Study on the photoelectrocatalytic performance of a WO 3 thin film electrode by constructing a BiOI/WO 3 heterojunction

To address the shortcomings of the narrow solar absorption range of WO 3 thin film electrodes and the high recombination rate of photogenerated electrons, a WO 3 thin film electrode containing a BiOI/WO 3 heterojunction was constructed using simple hydrothermal and electrodeposition methods. The photoelectrocatalytic activity was investigated through the degradation of methylene blue (MB) solution. By controlling the electrodeposition time, BiOI/WO 3 thin film electrodes with different BiOI contents and morphologies were obtained, and the electrodes were subjected to X-ray diffraction (XRD), scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). In addition, the photoelectrochemical properties of different electrodes were studied by electrochemical impedance spectroscopy (EIS), photoluminescence (PL), photocurrent, Mott–Schottky and other test methods. The results show that the BiOI/WO 3-120s thin film electrode achieves the best photoelectrocatalytic activity, with an electrodeposition time of 120 s and an applied voltage of −1.0 V. The efficiency of the photoelectrocatalytic degradation of MB by the BiOI/WO 3-120s film electrode can be as high as 86.7%, which is 3.6 times the photoelectrocatalytic degradation efficiency of a pure WO 3 film electrode. The increase in the photoelectrocatalytic activity is ascribed to the heterojunction structure formed by the combination of BiOI and WO 3 . The heterostructure photocatalytic electrode significantly improves the electron transport performance of photogenerated electrons and holes and reduces the band gap of the WO 3 electrode and photogenerated electron–hole pair recombination probability while expanding the solar absorption range of the electrode. The detailed mechanism of the photoelectrocatalytic performance of the BiOI/WO 3 heterojunction on the WO 3 thin film electrode is also discussed. This study provides a novel theoretical basis for the development of high-performance WO 3 photocatalytic materials.