Liying HuangHui XuYeping LiHuaming LiXiaonong ChengJixiang XiaYuanguo XuCai Guobin
Novel WO3/g-C3N4 composite photocatalysts were prepared by a calcination process with different mass contents of WO3. The photocatalysts were characterized by thermogravimetric analysis (TG), powder X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray spectrometry (EDS), high-resolution transmission electron microscopy (HRTEM), UV-vis diffuse reflection spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), photoluminescence (PL) and electrochemical impedance spectroscopy (EIS). The photocatalytic activity of the photocatalysts was evaluated by degradation of methylene blue (MB) dye and 4-chlorophenol (4-CP) under visible light. The results indicated that the WO3/g-C3N4 composite photocatalysts showed higher photocatalytic activity than both the pure WO3 and pure g-C3N4. The optimum photocatalytic activity of WO3/g-C3N4 at a WO3 mass content of 9.7% under visible light irradiation was up to 4.2 times and 2.9 times as high as that of the pure WO3 and pure g-C3N4, respectively. The remarkably increased performance of WO3/g-C3N4 was mainly attributed to the synergistic effect between the interface of WO3 and g-C3N4, including enhanced optical absorption in the visible region, enlarged specific surface areas and the suitable band positions of WO3/g-C3N4 composites.
Yeping LiShilong WuLiying HuangHui XuRongxian ZhangMinglan QuQiang GaoHuaming Li
Meiyin WangHui WangYuanhang RenCheng WangZhewei WengBin YueHeyong He
Yuexia JiJiafeng CaoLinqing JiangYaohong ZhangZhiguo Yi
Vien VoNguyen Van KimNguyễn Thị Việt NgaNguyễn Tiến TrungGiang Truong LePham Van HanhLục Huy HoàngSung‐Jin Kim
Yeping LiShilong WuLiying HuangJunli WangHui XuHuaming Li