Synthesis of Blend Polymer (PVA / PANI)/Copper (1) Oxide Nanocomposite: Thermal Analysis and UV-Vis Spectra Specifications

Copper (1) oxide nanoparticles together with matrix polymers of polyvinyl alcohol (PVA) and polyaniline (PANI) composite films were synthesized, as these materials are of importance in optoelectronic applications. ‎Nanoparticles of Cu2O were produced by chemical precipitation. Polymerization of aniline was carried out through polymerization in an acidic medium. Structural, thermal, and optical properties of PVA+PANI/Cu2O nanocomposite were inspected by x-ray diffraction (XRD), scanning electron microscopy (SEM), fourier-transform infrared (FTIR), differential scanning calorimeter (DSC) and ultraviolet-visible spectroscopy (UV-Vis spectroscopy). X-ray diffraction peaks at 29.53°, 36.34°, and 42.22° indicated the presence of cuprous oxide nanoparticles, having high dispersions and limited size distributions. The estimated average size of Cu2O nanoparticles was ~ 17.1525 nm. A characteristic peak at around 2θ = 18.5° was attributed to periodical parallel and perpendicular polymer chains, which denoted the formation of PANI. SEM results indicated the symmetrical dispersion of Cu2O nanoparticles inside the hybrid polymer of PVA and PANI matrix, being potentially useful for encapsulation and acting as a good capping agent. FTIR results established the formation of PANI and Cu2O with nanocrystalline nature. DSC results revealed the appearance of one single peak of Tg which decreased with Cu2O content of 4% wt, followed by an increase of that value by increasing Cu2O content up to 16%wt. Thermogram analysis of the PANI and PVA embedded with Cu2O form showed an exothermic peak at (240-292)℃ affiliated to the cross-linking reaction, while the Tm value of prepared nanocomposites is just about close to that of PVA polymer. The results indicated that there is an increase in thermal stability due to the presence of Cu2O NPS within the matrix of polymers. The distinguishing peaks at 330, 347, and 457 nm which refer to PANI are assigned to π−π* electron transitions among the benzenoid rings. The high absorption intensity of the peak at 470 nm for the blended PVA+PANI having 12% wt of Cu2O NPS is assigned due to the inter-band transitions for electrons of the core copper as well as copper oxide. This points out that the increasing quantity of Cu2O NPs leads to increases in the amounts of highly oxidized structures in PANI and decreases in the doping electrons and length of conjugation throughout the incorporation of Cu2O NPs into PANI matrix. Depending on the practical results, it can be said that these polymeric nanocomposites can be efficiently used in photovoltaic technology applications.

Development, Investigation, and Comparative Study of the Effects of Various Metal Oxides on Optical Electrochemical Properties Using a Doped PANI Matrix

A comparative study was performed in order to analyze the effect of metal oxide (MO) on the properties of a polymeric matrix. In this study, polyaniline (PANI)@Al2O3, PANI@TiC, and PANI@TiO2 nanocomposites were synthesized using in situ polymerization with ammonium persulfate as an oxidant. The prepared materials were characterized by various analytical methods such as X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), thermogravimetric analysis (TGA), UV/visible (UV/Vis) spectroscopy, Fourier-transform infrared spectroscopy (FTIR), and transmission electron microscopy (TEM). Furthermore, the conductive properties of the materials were tested using the four-point probe method. The presence of MO in the final product was confirmed by XPS, XRD, FTIR, and TEM, while spectroscopic characterization revealed interactions between the MOs and PANI. The results showed that the thermal stability was improved when the MO was incorporated into the polymeric matrix. Moreover, the results revealed that incorporating TiO2 into the PANI matrix improves the optical bandgap of the nanocomposite and decreases electrical conductivity compared to other conducting materials. Furthermore, the electrochemical properties of the hybrid nanocomposites were tested by cyclic voltammetry (CV) and galvanostatic charge/discharge (GCD). The obtained results suggest that the PANI@TiO2 nanocomposite could be a promising electrode material candidate for high-performance supercapacitor applications.

Pani:Cuo Nanocomposite as Electrolyte Material for Electrochemical Supercapacitor Application

PANI:CuO nanocomposite have been prepared by systematically adding different amounts of ammonium per sulfate as an oxidizing agent. Surface morphology shows the uniform distribution of CuO nanopowders in PANI matrix. TEM study gives the grain size of the as prepare PANI:CuO nanocomposite. FT-IR and UV-Vis studies confirm PANI is present and show the incorporation of CuO in polymer matrix. The data obtained by FT-IR measurements show the possible incorporation of CuO in PANI, rate of most interaction and the conductivity decrease due to the increase of APS content in the formed hybrid composites. A capacitance of polymeric materials is remarkably enhanced due to the synergistic effect between CuO and PANI. Moreover, the composite demonstrates good capacitive and charge/discharge properties.

The Effect of Variation Sensitivity Against Time For Magnesium Oxide (MgO) Doped Polyaniline Nanocomposites Influenced By Ammonium Persulfate

Polyaniline and doped polyaniline was prepared by the method of insitu chemical oxidative polymerization with ammonium persulfate as an oxidant agent. The composite polyaniline was mixing the magnesium oxide and polyaniline with the PANI matrix distributions. Polyaniline composite of MgO characterized like as x-ray diffractometer shows structural properties. The electrical properties of polyaniline and composite polyaniline as a conductivity increases with increase in frequency. The sensor property shows the sensitivity with the help of time obtained the sensitivities values the ranges from 120 to 160% from these composites in 50% composite the sensitivity is high.

Microporous MOF as nanogen facilitating diffusion-coupled charge transfer near the percolation threshold in a polyaniline pseudo-supercapacitor

A facile and potentially transferrable approach to enhance the PANI specific capacitance through the incorporation of MOF nanocrystals, as a microporous filler (nanogens), into the PANI matrix to provide ion-diffusion channels within the matrix.

Effect of SrTiO3 Nanoparticles in Conductive Polymer on the Thermoelectric Performance for Efficient Thermoelectrics

We present hybrid organic inorganic materials, namely, SrTiO3/polyaniline (PANI) composites, with high thermoelectric performance; samples with various SrTiO3 contents (10, 20, 30, and 50 wt.%) were prepared. The PANI component was obtained through the polymerization of aniline monomers, followed by camphosulfonic acid-doping to enhance its electrical conductivity. SrTiO3, with a high Seebeck coefficient, was used as the N-type inorganic componenet; it was synthesized via a one-pot solvothermal methods and, then, dispersed into the conductive PANI matrix. The SrTiO3 content influenced the Seebeck coefficient and electrical conductivity of the resulting composites. The variations in the thermoelectric properties of the SrTiO3/PANI composites consequently changed their power factor; at room temperature, the highest value was ~49.6 μW·m/K2, which is 17 times larger than that of pure PANI.

Triple Layer Tungsten Trioxide, Graphene, and Polyaniline Composite Films for Combined Energy Storage and Electrochromic Applications

Different polyaniline (PANI)-based hybrid films were successfully prepared by electro-polymerizing aniline monomers onto pre-spin-coated indium tin oxide (ITO) glass slides with WO3, graphene, or WO3/graphene films. Comparing with pristine PANI, the shifts of the characteristic peaks of PANI-based nanocomposites in UV-visible absorption spectra (UV-vis) and Fourier transform infrared spectroscopy (FT-IR) indicate the chemical interaction between the PANI matrix and the nanofillers, which is also confirmed by the scanning electron microscope (SEM) images. Corresponding coloration efficiencies were obtained for the WO3/PANI (40.42 cm2 C−1), graphene/PANI (78.64 cm2 C−1), and WO3/graphene/PANI (67.47 cm2 C−1) films, higher than that of the pristine PANI film (29.4 cm2 C−1), suggesting positive effects of the introduced nanofillers on the electrochromic performance. The areal capacitances of the films were observed to increase following the order as bare WO3 < WO3/graphene < pristine PANI < WO3/PANI < graphene/PANI < WO3/graphene/PANI films from both the cyclic voltammogram (CV) and galvanostatic charge-discharge (GCD) results. The enhanced energy storage and electrochromic performances of the PANI-based nanocomposite films can be attributed to the capacitance contributions of the introduced nanofillers, increased PANI amount, and the rougher morphology due to the embedment of the nanofillers into the PANI matrix. This extraordinary energy storage and electrochromic performances of the WO3/graphene/PANI film make it a promising candidate for combined electrochromic and energy storage applications.

Study of structural, electrical, optical and magnetic properties of Hexaferrite–Polyaniline nanocomposites

Y-type hexagonal ferrite (CaBaCo2Ga[Formula: see text]Fe[Formula: see text]O[Formula: see text]) was synthesized by sol–gel technique. The ferrite–polymer composites (1−x)CaBaCo2Ga[Formula: see text]Fe[Formula: see text]O[Formula: see text]+(x)polyaniline (x=0.25, 0.50, 0.75, 1) namely PF1, PF2, PF3 and polyaniline (PANI) were synthesized by in situ polymerization. The synthesized samples were characterized by XRD, SEM, electrical and dielectric measurements, optical and magnetic studies. XRD pattern reveals a broad peak of polyaniline which is an indication of amorphous nature of PANI. Room-temperature resistivity increases from 2.14 × 101 [Formula: see text]cm to 2.78 × 10[Formula: see text]cm as ferrite content increases due to resistive behavior of the ferrite particles dispersed in the PANI matrix. The value of dielectric constant decreases at fixed frequency with increasing concentration of ferrite filler which is predominantly due to exchange of electrons between Fe[Formula: see text] and Fe[Formula: see text] ions that ultimately results in enhancement of electric polarization and conductivity. The optical bandgap increases with increasing amount of ferrite in the composites. The saturation magnetization and remanence increase with the increase of ferrite filler amount in PANI matrix whereas coercivity decreases. The decrease in coercivity and increase in saturation magnetization are related to Brown’s relation. The present nanocomposite samples may be the best candidates for electromagnetic shielding.