.1 mm continuum emission at ∼0.″14 (55 au) resolution and CO (J = 2−1) emission at ∼1.″5 (590 au) resolution toward one prestellar (MMS 4), four Class 0 (MMS 1, MMS 3, MMS 5, and MMS 6), one Class I (MMS 7), and one flat-spectrum (MMS 2) sources in the Orion Molecular Cloud 3 region. The dust disk-like structures and clear CO outflows are detected toward all sources except for MMS 4. The diameters of these disk-like structures, ranging from 16 to 97 au, are estimated based on the deconvolved full width half maximum (FWHM) values obtained from the multi-Gaussian fitting. Polarized emissions are detected toward MMS 2, MMS 5, MMS 6, and MMS 7, while no polarized emission is detected toward MMS 1, MMS 3, and MMS 4. MMS 2, MMS 5, and MMS 7 show organized polarization vectors aligned with the minor axes of the disk-like structures, with mean polarization fractions ranging from 0.6% to 1.2%. The strongest millimeter source, MMS 6, exhibits complex polarization orientations and a remarkably high polarization fraction of ∼10% around the Stokes I peak, and 15%–20% on the arm-like structure, as reported by Takahashi et al. (2019). The origins of the polarized emission, such as self-scattering and dust alignment due to the magnetic field or radiative torque, are discussed for individual sources. Some disk-like sources exhibit a polarized intensity peak shift toward the nearside of the disk, which supports that the polarized emission originates from self-scattering.

Inversion of Forest above Ground Biomass in Mountainous Region Based on PolSAR Data after Terrain Correction: A Case Study from Saihanba, China

Accurate retrieval of forest above ground biomass (AGB) based on full-polarization synthetic aperture radar (PolSAR) data is still challenging for complex surface regions with fluctuating terrain. In this study, the three-step process of radiometric terrain correction (RTC), which includes polarization orientation angle correction (POAC), effective scattering area correction (ESAC), and angular variation effect correction (AVEC), is adopted as the technical framework. In the ESAC stage, a normalized correction factor is introduced based on local incidence angle and radar incidence angle to achieve accurate correction of PolSAR data information and improve the inversion accuracy of forest AGB. In order to verify the validity and robustness of this research method, the full-polarization SAR data of ALOS-2 and the ground measured AGB data collected in the Saihanba research area in 2020 were used for experiments. Our findings revealed that in the ESAC phase, the introduction of the normalized correction factor can effectively eliminate the ESA phenomenon and improve the correlation coefficients of the backscatter coefficient and AGB. Taking the data of 25 July 2020 as an example, ESAC increases the correlation coefficients between AGB and the backscattering coefficients of HH, HV, and VV polarization channels by 0.343, 0.296, and 0.382, respectively. In addition, the RTC process has strong robustness in different AGB statistical models and different date PolSAR data.

Exploration of structural and dielectric properties of orthorhombic Ta2O5 nanoplatelets towards the potential optoelectronic devices

The dielectric characteristics of tantalum pentoxide (Ta2O5) nanostructures, synthesized by hydrothermal process, have been investigated in the temperature range of 80 K to 400 K and frequency range of 20 Hz to 2 MHz. X-ray diffraction (XRD) confirms the formation of highly crystalline and orthorhombic phase of the nanostructures sintered at 950 ºC. The electron microscope images reveal that the synthesized nanostructures change their morphology to nanoplatelets upon increasing the sintering temperature. Further, UV–visible absorbance, FTIR and Raman spectra of the synthesized nanostructures were obtained to investigate their optical properties. The experimentally obtained dielectric results indicate that both the dielectric constant (ε) and dielectric loss (D) values increase with increasing operating temperature. Also, the dielectric constant increases to 20 while the dielectric loss decreases to <0.025 at room temperature on increasing the sintering temperature. At 300 K and 1 kHz, the value of ε becomes almost twice that of as-synthesized nanostructures i.e. from 10 to 20 on increasing the sintering temperature to 950 ºC. The enhancement in dielectric constant can be justified by the thermally activated orientational and interfacial polarization associated with the increase in the grain size of the Ta2O5 nanoplatelets at higher sintering temperatures. Furthermore, the frequency dependence of ε indicates the high effect of the distribution of relaxation time in the Ta2O5 nanoplatelets at lower frequencies. Overall, this study provides a better understanding of the structural and dielectric behaviour of Ta2O5 nanostructures in correlation with varying sintering temperature. The results suggest that the orthorhombic Ta2O5 nanoplatelets have potential applications as alternative dielectric materials in various electronic and optoelectronic devices.

Hydrophobic PI/SiO2 composites with excellent dielectric property and thermal stability via simple modification

Polyimide (PI) has been extensively used in 5G microelectronics however the relatively high dielectric constant (∼3.5) and moisture adsorption have greatly limit its practical applications in high-frequency region. Here hydrophobic PI/SiO2 composite films with low dielectric constant and excellent thermal stability were synthesized by dispersing methyl modified hollow silica nanospheres (MHS) into polyamic acid solution prior to imidization treatment. Comparing with unmodified hollow silica nanospheres (HS), the MHS obtained through methyl modification can disperse uniformly in the PI matrix. Thus, the relaxation and orientation polarization of the PI chains as well as their electron migration are suppressed, resulting in a significant decrease in dielectric constant. The PI/MHS-10% film exhibits a stable low dielectric constant (1.9–2.3) in the high-frequency range (8.2 GHz–12.4 GHz), meanwhile maintains a high breakdown voltage (192 kV/mm), mechanical properties (64 MPa) and an excellent thermal stability (Td5% = 546.5 °C; Tmax = 589.0 °C). Moreover. PI/MHS demonstrates much lower linear expansion coefficient of 25.0 ppm/K that better matches the substrate. The surface contact angle of PI/MHS increases from 73° to 110° and the water absorption rate decreases from 3.1% to 1.6%, effectively avoiding the moisture adsorption. This work provides a simple method to prepare high-performance composite films for 5G practical applications.

Investigating magnetization of permanent magnets by magnetic flux viewing film

Permanent magnets are used in many current industrial as well as home appliances today. Frequently, kitchen plastic magnets could be found at the refrigerators at home. However, the magnetic domain structure of such permanent plastic foils is not known and understood to the users at all. The purpose of this paper is to explain the magnetic domain structure of plastic magnets with Halbach array and ferrite or neodymium magnet polarization orientation. Principles of magnetic field visualization foils (magnetic flux detector and colour changing viewing film) is explained and demonstrated on multipole magnetic structures. Experiments with magnetic polarization reversal by the strong neodymium magnet in weaker ferrite magnetic material is demonstrated. All presented principles are collected in the simple magnetic set and suggested for education of school children of different ages. Elementary school children below 10 years age are mostly interested only in making hidden pictures in magnetic paper and ferrite magnet. Older school children of 11–12 years are able to absorb more knowledge about behaviour and properties of magnets.

Forked Vein Structure W/WO3- x with Dual Active Sites in W and Oxygen Vacancies to Enhance Methylene Self-Coupling for Efficient Conversion of Methane to Ethylene.

The directional conversion of methane to ethylene is challenging due to the dissociation of the C─H bond and the self-coupling of methyl intermediates. Herein, a novel W/WO3- x catalyst with the fork vein structure consisting of an alternating arrangement of WO3- x and W is developed. Impressively, the catalyst achieves an unprecedented C2H4 yield of 1822.73µmolg-1h-1, with a selectivity of 82.49%. The enhanced catalytic activity is ascribed to the multifunctional synergistic effect induced by oxygen vacancies and W sites in W/WO3- x. Oxygen vacancies provide abundant coordination of unsaturation sites, which promotes the adsorption and activation of CH4, thus reducing the dissociation energy barrier of the C─H bond. The CH2 coupling barrier on the metal W surface is significantly lower compared to WO3, so CH2 can migrate to the W site for coupling. Importantly, the W/WO3- x with high periodicity provides multiple ordered local microelectric fields, and CH2 intermediates with dipole moments undergo orientation polarization and displacement polarization driven by the electric field, thus enabling CH2 migration. This work opens a new avenue for the structural design and modulation of photocatalysts, and provides new perspectives on the migration of methylene between multiple active sites.

Texture in atomic layer deposited Hf0.5Zr0.5O2 ferroelectric thin films

HfO2-based ferroelectric materials have excellent CMOS compatibility and polarization even in ultrathin films, which is regarded as promising candidate material for memory devices and related electronic devices. However, as the ferroelectric layer thickness scaling down, the consistency of device performance is inevitably affected by the complex polyphase and polycrystalline nature of HfO2-based ferroelectric thin films. Therefore, obtaining and controlling the texture of HfO2-based ferroelectric thin films is extremely important for regulating polarization orientation and improving ferroelectric polarization. In this work, 10 nm Hf0.5Zr0.5O2 (HZO) films were prepared by atomic layer deposition (ALD) on Nb-doped SrTiO3 (NSTO) single crystal substrates. The texture and orientation of HZO films were analyzed through the state-of-the-art spherical aberration corrected transmission electron microscope (Cs-TEM) technique. The domain matching epitaxy between HZO films and NSTO substrate helps eliminate lattice mismatch and residual misfit strain, and ultimately leads to the formation of <112> texture in HZO ferroelectric films. The obtained results represent lattice and interface play an extremely important role in regulating the ferroelectricity of HfO2-based films, which provides a way to design ultra-thin HfO2-based materials with excellent ferroelectric polarization by controlling the crystal structure and orientation.

Secondary‐Bond‐Driven Construction of a Polar Material Exhibiting Strong Broad‐Spectrum Second‐Harmonic Generation and Large Birefringence

AbstractConsiderable effort has been invested in the development of non‐centrosymmetric (NCS) inorganic solids for ferroelectricity‐, piezoelectricity‐ and, particularly, optical nonlinearity‐related applications. While great progress has been made, a persistent problem is the difficulty in constructing NCS materials, which probably stems from non‐directionality and unsaturation of the ionic bonds between metal counter‐cations and covalent anionic modules. We report herein a secondary‐bond‐driven approach that circumvents the cancellation of dipole moments between adjacent anionic modules that has plagued second‐harmonic generation (SHG) material design, and which thereby affords a polar structure with strong SHG properties. The resultant first NCS counter‐cation‐free iodate, VO2(H2O)(IO3) (VIO), a new class of iodate, crystallizes in a polar lattice with VO2(H2O)(IO3)] zigzag chains connected by weak hydrogen bonds and intermolecular forces. VIO exhibits very large SHG responses (18 × KH2PO4 @ 1200 nm, 1.5 × KTiOPO4 @ 2100 nm) and sufficient birefringence (0.184 @ 546 nm). Calculations and crystal structure analysis attribute the large SHG responses to consistent polarization orientations of the VO2(H2O)(IO3)] chains controlled by secondary bonds. This study highlights the advantages of manipulating the secondary bonds in inorganic solids to control NCS structure and optical nonlinearity, affording a new perspective in the development of high‐performance NLO materials.

Secondary-Bond-Driven Construction of a Polar Material Exhibiting Strong Broad-Spectrum Second-Harmonic Generation and Large Birefringence.

Considerable effort has been invested in the development of non-centrosymmetric (NCS) inorganic solids for ferroelectricity-, piezoelectricity- and, particularly, optical nonlinearity-related applications. While great progress has been made, a persistent problem is the difficulty in constructing NCS materials, which probably stems from non-directionality and unsaturation of the ionic bonds between metal counter-cations and covalent anionic modules. We report herein a secondary-bond-driven approach that circumvents the cancellation of dipole moments between adjacent anionic modules that has plagued second-harmonic generation (SHG) material design, and which thereby affords a polar structure with strong SHG properties. The resultant first NCS counter-cation-free iodate, VO2 (H2 O)(IO3 ) (VIO), a new class of iodate, crystallizes in a polar lattice with VO2 (H2 O)(IO3 )] zigzag chains connected by weak hydrogen bonds and intermolecular forces. VIO exhibits very large SHG responses (18 × KH2 PO4 @ 1200 nm, 1.5 × KTiOPO4 @ 2100 nm) and sufficient birefringence (0.184 @ 546 nm). Calculations and crystal structure analysis attribute the large SHG responses to consistent polarization orientations of the VO2 (H2 O)(IO3 )] chains controlled by secondary bonds. This study highlights the advantages of manipulating the secondary bonds in inorganic solids to control NCS structure and optical nonlinearity, affording a new perspective in the development of high-performance NLO materials.

Constructing Novel High Dielectric Constant Polyimides Containing Dipolar Pendant Groups with Enhanced Orientational Polarization.

Polymer dielectrics with high dielectric constant are urgently demanded for potential electrical and pulsed power applications. The design of polymers with side chains containing dipolar groups is considered an effective method for preparing materials with a high dielectric constant and low loss. This study synthesizes and comprehensively compare the dielectric properties of novel polyimides with side chains containing urea (BU-PI), carbamate (BC-PI), and sulfonyl (BS-PI) functional groups. The novel polyimides exhibit relatively high dielectric constant and low dielectric loss values due to the enhanced orientational polarization and suppressed dipole-dipole interactions of dipolar groups. In particular, BU-PI containing urea pendant groups presents the highest dielectric constant of 6.14 and reasonably low dielectric loss value of 0.0097. The strong γ transitions with low activation energies derived from dielectric spectroscopy measurements have been further evaluated to demonstrate the enhanced free rotational motion of urea pendant dipoles. In energy storage applications, BU-PI achieves a discharged energy density of 6.92 J cm-3 and a charge-discharge efficiency above 83% at 500 MV m-1. This study demonstrates that urea group, as dipolar pendant group, can provide polymers with better dielectric properties than the most commonly used sulfonyl groups.

Robust valley quantum coherence in synthetic 3R-phase MoS2: A material for future valley based devices

Two-dimensional layered transition metal dichalcogenides (TMDCs) offer the ideal platform to optically initialize the qubits utilizing the superposition of valley polarized photons. However, in the commonly available 2H phase TMDCs, thickness sensitive crystal inversion symmetry demands the precise control over the number of layers, which makes the study of valley physics challenging. On the other hand, 3R-polymorphic phase TMDCs are non-centrosymmetric irrespective of the number of layers and therefore retain valley degree of freedom for all the thicknesses. Here, using polarization resolved photoluminescence measurements under linearly polarized excitations, we demonstrate the coherent superposition of the valley photons (known as valley coherence) in synthetic 3R-phase MoS2 with different numbers of layers ranging from 3 layers to 11 layers. With near-resonant excitation (633 nm for AX0), the degree of linear polarization (a measure of the valley coherence) is observed up to 70% at 80 K measurement temperatures and is found to be layer thickness independent. Robust valley coherence is attributed to the high optical quality and the 3R crystal symmetry of the MoS2. Using angle resolved polarization dependent measurements, it is established that the net dipolar emission aligns with the polarization orientations of the incident laser, which signifies the valley coherence to be independent of the crystal orientation. This study paves the way toward using 3R-phase MoS2 as a key material for the development of future quantum technologies utilizing valley polarized photons.