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Structural, morphological and electrical properties of the CNS/PANI composite have been studied as a function of composition of CNS. Morphological analysis by FESEM and TEM indicates an enhanced interaction between PANI and CNS as the CNS increases forming larger aggregated interconnected matrix network of CNS having hetero-structured molecular phases of sp2 and sp3. Raman spectroscopy reveals the presence of large tensile strain on the G and D bands of the CNS/PANI composite. Increase in the CNS percentage is seen to relax this large amount of strain. Electrochemical analysis of these composite structures as an active electrode gives a highest specific capacitance of 1470 Fg−1 for CNS/PANI composite with 75% of CNS with high cyclic stability.

Herein we have demonstrated facile synthesis approach to grow K+ and Na+ ions preinserted MnO2 (KxMnO2 and NaxMnO2) nanostructured thin films with the help of successive ionic layer adsorption and ...

Herein, by using chemical methods such as successive ionic layer adsorption and reaction (SILAR) and spin coating we have demonstrated a novel strategy for the synthesis of ternary hybrid to study photoelectrochemical (PEC) performance. To the best of our knowledge, for the first time we have represented a case study of achieving optimum SILAR cycles for Ag nanoparticles decoration on ZnO nanorods and a discussion was made on a role of multi-walled carbon nanotube (MWCNT) as a top layer over Ag–ZnO nanostructures for better PEC performance. Firstly, Ag nanoparticles loading over SILAR grown ZnO nanorods was varied for different SILAR cycles to optimize better photocurrent. This Ag–ZnO hybrid showed higher photocurrent density of 0.45 mA/cm2 at 1 V bias (vs SCE) and photoconversion efficiency (PCE) of 0.21% (0.45 V vs SCE). Thereafter, MWCNTs were garnished by using spin coating as a top layer on Ag–ZnO hybrid leading to the formation of ternary hybrid of MWCNT–Ag–ZnO for further enhancement of PEC activity. We believe that top layer of MWCNT plays a vital role of electron and hole transfer and bridges Ag decorated ZnO nanorods together leading to well-connected conducting pathways for efficient charge collection and transport. The appropriate band bending of MWCNT–Ag–ZnO hybrid leads to the formation of active interface helping out in charge separation leading to excellent photocurrent density of 0.56 mA/cm2 at 1 V bias (vs SCE) and photoconversion efficiency of 0.26% (0.45 V vs SCE). Enhanced light harvesting, higher donor density, appropriate band bending, lowest charge transfer radius of C–Ag–ZnO hybrid signifies that efficient charge transfer and restriction to charge recombination leading to the enhanced PEC performance.

Morphological forms of ZnO nanostructures play a vital role in deciding properties such as high internal surface area, efficient light scattering and harvesting, lowest charge transfer resistance, etc. which are important for photoelectrochemical (PEC) performance. Herein successful deposition of well oriented ZnO nanorods thin films over fluorine doped tin oxide (FTO) coated glass substrate is achieved by using simple, soft solution and scalable method known as successive ionic layer adsorption and reaction (SILAR). For the first time a compact ZnO layer over large area is deposited in one step synthesis approach, without any assistance of seed layer, by using hydrazine hydrate as a source of hydroxyl ions. The plausible growth mechanism of the morphological variation (alignment and orientation) happening with increasing SILAR cycles and its consequence on PEC performance are discussed in detail. All ZnO thin films show wurtzite crystal structure, however variations in their texture coefficients were found with SILAR cycles, which turns out to be a major aspect for PEC application. Anodic shift was observed in flat band potential values with increment in number of SILAR cycles. The ZnO thin films deposited for 120 cycles showed preferential orientation along (0002) plane and showed better PEC performance with photocurrent of 0.19 mA/cm2 (1 V) and maximum photo conversion efficiency of 0.084% at 0.45 V. On the other hand, film deposited for 60 (photocurrent of 0.11 mA/cm2 (1 V); efficiency of 0.055%) and 180 cycles (photocurrent of 0.15 mA/cm2 (1 V); efficiency of 0.063%) demonstrated inferior PEC performance.

Nickel nanoparticles were grown on graphite by using a comparatively simpler and cost effective method, namely successive ionic layer adsorption and reaction. Size and morphology of the nickel nanoparticles were observed using field emission scanning electron microscopy. X-ray diffraction, X-ray photoelectron spectroscopy and energy dispersive spectroscopy studies confirmed the presence of nickel. Electrocatalytic activity and stability of the grown nickel nanoparticles were investigated by recording cyclic voltammograms and chronoamperometry. Variations in growth parameters, such as reduction time, nickel chloride concentration and number of growth cycles affect the activity of the grown nickel nanoparticles. The grown nickel nanoparticles exhibited electrocatalytic activity towards ethanol electrooxidation reaction. The phase change as a result of mass change that occurred during the redox reactions and ethanol electrooxidation was studied using an electrochemical quartz crystal microbalance. The successive ionic layer adsorption and reaction method promises to be a viable option for growth of nickel nanoparticles for electrocatalytic applications.

Manganese oxide is an interesting material for electrochemical properties. It is well known that Mn3O4 (spinel) can be electrochemically converted to MnO2 (birnessite) via the electrochemical route during cyclic voltammetry (CV) cycling in aqueous Na2SO4 solution. Herein, the novel way is represented for the growth of highly adherent and compact Mn3O4 thin films by using successive ionic layer adsorption and reaction (SILAR) method. As grown Mn3O4 thin films are converted into MnO2 after chemical treatment by hydrochloric acid (HCl) via a disproportionate reaction. Mn3O4 thin films are converted into MnO2 by both chemical and electrochemical paths. During chemical conversion, at acidic pH, the crystal water insertion (H3O+) in Mn3O4 crystal provides the necessary driving force to transform it into MnO2 crystal. During electrochemical transformation, the specific capacitance was found to increase from 72 (1st CV cycle) to 393 F/g (1600th CV cycle). On the other hand, the specific capacitance was increased from 72 to 258 F/g through chemical transformation. Electrochemical and chemical conversion leads to ~5.5 and ~3.5 fold, respectively, improved supercapacitive performance than pristine Mn3O4 thin films. Both chemical and electrochemical conversion routes are extremely useful to recycle battery waste for supercapacitor applications.