Weak Polarization Research Articles

Effectiveness of Different Organic Solvent Additions to Water Samples for Reducing the Adsorption Effects of Organic Pesticides Using Ultra-High-Performance Liquid Chromatography-Tandem Mass Spectrometry.

This study systematically investigated the effect of organic solvent addition on the detection signal intensity of 15 organic pesticides in water using ultra-high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry (UHPLC-ESI-MS/MS). The analysis of chromatographic peak area ratios in ultrapure water (UPW) versus 30% methanol (MeOH)-UPW showed that the adsorption effects (AEs, mainly from injection vials with weaker polarity) were the main factor influencing the detection intensity of the organic pesticides. The AEs varied with pesticide type and concentration, especially for those with high logKow values and longer retention times, such as malathion, triadimefon, prometryn, S-metolachlor, diazinon, and profenofos. Significant differences were observed in the ability of five organic solvents (MeOH, dimethyl sulfoxide, isopropanol, acetonitrile, and acetone) to reduce AEs, with MeOH being the most effective. Optimal solvent ratios were determined to minimize AEs in aqueous solutions. Additionally, plastic injection vials caused greater AEs than glass injection vials, but the addition of organic solvents increased the detection intensity of the analytes for vials of both materials. Density functional theory calculations of the binding energies between pesticides (diazinon, malathion, and S-metolachlor) and vial materials further confirmed the effect of AE on the detection intensity of the analytes. This study showed that the addition of MeOH to real water samples effectively reduced or eliminated the effects of AEs, achieving a good linearity of calibration curves (0.05/0.1-5 μg/L, R2 = 0.9853-0.9998), high sensitivity (LOD = 5-32 ng/L), precision (RSD = 1.4-14.5%), and accuracy (average recoveries = 80.6-121.8%). These results provide technical and methodological support for mitigating the effects of AEs on pesticide detection in water using UHPLC-ESI-MS/MS.

Molecular dynamics analysis for aggregation phenomenon of aged asphalt and depolymerisation mechanism of regenerants

ABSTRACT The depolymerisation mechanism of various regenerants, when applied to the aged asphalt aggregate structure, was investigated to provide insights for the design and development of regenerants. This study focused on the molecular aggregation of the regenerant-aged asphalt system using molecular dynamics simulation technology. Simulation showcased that the uneven charge distribution in asphaltene molecules and the absence of charge in the central region are prerequisites for the electrostatic attraction of asphaltene molecules, which significantly affects their aggregation, and asphaltene molecules in heavy-aged asphalt are prone to forming stable aggregation structures. Among the four components of aged asphalt, asphaltene molecules exhibited the most significant self-aggregation, followed by saturates, while resin and aromatic molecules showed relatively weaker self-aggregation. Low temperatures encouraged aggregation, whereas high temperatures discouraged it, and ageing elevated the molecular self-aggregation, intensifying with the progression of asphalt ageing. Regenerants improved the depolymerisation of asphaltene aggregates, and fatty acid glycerides presented the most effective depolymerisation, followed by aromatic hydrocarbons and alkanes, while glycerol’s performance was the least effective. To choose regenerant composition materials, those with low electrical potential energy, weak polarity, low polar functional group content or non-polarity should be selected to ensure superior depolymerisation, permeation fusion, and regeneration effects.

Electric polarization induced by low magnetic field in the W-type hexaferrite BaCoFe17O27 single crystal

Recently, the noncollinear magnetic structure with varying Co/Zn ratios was reported in the W-type hexaferrites using neutron powder diffraction. It is believed that these noncollinear spin orderings may stimulate magnetoelectric (ME) effect in the W-type hexaferrite. Herein, we present distinct evidence of ME response through systematic investigation on the magnetic and ferroelectric properties in BaCoFe17O27. Magnetization exhibits two different anomalies at TC1 ∼ 350 K and TC2 ∼ 150 K, indicating the formation of long-range longitudinal spin configurations and the spin reorientation transition, respectively. We have found that the low field-driven electric polarization has been observed under the ME poling condition of E ⊥ (H ⊥ c, and c). Spin current mechanism is mainly considered as the physics origin in its ME response, corresponding to the other hexaferrites as reported early. In addition, the weak electric polarization observed with E(⊥c)//H(⊥c) suggests that the p–d hybridization mechanism should also be contributed to the ME response in this compound. Therefore, BaCoFe17O27 presents an intrinsic magnetoelectric effect and provides a thought for people to seek and study the more single-phase ME compounds from the viewpoint of foundational and applications.

Two-Dimensional Rare-Earth Metal Phosphides: From Weyl Semimetal to Semiconductor.

Two-dimensional (2D) nanomaterials have garnered extensive attention owing to their unique properties and versatile application. Here, a family of 2D rare-earth metal phosphides (M2P, M = Sc, Y, La) and their derivatives M2POT (T = F, OH) is developed to find their topological and electronic properties on the basis of density functional theory simulations. We show that the 2D M2P compounds are most possibly obtained from thermodynamically stable M2InP by chemical exfoliation. The In with a substantial atomic radius of 156 pm exhibits weak polarization ability, resulting in homogeneity of the electron cloud and a weakening of the M-In bond relative to the M-P bond. Upon exfoliation of the In layer, the M22+P3-:e- emerges as an electride with surface electrons, which is attributed to the larger ion radius and lower electronegativity of M2+ ions in M2P. The metallic M2P is found to be a Weyl semimetal derived from the contribution of surface electrons. Further, by leveraging the high reactivity of surface electrons, surface functionalization can produce M2POT compounds with the increased valence state of M3+, which results in their semiconducting properties characterized by high carrier mobilities and strong built-in electronic fields. These distinct topological and electronic characteristics position the 2D M2P and M2POT as promising candidates for a wide range of applications.

Polarization-rotation-driven modulation of second harmonic generation in van der Waals layered ferroelectric CuInP2S6

Two-dimensional van der Waals (vdW) ferroelectrics, renowned for their spontaneous breaking of inversion symmetry and finite electric polarization, are pivotal in nonlinear optics and low-power nanoelectronics. Prior studies primarily focused on materials exhibiting out-of-plane or in-plane ferroelectric polarization, whose rotational degrees of freedom are commonly overlooked. Herein, we experimentally validate the existence of a weak yet symmetry-allowed in-plane polarization in the low-symmetry vdW ferroelectric CuInP2S6 by rigorous structural analysis and vectorial property characterizations. Remarkably, the magnitude of this in-plane polarization is tunable via an interface-induced electric field, leading to a significant contrast in second harmonic generation between oppositely polarized domains. Based on this unique rotational capability of electric polarization, we demonstrate an electrically tunable second-order optical emission in a fabricated vdW ferroelectric capacitor. Our findings highlight the intricate interplay between crystal symmetry and tensorial physical properties, providing a novel pathway for manipulating nonlinear optical functionalities in vdW layered ferroelectrics.

Gate-tunable high tunneling magnetoresistance induced by hybrid interface states in Ni-electrode single-molecule junctions

Based on the density functional theory and non-equilibrium Green's function method, the modulation effects of gate voltage on the spin transport properties of Ni/triphenylene/Ni single-molecule junctions are investigated. The plane-, platform-, and tip-shaped electrode configurations are considered in the calculations. The numerical results show that the electrode configuration and gate voltage significantly influence the hybrid interface states (HIS) and further the spin transport properties of the molecular junctions. The molecular junctions with plane- and platform-shaped electrode configurations show weak spin polarization (SP) and tunneling magnetoresistance (TMR). Still, they exhibit excellent field effect transistor behaviors with the modulation of the gate voltage. Due to the delocalized spin-down HIS located at the Fermi level, the molecular junction with tip-shaped electrode configuration presents high and controllable SP and TMR behaviors through the gate voltage modulation. The calculations demonstrate that high spin-polarized HIS located at the Fermi level are extremely significant for the generation of excellent spin transport properties in molecular junctions composed of non-magnetic molecule and magnetic electrodes.

Ultrafast Ion Transport in 2D Confined MXene for Improved Electrochemical Performance: Boron-Atom-Substituted -OH Termination.

Regulating the surface termination of a confined space to achieve ultrafast ion transport remains an ongoing challenge. Two-dimensional (2D) MXenes possess adjustable structures and interlayer spacing, which provide an ideal platform for in-depth investigation of ion transport in 2D confined space; however, the strong interaction of the negatively charged terminations in MXenes hinders the transport of intercalated cations. In this work, we proposed a strategy that precisely regulates the surface modification of Ti3C2Tx MXene with the weak polarity of boron atoms (SCB-MXene) via the distinct effect of supercritical CO2. This not only could effectively substitute -OH termination in MXene but also can prevent the loss of -O active sites, and then, both ultrafast ion transport and high volumetric capacitance can be achieved simultaneously. Ideally, a volumetric capacitance up to 742.7 C cm-3 at 1000 mV s-1 for the SCB-MXene film as pseudocapacitive materials that provides an energy density of 66.3 Wh L-1 even at an ultrahigh power density of 132.5 kW L-1 is obtained, which is a prominent record of energy density and power density reported up to now. Subsequently, it can be used in large-scale energy storage and conversion devices.

The solid–liquid equilibrium behavior of ε-CL-20 in 10 pure solvents and its molecular mechanism

The solubility performance of 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane has been investigated by the combination of experimental measurement, solvent parameter analysis, and molecular simulation methods. The solubility in 10 pure solvents at 293.15 K to 343.15 K was determined. It was found that the solubility in nine solvents increased with temperature, except for isoamyl propionate. However, it has the largest solubility in isoamyl propionate (4.36 × 10−2 ∼ 5.39 × 10−2). Additionally, a correlation analysis was performed using four equations, which showed that the NRTL equation provided the best fit (overall average relative deviation = 3.74 %, overall coefficient of determination = 0.991). Moreover, the solvent effect was analyzed by Hansen solubility parameters, predicting good solubility in solvents with Ra(V) ≤ 12.47 MPa0.5 or Δδt ≤ 7.77 MPa0.5, indicating weak polarity of solvent and weak solvent–solvent intermolecular hydrogen bonds enhance dissolution. Furthermore, molecular electrostatic potential surface and radial distribution function analyses provided that weak hydrogen bonding C-H···O promotes dissolution.

Enhanced piezo-photocatalytic activity of ZnS/Fe2O3: Benefit from type I junction and weak water flow-induced piezoelectric polarization

Photocatalysis is considered to be a sustainable and less polluting environmental purification technology, however, the limited photogenerated charge separation efficiency and light absorption hinder its large-scale application. Encouragingly, piezocatalysis is proposed as an emerging and appealing strategy to drive the migration and separation of photoinduced carriers. Nevertheless, the source of piezocatalysis is usually derived from high energy-consuming ultrasonic vibration. Herein, we realize superior piezo-photocatalytic chlortetracycline hydrochloride degradation performance stimulated by low-frequency water flow-driven piezoelectric polarization of I-type ZnS/Fe2O3 junction. The integration of Fe2O3 is beneficial to extend the light absorption from ultraviolet region to visible range and boost the charge separation efficiency of ZnS/Fe2O3. Meanwhile, the piezoelectric polarization triggered by weak water flow further promotes the directional separation of photogenerated carriers. With all these merits, the optimized ZnS/Fe2O3 shows a piezo-photocatalytic chlortetracycline hydrochloride (CTC) degradation rate of 73.2 % within 20 min, which is 2.8 and 2.1 times that of Fe2O3 and ZnS, respectively, and 17.4-fold and 1.1-fold that of single stirring and light, respectively. This work provides a feasible guidance for designing efficient piezo-photocatalysts for in-situ purification of wastewater in natural environmental with effective visible light responsiveness and sensitivity to weak mechanical stress.

Exploring the mechanisms of benzanilide crystal growth and morphology: Crystal surface structure, solvent diffusion and solvent-interface interactions

Flaky crystals are fragile, rendering them unsuitable for various applications including use, processing, storage and transportation. This work investigates the growth and morphology regulation mechanisms of flaky crystals using benzanilide as a model material. Initially, block-like crystals are prepared by solvent screening and cooling crystallization with its morphology greatly improved. Subsequently, growth kinetics of (111), (1–10) and (020) faces are established with crystal growth experiments. The crystal growth of (001) face is also determined to follow a two-dimensional nucleation model with the microscopic surface analysis using atomic force microscopy. The changes of the surface integration resistance and the growth step height are regarded as kinetic mechanisms of the growth behavior and crystal morphology modulation by solvent and supersaturation. Finally, the molecular mechanism of the modulation of the solvent in crystal morphology is revealed base on crystal surface structure analysis and molecular dynamics simulations. The weak solvent-interface polar interactions facilitate the incorporation of benzanilide molecules into the weak polarity (001) face, leading to the surface roughening and increased crystal thickness when employing strongly polar solvents such as acetonitrile. Unlike the former, the relatively weak hydrogen bonding interactions between solvents and strong polarity (020) face, and the higher diffusion ability of molecules promote the rapid growth and disappearance of (020) face in ethanol and acetonitrile with strong hydrogen bond formation ability. This study can contribute to a deeper understanding of the solvent effect on crystal morphology and provide guidance for optimizing crystallization conditions to obtain shape-tailored crystal products.

Realizing Ultrahigh Energy Storage Density in (Bi0.5Na0.5)0.94Ba0.06TiO3-Based Ceramics via Manipulating the Domain Configuration and Grain Boundary Density.

Dielectric capacitors with a high power density are widely used in various pulsed power electronic systems. However, their low comprehensive energy storage performance severely limits the development of these systems in terms of miniaturization and lightweight design. Herein, we achieved decent energy storage performance in a class of (Bi0.5Na0.5)0.94Ba0.06TiO3 (BNTBT)-based ceramics by synergistically manipulating domain configurations and grain boundary densities. High-resolution transmission electron microscopy and piezoresponse force microscopy confirm that composition-driven refined domain configurations with weak polarity effectively improve the polarization response of BNTBT-based ceramics. The results of experimental and phase-field simulation analysis indicate that the refined grain size contributes to its high breakdown electric strength (Eb). Benefiting from the high polarization difference (ΔP) of 32.62 μC/cm2, delayed saturation polarization behavior, and an ultrahigh Eb of 815.00 kV/cm, BNT-based ceramics simultaneously achieve a high energy storage density (Wrec) of ∼12.25 J/cm3 and an efficiency (η) of ∼86.90%. Because of these structure-induced advantages, the ceramics also exhibit good energy storage temperature stability in the range of 30-150 °C. We believe that the findings of this work may provide practical guidance for the development of high-performance energy storage ceramics.

The Impact of Fractures on Shale Oil and Gas Enrichment and Mobility: A Case Study of the Qingshankou Formation in the Gulong Depression of the Songliao Basin, NE China

To study the impact of faults on the enrichment and mobility of shale oil in the Gulong area, representative rock samples were selected in this paper. Based on geochemical data and chemical kinetics methods, coupled with shale oil enrichment and mobility analysis techniques, the shale oil generation quantity and in situ oil content were evaluated from the perspectives of shale oil generation and micro migration, and the mobility of shale oil was revealed. At the same time, the hydrocarbon expulsion efficiency (HEE) of shale was qualitatively and quantitatively characterized, combined with the development of faults. The research results indicate that the study area mainly develops organic-rich felsic (ORF)/organic-containing felsic (OCF) shale, their proportion in both wells exceeds 65%, and the resource amount is the largest in this type of lithofacies. The development of a fault controls the enrichment of shale oil, and the in situ oil content and oil saturation index (OSI) of the shale in well Y58, which is close to the fault, are significantly worse than those in well S2. Well Y58 has 9.52 mg/g and 424.83 mg/g TOC respectively, while well S2 has 11.34 mg/g and 488.73 mg/g TOC respectively. The fault enhanced the migration of shale oil, increasing the efficiency of oil expulsion. As a result, the components with weak polarity or small molecules, such as saturated hydrocarbons and low carbon number n-alkanes, are prone to migration, reducing the mobility of shale oil.

Full-speed domain position sensorless control strategy for PMSM based on a novel phase-locked loop

This paper proposes a full-speed-domain position-sensor-less control strategy for precise control under forward and reverse rotation conditions to address the weak convex polarity of surface-mounted permanent magnet synchronous motor (SPMSM). The strategy comprises several key stages: pre-positioning of the rotor, constant current variable frequency (I/F) start-up, construct the Luenberger State Observer, and utilization of an improved phase-locked loop (PLL) for position estimation. In the pre-positioning stage, a constant amplitude current is applied to drag the rotor to a predetermined position. Subsequently, the I/F start-up stage accelerates the motor to a predetermined speed before transitioning to the Luenberger observer for closed-loop speed control, which is based on an extended back electromotive force (back-EMF) a two-phase rotating coordinate system. The improved PLL for position and speed estimation features three components: a phase discriminator (PD), a voltage-controlled oscillator (VCO), and loop filter (LF). Experimental results demonstrate the efficacy of the proposed strategy, showing quick start-up response, speed estimation error below 2 RPM, rotor position estimation error under 0.6 degrees post-loop closure, stable tracking during rapid speed changes, and consistent accuracy and stability even under reverse rotation conditions, thereby meeting the control strategy’s objectives.

Regional polarity in the laminar premixed flame considering the combined effect of positive and negative charge

The study of flame charge is helpful in analyzing the combustion regime, which is significant for optimizing energy conversion in the combustion. In this article, a method to calculate the charge density considering polarity (CDCP) for flame is presented. The charge in the flame local area is obtained by combining the effect of charged particles with positive and negative polarity. The CDCP in different zones of the premixed methane flame with three equivalence ratios of 0.9, 1.0, and 1.3 is measured in the Langmuir probe measurement experiment. The experiment result found that the regional polarity is shown in the premixed flame. Subsequently, the premixed methane flame was simulated using Fluent, and then the simulation distribution of CDCP in the premixed methane flame was obtained. The CDCP and polarity across the reactant, preheat, reaction, and product zones of the premixed flame are analyzed based on the experiment and simulation results. The CDCP of the reaction zone is greater than 0 C/m3 and reaches a peak, showing obvious positive polarity. The CDCP of the reactant zone is less than 0 C/m3, showing negative polarity. The CDCP changes rapidly from less than 0 C/m3 to greater than 0 C/m3 with the approach of the reactant zone to the preheating and reaction zones. The CDCP in the product zone gradually decreases with the increase of the distance from the reaction zone and finally less than and close to 0 C/m3, showing weak negative polarity. Finally, the cause of regional polarity formation is discussed based on the net production rate of charged particles and the velocity distribution of the flow field in the simulation results. The distribution of positive ions and electrons in the premixed flame is different due to the effect of the flow field and the different diffusion properties of charged particles. Thus, the regional polarity is exhibited in the premixed flame.

Giant Tunneling Electro‐Resistance in Ultrathin Ferroelectric Tunnel Junctions: The Interface Barrier Gain Mechanism

AbstractUltrathin ferroelectric tunnel junctions (FTJs) hold considerable promise for next‐generation, high‐speed, low‐power, and high‐density nonvolatile memory applications. Achieving a substantial tunneling electro‐resistance (TER) remains a challenge as the ferroelectric layer is thinned to nanoscale dimensions, often resulting in a diminished or lost polarization. An innovative interface barrier gain mechanism is introduced, employing interface electronic state modulation to precisely control the size of an additional interface barrier. This strategy lessens the dependency of the tunneling barrier on ferroelectric polarization strength, facilitating a remarkable TER even at ferroelectric thicknesses as minimal as ≈1 nm. The focus is on composite FTJs using In2Se3/MTe2 (M = Mo, W), where the inclusion of an MTe2 monolayer disrupts the asymmetric electrode configuration. The weak ferroelectric polarization reversal of the In2Se3 monolayer effectively modulates the electronic state coupling at the In2Se3/MTe2 interface. This modulation leads to variations in the width and height of the Schottky barrier at the heterojunction‐electrode interface corresponding with the ferroelectric polarization reversal, establishing a beneficial Ohmic contact in the “on” state and resulting in an exponential TER increase up to 5.4 × 106%. This work introduces a universal mechanism to overcome the thickness limitations traditionally associated with enhancing TER, marking a significant advancement in the development of ultrathin ferroelectric nonvolatile devices.

Enhanced Self-Assembly and Spontaneous Separation for Ultrathin, Air‒Floating Graphene Macrofilms and their Application in Ultrasensitive In-Site Growth Sensors.

Self-assembled graphene films at air-liquid interface have great potential for multiple applications. However, the large size and ultrathin thickness for graphene-based films are hardly achieved simultaneously because of poor assembly ability of graphene oxide (GO) and cautious film transfer process (FTP). Herein, the ethanol-based binary solution with supramolecular clusters and weak polarity is introduced to enhance the assembly performance of GO. In this regime, GO film is formed within 52 s, and its formation temperature can be as low as -20°C. More importantly, the attractive force between the formed GO film and this binary solution is 62% lower than that between GO film and traditional aqueous solution. On this basis, for the first time a spontaneous separation of the self-assembled GO film from solution is reported, and the air‒floating graphene films (AGFs) with nanoscale thickness and centimeter-scale diameter are prepared without FTP. By means of this separation behavior, the in situ growth AGFs sensors are fabricated, and they express fast response and ultrahigh sensitivity to imperceptible change in temperature and disturbances that are hardly recognized by common sensors. Therefore, a new accessible strategy is demonstrated to prepare ultrathin graphene macrofilms, which can be the excellent candidates for multifunctional, ultrasensitive sensors.

Quantum theory of polariton weak lasing and polarization bifurcations

Quantum theory of polariton weak lasing and polarization bifurcations

Research on interfacial fusion characteristics of rejuvenator-aged asphalt system: Wettability, permeability and molecular simulation

The research aims to illuminate the interfacial fusion mechanism of rejuvenator-aged asphalt to guide the development of high-performance rejuvenators and foster the high-value utilization of waste asphalt pavement materials. In the research, the contact angle between rejuvenator and aged asphalt was measured to assess its interface wettability, and the permeability and contributing factors in aged asphalt were profiled based on the permeation test and permeation degree parameter. Concurrently, the molecular dynamics simulations of the fusion behavior between rejuvenator and aged asphalt were conducted to comprehend the fusion mechanism deeply. Results reveal that thermal oxygen and photo-oxygen aging enhanced the asphalt mixture’s hydrophobicity with similar effects, and they also had comparable impacts on the wettability of rejuvenator-aged asphalt interface. A more considerable asphalt aging eventuated a more challenging for the rejuvenator to wet the asphalt surface naturally. Waste vegetable oil rejuvenators tended to have a superior wetting effect on the aged asphalt surface compared to mineral oil rejuvenators. Higher permeation temperatures and permeation durations facilitated the rejuvenator’s fusion with aged asphalt, and the permeability varied across different rejuvenators, hinging on the rejuvenator’s permeation performance and composition. The rejuvenator’s permeation process into light aged asphalt or aged matrix asphalt was prone to occur. The aging effect of asphalt negatively impacted the fusion process of the layered system. Compared to oleic acid, aromatic hydrocarbons exhibited superior permeation ability and better fusion effect with aged asphalt. Rejuvenator composition materials yielding high permeation and fusion effects should display the following characteristics: lower viscosity, weak molecular polarity, small molecular weight, linear molecular structure, or end phenyl ring structure.

Macroporous polymeric resin for the purification of flavonoids from medicinal plants: A review.

The purification of flavonoids using the macroporous polymer resin method has gained attention in recent years due to its simplicity, precision, cost-effectiveness, and the ability to separate flavonoids from other constituents. Several studies have been conducted to investigate the efficiency and effectiveness of macroporous polymer resin in purifying flavonoids from various plant sources. This review aims to evaluate the existing literature on macroporous polymer resin purification of flavonoids and provide a comprehensive analysis of the current research trends and advancements in this field. It also highlights the importance of optimizing the adsorption parameters and conditions such as resin type, resin concentration, pH, and temperature for efficient purification of flavonoids using macroporous polymer resin. The key findings of this review reveal that macroporous resins with weak polarity, large surface areas, and pore diameters have a stronger adsorption capacity for flavonoids compared to polar resins. Furthermore, ultrasonic-solvent assisted extraction often combines with macroporous resin for effective the extraction and purification of flavonoids.

Surface phonon activation for broadband high emissivity via textured structure on TiO2 coating

In the pursuit of developing broadband high emissivity coatings for metallic radiation thermal protection, conventional approaches often involve complex photonic structures or the incorporation of transition metals and rare earth additives, which pose significant technological challenges and environmental concerns. Here, we present a straightforward and eco-friendly surface structuring strategy for creating a high emissivity TiO2 coating on titanium, eliminating the need for environmentally hazardous additives. By controlling surface micropore diameter to ∼6 um through soft-sparking discharge, we successfully engineered a textured surface that effectively mitigates the intrinsic emissivity dip of planar TiO2 at wavelengths with weak polarization extinction (3–8 µm) and strong polarization resonance (>12 µm). Finite-difference time-domain (FDTD) simulations highlighted the crucial role of micropores in confining the incident electric field, maximizing the absorption potential of surface phonon polaritons. This improvement yields an impressive emissivity of 0.83 across the thermal infrared spectrum. The coating also demonstrated robust resistance to oxidation and retained its high emissivity at elevated temperatures, presenting a promising solution for sustainability in spacecraft and electronic applications.