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Abstract Counter electrode (CE) is an essential part of dye‐sensitized solar cells (DSSCs) in determining their efficiency. Ultimately, the high catalytic activity and conductivity of a CE are dependent on the type of electrode material. The utilization of polyaniline (PANI) coatings for surface modification of CE has proven to be worth. Though it is a bit difficult to optimize the efficiency of a polymeric material, a proper combination of inorganic‐organic dopants can impart positive synergistic effects to the resulting PANI in terms of good conductivity, electrocatalytic activity, and low resistance. This work reports on the effect of the combination ration of an organic dopant (ammonium lauryl sulfate, ALS) and an inorganic dopant (sulfuric acid) on the catalytic activity of CEs modified with PANI for DSSCs. The results are compared with those of platinum counter electrode (Pt CE). The maximum conversion efficiency of DSSC with optimized case reaches 4.54%, which is higher than that of Pt counter electrode (4.02%). This organic–inorganic acids doped polymeric material showing an enhanced photoelectrochemical activity might be exploited in the future as a promising material for application in next‐generation solar devices.

Conducting polymers integrated with metal oxides create opportunities for hybrid capacitive electrodes. In this work, we report a one-pot oxidative polymerization for the synthesis of integrated conductive polyindole/nickel oxide (PIn/NiO), polyindole/zinc oxide (PIn/ZnO), and polyindole/nickel oxide/zinc oxide (PNZ). The polymers were analyzed thoroughly for their composition and physical as well as chemical properties by X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), ultraviolet–visible spectroscopy (UV–Vis), and thermogravimetric analysis (TGA). The PIn and its composites were processed into electrodes, and their use in symmetrical supercapacitors in two- and three-electrode setups was evaluated by cyclic voltammetry (CV), galvanostatic discharge (GCD), and electrochemical impedance spectroscopy (EIS). The best electrochemical charge storage capability was found for the ternary PNZ composite. The high performance directly correlates with its uniformly shaped nanofibrous structure and high crystallinity. For instance, the symmetrical supercapacitor fabricated with PNZ hybrid electrodes shows a high specific capacitance of 310.9 F g−1 at 0.5 A g−1 with an energy density of 42.1 Wh kg−1, a power density of 13.2 kW kg−1, and a good cycling stability of 78.5% after 5000 cycles. This report presents new electrode materials for advanced supercapacitor technology based on these results.

Eco-friendly inhibitors have attracted considerable interest due to the increasing environmental issues caused by the extensive use of hazardous corrosion inhibitors. In this paper, environmentally friendly PDG-g-PANI/Al2O3 composites were prepared by a low-cost inverse emulsion polymerization for corrosion inhibition of mild steel (MS) and stainless steel (SS). The PDG-g-PANI/Al2O3 composites were characterized by different techniques such as X-ray diffraction (XRD), UV/Vis, and FTIR spectroscopy. XRD measurements show that the PDG-g-PANI/Al2O3 composite is mostly amorphous and scanning electron micrographs (SEM) reveal a uniform distribution of Al2O3 on the surface of the PDG-g-PANI matrix. The composite was applied as a corrosion inhibitor on mild steel (MS) and stainless steel (SS), and its efficiency was investigated by potentiodynamic polarization measurement in a 3.5% NaCl and 1 M H2SO4 solution. Corrosion kinetic parameters obtained from Tafel evaluation show that the PDG-g-PANI/Al2O3 composites protect the surface of MS and SS with inhibition efficiencies of 92.3% and 51.9% in 3.5% NaCl solution, which is notably higher than those obtained with untreated epoxy resin (89.3% and 99.5%). In particular, the mixture of epoxy/PDG-g-PANI/Al2O3 shows the best performance with an inhibition efficiency up to 99.9% on MS and SS. An equivalent good inhibition efficiency was obtained for the composite for 1M H2SO4. Analysis of activation energy, formation enthalpy, and entropy values suggest that the epoxy/PDG-g-PANI/Al2O3 coating is thermodynamically favorable for corrosion protection of MS and exhibits long-lasting stability.

The lack of an eco-friendly approach towards application of polyaniline as a coating material has been one of the most challenging tasks. Herein, the synthesis of green Prunus domestica gum grafted polyaniline (PDG-g-PANI) composite is reported by a cost-effective emulsion polymerization for application as an efficient anti-corrosion material for mild steel (MS) and stainless steel (SS) in a strong corroding environment. The composite formation was confirmed by Ultraviolet Visible (UV-Visible) and Fourier Transformed Infrared (FTIR) spectroscopies. X-ray diffraction data revealed the amorphous nature of the PDG-g-PANI. Scanning Electron Microscopic (SEM) images showed a bi-layered structure having a parent porous layer of PANI coated with afibrous layer of PDG. The solubility test confirmed the dissolution of PDG-g-PANI in common organic solvents such as acetone, ethanol, propanol, butanol, chloroform, N-Methyl-2-pyrrolidone, dimethyl sulfoxide, and the mixture of propanol and chloroform. The polarization curve, open circuit potential, electrochemical impendence spectroscopy (EIS), and gravimetric analysis were applied to investigate the corrosion protection behavior of the composite on MS and SS in 3.5% NaCl and 1 M H2SO4 solution. The PDG-g-PANI-coated MS exhibited 96% corrosion inhibition efficiency as compared to 86% and 43% for pristine PANI and PDG in 3.5% NaCl solution while PDG-g-PANI-coated SS showed 98% corrosion inhibition efficiency. Moreover, 99% and 96.6% corrosion protection was observed for PDG-g-PANI-coated MS and SS in 1 M H2SO4 solution. Gravimetric studies revealed that PDG-g-PANI coating can protect MS up to 93% for 14 days in salt solution while 97% corrosion inhibition efficiency was retained for 2 months in open air.

A polybenzopyrrole@nickel oxide (Pbp@NiO) nanocomposite was synthesized by an oxidative chemical one-pot method and tested as an active material for hybrid electrodes in an electrochemical supercapattery device. The as-prepared composite material exhibits a desirable 3D cross-linked nanostructured morphology and a synergistic effect between the polymer and metal oxide, which improved both physical properties and electrochemical performance. The unprocessed material was characterized by X-ray diffraction, FTIR and UV–Vis spectroscopy, scanning electron microscopy/energy disperse X-ray analysis, and thermogravimetry. The nanocomposite material was deposited without a binder on gold current collectors and investigated for electrochemical behavior and performance in a symmetrical two- and three-electrode cell setup. A high specific capacity of up to 105 C g−1 was obtained for the Pbp@NiO-based electrodes with a gravimetric energy density of 17.5 Wh kg−1, a power density of 1925 W kg−1, and excellent stability over 10,000 cycles.

Fabrication of composites by developing simple techniques can be an efficient way to modify the desire properties of the materials. This paper presents a detailed study on synthesis of low cost and efficient nitrogen doped reduced graphene oxide nickle-silver (N-rGO-Ni/Ag) and nickel-cobalt (N-rGO-Ni/Co) nanocomposites as electrocatalysts in fuel cell using one-pot blended reflux condensation route. An admirable correlation in the structures and properties of the synthesized nanocomposites was observed. The Oxygen Reduction Reaction (ORR) values for N-rGO-Ni/Ag and N-rGO-Ni/Co calculated from the onset potential, using Linear Sweep Voltammetry (LSV), were found to be 1.096 and 1.146. While the half wave potential were determined to be 1.046 and 1.106, respectively, N-rGO-Ni/Ag and N-rGO-Ni/Co. The Tafel and bi-functional (ORR/OER) values were calculated as 76 and 35 mV/decade and 1.23 and 1.12 V, respectively, for N-rGO-Ni/Ag and N-rGO-Ni/Co. The lower onset and half wave potential, low charge transfer resistance (Rct = 1.20 Ω/cm2) and internal solution resistance (Rs = 8.84 × 10−1 Ω/cm2), lower Tafel values (35 mV), satisfactory LSV measurements and mass activity (24.5 at 1.056 V for ORR and 54.9 at 1.056 for OER) demonstrate the remarkable electrocatalytic activity of N-rGO-Ni/Co for both ORR and OER. The chronamperometric stability for synthesized nanocomposites was found satisfactory up to 10 h.

Electronically conducting poly (aniline-co-2-hydroxyaniline) (PACHA), a copolymer of aniline and 2-hydroxyaniline (2HA), was electrochemically coated on gold substrate for methanol electrooxidation in alkaline media. The electrochemical behavior of PACHA coated gold electrode towards methanol electrooxidation was investigated via cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) for application in an alkaline fuel cell. Methanol electrooxidation was observed at two different electrode potentials depending on the concentration of the base. At the PACHA coated gold electrode, the methanol oxidation peak was observed at lower overpotential (at 0.19 V) in a solution of high base concentration (1.8 M NaOH), which was 30 mV lower than the peak for the uncoated gold electrode. In addition, the Faradic current Imax obtained on the PACHA coated electrode (20 mA) was two times higher as compared to the Faradic current Imax of the un-modified gold electrode (10 mA). In solution of lower base concentration (0.06 M NaOH), the electrooxidation of methanol became sluggish on both electrodes, as indicated by peak shifting towards positive potential and with reduced faradaic current (at 0.74 V on PACHA coated electrode; Imax 10 mA). The electrooxidation of methanol at both lower and higher electrode potentials was analyzed mechanistically and discussed in light of the literature. EIS results were interpreted using Nyquist and Bode plots. The charge transfer resistance was decreased and pseudo-capacitive behavior changed to conductive behavior when external applied potential was increased from 0.1 V to 0.4 V.