In situtailoring the morphology of In(OH)3nanostructures via surfactants during anodization and their transformation into In2O3nanoparticles.

The present work reports the effect of various surfactants on the morphology of In(OH)3nanostructures prepared via anodization. In-sheets were anodized in an environmentally benign electrolyte containing a small quantity of CTAB, CTAC, and PDDA surfactants at room temperature. The produced nanostructures were characterized using XRD, HRTEM, SAED, and EDAX. The morphology of indium hydroxide (In(OH)3) nanostructures was successfully tailoredin situwith the help of surfactants in 1 M KCl aqueous electrolyte. XRD results confirmed the formation of In(OH)3and indium oxyhydroxide (InOOH) nanostructures in the pristine form which were transformed into single-phase cubic In2O3nanoparticles (NPs) after calcination. HRTEM analyses showed that the morphology and size of the In(OH)3nanostructures can be tuned to form nanorods, nanosheets and nanostrips using different surfactants. The results revealed that CTAC and PDDA surfactants have a profound effect on the morphology of In(OH)3nanostructure compared to CTAB due to the higher concentration of Cl-ion. The possible mechanism of surfactants effect on the morphology is proposed. Furthermore, annealing converted the In(OH)3nanostructures into spherical In2O3NPs with uniform and homogeneous size. We anticipate that the morphology of other metal-oxides nanostructure can be tuned using this simple, facile and rapid technique. In2O3NPs prepared without and with CTAB surfactant were further explored for the non-enzymatic detection of hydrogen peroxide (H2O2). Electrochemical measurements showed enhanced electrocatalytic performance with fast electron transfer (∼2s) between the redox centers of H2O2and electrode surface. The In2O3NPs prepared using CTAB/Au electrode exhibited about 4-fold increase in sensitivity compared to the bare Au electrode. The biosensor also demonstrated good reproducibility, higher selectivity, and increased shelf life.