ABSTRACT
The present investigation deals with controlled synthesis of nanostructured NiCo2O4 thin films directly on stainless steel substrates by facile and economical chemical bath deposition technique, without adding a surfactant or a binder. The consequences of different compositions of solvents on morphological and electrochemical properties have been studied systematically. We used different solvent composition as Double Distilled Water (DDW), DDW:Ethanol (1:1) and DDW: N, N dimethylformamide (1:1). The films have been named as NCO-W for DDW, NCO-WE for DDW: Ethanol (1:1) solvent and NCO-WD for DDW: N, N dimethylformamide (1:1) solvent. The morphologies of NiCo2O4 thin films modify substantially with change in a solvent. NCO-W exhibited the spikes of Crossandra infundibuliformis like nanostructures. The NCO-WE favored the formation of uniformly distributed leaf-like nanostructure whereas NCO-WD showed randomly oriented nanoplates all over the surface area. The Electrochemical performance of these NiCo2O4 thin films were studied using cyclic voltammetry, chronopotentiometry, and electrochemical impedance spectroscopy techniques. The NCO-W, NCO-WE and NCO-WD electrodes showed specific capacitance values of 271, 553 and 140 F/g respectively at the current density of 0.5 mA/cm2 and excellent capacitance retention of 90%, 91% and 80% after 2000 cycles for NCO-W, NCO-WE and NCO-WD samples respectively. This result reveals that NiCo2O4 is a prominent electrode material for supercapacitor application.
ABSTRACT
Gold in the form of bulk metal mostly does not react with gases or liquids at room temperature. On the other hand, nanoparticles of gold are very reactive and useful as catalysts. The reactivity of nanoparticles depends on the size and the morphology of the nanoparticles. Gold nanostars containing copper have rough surfaces and large numbers of active sites due to tips, sides, corners, and large surface area-to-volume ratios due to their branched morphology. Here the sensitivity of the gold nanostar-polyaniline composite (average size of nanostars â¼170 nm) toward ammonia gas has been investigated. For 100 ppm ammonia, the sensitivity of the composite increased to 52% from a mere 7% value for pure polyaniline. The gold nanostar-polyaniline composite even showed a response time as short as 15 s at room temperature. The gold nanostars act as a catalyst in the nanocomposite. The stability and sensitivity at different concentrations and the selectivity for ammonia gas were also investigated.
