Polarization Effects Research Articles

Spatiotemporal Changes and Influencing Factors of the Coupled Production–Living–Ecological Functions in the Yellow River Basin, China

The imbalance in the “production–living–ecology” function (PLEF) has become a major issue for global cities due to the rapid advancement of urbanization and industrialization worldwide. The realization of PLEF coupling and coordination is crucial for a region’s sustainable development. Existing research has defined the concept of PLEF from the perspective of land function and measured its coupling coordination level using relevant models. However, there is still room for improvement in the indicator system, research methods, and other aspects. This work builds a PLEF coupling coordination evaluation-index system based on the perspective of human habitat using multi-source data in order to examine the spatial differences in PLEF coupling coordination level and the influencing factors in the Yellow River Basin (YRB). Using the modified coupling coordination model, the Moran index, spatial Markov chain model, and geographically weighted random forest model were introduced to analyze its spatial and temporal differentiation and influencing factors. The results found that (a) the level of PLEF coupling coordination in the YRB from 2010 to 2022 has been improving, and the number of severely imbalanced cities has been reduced from 23 to 15, but the level of downstream cities’ coupling coordination is significantly higher than that of upstream cities. The probability of cities maintaining their own level is greater than 50%, and there is basically no cross-level transfer. (b) The Moran index of the PLEF coupling coordination level has risen from 0.137 to 0.229, which shows a significant positive clustering phenomenon and is continually strengthening. The intercity polarization effect is being continually enhanced as seen in the LISA clustering diagram. (c) There is significant heterogeneity between the influencing factors in time and space. In terms of importance level, the series is per capita disposable income (0.416) > nighttime lighting index (0.370) > local general public budget expenditure (0.332) > number of beds per 1000 people (0.191) > NO2 content in the air (0.110). This study systematically investigates the dynamic evolution of the coupled coordination level of PLEF in the YRB and its influencing mechanism, which is of great practical use.

SUSTAINABLE CONVERSION OF BANANA WASTE INTO ELECTRICAL INSULATION MATERIALS FOR HIGH VOLTAGE APPLICATIONS

<p style="text-align:justify;"><span style="font-family:"Times New Roman","serif";font-size:12.0pt;line-height:150%;text-justify:inter-ideograph;">The study examined the electrical characteristics of epoxy composites that were reinforced with fibers derived from banana leaves and pseudostems. Specifically, the study focused on analysing the dissipation factor, loss factor, and dielectric constant of these composites. The study found that composites containing banana leaf fibers demonstrated enhanced dielectric properties in comparison to pure epoxy composites. This improvement can be attributed to the effective interlocking between the fibers and the matrix, as well as the polarization effects. Enhancing the amount of fibre in the material resulted in greater dielectric constants, reaching a maximum at a critical volume of 17.2%. However, at higher frequencies, the dielectric constants fell due to decreasing polarization. Chemical treatments, such as alkali and peroxide solutions, improved the bonding between the fibers and the matrix, leading to higher resistance to water and greater electrical insulation. The results also showed that banana leaf fibers had superior dielectric performance compared to pseudostem fibers, mostly because of enhanced nanoparticle bonding. Using banana fibers is particularly noteworthy since it contributes to environmental sustainability by recycling agricultural waste, hence mitigating the ecological consequences of synthetic products.</span></p>

Fe-loaded two-dimensional nitrogen-doped carbon for electromagnetic wave absorption

Abstract Electromagnetic wave absorbing materials are particularly important in modern electronics, especially in the fields of stealth and communications. Carbon-based materials show great promise in the production and application of efficient wave-absorbing materials due to their rich structure, ultra-light weight, good corrosion resistance, and low cost. Among them, nitrogen-doped carbon-based two-dimensional materials have a stronger depletion effect on electromagnetic waves due to their higher specific surface area and abundant polarization states. In this article, nitrogen-doped carbon 2D flakes (NC) were successfully synthesized by a hydrothermal method. Furthermore, Fe single atoms were successfully loaded onto their surfaces, creating Fe@NC. The wave-absorbing properties of Fe@NC samples were significantly enhanced, with the minimum reflection loss (RLmin) reaching -69.22 dB at 11.48 GHz and the effective absorption bandwidth (EAB) extending to 5.79 GHz. The enhancement of electromagnetic wave absorption is attributed to the synergistic effects of magnetic loss, relaxation processes, dipole polarization, and electrical conduction loss. The successful preparation of Fe@NC offers new possibilities for the development of atomically dispersed wave-absorbing materials.

Computational Fluid Dynamics Modeling of Pressure-Retarded Osmosis: Towards a Virtual Lab for Osmotic-Driven Process Simulations

Pressure-Retarded Osmosis (PRO) is an osmotically driven membrane-based process that has recently garnered significant attention from researchers due to its potential for clean energy harvesting from salinity gradients. The complex interactions between mixed-mode channel flows and osmotic fluxes in real PRO membrane modules necessitate high-fidelity modeling approaches. In this work, an efficient CFD framework is developed for the 3D simulation of osmotically driven membrane processes. This approach is based on a two-way coupling between a CFD solver, which captures external concentration polarization (ECP) effects, and an analytical representation of internal concentration polarization (ICP). Consequently, the osmotic water flux and reverse salt flux (RSF) can be accurately determined, accounting for all CP effects without any limitations on the geometrical complexity of the membrane chamber or its flow mode/regime. The proposed model is validated against experimental data, showing good agreement across various PRO case studies. Additionally, the model’s flexibility to simulate other types of osmotically driven processes such as forward osmosis (FO) is examined. Thus, the contributions of ECP and ICP effects in local osmotic pressure drop along the membrane chamber are comprehensively compared for FO and PRO modes. Finally, the capability of the CFD model to simulate a lab-scale PRO module is demonstrated across a range of Reynolds numbers from low-speed laminar up to turbulent flow regimes.

Theoretically grounded approaches to account for polarization effects in fixed-charge force fields.

Non-polarizable, or fixed-charge, force fields are the workhorses of most molecular simulation studies. They attempt to describe the potential energy surface (PES) of the system by including polarization effects in an implicit way. This has historically been done in a rather empirical and ad hoc manner. Recent theoretical treatments of polarization, however, offer promise for getting the most out of fixed-charge force fields by judicious choice of parameters (most significantly the net charge or dipole moment of the model) and application of post facto polarization corrections. This Perspective describes these polarization theories, namely the "halfway-charge" theory and the molecular dynamics in electronic continuum theory, and shows that they lead to qualitatively (and often, quantitatively) similar predictions. Moreover, they can be reconciled into a unified approach to construct a force field development workflow that can yield non-polarizable models with charge/dipole values that provide an optimal description of the PES. Several applications of this approach are reviewed, and avenues for future research are proposed.

Solid-State NMR Analysis of the Dynamics of Cofactors: Comparison of Heliobacterial and Purple Bacterial Reaction Centers.

Photosynthetic reaction centers (RCs) serve as natural engines converting solar energy to chemical energy. Understanding the principles of efficient charge separation and light-induced electron transfer (ET) between the chlorophyll-type pigments might guide the synthesis for artificial photosynthetic systems. We present detailed insight into the dynamics at the atomic level using solid-state NMR techniques applied to the RCs of Heliobacillus (Hb.) mobilis (HbRCs) and the purple bacterium Rhodobacter (R.) sphaeroides (PbRCs). It is assumed that heliobacteria were among the first phototrophic organisms; therefore, their RC can be regarded as ancient. They are constructed homodimerically with perfect C2 symmetry, enabling ET over both branches of cofactors. Modern RCs of R. sphaeroides wild-type (WT) have higher redox power and are functionally highly asymmetric. The dynamics of the cofactors in both RCs has been explored using nuclear hyperpolarization, induced by the solid-state photochemically induced dynamic nuclear polarization (photo-CIDNP) effect. Based on the individual incorporation of 13C positions of the cofactors (through supplementation by 13C-δ-aminolevulinic acid), photo-CIDNP magic-angle spinning (MAS) NMR experiments provide access to the local dynamics of the cofactors along the ET path over a broad range of time scales. Theoretical analysis of the dynamic deformation of these macrocycles is also discussed in terms of function. The dynamics observed in HbRCs appears to be correlated to ET. The cofactors in PbRC are significantly less dynamic than those in the HbRC. Relevance for efficiency and redox properties are discussed.

Effect of Liquid Properties on the Non-Newtonian Rheology of Concentrated Silica Suspensions: Discontinuous Shear Thickening, Shear Jamming, and Shock Absorbance.

Concentrated particle suspensions exhibit rheological behavior, such as discontinuous shear thickening (DST) and dynamic shear jamming (SJ), which affect applications such as soft armors. Although the origin of this behavior in shear-activated particle-particle interactions has been identified, the effect of chemical factors, especially the role of liquids, on this behavior remains unexplored. Hydrogen bonding in suspensions has been proposed to be essential for frictional contacts between particles, and therefore, most studies on DST and SJ have focused on aqueous and protic organic media with a definite hydrogen bonding ability. To identify an alternative molecular mechanism, this study explored the effects of liquid polarity and an aprotic nature on the rheological behavior of concentrated suspensions of silica microparticles. Owing to their excellent particle dispersion, the DST behavior of polar liquids was observed, independent of protic and aprotic liquids. In contrast, nonpolar liquids formed particle agglomerates because of the particle-particle attraction and became a paste at a high particle fraction. The SJ behavior was confirmed for three aprotic organic liquids (propylene carbonate, 1,3-dimethyl-2-imidazolidinone, and 1,3-dimethylpropyleneurea), suggesting the hydrogen bonding ability of these aprotic liquids. The diverse mechanisms of shear-activated interactions between particles present material design possibilities for the non-Newtonian rheology of concentrated particle suspensions.

Out-of-plane polarization induces a picosecond photoresponse in rhombohedral stacked bilayer WSe2.

Constructing van der Waals materials with spontaneous out-of-plane polarization through interlayer engineering expands the family of two-dimensional ferroelectrics and provides an excellent platform for enhancing the photoelectric conversion efficiency. Here, we reveal the effect of spontaneous polarization on ultrafast carrier dynamics in rhombohedral stacked bilayer WSe2. Using precise stacking techniques, a 3R WSe2-based vertical heterojunction was successfully constructed and confirmed by polarization-resolved second harmonic generation measurements. Through output characteristics and the scanning photocurrent map under zero bias, we reveal a non-zero short-circuit current in the graphene/3R WSe2/graphene heterojunction region, demonstrating the bulk photovoltaic effect. Furthermore, the out-of-plane polarization enables the 3R WSe2 heterojunction region to achieve an ultrafast intrinsic photoresponse time of approximately 3 ps. The ultrafast response time remains consistent across varying detection powers, demonstrating environmental stability and highlighting the potential in optoelectronic applications. Our study presents an effective strategy for enhancing the response time of photodetectors.

Effects of Over-Time Exposure to Partisan Media and Coverage of Polarization on Perceived Polarization

ABSTRACT America is said to be more polarized than ever before, and extensive research examines the causes and effects of political polarization. A less studied but more pronounced trend is that citizens perceive society and politics as sharply divided. We focus on news exposure as a key reason for these perceptions. We disentangle the unique effects of exposure to partisan outlets and to news coverage of polarization in general, whether in partisan or centrist news media. We rely on 9 months of online behavioral data (127,400,000 visits) from large samples in the U.S. and Poland (total N = 2,462 & 2,120), paired with a three-wave panel survey on participants' attitudes and perceptions. We measure individual exposure, over-time and unobtrusively, to partisan outlets as well as to news coverage of polarization through a fine-tuned BERT-based machine learning classifier. We find that both exposures increase perceived polarization, independently, in both countries. Yet, in both contexts, it is news coverage of polarization, regardless of whether it is ideologically left, right, or centrist news outlets, that is the strongest driver of perceived polarization. These changes are confined to personal-level polarization (perceived distance between oneself and members of the opposing party), while no measure significantly influences perceptions of society, more generally, as being polarized. These findings have important implications for our understanding of how the media’s increasing tendency to focus on conflict as a central reporting frame can be the driver of often exaggerated perceptions of partisan divisions.

Alluring or Alarming? The Polarizing Effect of Forbidden Knowledge in Political Discourse.

"Forbidden knowledge" claims are central to conspiracy theories, yet they have received little systematic study. Forbidden knowledge claims imply that information is censored or suppressed. Theoretically, forbidden knowledge could be alluring or alarming, depending on alignment with recipients' political worldviews. In three studies (N = 2363, two preregistered), we examined censorship claims about (conservative-aligned) controversial COVID-19 topics. In Studies 1a and 2 participants read COVID-19 claims framed as censored or not. Conservatives reported more attraction to and belief in the claims, regardless of censorship condition, while liberals showed decreased interest and belief when information was presented as censored. Study 1b revealed divergent interpretations of suppression motives: liberals assumed censored information was harmful or false, whereas conservatives deemed it valuable and true. In Study 2, conservatives made more critical thinking errors in a vaccine risk reasoning task when information was framed as censored. Findings reveal the polarizing effects of forbidden knowledge frames.

The Polarization Loop: How Emotions Drive Propagation of Disinformation in Online Media—The Case of Conspiracy Theories and Extreme Right Movements in Southern Europe

This paper examines the influence of emotions on political polarization, looking at online propagation of conspiracy thinking by extreme right movements in Southern Europe. Integrating insights from psychology, political science, media studies, and system theory, we propose the ‘polarization loop’, a causal mechanism explaining the cyclical relationship between extreme messages, emotional engagement, media amplification, and societal polarization. We illustrate the utility of the polarization loop observing the use of the Great Replacement Theory by extreme right movements in Italy, Portugal, and Spain. We suggest possible options to mitigate the negative effects of online polarization in democracy, including public oversight of algorithmic decission-making, involving social science and humanities in algorithmic design, and strengthening resilience of citizenship to prevent emotional overflow. We encourage interdisciplinary research where historical analysis can guide computational methods such as Natural Language Processing (NLP), using Large Language Models fine-tunned consistently with political science research. Provided the intimate nature of emotions, the focus of connected research should remain on structural patterns rather than individual behavior, making it explicit that results derived from this research cannot be applied as the base for decisions, automated or not, that may affect individuals.

Solid-state solvatochromism of oxazolidine in multi-functionalized copolymer nanoparticles: Development of advanced materials with multi-color fluorescence

Investigating the solvatochromism of stimuli-chromic compounds such as oxazolidine in polymer matrices with various polarities or functionalities is a unique approach to developing advanced materials for anticounterfeiting, sensor, optoelectronic, and displayers. In a novel strategy, multi-functionalized copolymer nanoparticles were synthesized by copolymerization of methyl methacrylate (MMA) with various functional comonomers in emulsion media for post-polymerization modification with oxazolidine and investigation of its solvatochromism in both colloidal solution and solid phase. The particle size and morphology of nanoparticles were influenced significantly by the polarity of functional groups, and the morphology evolution from sphere to anisotropic shapes was observed by increasing the polarity of functional groups. Investigation of oxazolidine solvatochromism in colloidal solution and solid polymer powders indicated different mechanisms for solvatochromism, in which the polarity of media is the main effective parameter in colloidal solution and the polarity of functional groups in the polymer structure is the main effective parameter in solid polymer phase. The solvatochromism of oxazolidine was confirmed by observed red shift and blue shift in UV–Vis and fluorescence spectra, in which the intensity of absorbance and emission peaks was changed as a function of the polarity of functional groups. Solvatochromic photoluminescent polymer nanoparticles were used for several advanced applications such as solid anticounterfeiting inks to information encryption, dual-mode visualization of latent fingerprints, and also development of organic light-emitting diodes (OLEDs). For the first time, the results indicate a significant effect of polymer chain local polarity induced by functional groups on the tuning of optical properties of the oxazolidine by the solid-state solvatochromic phenomenon. Solvatochromism of oxazolidine in functionalized polymer nanoparticles is an interesting approach to developing novel intelligent materials that have advanced applications in different fields such as anticounterfeiting and information encryption, optoelectronic, polarity sensor, and visualization of latent fingerprints.

Cu Pillar Electroplating Using a Synthetic Polyquaterntum Leveler and Its Coupling Effect on SAC305/Cu Solder Joint Voiding

With the advancement of high-integration and high-density interconnection in chip manufacturing and packaging, Cu bumping technology in wafer- and panel- level packaging is developed to micrometer-sized structures and pitches to accommodate increased I/O numbers on high-end integrated circuits. Driven by this industrial demand, significant efforts have been dedicated to Cu electroplating techniques for improved pillar shape control and solder joint reliability, which substantially depend on additive formulations and electroplating parameters that regulate the growth morphology, crystal structure, and impurity incorporation in the process of electrodeposition. It is necessary to investigate the effect of an additive on Cu pillar electrodeposition, and to explore the Kirkendall voids formed during the reflowing process, which may result from the additive-induced impurity in the electrodeposited Cu pillars. In this work, a self-synthesized polyquaterntum (PQ) was made out with dual suppressor and leveler effects, and was combined with prototypical accelerator bis- (sodium sulfopropyl)-disulfide (SPS) for patterned Cu pillar electroplating. Then, Sn96.5/Ag3.0/Cu0.5 (SAC305) solder paste were screen printed on electroplated Cu pillars and undergo reflow soldering. Kirkendall voids formed at the joint interfaces were observed and quantified by SEM. Finally, XRD, and EBSD were employed to characterize the microstructure under varying conditions. The results indicate that PQ exhibits significant suppressive and levelled properties with the new structure of both leveler and suppressor. However, its effectiveness is dependent on liquid convection. PQ and SPS work synergistically, influencing the polarization effect in various convective environments. Consequently, uneven adsorption occurs on the surface of the Cu pillars, which results in more Kirkendall voids at the corners than at the center along the Cu pillar surface.

A Multipole-Based Reactive Force Field for Hydrocarbons.

The computational complexity of quantum chemistry methods has prompted the development of reactive force fields, facilitating practical applications of molecular dynamics simulations for large-scale reactive systems. Current reactive force fields typically employ intricate corrections based on prior chemical knowledge, which severely impedes their further advancement. This study presents a new atomic multipole-based reactive model with bond free (OPERATOR). The force field is constructed on a simple, physically motivated model within the AMOEBA framework that closely resembles the physical representation of the chemical reaction processes. In the force field, the atomic multipoles are generated dynamically according to the atomic environments, aiming to effectively capture significant changes in the electrostatic environments during chemical reactions. Subsequently, atomic multipole-based charge penetration, polarization, and charge transfer effects are incorporated into the force field to describe the complex electrostatic interactions in the system. The force field also includes van der Waals interactions and three-body potentials. In addition, to extend these nonreactive interactions to chemical reactions, the atom distribution multipole moments are used to characterize different chemical environments. The force field has been optimized using the dataset of potential energy surfaces (PESs) of hydrocarbons derived from DFT results of millions of conformations with six degrees of freedom (DOFs). The results demonstrate that the new force field effectively replicates both the monopoles and the energies. In comparison to ReaxFF, the new force field exhibits comparable or superior performance. Furthermore, molecular dynamics simulations of n-heptane decomposition effectively reproduce the primary products and reactions observed in the experiments. Given the simplicity and physically motivated nature of the model, it is expected that the new force field will be utilized in future studies to investigate chemical reaction mechanisms involving more elements.

Spin polarization effect on linear polarization of photon emission following resonant electron capture of lithiumlike ions

Spin polarization effect on linear polarization of photon emission following resonant electron capture of lithiumlike ions

Investigation of linear and microscopic nonlinear optical responses of 1-indanone compounds in different environments based on polarity models

Molecular spectroscopic and nonlinear features can indicate positive changes by solvent molecules. In this work, DFT and spectroscopic techniques were used to study the polarity effects of different solvent environments. Polarity-based models were used for studying solvent induced interactions on the optical features of new groups of biomolecules. Despite the significant contribution of general effects on the molecular absorption spectra, there is considerable competition between general and specific environmental effects on the molecular emission properties. Under this condition, strong hydrogen bonds tend to increase molecular nonlinear responses. The same results were observed for the low order (first and second order) nonlinearity of biomolecules. Therefore, the studies on the environment effects on the biomolecules’ first order nonlinearity can give valuable information about higher-order optical responses. Moreover, 1-Indanone compounds with high nonlinearity can be considered as an effective element in designing optical devices.

Evaluation of ion recombination and polarity effect on photon depth dose measurements using mini- and micro-ion chamber.

To investigate the effect of ion recombination ( ) and polarity ( ) correction factors on percentage depth dose (PDD) curves for three ion chambers, using flat and flattening filter free (FFF) beams, across different broad field sizes. A method to assess these effects and their corresponding corrections is proposed. and were evaluated following the IAEA TRS-398 protocol for three ion chambers: PTW Semiflex-3D-31021, PinPoint-3D-31022, and Semiflex-31010. PDD measurements were acquired from dmax to 32cm depth at four voltages (±400V or±300V, and±100V) for field sizes 4×4, 10×10, 20×20, and 40×40 cm2. The values were computed after the correction at each applied voltage. This study aimed to assess the variation of the factors along scanning depths for different field sizes, to evaluate the need for correcting the scanning data. was independent of depth and field size for Semiflex-3D, while it presented an increasing value with depth for the PinPoint-3D. increased with dose rate, i.e., decreased with depth. The variation of this perturbation effect over the PDD range was about 0.1% for flat beams with all three ion chambers. With FFF beams, it was around 0.3% with PinPoint-3D, and 0.8% for 10FFF with Semiflex-3D. A second-order polynomial fit can be determined to directly correct the raw data scanned along the beam axis for both and . can significantly affect the PDD scanning measurements in FFF beams acquired with Semiflex-3D. An error close to 1% at large depths could be present, meaning an error of less than 0.3% relative to the dose at the depth of dmax.

Investigating the effect of finite ionic size and solvent polarization on induced charge electro-osmosis around a perfectly polarizable cylinder

Many industrially relevant microfluidic applications use concentrated solutions of macro-molecular solutes dissolved in polar solvents like water, which are typically deployed at high voltages. In this study, we investigate the effect of finite ionic sizes and solvent polarization on induced charge electro-osmotic flow around a perfectly polarizable cylinder, at high electric field strengths and ionic concentrations. The flow is actuated by means of a direct current electric field, and the step response of various flow parameters are studied numerically. Finite ionic sizes, defined through a steric factor ν, are modeled using the modified Poisson–Nernst–Planck model. Additionally, a field-dependent permittivity, characterized by a solvent polarization number A, accounts for molecular re-orientation effects. Our findings reveal an ion-size modulated decrement in charge concentration in the electrical double layer and an augmentation in the electric field. Remarkably, the resulting flow velocities increase with ion size. Solvent polarization, on the other hand, results in a marked reduction in flow velocities. Steric effects, however, dominate over a large range of parameter space (applied voltage and bulk ionic concentration) as compared to solvent polarization. Finally, we demonstrate that unequal ionic sizes result in flow asymmetries at the steady-state, thereby generating net electro-phoretic motion of suspended particles.

Manipulation of ionic transport behavior in smart nanochannels by diffuse bipolar soft layer

Soft bipolar nanochannels provide distinct and valuable understanding of the intricate relationship among shape, charge distribution, concentration, and flow dynamics. This study investigates the intriguing realm of nanoscale structures, where two distinct configurations of soft layers with varying charges provide an intricate but appealing setting for the movement and management of ions, as well as the regulation and control of ionic species in nanochannels with five various geometries. It generates cylindrical, trumpet, dumbbell, hourglass, and conical forms. The nanochannels are coated with a diffuse polyelectrolyte layer, and the charge density distribution in the soft layer is described using the soft step distribution function. To enhance accuracy, the impact of ionic partitioning is taken into account. To investigate the effect of soft layer polarity, two types were considered: Type I and Type II. In Type I, the negative pole is at the start, while in Type II, the positive pole is at the start. Thus, Type I features a bipolar soft layer arrangement of negative–positive (NP), whereas Type II has a positive–negative (PN) configuration. The research was conducted under stationary conditions using the finite element method, Poisson–Nernst–Planck, and Navier–Stokes equations. By manipulating variables such as the arrangement order, charge density of the soft layer, and bulk concentration, a numerical analysis was performed to investigate the impact of these variables on current–voltage parameters. The results demonstrate the soft layer with a positive charge serves as a more effective receiver layer for generating greater rectification. For instance, the dumbbell-shaped nanochannel exhibits a rectification of 2046 at a concentration of 1 mM and the lowest charge density in the soft layer. From an alternative perspective, the conductivity in bipolar nanochannels is significantly influenced by the bulk concentration. The study's findings on the fundamental principles of soft bipolar nanochannels have profound implications for the diverse applications of nanochannels. The capacity to regulate and manipulate ion transport through these nanochannels can result in enhanced efficiency, selectivity, and performance in various processes.

Influence of the induced Na+/Cl− ionic polarization effects on multi-scale structures of maize starch during radio frequency heating

Influence of the induced Na+/Cl− ionic polarization effects on multi-scale structures of maize starch during radio frequency heating