Abstract

Herein, the effects of the precursor solution's acidity level on the crystal structure, morphology, nucleation, and growth of WO3·nH2O and WO3 nanostructures are reported. Structural investigations on WO3·nH2O using X-ray diffraction and Fourier-transform infrared spectroscopy confirm that the quantity of hydrate groups increases due to the interaction between H+ and water molecules with increasing HCl volume. Surface analysis results support our claim that the evolution of grain size, surface roughness, and growth direction on WO3·nH2O and WO3 nanostructures rely on the precursor solution's pH value. Consequently, the photocurrent density of a WO3 photoanode using a HCl-5 mL sample achieves the best results with 0.9 mA/cm2 at 1.23 V vs. a reversible hydrogen electrode (RHE). We suggest that the improved photocurrent density of the HCl-5 mL sample is due to the efficient light absorption from the densely grown WO3 nanoplates on a substrate and that its excellent charge transport kinetics originate from the large surface area, low charge transfer resistance, and fast ion diffusion through the photoanode/electrolyte interface.

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