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Metal‐free mesoporous P and N co‐doped carbon (PNDC) composites are evaluated for their electrocatalytic activity towards the oxygen reduction reaction (ORR). Carbonization of melamine and hexamine‐modified tannin in the presence of polyphosophoric acid produces PNDCs with prominent oxygen reduction properties in alkaline media. The effect of the P and N content in the carbon material is evaluated in terms of the ORR activity. The compound containing a high amount of N (8.3 atom %) and P (6.8 atom %), denoted PNDC‐1, shows high electrocatalytic activity, stability, durability, and selectivity towards the ORR. PNDC‐1 has an onset potential of 0.10 V versus a reversible hydrogen reference electrode and shows a significantly improved performance in comparison to the carbon materials containing less P and N dopant atoms. PNDCs exhibit superior ORR current densities to that of the 20 % Pt/C catalyst because of the synergetic effect of P and N co‐doping. X‐ray photoelectron spectroscopy studies indicate the presence of pyridinic and graphitic N species, which are responsible for oxygen reduction that results in higher current densities. Rotating disk electrode and rotating ring‐disk electrode studies support a four electron oxygen reduction to water, with negligible generation of hydrogen peroxide.

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In this work, polyaniline (PANI) protonated with various levels of camphor sulfonic acid (HCSA) has been used as a hole‐transport layer (HTL) in organic bulk‐heterojunction solar cells. Polyaniline with three different protonation levels was inserted between poly(3‐hexylthiophene‐2,5‐diyl):[6,6]‐phenyl‐C61‐butyric acid methyl ester (P3HT:PCBM) and the indium‐tin oxide (ITO) glass transparent electrode to explore the effects of varying the protonation level to optimize the hole‐transport properties. The three protonation concentrations (in molar ratios) of PANI are zero‐protonated (PANI/HCSA, 1:0), half‐protonated (PANI/HCSA, 1:1), and fully protonated (PANI/HCSA, 1:2) thin films. Current–voltage measurements under AM 1.5 conditions revealed that a conversion efficiency of 1.3 % was achieved if half‐protonated PANI was used as the HTL. Several analytical methods were utilized for characterizing PANI to understand the effects of the protonation level on the electrical, optoelectronic, and structural characteristics, and their correlation with final device properties.

Poly(3-hexylthiophene) (P3HT)-graphene nanocomposites were synthesized via in situ oxidative polymerization of 3-hexylthiophene monomer in the presence of graphene. The main thrust was to investigate the structural and optoelectronic properties of P3HT-graphene nanocomposites with various graphene concentrations. NMR spectroscopy was used to determine the regioregularity of the polymer composites, whereas Fourier transform infrared spectroscopy and differential scanning calorimetry were used to study their structural and thermal properties. Moreover, cyclic voltammetry was employed to evaluate the HOMO levels of the nanocomposites, while optical spectrophotometry (UV-Vis-NIR) was utilized to determine the optical bandgap of the composites. The information from the aforementioned techniques was used to estimate the HOMO-LUMO energy levels. The results revealed changes in the optical bandgap of P3HT with increasing graphene content. Furthermore, an extensive study aiming at the effect of graphene content on the optical constants of P3HT was conducted using ellipsometry. Photoluminescence analysis of the samples showed no quenching effect of photoluminescence emission with increasing graphene content. Our studies indicate that the inclusion of graphene impacts the optoelectronic properties of P3HT, which can further be used for advanced applications, such as organic solar cells, organic light emitting diodes, organic field-effect transistors, and polymer batteries.