Facile synthesis and excellent electromagnetic wave absorption properties of flower-like porous RGO/PANI/Cu<Subscript>2</Subscript>O nanocomposites

Novel porous ternary nanocomposite systems containing reduced graphene oxide (RGO)/polyaniline (PANI)/cuprous oxide (Cu₂O) were prepared via one-step in situ redox method. The RGO/PANI/Cu₂O nanocomposites present a flower-like structure with an average size of 2.0 μm in diameter. The morphologies and properties of the products can be controlled by adjusting the molar ratios of aniline to Cu²⁺. When the molar ratio of aniline to Cu²⁺ is 1:1, the product exhibits excellent microwave absorption property in the frequency range of 2–18 GHz. It can be seen that the maximum reflection loss (RL) of the ternary composite is up to ?52.8 dB at 2.7 GHz with a thickness of only 2 mm, and the absorption bandwidth corresponding to ?10 dB (90% of EM wave absorption) is 13.2 GHz. The microwave absorption property of ternary RGO/PANI/Cu₂O composite is significantly improved due to its special flower-like porous structure, dielectric loss property and well impedance matching characteristics, which is 8.12 times than that of pure RGO and 5.28 times than that of pure PANI. Therefore, our study paves a new way to prepare the promising lightweight and high-performance composite materials combined with the characteristics of three components for electromagnetic absorption.     

Fabrication and microwave absorption performances of hollow-structure Fe<Subscript>3</Subscript>O<Subscript>4</Subscript>/PANI microspheres

The hollow polyaniline (PANI) microspheres were prepared by controlling the mass ratio of the aniline to polystyrene (PS) via a template method, and Fe₃O₄/PANI composite microspheres have been fabricated by blending the hollow PANI microspheres with Fe₃O₄ magnetic particles. The effects of the mass ratio of aniline/PS on the microwave absorption performances of Fe₃O₄/PANI microspheres were investigated. It was found that the value of minimum reflection loss (RL_min) of the microspheres were respectively ?14.06, ?22.34 and ?24.3 dB, corresponding to the mass ratio of aniline/PS of 1:1.5, 1:3, and 1:6. In addition, when the mass ratio of aniline/PS was 1:6, with the thickness of 1.5 and 2.0 mm, the bandwidth below ?10dB were respectively 2.48 GHz (15.52–18 GHz) and 4.64 GHz (11.04–15.68 GHz), indicating that the Fe₃O₄/PANI microspheres could be a potential electromagnetic wave absorbing material in X (8–12 GHz) and Ku (12–18 GHz) bands.     

Structural and magnetic properties of nanocomposites based on nanostructured polyaniline and titania nanotubes

Nanocomposites consisting of self-assembled polyaniline (PANI) nanostructures and titania nanotubes (TiO₂-NT) were synthesized by the oxidative polymerization of aniline with ammonium peroxydisulfate in an aqueous dispersion of TiO₂-NT (outer diameter ~10 nm), without added acid. The influence of initial mole ratio of aniline to TiO₂ (80, 20, and 5) on the morphology, electrical conductivity, molecular structure, crystallinity, and magnetic properties of synthesized PANI/TiO₂ nanocomposites was studied. Transmission electron microscopy, Raman spectroscopy, and X-ray powder diffraction proved that the shape and structure of TiO₂-NT in the final nanocomposites were preserved. The shape of PANI nanostructures formed in the nanocomposites was influenced by the initial aniline/TiO₂-NT mole ratio. Nanotubes and nanorods are predominant PANI nanostructures in the nanocomposite prepared with the highest aniline/TiO₂ mol ratio of 80. The decrease of aniline/TiO₂ molar ratio induced more pronounced formation of nanorod network. The electrical conductivity of PANI/TiO₂ nanocomposites was in the range (1.3–2.4) × 10^?3 S cm^?1. The nanocomposites exhibit weak ferromagnetic behavior. Approximately order of magnitude lower values of coercive field and remanent magnetization were obtained for nanocomposite samples in comparison to pure PANI.     

Preparation of new antimony(0)/polyaniline nanocomposites by a one-pot solution phase method

The new Sb(0)/PANI nanocomposite was successfully synthesized by a one-pot solution phase method. Sb(0) particles were first prepared by the reduction of SbCl₅ or SbCl₃ using t-BuONa-activated NaH in THF. A ligand exchange with aniline on t-BuONa-stabilized Sb(0) particles yielded aniline-stabilized particles. The Sb(0)/PANI nanocomposite was finally obtained by polymerizing aniline-stabilized Sb(0) particles by using ammonium persulfate. The morphology and the structure of the nanocomposite was examined by transmission electron microscopy (TEM), selected-area electron diffraction (SAED), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). Results obtained show that the Sb(0) precursor has a great influence on the size and the crystallinity of Sb(0) nanoparticles dispersed in PANI.     

Preparation, characterization and photocatalytic activity of TiO2/polyaniline core-shell nanocomposite

Polyaniline (PANI) as a promising conducting polymer has been used to prepare polyaniline/TiO₂ (PANI/TiO₂) nanocomposite with core-shell structure as photocatalyst. Titanium dioxide (TiO₂) nanoparticles with an average crystal size of 21?nm were encapsulated by PANI via the in situ polymerization of aniline on the surface of TiO₂ nanoparticles. FT?CIR, UV-Vis-NIR, XRD, SEM and TEM techniques were used to characterize the PANI/TiO₂ core-shell nanocomposite. Photocatalytic activity of PANI/TiO₂ nanocomposite was investigated under both UV and visible light irradiations and compared with unmodified TiO₂ nanoparticles. Results indicated deposition of PANI on the surface of TiO₂ nanoparticles which improved the photocatalytic activity of pristine TiO₂ nanoparticles.     

Preparation of nanocomposite of polyaniline and gamma-zirconium phosphate (γ-ZrP) by power ultrasonic irradiation

The high-intensity ultrasound was applied to the preparation of nanocomposite of polyaniline (PANI) and gamma-zirconium phosphate (γ-ZrP) by intercalation of aniline into γ-ZrP. The intercalation rate was enhanced greatly and the interlayer distance of aniline-intercalated γ-ZrP was determined to be 16.0 Å. The intercalated aniline polymerized at low pH during the sonication by initiator (NH₄)₂S₂O₈ and nanocomposite of exfoliation of γ-ZrP in PANI bulk was obtained. The intercalated or exfoliated compounds were characterized by XRD, FTIR, TEM, UV-Vis spectrum, and TG-DTA.     

Synthesis of PANI/TiO<Subscript>2</Subscript>–Fe<Superscript>3+</Superscript> nanocomposite and its photocatalytic property

A convenient method for synthesizing highly photocatalytic activity PANI/TiO₂–Fe³⁺ nanocomposite was developed. The effect of calcination temperature on the phase composition of TiO₂ nanopowder was investigated. It was found that higher temperature could promote the formation of rutile phase. The nanocomposite was characterized by atomic force microscopy (AFM), transmission electron microscopy (TEM), infrared spectroscopy (IR) and X-ray diffraction (XRD). The results indicated that the nanohybrid was composed of TiO₂, Fe³⁺ and PANI. The photocatalytic property of the nanocomposite was evaluated by the degradation of methyl orange. In the presence of this catalyst, the degradation rate of methyl orange of 95.2% and 70.3% could be obtained under the UV and sunlight irradiation within 30 min, respectively. The apparent rate constant was 5.64 × 10⁻² which is better than that of the Degussa P25.     

Synthesis and ferrimagnetic properties of novel Sm-substituted LiNi ferrite–polyaniline nanocomposite

Polyaniline (PANI)–LiNi_0.5Sm_0.08Fe_1.92O₄ nanocomposite was synthesized by an in situ polymerization of aniline in the presence of LiNi_0.5Sm_0.08Fe_1.92O₄ ferrite. The products were characterized by powder X-ray diffractometer (XRD), Fourier transform infrared (FTIR) and UV–visible absorption spectrometer, thermogravimetric analyser (TGA), atomic force microscope (AFM) and vibrating sample magnetometer (VSM). The results of XRD, FTIR and UV–visible spectra confirmed the formation of PANI–LiNi_0.5Sm_0.08Fe_1.92O₄ composite. AFM study showed that ferrite particles had an effect on the morphology of the composite. TGA revealed that the incorporation of ferrite improved the thermal stability of PANI. The nanocomposite under applied magnetic field exhibited the hysteresis loops of ferrimagnetic nature at room temperature. The bonding interaction between ferrite and PANI in the nanocomposite had been studied.     

Enhancing the thermoelectric performance by defect structures induced in p-type polypyrrole-polyaniline nanocomposite for room-temperature thermoelectric applications

Organic thermoelectric materials mainly conducting polymers are green materials that can convert heat energy into electrical energy and vice versa at room temperature. In the present work, we investigated the thermoelectric properties of polymer nanocomposite of polypyrrole (PPy) and polyaniline (PANI) (PPy/PANI) by varying the pyrrole: aniline monomer ratios (60:40, 50:50, and 40:60). The PPy/PANI composite is prepared by in-situ chemical polymerization of PPy on PANI dispersion. It has been observed that the combination of two conducting polymers has enhanced the electrical and thermal properties in the PPy/PANI composite due to the strong π–π stacking and H-bonding interaction between the conjugated structure of PPy and conjugated structure of PANI. The maximum electrical conductivity of 14.7 S m^?1 was obtained for composite with high pyrrole content, whereas the maximum Seebeck coefficient of 29.5 μV K^?1 was obtained for composite with high aniline content at 366 K. Consequently, the PPy/PANI composite with pyrrole to aniline monomer ratio of 60:40 exhibits the optimal electrical conductivity, Seebeck coefficient, and high power factor. As a result, the maximum power factor of 2.24 nWm^?1 K^?2 was obtained for the PPy/PANI composite at 60:40 pyrrole to aniline monomer ratio, which is 29 times and 65.8 times higher than PPy (0.077 nWm^?1 K^?2) and PANI (0.034 nWm^?1 K^?2), respectively.

     

Effect of polyaniline concentration on the photoconversion efficiency of nano-TiO<Subscript>2</Subscript> based dye sensitized solar cells

Extensive research have been made in improving the dye sensitized solar cells (DSSC) performance by designing, tailoring and enhancing the photoconversion properties of the matrix. The approaches used are material synthesis, dye permutation combinations, use of natural extracts or using several sensitizers. The polymers are also being explored in this regards in their pristine or composite forms. Therefore, in this study an attempt is made to synthesize a mesoporous polyaniline–titanium dioxide (PANI–TiO₂) nanocomposites with one pot synthesis approach at different concentrations of PANI (0.3–0.7 ml). Titanium isopropoxide was used as precursor for TiO₂ with aniline and the material was synthesized at ice bath temperature. Morphological observations showed that the composite is a mesoporous material with tubular structure where TiO₂ particles are seen entrapped in the polymer matrix and found that intercalation can be tailored with PANI concentration. Structural, functional and optical characterization indicate anatase phase of TiO₂, with several functional bands that can help in dye interaction and broad absorption bands within visible region. The photocurrent-voltage response was measured with simulated light and source-meter. It is interesting to note that increasing PANI concentration enhances the mesoporous structure and hence increases the dye loading capacity and photoconductivity of the material. The efficiency increased by about 22 % with addition of 0.5 ml of PANI from 0.3 ml. The proposed study has indicated that such material have the potential to be used for DSSC fabrication with which the device performance can further be increased to a better levels.     

Preparation and characterization of polyaniline/cerium dioxide (CeO2) nanocomposite via in situ polymerization

Crystalline ceria (CeO₂) nanoparticles have been successfully synthesized by a microwave-assisted solution method. Polyaniline (PANI)/cerium dioxide (CeO₂) nanocomposite was synthesized by in situ polymerization of aniline in the presence of CeO₂ nanoparticles. Characterization of CeO₂ and PANI/CeO₂ nanomaterials are carried out using various studies such as powder X-ray diffraction, infrared spectral and UV–Vis absorption spectral analyses, scanning electron microscopic and high-resolution transmission electron microscopic (HRTEM) studies and thermal analysis. The HRTEM of the images indicate that the CeO₂ nanoparticles were embedded in the PANI matrix forming the core–shell structure.     

Structural,dielectric, ac conductivity and electromagnetic shielding properties of polyaniline/Ni<Subscript>0.5</Subscript>Zn<Subscript>0.5</Subscript>Fe<Subscript>2</Subscript>O<Subscript>4</Subscript> composites

A conducting polymer, polyaniline (PANI)/Ni_0.5Zn_0.5Fe₂O₄ composites with high dielectric absorbing properties and electromagnetic shielding effectiveness at low frequencies were successfully synthesized through a simple in situ emulsion polymerization. PANI was doped with hydrochloric acid to improve its electrical properties and interactions with ferrite particles. PANI/Ni_0.5Zn_0.5Fe₂O₄ composites were characterized by X-ray diffraction analysis, scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy and thermal gravimetric analysis. Frequency dependence of dielectric and ac conductivity (σ_ac) studies have been undertaken on the PANI/Ni_0.5Zn_0.5Fe₂O₄ composites in the frequency range 50 Hz–5 MHz. The electrical conduction mechanism in the PANI/Ni_0.5Zn_0.5Fe₂O₄ is found to be in accordance with the electron hopping model. Further, frequency dependence of electromagnetic interference (EMI) shielding effectiveness (SE) is studied. The EMI shielding effectiveness is found to decrease with an increase in the frequency. The maximum value 55.14 dB of SE at 50 Hz was obtained at room temperature for PANI/Ni_0.5Zn_0.5Fe₂O₄ composites in the 50 Hz–5 MHz frequency range. PANI/Ni_0.5Zn_0.5Fe₂O₄ composites were demonstrated as a promising functional material for the absorbing of electromagnetic waves at low frequencies because of a large amount of dipole polarizations in the polymer backbone and at the interfaces of the Ni–Zn ferrite particles and PANI matrix.     

Hierarchical structures based on Li<Subscript>0.35</Subscript>Zn<Subscript>0.3</Subscript>Fe<Subscript>2.35</Subscript>O<Subscript>4</Subscript>/polyaniline nanocomposites: synthesis and excellent microwave absorption properties

For the first time, the hierarchical structures of Li_0.35Zn_0.3Fe_2.35O₄(LZFO)/polyaniline nanocomposites were successfully synthesized by interfacial polymerization. Firstly, the LZFO particles were prepared by the sol–gel method, and subsequently the PANI nanorods, composed of nanoneedle-like PANI, were grafted on the surface of the LZFO. A novel microtopography, urchin-like, of LZFO/PANI was prepared by a simple, efficient and controllable two-step method. The crystal structure, chemical bonding states and morphology of samples were characterized by means of Fourier transform infrared spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, Scanning and Transmission electron microscopy (SEM/TEM). The bandwidth of reflection loss exceeds 10 dB in the frequency was 5.56 GHz (3.36–8.48, 10.32–10.76 GHz), and the maximum reflection loss can reach ??49.4 dB at 4.96 GHz with the thickness of 5.1 mm. The enhanced microwave absorption properties of LZFO/PANI nanocomposites are mainly ascribed to the multi-level structure and the improved impedance matching, and make it a potential candidate for microwave absorption materials.     

Synthesis and microwave absorption property of ternary composites: polyaniline/CoFe<Subscript>2</Subscript>O<Subscript>4</Subscript>/Ba<Subscript>3</Subscript>Co<Subscript>2</Subscript>Fe<Subscript>24</Subscript>O<Subscript>41</Subscript>

Polyaniline (PANI)/CoFe₂O₄/Ba₃Co₂Fe₂₄O₄₁ composite was prepared by an in-situ polymerization method. The phase structure, morphology and magnetic properties of the as-prepared PANI/CoFe₂O₄/Ba₃Co₂Fe₂₄O₄₁ composite were characterized by XRD, FT-IR, SEM, TEM, and VSM, respectively. The microwave absorption properties of the composite were investigated by using a vector network analyzer in the 2–18 GHz frequency range. The results show that the maximum reflection loss value of the PANI/CoFe₂O₄/Ba₃Co₂Fe₂₄O₄₁ composite reaches ?30.5 dB at 10.5 GHz with a thickness of 3 mm and the bandwidth of reflection loss below ?10 dB reaches up to 1.2 GHz. The excellent microwave absorption properties of the as-prepared PANI/CoFe₂O₄/Ba₃Co₂Fe₂₄O₄₁ composite due to the enhanced impedance match between dielectric loss and magnetic loss.     

Thermostable nitrogen-doped HTiNbO5 nanosheets with a high visible-light photocatalytic activity

Nitrogen-doped HTiNbO₅ nanosheets have been successfully synthesized by first exfoliating layered HTiNbO₅ in tetrabutylammonium hydroxide (TBAOH) to obtain HTiNbO₅ nanosheets and then heating the nanosheets with urea. The resulting samples were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), Energy-dispersive X-ray (EDX), X-ray photoelectron spectroscopy (XPS), UV-vis spectroscopy and N₂ adsorption-desorption measurements. It was found that N-doping resulted in a much higher thermostability of the layered structure, intrinsic bandgap narrowing and a visible light response. The doped nitrogen atoms were mainly located in the interstitial sites of TiNbO₅ ⁻ lamellae and chemically bound to hydrogen ions. Compared with N-doped HTiNbO₅, N-doped HTiNbO₅ nanosheets had a much larger specific surface area and richer mesoporosity due to the rather loose and irregular arrangement of titanoniobate nanosheets. Both N-doped layered HTiNbO₅ and HTiNbO₅ nanosheets showed a very high visible-light photocatalytic activity for the degradation of rhodamine B (RhB) aqueous solution. Moreover, due to the considerably larger surface area, richer mesoporosity and stronger acidity, N-doped HTiNbO₅ nanosheets had an even higher activity than N-doped HTiNbO₅, although the latter had a stronger absorption in the visible region. The dye molecules were mainly degraded to aliphatic organic compounds and partially mineralized to CO₂ and/or CO, rather than being simply decolorized. The effect of photosensitization was insignificant and RhB was degraded mainly via the typical photocatalytic reaction routes. Two different reaction routes for the photodegradation of RhB under visible light irradiation over N-doped HTiNbO₅ nanosheets have been proposed. The present method can be extended to a large number of layered metal oxides that have the characteristics of intercalation and exfoliation, thus providing new opportunities for the fabrication of highly effective and potentially practical visible-light photocatalysts.      

Lightweight glass/Fe<Subscript>3</Subscript>O<Subscript>4</Subscript>-polyaniline composite hollow spheres with conductive and magnetic properties

Lightweight composite hollow spheres with conductive and magnetic properties were prepared by using Hollow Glass Spheres (HGS) as substrate. The morphology, composition, conductive, and magnetic properties of the resultant products were characterized by SEM, EDX, XRD, FTIR spectra, conductivity measurement, and vibrating-sample magnetometry. Polyaniline (PANI) were in situ polymerized on HGS with increasing ratios of PANI to HGS, resulting in the enhanced conductivity of HGS/PANI composites from 1.3 × 10⁻² S/cm to 4.4 × 10⁻² S/cm. Lightweight glass/Fe₃O₄-PANI composite hollow spheres (HGS/Fe₃O₄-PANI) with conductivity of 5.4 × 10⁻³ S/cm and magnetization of 9.25 emu/g were prepared by deposition of Fe₃O₄ nanoparticles onto HGS via electrostatic adsorption first, and then polymerization of aniline onto HGS/Fe₃O₄. The glass/PANI-Fe₃O₄ composite hollow spheres (HGS/PANI-Fe₃O₄) composed of Fe₃O₄ as the outmost layer and PANI as the inner layer were prepared for comparison. The conductivity and magnetization of HGS/PANI-Fe₃O₄ were 1.1 × 10⁻⁴ S/cm and 2.61 emu/g, respectively.     

Synthesis of polyaniline/ZrO<Subscript>2</Subscript> nanocomposites and their performance in AC conductivity and electrochemical supercapacitance

Polyaniline/zirconium oxide (PANI/ZrO₂) nanocomposites have been synthesized by incorporating ZrO₂ nanoparticles into the PANI matrix via liquid–liquid interfacial polymerization method. The composite formation and structural changes in PANI/ZrO₂ nanocomposites were investigated by powder X-ray diffraction (PXRD), scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FT-IR). PXRD pattern of PANI/ZrO₂ nanocomposites exhibited sharp and well-defined peaks of monoclinic phase of ZrO₂ in PANI matrix. SEM images of the composites showed that ZrO₂ nanoparticles were dispersed in the PANI matrix. The FT-IR analysis revealed that there was strong interaction between PANI and ZrO₂. AC conductivity and dielectric properties of the nanocomposites were studied in the frequency range, 50–10⁶ Hz. AC conductivity of the nanocomposites obeyed the power law indicating the universal behaviour of disordered media. The nanocomposites showed high dielectric constant in the order of 10⁴, which could be related to dielectric relaxation phenomenon. Further, the materials were checked for their supercapacitance performance by using cyclic voltammetry (CV), chronopotentiometry (CP) and electrochemical impedance spectroscopy (EIS). Among the synthesized nanocomposites, PANI/ZrO₂-25 wt.% showed a higher specific capacitance of 341 F g^?1 at 2 m Vs^?1 and good cyclic stability with capacitance retention of about 88% even after 500 charge–discharge cycles.     

Microstructure,electrical and humidity sensing properties of TiO<Subscript>2</Subscript>/polyaniline nanocomposite films prepared by sol–gel spin coating technique

High sensitive resistive type humidity sensor based titanium oxide/polyaniline (TiO₂/PANI) nanocomposite thin films prepared by a sol–gel spin coating technique on an alumina substrate. The resultant nanocomposites were characterized by using X-ray diffraction (XRD), Field emission electron microscopy, Fourier transform infrared spectroscopy (FTIR), UV–Vis absorbance and energy dispersive spectra analysis. In the XRD patterns of both pure and TiO₂/PANI composite confirms the deposition of PANI on TiO₂ and the average size of the composite particle was found to be 32 nm. Large number of nano grain surface being covered by PANI, which agrees very well with the results obtained by XRD studies. FTIR and UV–Vis spectra reveal that the PANI component undergoes an electronic structure modification as a result of the TiO₂ and PANI interaction. The room temperature resistivity was found to be for TiO₂ and TiO₂/PANI nanocomposite films 1.42?×?10⁶ and 2.56?×?10³ Ω cm respectively. The obtained TiO₂/PANI nanocomposites sensor exhibited higher humidity sensing performance such as high sensitivity, fast response (20 s) and recovery time (15 s) and high stability.     

Preparation and microwave absorption properties of BiFeO<Subscript>3</Subscript> and BiFeO<Subscript>3</Subscript>/PANI composites

BiFeO₃(BFO) particle was successfully synthesized by normal citric acid sol–gel method and the size of BiFeO₃ particle is about 200 nm. BiFeO₃/polyaniline (PANI) composites with the different weight ratio were synthesized by in situ emulsion polymerization. The citric acid doped PANI is fibrous and form a loose structure outside the BFO particle. With the increasing of PANI, the conductivity value of composites are increasing to 9.34?×?10^?2 S/cm. Moreover, the permittivity also enhance with the increasing of conductivity, which contribute to the improvement of dielectric loss. Microwave absorbing properties were investigated with a vector network analyzer in 1–18 GHz. The minimum reflection loss (RL) value is about ?40.2 dB at 8.3 GHz when the thickness is 3.5 mm, and the maximum bandwidth less than ?10 dB is 3.5 GHz (from 13.5 to 18 GHz) at the thickness of 2 mm. 3 mm millimeter-wave-attenuation properties were also tested, and the maximum attenuation value of BFO/PANI composites reach 15.71 dB. The composites can dissipate microwave energy into heat effectively by dielectric relaxation because of the suitable conductivity. The interface scattering and multiple reflections also play a important role because of the increasing of a loose structure. The BFO/PANI composite can be taken as a promising lightweight and multiband microwave absorber.     

Solid-state synthesis and electrical properties of polyaniline/Cu-montmorillonite nanocomposite

In this paper, the solid-state synthesis of polyaniline/Cu-montmorillonite nanocomposite is reported. Mixture of anilinium chlorure and Cu exchanged montmorillonite was grinded at room temperature while we vary the molar rate of aniline to interlayer Cu²⁺ cations (R) from 0.5 to 6. The properties of the hybrid compounds are characterized by X-ray diffraction, thermogravimetric analysis, SEM, FTIR and impedance spectroscopy. The results showed that the structure and the conductivity of PANI in hybrid materials depend on R. The ac conduction showed a regime of constant dc conductivity at low frequencies and a crossover to a frequency-dependent regime of the type A ω^s at high frequencies.