Abstract

Hematite (α-Fe2O3, bandgap ~2.1 eV) is a potential photoanode candidate for photoelectrochemical water splitting. In this work, we report the preparation of Fe2O3 with Ti4+ doping by hydrothermal treatment at 393 K and then annealing in the air at 873 K, with a second round of annealing in argon at 473 K. The two-step annealing process increased the photoelectrochemical performance of Ti-doped Fe2O3 on a fluorine-doped tin oxide (FTO)-coated glass substrate (FTO/Ti-Fe2O3) for water oxidation in 0.1 mol L−1 NaOH solution. Ti4+ doping was sourced from TiCl4 in ethanol solutions of various concentrations. An energy-dispersive X-ray spectrometer (EDS) analysis confirmed that the optimized Ti/Fe atomic ratio in the solution was ~3%, which showed the highest photocurrent densities in the linear sweep voltammetry and chronoamperometry measurements. The two-step annealed FTO/Ti-Fe2O3 generated a photocurrent density of 0.55 mA cm−2 at 1.50 V vs. reversible hydrogen electrode (RHE) under simulated one-sun illumination, which was approximately 3 times higher than that of the photoanodes annealed in air. Four-point probe resistivity measurements revealed that the two-step annealing resulted in a higher electrical conductivity than that of the samples annealed in air. The conductivity improvements induced by additional argon annealing at 473 K were ascribed to the increased donor density, which was confirmed by Mott–Schottky analysis and diffuse reflectance UV–visible–near-infrared spectra. We found that the strategy of Ti4+ doping and two-step annealing helped fabricate Fe2O3-based photoanode materials with better photocurrent density attributed to high electrical conductivity successfully.

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