Dipole Polarizability Research Articles

Tensorial Properties via the Neuroevolution Potential Framework: Fast Simulation of Infrared and Raman Spectra.

Infrared and Raman spectroscopy are widely used for the characterization of gases, liquids, and solids, as the spectra contain a wealth of information concerning, in particular, the dynamics of these systems. Atomic scale simulations can be used to predict such spectra but are often severely limited due to high computational cost or the need for strong approximations that limit the application range and reliability. Here, we introduce a machine learning (ML) accelerated approach that addresses these shortcomings and provides a significant performance boost in terms of data and computational efficiency compared with earlier ML schemes. To this end, we generalize the neuroevolution potential approach to enable the prediction of rank one and two tensors to obtain the tensorial neuroevolution potential (TNEP) scheme. We apply the resulting framework to construct models for the dipole moment, polarizability, and susceptibility of molecules, liquids, and solids and show that our approach compares favorably with several ML models from the literature with respect to accuracy and computational efficiency. Finally, we demonstrate the application of the TNEP approach to the prediction of infrared and Raman spectra of liquid water, a molecule (PTAF-), and a prototypical perovskite with strong anharmonicity (BaZrO3). The TNEP approach is implemented in the free and open source software package gpumd, which makes this methodology readily available to the scientific community.

Controllable surface functionalization of rice husk-derived porous carbon by atomic layer deposition for highly-efficient microwave absorption

Multilayer absorbers, characterized by their distinctive structures and numerous heterogeneous interfaces, possess the potential to become exceptionally efficient and stable electromagnetic wave absorbers. Herein, we have ingeniously engineered multilayer ZnO/NiCo/C (ZNC) composite absorbers, utilizing a combination of an annealing procedure and atomic layer deposition (ALD) process. From the SEM images, the ZnO layers composed of ZnO nanoparticles (NPs) fabricated via ALD almost completely cover the surface of rice husk-derived carbon and the NiCo NPs residing on the surface. Benefiting from the specific multilayer structure, the well-designed ternary dielectric/magnetic components, and the synergistic interplay between dipole polarization relaxation and interfacial polarization relaxation, coupled with good impedance matching, the ZNC150 and ZNC200 composites exhibit best microwave absorption capacities. Through the precise control of the electromagnetic parameters by the deposition circle modifications, the minimum reflection loss reaches −52.5 dB and the effective bandwidth extends to 4.96 GHz with thin thickness of 1.52 mm.

Effect of metal doping on the microwave absorption performance of multi-element (metal, N, and Cl) doped carbon composites

Multi-element-doped carbons are actively being pursued as efficient lightweight microwave absorbers. In this work, metal, nitrogen and chlorine codoped carbons (metal,N,Cl–C, where metals = Ni, Co, Mn, or Zn) were synthesized through the high-temperature carbonization of polypyrrole doped with hydrochloric acid (PPy-HCl) and prepared in the presence of certain metal chloride salts (NiCl2, CoCl2, MnCl2, or ZnCl2). The dielectric parameters and microwave absorption properties of the metal,N,Cl–C composites could be regulated by simply altering the type of metal salt. Compared with N,Cl–C, it was discovered that Co,N,Cl–C and Ni,N,Cl–C possessed higher graphitization degrees, smaller particle sizes and more surface chemical functional groups (metal−N), which significantly improved the conduction loss and polarization loss effects including interfacial polarization and dipole polarization. At a filler ratio of 9.0 wt%, Ni,N,Cl–C displayed a wide effective absorption bandwidth (EAB, RL ≤ −10 dB) of 7.1 GHz at a thickness of 2.5 mm and a minimum reflection loss (RLmin) of −29.7 dB at 9.7 GHz and 3.5 mm thickness. Similarly, Co,N,Cl–C offered an RLmin value of −48.2 dB at 11.3 GHz and a thickness of 3.0 mm and an EAB of 6.0 GHz at a thickness of 2.5 mm. These results showcase the advantages of metal,N,Cl–C composites as microwave absorbers.

Bound state energies and critical bound region in the semiclassical dense hydrogen plasmas

We calculate the bound state energies of the hydrogen atom in semiclassical dense hydrogen plasmas modeled by the effective screened interaction potential developed by Ramazanov et al. [Phys. Rev. E 92, 023104 (2015)]. It is shown that the quantum degenerate and exchange-correlation effects of plasma electrons do not play significant roles in the region where the system exhibits bound states. The bound-continuum critical transition lines and the distribution of the ground state energies in the plasma density-temperature phase diagrams are obtained, both with and without taking into account the screening effect of the plasma ions. The dipole transition oscillator strengths and static dipole polarizabilities of the electron-ion subsystems in semiclassical dense hydrogen plasmas are calculated in a wide range of plasma parameters.

Virtual and bound states in low-energy positron scattering by atoms and molecules via modified effective range theory

Modified effective range theory is applied as a tool to determine bound and virtual state energies in low-energy positron elastic scattering by atoms and molecules. This is achieved by the S-matrix continuation into the complex momentum plane, allowing to identify poles related to shallow energy states. The influence of the long-range polarization potential (∼r −4) on the bound and virtual-state pole positions is analyzed for noble gases and nonpolar molecules such as H2, N2, and CH4. The quantitative relations between the S-matrix poles and the s-wave scattering length accounting for dipole polarization are introduced.

Construction of gradient hierarchical and hetero-interfaces structure for ultra-broad microwave absorption

Currently, carbon materials derived from biomass are widely sought after as electromagnetic absorbing(EMWA) materials owing to the unique structure, as well as the wide range of natural acquisition pathways, economic viability, and simple processing. However, due to the high dielectric properties, mismatched impedance and single attenuation mechanism, they cannot achieve efficient EMWA performance. Herein, the biomass carbon/Co/porous carbon magnetic composites with a layered gradient structure were fabricated by in-situ deposition of ZIF-67 on the lotus leaf base and then pyrolysis at high temperature. By adjusting the pyrolysis temperature, the sample obtained at 650 ​°C achieved a minimum reflection value (RLmin) of −34.2 ​dB at a matching thickness of 2.6 ​mm, and a maximum effective absorption bandwidth (EAB) of 7.12 ​GHz. The results indicate that this magnetic composite with a multi-sized layered gradient porous structure has a good electron transport network, a large number of heterogeneous interfaces, and dipole polarization centers, which are conducive to multiple reflection and scattering of microwaves, conduction loss, interface loss, magnetic loss, and impedance matching of materials. Therefore, this work provided a reference for optimizing the EMWA performance of carbon materials and designing a layered gradient porous magnetic composite with multi-sized structure.

Comparative study of 4-((4-aminophenyl)diazenyl)-2-((2-phenylhydrazono)methyl)phenol and N-(4-((4-hydroxy-3-((2-phenylhydrazono)methyl)phenyl)diazenyl)phenyl)acetamide - DFT method

Theoretical calculation of 4-((4-aminophenyl)diazenyl)-2-((2-phenylhydrazono)methyl) phenol (1) and N-(4-((4-hydroxy-3-((2-phenylhydrazono)methyl)phenyl)diazenyl)phenyl) acetamide (2) was studied by DFT/B3LYP/6-311+G(d,p) basis set. The calculated values of geometric structural parameters, Fourier transform infrared spectral data, highest occupied molecular orbital and lowest unoccupied molecular orbital, natural bond orbital, nucleus-independent chemical shifts, Fukui function, polarizability, hyperpolarizability, and UV data of compounds 1 and 2 clearly indicate that substitution of the amino group alters the physical properties of compound 2. The nucleus-independent chemical shift values of the amino-substituted phenyl ring reduces the aromatic character due to the lone pair electron on nitrogen involved in inductive and conjunction effects, as well as due to OH, NH2 and OH, NHCOCH3 in compounds 1 and 2, respectively. The effect of the solvent on different parameters was studied, and it was found that increasing the dielectric constant increased the parameter studied. The stability and planarity of the molecule’s effects on dipole moment, energy, polarizability, and hyperpolarizability were studied extensively.

High-performance electromagnetic wave absorption by two-dimensional mesoporous monolayer Ti3C2Tx MXene

Transition metal carbide MXene, with its unique chemical composition, structure and sizeable particular surface area, is widely applied in wave absorption. However, the high conductivity of MXene resulted in an impedance mismatch that prevented electromagnetic waves from entering the material to achieve dissipation, and thus, tuning the intrinsic properties of pure MXene to obtain excellent electromagnetic wave absorption is still a challenge. Here, we strengthen the absorption of electromagnetic waves by generating titanium vacancies through hydrogen peroxide etching and thus forming micro-sized wrinkles with porous MXene. Porous MXene possesses an excellent microstructure and surface state, abundant porous defects, and moderate electrical conductivity, allowing it to achieve well-matched impedance, dipole polarization, and conduction loss, thus inheriting excellent electromagnetic wave absorption (EWA) properties. Therefore, the porous MXene achieves a strong absorption of − 63.31 dB and an adequate absorption bandwidth (EAB) of 6.88 GHz at a matched thickness of 2.39 mm with a fill ratio of 6 wt%.

Reversible Hydrogen Electrode (RHE) Scale Dependent Surface Pourbaix Diagram at Different pH.

In the analysis of electrocatalysis mechanisms and the design of catalysts, the effect of electrochemistry-induced surface coverage is a critical consideration that should not be overlooked. The surface Pourbaix diagram emerges as a fundamental tool in this context, providing essential insights into the surface coverage of adsorbates generated via electrochemical potential-driven water activation. A classic surface Pourbaix diagram considers the pH effects by correcting the free energy of H+ ions by the concentration-dependent term: -kBT ln(10) × pH, which is independent of the reversible hydrogen electrode (RHE) scale. However, this is sometimes inconsistent with the experimentally observed potential-dependent surface coverage at an RHE scale, especially under high-pH conditions. Here, we derived the pH-dependent surface Pourbaix diagram at an RHE scale by considering the energetics computed by density functional theory with the Bayesian Error Estimation Functional with van der Waals corrections (BEEF-vdW), the electric field effects, the derived adsorption-induced dipole moment and polarizability, and the potential of zero-charge. Using Pt(111) as the typical example, we found that the surface coverage predicted by the proposed RHE-dependent surface Pourbaix diagram can significantly minimize the discrepancy between theory and experimental observations, especially under neutral-alkaline, moderate-potential conditions. This work provides a new methodology and establishes guidelines for the precise analysis of the surface coverage prior to the evaluation of the activity of an electrocatalyst.

Anomalous polarization-switching phenomena and noteworthy pyroelectricity in ferroelectric Hf0.5Zr0.5O2 polycrystalline films

Hafnia-based oxide thin films exhibit unconventional robust ferroelectricity at the nanoscale, paving the way for advancements in next-generation nanoelectronics. However, the stability and dynamics of ferroelectric polarization in hafnia-based oxides films, particularly at the nanoscale, warrant further exploration. In this study, we delve into the factors influencing the formation of the ferroelectric phase. Our findings illuminate that the confinement effect of the capped layer enhances the stabilization of the metastable orthorhombic phase, thereby bolstering its ferroelectricity and endurance. Furthermore, we identify an unprecedented polarization-switching behavior in HfO2-based ferroelectric films, characterized by a decrease in the remanent polarization and an increase in the coercive field as the temperature drops. This peculiar phenomenon can be ascribed to the reduction in the long-range interaction of polarization dipoles upon cooling, as evidenced by the dielectric spectrum. The diminished long-range interaction results in the emergence of nanodomains and a re-entrant relaxer behavior, offering novel insights into the origin of ferroelectricity and the stability of ferroelectric polarization in hafnia-based thin films. Given the commendable compatibility of Hf0.5Zr0.5O2 films with Si substrates and a pyroelectric coefficient of −62.1 μC/m2·K, they emerge as a prime candidate for sensor device applications.

Bead-like Co/C@MoS2Composites connected by Multi-Walled carbon nanotubes for high-efficiency electromagnetic wave absorption

This study presents a novel approach to synthesize a composite material composed of bead-like Co/C nanoparticles anchored on MWCNTs, encapsulated by MoS2 nanosheets through a combination of carbonization and hydrothermal treatment using ZIF-67 as the precursor. The resulting composite demonstrates exceptional electromagnetic wave (EMW) absorption performance, with a minimum reflection loss (RL) of −63 dB at a thickness of 2.44 mm and an effective absorption bandwidth (EAB) of 7.2 GHz when RL is below 10 dB together with an expanded EAB of 12.3 GHz (d = 5 mm).The superior absorption capabilities arise from a well-thought-out design of material composition and structure. The synergy of Co/C and MWCNTs enhances ferromagnetic resonance, conductivity, and polarization loss, while sulfur vacancies in MoS2 act as polarization centers, facilitating dipole polarization and efficient conversion of electromagnetic wave energy. The core–shell structure and heterogeneous interfaces introduce various energy loss mechanisms, including multiple polarizations, scattering effects, and dielectric loss. This work introduces a facile method for synthesizing a composite material with outstanding EMW absorption performance. The synergistic combination of unique material components and the carefully engineered structure make this composite a promising candidate for advanced applications in electromagnetic wave absorption technology.

Enhanced electromagnetic wave absorption in YAG-modified SiC foam

Electromagnetic technology applications are escalating, leading to increased human exposure to electromagnetic radiation. In addressing the challenges posed by this radiation, electromagnetic wave absorbing materials stand out due to their distinguished properties. This study focused on developing porous fibrous SiC three-dimensional (3D) foams. These were synthesized by freeze-drying SiC nanofiber dispersions followed by high-temperature sintering. Measurements demonstrated that the resulting SiC foams possess a relatively low density, approximating 0.1 g cm−3. Upon microscopic analysis, it became evident that the foam's porous structure is predominantly made up of SiC fibers intermixed with yttrium aluminum garnet granules. These tailored SiC foams delivered outstanding electromagnetic wave absorption characteristics, recording a minimum reflection loss value of −63 dB. Furthermore, an expansive effective absorption bandwidth of 6.9 GHz (spanning from 9.3 to 16.2 GHz) was noted for a sample thickness of 3.15 mm. Several factors contribute to this high absorption efficacy, including multiple reflections and both interface and dipole polarizations. It is also worth noting that the SiC foam displayed commendable oxidation resistance when exposed to elevated temperatures. Cumulatively, these findings underscore the promising potential of porous fibrous SiC 3D foams in electromagnetic wave absorption applications, especially in extreme conditions.

Porous CoZn@NC skeletons supported NiCo2S4 nanorods for efficient electromagnetic wave absorption

Bimetallic sulfides are promising in electromagnetic wave (EMW) absorption due to their moderate permittivity and high dielectric loss. However, the impedance mismatching and insufficient loss mechanism of bimetallic sulfides result in limited EMW absorption performance. Herein, bimetallic sulfide (NiCo2S4) nanorods were loaded onto nitrogen-doped carbon embedded with CoZn nanoparticles (CoZn@NC) derived from CoZn-based metal organic framework (CoZn-MOF) through simple hydrothermal and vulcanization processes. Importantly, during the vulcanization process, CoZn@NC undergoes structural reorganization and evolves into defect-rich porous nanosheets, which promotes dipole polarization and enhance EMW absorption ability. Additionally, the formed NiCo2S4 nanorods are tightly anchored on the porous CoZn@NC skeletons, forming a large number of heterostructures, and promoting interfacial polarization. In addition, the carbon nanotubes (CNTs) formed during the pyrolysis process of CoZn-MOF contribute to the conduction loss of the heterostructure and motivate dielectric loss. Therefore, CoZn@NC/NiCo2S4 heterostructures inherit excellent EMW absorption performance and obtain a reflection loss (RL) value of −32.53 dB at a matching thickness of 2.1 mm, while exhibiting an effective absorption bandwidth (EAB) of 4.1 GHz. Radar cross-sectional area (RCS) simulation shows that the potential of CoZn@NC/NiCo2S4 heterostructure in practical anti radar detection. This work puts up great potential for the development of advanced bimetallic sulfides-based EMW absorbers.

Multi-dimensional nano-microstructures design of MOF-derived CoSe2@N–C composites toward excellent microwave absorption

Nano-microstructures design enabled the controlled tuning of electromagnetic parameters to obtain high-performance microwave absorption materials (MAM). Herein, Metal-Organic Frameworks-derived (MOFs-derived) CoSe2@Nitrogen-doped Carbon (CoSe2@N–C) materials with controllable nano-microstructures also exhibit tunable morphologies from dodecahedra-, cube-, fusiform-to sheet-like by adjusting the solvent and the molar ratio of cobalt/ligand. The organic frameworks are maintained by pyrolysis selenization, forming a unique CoSe2@N–C three-dimensional conduction network that broadens electron transport and electromagnetic wave multiple reflection routes, enhances conduction loss capability, and optimizes impedance matching. The confinement of ligand-derived carbon can avoid the agglomeration of CoSe2, forming rich heterogeneous interfaces within CoSe2@N–C, enhancing interfacial polarization loss. Symmetric models are developed to reveal the importance of destructive interference on the microwave absorption property. In addition, dipole polarization of defects and doped-nitrogen further encourages the enhancement of the microwave absorption properties of CoSe2@N–C. The CoSe2@N–C-d exhibits the best microwave absorption properties with a minimum reflection loss (RLmin) of −42.31 dB at 15.62 GHz in a thickness of 1.5 mm, and an effective absorption bandwidth of 4.25 GHz. The excellent absorption performance of CoSe2@N–C paves the way for the design and synthesis of high-performance absorbers.

2D/3D structure engineering of dual-phase Mo2C/MoO2-decorated rGO aerogels for electromagnetic waves absorption

The rational design of structure and regulation of composition in micro/nano-scale is of great significance for broadband absorbing properties of lightweight aerogels. Herein, the controllable dual phase Mo2C/MoO2-decorated rGO aerogels are prepared by designing the Mo-rGO precursor, which possesses heterostructure interfaces and three-dimensional structures. The dual-phase of Mo2C/MoO2 was controlled and nanoparticles were dispersed on the surface of graphene. The interconnected rGO sheets construct continuous network for electron transport, which facilitates conduction loss and multiple reflections inside the aerogel. The Mo2C/MoO2 nanoparticles decorated on rGO sheets contribute sufficient interfacial and dipole polarization, and improve the impedance matching and strengthen the loss capacity of electromagnetic waves. The as-prepared Mo2C/MoO2/rGO aerogel exhibits considerable electromagnetic wave absorption performance with a minimum reflection loss of −42.1 dB at 12.5 GHz and an effective absorption bandwidth of 5.6 GHz (10.6–16.2 GHz) at a thin thickness of 2.2 mm with a low density of 9.8 mg·cm−3. This Mo2C/MoO2/rGO aerogel would be a promising material for electromagnetic wave absorption in wide application fields, and it also provides a universal idea for constructing low-density broadband microwave absorption material by structural and composition engineering.

Abundant vacancies induced high polarization-attenuation effects in flower-like WS2 microwave absorbers

Defect engineering could provide new ideas for the design of transition metal disulfide electromagnetic wave (EMW) absorbers with high performance. Since the effects of dipoles on impedance matching and EMW absorption are crucial for the development of novel absorbers, the polarization attenuation dependence on defect engineering should be understood at micro- and macro-scales. In this paper, it is found that the defect-rich WS2 nanoflowers synthesized by the cold plasma method possess excellent EMW absorption properties. Cold plasma treatment of materials is easy to perform and maintains the original shape of the material to a high degree. The formation of defects results in abundant electrochemically active sites, increased multiple reflection losses, improved dielectric properties and impedance matching in the materials. The RLmin of the defect-rich material with a thickness of 3.19 mm is as high as −54.36 dB at 8.16 GHz, and the effective absorption bandwidth is 4.72 GHz. The results reveal that the formation of defective vacancies enhances the effects of dipole polarization of the material on improving its EMW absorption properties. Thus, this work provides not only a facile preparation route for novel EMW-absorbing materials, but also a new strategy for tunning defects in transition metal disulfides.

Lightweight broadband electromagnetic wave absorption achieved by a like-clustered CNTs spheres modified SiC nanowires

Developing lightweight, broadband, and highly absorptive electromagnetic (EM) wave absorption materials by effectively utilizing the agglomeration effect of one-dimensional nanowires is challenging. In this work, a SiCnws/CNTs aerogel with a like-clustered CNTs sphere-modified SiCnws structure was prepared via simple freeze-drying and heat treatment techniques, where the CNTs content was controlled to adjust the quantity and volume of the CNTs spheres. This allows for effective regulation of the impedance matching characteristics and dielectric loss capability. Specifically, the SiCnws/CNTs aerogel exhibited remarkable dissipation of EM waves through the enhancement of the interface and dipole polarization, achieved by significantly increasing the presence of multiple interfaces and defects. Moreover, the aerogel structure induces conduction loss and amplifies multiple reflections and scattering, facilitating efficient dissipation of EM wave energy across multiple levels. The minimum reflection loss (RLmin) of the SiCnws/CNTs aerogel (SN-3 sample) achieves −43.4 dB at 11.2 GHz with a matching thickness of 2.6 mm. Its effective absorption bandwidth (EAB) spans from the C band to the Ku band (7.4–18 GHz) at thicknesses ranging from 2.1 to 4.4 mm. Additionally, when the matching thickness is 3.4 mm, the broadened EAB extends up to 9.8 GHz (covering the whole X and Ku bands). Furthermore, CST simulations clearly demonstrate a remarkable suppression of the incident EM wave by the samples under real-world conditions, with a substantial reduction of 42.5 dBm2 in the RCS. Considering this, SiCnws/CNTs aerogel materials pave the way for new opportunities in lightweight, broadband, and high-absorption materials.

Carbon microspheres/carbon sheets as efficient electromagnetic wave absorbers

To address the issue of weak absorption intensity and narrow frequency band in pure dielectric electromagnetic wave (EMW) absorbing materials, this study adopts a simple method to successfully prepare a pure dielectric EMW absorption material by modifying acrylonitrile–methylmethacrylate copolymer carbon microspheres (co-AN-MMA@CS) with capsaicin-like 3,5-dimethylphenol derivative (DMPD). The introduction of DMPD into the carbon microspheres increases the heteroatoms (N, O) in the carbon material, thus resulting in functional groups (-C-N, –NO, and C–O) that enable energy loss through dipole polarization. Additionally, the special morphology of carbon microspheres attached or embedded in carbon sheets derived from DMPD increases the inhomogeneous interfaces, thereby increasing the interface polarization relaxation and further attenuating EMWs. The resulting carbon material with the optimal structure (denoted as CNO-2) exhibits superior EMW absorption properties. At a thickness of 2.50 mm, the minimum reflection loss (RLmin) reaches −63.10 dB at 13.14 GHz, whereas the maximum effective absorption bandwidth (EABmax) reaches 6.81 GHz (8.95–15.76 GHz). CNO-2 has excellent EMW absorption capabilities due to the controllable complex dielectric constant and multiple attenuation mechanisms, including interfacial polarization, dipole polarization, and conduction loss. The CNO absorbers prepared in this study can be used as efficient microwave absorbers for electromagnetic protection applications.

Integrated design of MOFs-derived 0D/1D/2D/3D hierarchical network for high-efficiency electromagnetic wave absorption

To overcome electromagnetic pollution issues, multi-dimensional carbon-magnetic composites have gained attention. In this study, a 2D nanosheets stacked 3D network with 0D Co particles and 1D CNTs was synthesized via hydrothermal and annealing method. The nitrogen-doped porous 3D crosslinked network constructed with intertwined 1D and 2D components (CNTs, PDA-derived carbon, and MOFs-derived carbon) effectively extends the propagation pathway, providing superior conductive loss. Moreover, the 3D magnetic-electrical porous heterostructure greatly enhances the multiple scattering and reflection of the incident waves, as well as induces excellent eddy current loss. In addition, 0D Co nanoparticles exhibit multi-mode magnetic resonances and optimize impedance matching characteristics to capture more electromagnetic waves (EMWs). The microstructures, consisting of rich defects and multilevel heterogeneous interfaces, stimulate multidimensional advantages to regulate relaxation time for optimized dipolar polarization and interface polarization. Consequently, the multidimensional Co/CNTs@C heterostructure displays an optimum absorption of −59.1 dB at 11.3 GHz (loading of 10 wt%) and an ultra-width effective absorption band (EAB) of 8.1 GHz (20 wt%). Relevant simulation experiments demonstrate the strong absorption and extremely poor reflection, testifying its surprising performance. Overall, this work provides a novel strategy for preparing MOFs-derived multidimensional EMW absorbing materials.

ДЖОНШЕРОВСКИЙ УНИВЕРСАЛЬНЫЙ ДИНАМИЧЕСКИЙ ОТКЛИК В ТОНКИХ ПЛЕНКАХ ПОЛИДИФЕНИЛЕНФТАЛИДА

It is known that the supramolecular structure of organic materials can have a significant effect on the conductivity of polymer films in both constant and alternating fields. In particular, the presence of associative supramolecular formations can lead to a significant increase in the local dielectric constant. At the same time, the presence of different types of supramolecular ordering can lead to the predominance of certain charge transfer mechanisms in polymer films, and, consequently, to the presence of a dependence of conductivity on the electric field strength. The degree of molecular ordering, both on the surface and in the bulk of a polymer film, can also have a significant effect on polarization. In this regard, studying the influence of the supramolecular structure on the conductivity of polymer films in an alternating electric field is an urgent task.Previously, using various methods, it was established that the supramolecular structure of films with a thickness of more than 300 nm is determined mainly by supramolecular formations of an associative structure. The structure of films with a thickness of 100 to 300 nm is determined by the mixed structure of globular and associative formations. The structure of films less than 100 nm thick is determined by supramolecular formations of a globular. It was also established by the method of thermally stimulated depolarization that three regions are observed on the dependence of the activation energy of capture centers on the thickness of the polymer film, corre- sponding to different supramolecular organizations.In this work, the dependence of the conductivity of poly (diphenylene phthalide) films in an alternating electric field in the low-frequency range from 0.1 to 106 Hz on the supramolecular structure of polymer films was studied. It was found that the type of dependence of the conductivity of polymer films on the frequency of an alternating field depends on the thickness and supramolecular structure of the polymer films, as well as the electric field strength. The applicability of the Jonsher’s model, which describes the conductivity of amorphous materials in an alternating electric field, for thin polymer films is discussed. A correlation between the power-law dependence index and the supramolecular structure of the polymer film and the influence of dipole polarization and injection of charge carriers into the bulk of the polymer film on the conductivity of the polymer film have been revealed.