摘要
Choosing suitable photoanode materials is the most critical aspect for photoelectrochemical (PEC) water splitting. The low efficiency of PEC water splitting photoanodes restricts their widespread application for large-scale H 2 production. Herein, we prepared WO 3 photoanodes with controllable structures via hydrothermal-electrophoretic deposition and seed-mediated hydrothermal synthesis, achieving ex situ assembly and in situ growth on FTO glass substrates. Under simulated sunlight irradiation, the photoelectric current density of the WO 3 photoanode prepared by in situ hydrothermal synthesis exceeds 1.0 mA/cm² (at 1.23 V vs. RHE), significantly higher than that of the WO 3 photoanode prepared by ex situ assembly (which is less than 0.3 mA/cm² at 1.23 V vs. RHE). By contrast, the in situ preparation of the WO 3 photoanode using tungsten powder and H 2 O 2 as raw materials exhibits the enhanced photocurrent density of 1.27 mA/cm² at 1.23 V vs. RHE. The excellent PEC performance of the resulting sample could be attributed to the ordered charge transport channels from the two-dimensional (2D) nanoplates structure, the enhanced electron-hole pairs separation from the superior crystallinity of WO 3 and the strong binding between the WO 3 nanoplates and the FTO substrate. Additionally, the effect of calcination temperature on the PEC performance of the prepared WO 3 was further investigated. This work provides a way for the synthesis of environmentally friendly and cost-effective photoanodes for efficient photoelectrochemical water splitting.
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