Synthesis of ZrO2 nanowires by ionic-liquid route

Zirconia precursor nanowires were synthesized via the solvothermal reaction of zirconium tetra-n-propoxide Zr(OPrn)4 with ethylene glycol and 1-butyl-3-methyl imidazolium tetrafluoroborate ionic liquid at 160 °C. The as-synthesized nanowires were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), powder X-ray diffraction (XRD), thermogravimetric and differential scanning calorimetric (TG-DSC) analysis, and infrared spectroscopy (IR), etc. The length of the as-synthesized nanowires reaches ∼20 μm, and the width ∼50 nm, giving an aspect ratio of a few hundreds. Upon calcination at elevated temperatures, the zirconia precursor nanowires transform from relative dense structure into highly porous ZrO2 nanowires consisting of interconnected nanocrystallites; in addition the length of the nanowires is greatly reduced. Cyclic voltammetry measurement shows that the modification of the graphite electrode with the ZrO2 nanowires greatly enhances sensitivity of the detection of vanadium, suggesting that ZrO2 nanowires may find important applications in vanadium(V) determination using electroanalytical methods with chemically modified electrode technique.

Graphical abstractZirconia precursor nanowires with high aspect ratio were synthesized by a novel, facile solvothermal reaction of zirconium tetra-n-propoxide Zr(OPrn)4 with ethylene glycol and l-butyl-3-methyl imidazolium tetrafluoroborate ionic liquid.Figure optionsDownload full-size imageDownload as PowerPoint slide