Poly Aryl Ether Ketone Research Articles

Poly aryletherketone chemically modified multi-walled carbon nanotubes/poly etheretherketone electromagnetic interference shielding foam suitable for high temperature and strong corrosive media

Poly aryletherketone chemically modified multi-walled carbon nanotubes/poly etheretherketone (PAEK-m-CNTs/PEEK) electromagnetic interference (EMI) shielding foams were fabricated using supercritical carbon dioxide (Sc-CO2) foaming technique saturated near-melting point (Tm). The percolation thresholds for conductivity and EMI shielding of PAEK-m-CNTs/PEEK foams were both significantly reduced by the presence of the porous structure, reaching to 0.0457 vol% and 0.123 vol%, respectively. These reductions were observed to be 87.72% and 75.20% of those of PAEK-m-CNTs/PEEK composites. This could be attributed to the heterogeneous nucleation of PAEK-m-CNTs, which are uniformly dispersed in PEEK, in addition to the Sc-CO2 foaming technique saturated near Tm. By comparison, it could be observed that the specific total electromagnetic shield effectiveness (SSETotal) of PAEK-m-CNTs/PEEK foam with a filler content of 0.440 vol% was 687.9% higher than that of PAEK-m-CNTs/PEEK composite with a filler content of 0.496 vol%. Moreover, the introduction of the porous structure transformed the electromagnetic shielding material from reflective to absorptive. In addition, PAEK-m-CNTs/PEEK foams demonstrated the capacity to maintain stable performance even in high temperatures of up to 315 °C and in the presence of strong corrosive media.

Carbon Fiber Reinforced Hybrid Polyaryl–Ether–Ether–Ketone (PEEK) Spinal Fixation System: Technical Features and Preliminary Clinical Trial

Carbon Fiber Reinforced Hybrid Polyaryl–Ether–Ether–Ketone (PEEK) Spinal Fixation System: Technical Features and Preliminary Clinical Trial

Mechanical characterization of FDM components made of polyaryletherketone (PAEK) for aerospace applications: a comparison of direct printing and box-cut sample manufacturing strategies

This study delves into the manufacturing strategies employed for fabricating tensile samples utilized in the mechanical characterization of material extrusion (MEX) components constructed with polyaryletherketone (PAEK) for aerospace applications. Two distinct methods were investigated for obtaining tensile test samples: direct cutting and extraction from a box. These methods were examined under both as-printed and annealing conditions. Quasistatic tensile tests were conducted along the building direction to evaluate the impact of processing conditions on the adhesion of overlying layers. The results unveiled significant disparities in mechanical behavior and crystallinity between directly printed samples and those derived from the box. The Young’s modulus exhibited marginal influence; however, the tensile strength of directly printed samples measured at 30 MPa (prior to annealing), corresponding to 50% of the strength observed in samples cut from the box (60 MPa). Moreover, the elongation at rupture of directly printed samples was found to be less than 2%, while that of cut samples exceeded 8%. Notably, directly printed samples exhibited a significant degree of incipient crystallization (12.18%), contrasting with the lower level of crystallinity observed in samples cut from the box (3.27%). These findings underscore the importance of recognizing the limitations associated with direct sample printing, emphasizing its crucial role in accurately characterizing components destined for the aerospace industry. Furthermore, this understanding is pivotal for optimizing the performance and reliability of MEX-printed PAEK components in aerospace engineering applications.

An effective strategy to enhance phosphoric acid retention and proton conductivity stability: Construction of proton transfer channels with starch rather than H3PO4

To enhance the phosphoric acid (PA) retention as well as maintain high proton conductivity of phosphoric acid doped proton exchange membranes at high temperature, we successfully design a series of phosphoric acid doped biobased composite membranes by incorporation of starch and graphene oxide (GO) into poly arylene ether ketones (PAEK). Proton transfer channels should be mainly built through dense hydrogen bonds formed from massive oxygen-containing groups of starch mainchain, which is confirmed by Molecular dynamics (MD) simulation, FT-IR and XRD analysis. The dense hydrogen-bond structure could construct fast proton transfer channels with extreme low doping level (0.00484 molH3PO4). The excellent PA retention properties with almost unchanged proton conductivity at high temperature (200 °C) for 600 min indicates that PA molecules are firmly fixed into membranes. Thus, in this study, we suggest a novel strategy for stablizing proton conductivity at high temperature and improving PA retention properties of PA doped membranes, which is building dense hydrogen-bond structure with low PA doping level.Based on the results in this study and the Grotthuss proton transfer mechanism, dense hydrogen-bonds from oxygen-containing groups in polymer backbones should be more stable than hydrogen-bonds from massive H3PO4 molecules with high acid doping levels to promote proton conduction.

Characterization and modeling of laser transmission welded polyetherketoneketone (PEKK) joints: Influence of process parameters and annealing on weld properties

Welding high-performance thermoplastics has gained popularity across various industries such as automotive, aerospace, and medical. Laser transmission welding (LTW) has emerged as an effective method for joining thermoplastic parts due to its precise control and high joint quality. PAEK (polyaryletherketone) are wide spreading over various industrial applications as a substitute to metals and thermosets when high durability and performance are required. Polyetherketoneketone (PEKK) is one of these PAEK and it has received less attention than PEEK until now. PEKK, being a semi-crystalline thermoplastic, requires additional care during processing due to its propensity to crystallize. This study presents both experimental and numerical investigations into LTW of PEKK molded parts, aiming to understand the influence of welding parameters and crystallinity on weld joint morphology and mechanical properties. PEKK plates, prepared in amorphous and semi-crystalline states, are subjected to LTW using a 975 nm diode laser. Material characterization confirms differences in crystallinity between the samples, which affect their thermal and optical properties, which are crucial for welding. Welding tests are conducted with varying laser power (between 75 and 95 W) and semi-transparent part thickness (2 and 4 mm). The morphology of joints is analysed. Assemblies undergo post-weld annealing treatment to examine its influence on weld crystallinity and consequent mechanical properties. Results reveal an anisotropic distribution of crystallinity within the heat-affected zone (HAZ). The depths of the molten layer (ML) and semi-crystalline layer (scL) vary with laser power and assembly type. A notable decrease in weld strength with laser power is highlighted, while annealing leads to enhanced crystallinity and improved weld strength. Despite variations, high weld strengths are achieved with annealing. Computational modelling elucidates the complex interplay between laser irradiation, temperature distribution, and crystallization kinetics observed experimentally. Overall, this comprehensive investigation provides valuable insights into optimizing LTW parameters for PEKK parts.

Influence of Extrusion Parameters on the Mechanical Properties of Slow Crystallizing Carbon Fiber-Reinforced PAEK in Large Format Additive Manufacturing.

Additive Manufacturing (AM) enables the automated production of complex geometries with low waste and lead time, notably through Material Extrusion (MEX). This study explores Large Format Additive Manufacturing (LFAM) with carbon fiber-reinforced polyaryletherketones (PAEK), particularly a slow crystallizing grade by Victrex. The research investigates how extrusion parameters affect the mechanical properties of the printed parts. Key parameters include line width, layer height, layer time, and extrusion temperature, analyzed through a series of controlled experiments. Thermal history during printing, including cooling rates and substrate temperatures, was monitored using thermocouples and infrared cameras. The crystallization behavior of PAEK was replicated in a Differential Scanning Calorimetry (DSC) setup. Mechanical properties were evaluated using three-point bending tests to analyze the impact of thermal conditions at the deposition interface on interlayer bonding and overall part strength. The study suggests aggregated metrics, enthalpy deposition rate and shear rate under the nozzle, that should be maximized to enhance mechanical performance. The findings show that the common practice of setting fixed layer times falls short of ensuring repeatable part quality.

Improving the interfacial properties of carbon fiber/low melting point PAEK composites by embellishing of bio-based PAEK sizing agent

In this study, a bio-based polyarylene ether ketone (bio-PAEK) was synthesized to prepare water-based sizing agents for enhancing the interfacial adhesion between carbon fiber (CF) and matrix. Thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) results indicated that the bio-PAEK exhibited good thermal properties. To improve the processability and reduce the processing temperature, PAEK with a low melting point (LMPAEK) was also used as the matrix resin. The glass-transition temperature (Tg) of LMPAEK was slightly higher than that of polyether ether ketone (PEEK), but its melting temperature (Tm) was lower 48.5 °C. A strong interface was created after introducing sizing agents onto the CF surface due to good compatibility between fibers and matrix. The interlaminar shear strength (ILSS), interfacial shear strength (IFSS) and flexural strength of CF2/LMPAEK composites increased by 54.7 %, 56.0 % and 46.6 %, respectively, compared with the untreated composites. This study provided a novel approach to prepare water-based bio-PAEK sizing agents for CF composites with a low melting point matrix to be applied in additive manufacturing.

Effects of handheld nonthermal plasma on the biological responses, mineralization, and inflammatory reactions of polyaryletherketone implant materials

Background/purposeThe handheld nonthermal plasma (HNP) treatment may alter the surface properties, bone metabolism, and inflammatory reactions of polyaryletherketone (PAEK) dental implant materials. This study tested whether the HNP treatment might increase the biocompatibility, surface hydrophilicity, surface free energies (SFEs), and the cell adhesion and mineralization capability of PAEK materials. Materials and methodsDisk-shaped samples of titanium (Ti), zirconia (Zr), polyetheretherketone (PEEK [PE]), and polyetherketoneketone (PEKK [PK]) were subjected to HNP treatment and termed as TiPL, ZrPL, PEPL, and PKPL, respectively. Water-surface reactions were examined using a goniometer. MG-63 cells were cultured on all samples to assess the cell viability, cytotoxicity, cell attachment, and mineralization characteristics. The expression of pro-inflammatory cytokines (tumor necrosis factor-alpha and interleukin-6) and key mineralization markers (alkaline phosphatase [ALKP], osteopontin [OPN], and dentin matrix protein 1 [DMP1]) was measured using enzyme-linked immunosorbent assay kits. ResultsThe HNP-treated samples exhibited significantly enhanced surface hydrophilicities and SFEs compared to the untreated samples. The cell viability remained high across all samples, indicating no cytotoxic effects. The HNP treatment significantly enhanced MG-63 cell adherence and proliferation. Elevated levels of ALKP and OPN were observed for the plasma-treated PEPL and PKPL specimens, while DMP1 levels increased significantly only in the PKPL specimen. Pro-inflammatory cytokine levels were low across all samples, suggesting no inflammatory response. ConclusionThe HNP-treated PAEKs have enhanced the surface hydrophilicity and SFEs as well as superior cell adhesion and mineralization capability, and thus may be good clinical dental implant materials.

Non-covalent functionalization at Titanium carbide nano-particles for strengthening the interface with polyaryletherketone matrix for developing high-strength adhesives

In this study, a highly effective cationic polymer, Poly (diallyldimethylammonium chloride) (PDDA), was used to bond Titanium Carbide (TiC) nano-particles (NPs) non-covalently with matrix polyaryletherketone (PAEK). Functionalization of PDDA to TiC NPs was confirmed using Fourier-transform infrared spectroscopy (FT-IR), Zeta potential, and Field Emission Scanning Electron Microscopy (FE-SEM). Both TiC NPs (3 wt%) (untreated and PDDA-treated) were added to PAEK, as a filler for reinforcement and elevating friction. The addition of TiC NPs (untreated and treated) in the PAEK led to an improvement in selected performance properties such as thermal stability (by 11 and 13 °C), surface free energy (17 and 29%), and lap shear strength (LSS) (116 and 161%) respectively. Plastic deformation, cup formaion and micro-striation formation were the major failure mechanisms. PDDA treatment to TiC NPs resulted in better and more uniform deagglomeration in the PAEK matrix, strengthened particle-matrix interface, higher surface energy, and hence more adhesion with the adherend. The improved strengthening of both the interfaces (NPs with the matrix and nanocomposite with the metallic adherend) led to an enhanced performance by the treated NPs.

Poly (arylene ether ketone sulfone)s functionalized with diethylenetriamine-modified graphene oxide as proton exchange membranes for fuel cells

In this paper, composite proton exchange membranes (PEMs) based on functionalized graphene oxide (NGO) and carboxylated sulfonated poly aryl ether ketone sulfone (C-SPAEKS) were successfully synthesized. Functionalized graphene oxide was synthesized using graphene oxide as a substrate, and then diethylenetriamine (DETA) was chemically bound to the graphene oxide. The 1H NMR, FT-IR and XPS were used to characterize the NGO and composite membranes. The results show that the composite membranes have good proton conductivity, dimensional stability and electrochemical performance. The swelling rate of all the composite membranes was less than 18%, which indicates that they have good dimensional stability. Compared to C-SPAEKS membrane (34.8 mS cm-1 at 20 °C, 109.8 mS cm-1 at 90 °C), the proton conductivities of C-SPAEKS/GO-0.75 membrane (52.4 mS cm-1 at 20 °C, 171.1 mS cm-1 at 90 °C) were significantly improved. Meanwhile, the C-SPAEKS/NGO-0.75 achieved peak power density of 407.77 mW cm-2 at high OCV of 0.9576 V. Such a result is much superior to the C-SPAEKS membrane (0.8973 V, 190.72 mW cm-2) and the Nafion 117 (0.99 V, 302 mW cm-2), and demonstrated good single-fuel cell performance. In summary, it can be well concluded that functionalized GO as filler makes an significant contribution in improving the overall performance of the composite membranes.

Influence of handheld nonthermal plasma on shear bond strength of polyaryletherketone to resin-matrix cement

Background/purposeChallenges exist regarding the bonding efficiency of polyaryletherketone (PAEK), a high-performance thermoplastic, attributed to its chemical inertness and hydrophobic surface, hindering effective bonding with resin-matrix cement. This research explored the impact of handheld nonthermal plasma (HNP), under varying operational parameters, on PAEK surface wettability and changes in bonding performance with cement. Materials and methodsThree types of disc-shaped PEAK specimens were prepared, with surface treatments categorized as grinding, airborne-particle abrasion (APB), and HNP. Surface wettability was analyzed using a contact angle analyzer (n = 10). Specimens were bonded with resin cement and subjected to artificial aging tests: distilled water bath (NA), thermocycling, and highly accelerated stress tests (n = 10 for each test). Shear bond strength (SBS) was measured, failure modes were analyzed, and statistical analyses were conducted. ResultsThe HNP markedly improved PAEK surface wettability, achieving superhydrophilicity (P < 0.05). This effect intensified with extended operation times (30 or 60 s) and reduced elapsed times (<30 s). HNP-treated PAEK exhibited higher SBS than APB (P < 0.05) and maintained bonding durability after artificial aging, particularly in ketone-enriched variants. Failure analysis revealed predominantly adhesive failure under APB–NA treatment, mixture failures under HNP–NA treatment and postaging, but no cohesive failure. ConclusionThe HNP device benefits dental settings by transforming the PAEK surface into superhydrophilic properties, thereby improving PAEK–cement bonding. It significantly enhances bond durability within 30 s of operation and after a 30 s elapsed period. It is noteworthy that ketone-enriched PAEK demonstrates markedly improved bonding performance.

Targeted Synthesis of Thermo- and Heat-Resistant Polyarylene Ether Ketones with a Complex of Valuable Functional Properties

Targeted Synthesis of Thermo- and Heat-Resistant Polyarylene Ether Ketones with a Complex of Valuable Functional Properties

Application of Polyether Ketone in Oral Implantology and Prosthodontics.

Polyetheretherketone (PEEK) is a polymer that has a comprehensive range of possible uses in dental treatment. The goal of this study was to compile research findings on the substance of dental claims and highlight the upcoming predictions of PEEK in clinical dentistry. PEEK is a novel polymeric material that is yet in its preliminary stage of evolution. Biomolecules are elastic materials with remarkable mechanical strength, barrier properties, and heat resistance compared to other matrix materials. The efficacy of PEEK in clinical dentistry has been acknowledged. Polyetherketone (PEKK) and PEEK are the most commonly mentioned members of the polyaryletherketone (PAEK) family. PEEK has also found significant use in dentistry, notably in prosthodontics and implant dentistry. It also offers exceptional mechanical qualities, including high strength and toughness, making it ideal for dental implants and prostheses. It can endure the stresses of chewing and grinding, resulting in long-lasting restorations. PEEK's tooth-colored look and ability to simulate natural tooth translucency make it suitable for use in dental prostheses such as crowns and bridges. This makes it a more esthetically acceptable alternative to standard metal-based repairs.

Comparison of biomechanical performance of titanium and polyaryletheretherketone miniscrews at different insertion angles: A finite element analysis.

Only miniscrews [temporary anchoring devices, (TADs)] can provide absolute anchorage during orthodontic treatment. Titanium (Ti) is a fundamental material used in the production of miniscrews, but it has many disadvantages. Polyaryletheretherketone (PEEK) may have various benefits in the production of miniscrews. Finite element analysis (FEA) is a valid and reliable method for calculating stress, strain, and loading forces on complex structures and can be more time- and cost-efficient. To investigate the biomechanical performance of Ti and PEEK as miniscrew biomaterials employing FEA. This study is a 3-D (3D) simulation with FEA. First, 3D miniscrew modeling is done using Ti base material and PEEK (1.4 mm × 6 mm size), as well as 3D inter-radicular space bone modeling. The simulation was performed by modeling the insertion angles (30°, 60°, and 90°) and applying a 200-gram loading force. The biomechanical performance of the miniscrew was then determined using FEA. As the angle of insertion increases, the tension on the bone decreases, the stress on the TADs increases, and the bone deformation decreases. Compared to TADs made of Ti and PEEK, TADs made of PEEK alone cause more bone stress than TADs made of Ti. The distortion in the maxilla is observed to be larger than in the mandibular. PEEK has greater stress on the bones than Ti and may be prospected as an alternative biomaterial for TAD fabrication, as documented in the FEA.

Characteristics of in-situ automated fiber placement carbon-fiber-reinforced low-melt polyaryl ether ketone laminates part 1: Manufacturing influences

This study presents an investigation into mechanical and thermal properties, as well as the microstructure of Automated Fiber Placement-manufactured laminates using a novel carbon fiber-reinforced low-melt polyaryl ether ketone polymer material. The material’s lower melting temperature and lower melt viscosity as compared to established high-temperature thermoplastic materials as PEEK, promises favourable characteristics for the Automated Fiber Placement process. This work aims at in-situ consolidation and the influence of a heated tooling and a post process tempering step, which both turned out to be promising in previous investigations. Laminates were manufactured using a cold tooling, a heated tooling configuration, a cold tooling with a subsequent tempering process step and a hot-pressed reference laminate. Differential Scanning Calorimetry showed that crystallinity values more than doubled for the heated tooling and post process tempering configurations, compared to the cold tooling, reaching 24% and 30%, respectively. Mechanical strength values showed an increase in interlaminar shear strength and compression strength but did not increase to the same extent as was expected from the increase in crystallinity. With Scanning Electron Microscopy differences in the microscopic structure of the polymer matrix could be detected. While the post process tempering step leads to a mostly lamellar crystalline structure, the heated tooling configuration and the post process hot pressing induce a predominance of crystalline spherulites, which might positively affect the mechanical performance. Computed Tomography scans revealed a high amount of porosity in the in-situ-manufactured samples and unprocessed tape material, which likely mitigated the positive effect of increased crystallinity.

Sandwich-structured nano-adhesive based on the synergistic action of two nanoparticles (SiC and MWCNTs)

This study encompasses the development of sandwich-structured adhesive reporting the synergism in the functioning of two kinds of nanoparticles (NPs)-SiC (Silicon carbide) and MWCNTs (multiwalled carbon nanotubes). Two adhesives using MWCNTs and NPs of SiC in selected amounts were developed using Polyaryletherketone (PAEK) thermoplastic polymer as a base matrix. Fabricated joints using these adhesives were characterized for degglomeration and dispersion of NPs, lap shear strength (LSS), and failure modes. Based on the data on the LSS, the advantages and disadvantages of using individual NPs were analyzed, and the third adhesive was designed in a sandwich manner, where positive points of both the NPs were expected to work synergistically. The sandwich adhesive showed higher LSS than the individual ones, i.e., an 8.6% and 26% improvement to SiC-based and MWCNT-based adhesives, respectively. It was concluded that the strengthening mechanism of MWCNTs of bulk polymer in the central portion was beneficial. The two outer layers of SiC NPs in PAEK interacting with the two steel surfaces of coupons proved helpful in increasing friction and, hence, synergistically increasing the LSS of sandwich adhesive.

Protecting Orthopaedic Implants from Infection: Antimicrobial Peptide Mel4 Is Non-Toxic to Bone Cells and Reduces Bacterial Colonisation When Bound to Plasma Ion-Implanted 3D-Printed PAEK Polymers.

Even with the best infection control protocols in place, the risk of a hospital-acquired infection of the surface of an implanted device remains significant. A bacterial biofilm can form and has the potential to escape the host immune system and develop resistance to conventional antibiotics, ultimately causing the implant to fail, seriously impacting patient well-being. Here, we demonstrate a 4 log reduction in the infection rate by the common pathogen S. aureus of 3D-printed polyaryl ether ketone (PAEK) polymeric surfaces by covalently binding the antimicrobial peptide Mel4 to the surface using plasma immersion ion implantation (PIII) treatment. The surfaces with added texture created by 3D-printed processes such as fused deposition-modelled polyether ether ketone (PEEK) and selective laser-sintered polyether ketone (PEK) can be equally well protected as conventionally manufactured materials. Unbound Mel4 in solution at relevant concentrations is non-cytotoxic to osteoblastic cell line Saos-2. Mel4 in combination with PIII aids Saos-2 cells to attach to the surface, increasing the adhesion by 88% compared to untreated materials without Mel4. A reduction in mineralisation on the Mel4-containing surfaces relative to surfaces without peptide was found, attributed to the acellular portion of mineral deposition.

Characteristics of in-situ automated fiber placement carbon-fiber-reinforced low-melt polyaryl ether ketone laminates part 2: Effect of prepreg composition

This paper presents an investigation into prepreg tape composition and its impact on the consolidation quality of in‐situ Automated Fiber Placement-manufactured laminates. Three different prepreg tape materials were investigated in terms of fiber distribution, porosity and surface roughness. Laminates were manufactured using the in-situ Automated Fiber Placement process and subsequently tested using microanalysis and mechanical testing methods. Higher quality prepreg tape material yielded lower porosity laminates and increased mechanical strength results. The best in-situ Automated Fiber Placement-manufactured laminates achieved 82 % and 88 % of hot-pressed reference tensile- and compressive strength, respectively. Prepreg tape with disadvantageous composition for in‐situ consolidation yielded up to 74 % knockdown compared to the best in-situ consolidated laminates. A five-point bending test was successfully used to determine interlaminar shear strength with significant results relating to consolidation quality. A correlation was successfully established between prepreg composition, resulting laminate consolidation quality and mechanical properties.

Construction of fluorinated hyperbranched polyaryletherketone-based UV-cured films with low dielectric and enhanced mechanical properties

The incorporation of hyperbranched structure into the polyaryletherketone (PAEK) is a crucial method for achieving a low dielectric constant (Dk), and the inclusion of crosslinked structure effectively reduces the dielectric loss (Df). This approach is of great significance in the development of high-quality communication at high frequencies. However, it is still a significant challenge for maintaining its mechanical properties and reducing Dk and Df due to the poor film-forming properties and low ductility of hyperbranched polymers. In this study, we synthesized a novel acrylate-based fluorinated hyperbranched photosensitive polyaryletherketone (hb-P6FAEK-Ace) as a prepolymer with various bifunctional aliphatic active and 4-acryloyl morpholine as the reactive solvent. Upon UV irradiation, cured films were obtained. This method significantly improved the mechanical properties of the hyperbranched UV-cured resin, with the tensile strength of CF-DCDDA of 83.2 MPa and the elongation at break of 7.61%. Additionally, the five prepared photosensitive resins exhibited excellent rheological properties (from 71.6 mPa s to 134.7 mPa s at 100 °C), rapid curing rates (within tens of seconds), and minimal volume shrinkage (<7%). Meanwhile, the Dk of CF-DCDDA was measured to be 2.87, with a Df of 0.0126 at the frequency of 20 GHz. This low dielectric expression for the crosslinked cured films could be ascribed to the confinement of electronic polarization caused by the crosslinked and hyperbranched structures. This work provides a simple, green, and promising strategy for enhancing the dielectric and mechanical properties of hb-PAEK.

ИССЛЕДОВАНИЕ ФИЗИКО-ХИМИЧЕСКИХ ОСОБЕННОСТЕЙ СТРОЕНИЯ И ЭЛЕКТРОННЫХ СВОЙСТВ СОПОЛИАРИЛЕНЭФИРКЕТОНОВ

In this work model compounds for copolymers of polyarylene ether ketones (co-PAEK) were modeled and analyzed, and optical and electrophysical studies were carried out. Quantum chemical calculations of the structures were carried out using the density functional theory (DFT) method in the B3LYP/6-31+G(d) approximation. The optical properties of the films were studied using the optical absorption method in the UV-visible region. The study of the current-voltage characteristics and time dependences was carried out on the MPI ETS50 probe station.