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Presenting instant microwave-synthesized hierarchical nanostructures (HNSs) of titania with huge surface area and light scattering, thus greater absorption, for better performance in DSSCs.

Conductive polymers have become a remarkable candidate for electrode materials of supercapacitors. Polyaniline (PANI) is the most promising contender for supercapacitors because of its easy method of synthesis, low cost, and higher choice in the improvement of energy storage applications. The main issue in the use of PANI in supercapacitors is its lower stability. In this work, PANI@Fe−Ni codoped Co 3 O 4 (PANI@FNCO) nanocomposite has been prepared by in situ addition of 10 wt % FNCO as fillers in the PANI matrix. The nanocomposites were then characterized via scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy, thermogravimetric analysis, and differential scanning calorimetry to observe the morphology, crystal structure, functional groups, and thermal stability of samples, respectively. SEM results showed that FNCO was fairly dispersed in the PANI matrix, while XRD results showed a broad peak for nanocomposites because of the semicrystalline nature of polymers. The electrochemical properties of the samples were analyzed via cyclic voltammetry, galvanostatic charge and discharge, and electrochemical impedance spectroscopy. PANI@FNCO nanowires are found to overcome the shortcomings in electrochemical energy storage devices by exhibiting a higher value of specific capacitance of 1171 F g −1 and energy density of 144 W h kg −1 at a current density of 1 A g −1 . Moreover, the FNCO nanowires also showed a cyclic charge/ discharge stability of 84% for 2000 cycles.

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Polyvinyl alcohol (PVA)-stabilized graphene nanosheets (GNS) of lateral dimension (L) ~1 μm are obtained via liquid phase exfoliation technique to prepare its composites in the PVA matrix. These composites show low levels of reinforcements due to poor alignment of GNS within the matrix as predicted by the modified Halpin-Tsai model. Drawing these composites up to 200 % strain, a significant improvement in mechanical properties is observed. Maximum values for Young’s modulus and strength are ~×4 and ~×2 higher respectively than that of neat PVA. Moreover, the rate of increase of the modulus with GNS volume fraction is up to 700 GPa, higher than the values predicted using the Halpin-Tsai theory. However, alignment along with strain-induced de-aggregation of GNS within composites accounts well for the obtained results as confirmed by X-ray diffraction (XRD) characterization.

Silver (Ag) and/or aluminum (Al)-doped zinc oxide (ZnO:Ag, ZnO:Al) films with different concentrations were produced using sol-gel process and investigated for wettability and photocatalysis. Water contact angle (CA) measurements indicated the films to be hydrophilic with reduced solid/liquid interfacial surface energy upon metal doping. The films were highly transparent (>94%) with red or blue shift in the absorption edge depending on the dopant type (Ag or Al) owing to the Burstein–Moss effect. The ZnO:Ag and ZnO:Al films with 0.5 and 1.0 wt.% metal dopant showed high degradation efficiency in methylene blue (MB) solution under UV irradiation, mainly due to an increase in the photogenerated electron–hole pair recombination time and hydroxyl radicals (·OH) generation. The MB degradation followed pseudo-first-order reaction with maximum apparent reaction rate constant of 2.40 h−1 for the 0.5 wt.% ZnO:Al film. ZnO films with 1.0 wt.% dopant demonstrated excellent photostability and recyclability even after several runs presumably due to reduced Zn2+ dissolution as well as blocking of the active surface area. ZnO:(Ag + Al) film containing 0.5 wt.% Al and Ag showed excellent UV photodegradation of MB and rhodamine blue (RhB) with high levels of photostability over five cycles.