光催化
X射线光电子能谱
石墨氮化碳
异质结
材料科学
亚甲蓝
降级(电信)
反应速率常数
激进的
氮化碳
光化学
催化作用
复合数
化学工程
可见光谱
动力学
化学
有机化学
复合材料
光电子学
电信
物理
量子力学
计算机科学
工程类
作者
Sanjeevamuthu Suganthi,Thirumuruganantham Sivakumar,P. Nethaji,S. Vignesh,Tae Hwan Oh
标识
DOI:10.1016/j.inoche.2023.111658
摘要
The g-C3N4/TiO2 heterostructure photocatalysts (PCs) were successfully synthesized in a facile way. Powder XRD, FT-IR, XPS, SEM, HR-TEM, and UV–Vis spectra were used for structural, morphological, and optical characterization. The photocatalytic action of the as-synthesized GTO2 catalyst samples was examined via methylene blue (MB) dye and the degradation efficiency under light exposure was 80.8 % in 160 min. The outcomes exhibited that the photocatalytic MB dye degradation confirmed pseudo-first-order kinetic fitting, and the kinetic constant of GTO2 was 5.04 folds higher than those of GCN and 3.21 folds higher than those of TiO2, respectively. The enhanced photocatalytic activity of GTO2 PCs was due to the heterostructure formation on the TiO2/g-C3N4 interface. Formation of efficient GTO2 heterostructure PCs resulted in the suppression of photo-produced electron–hole (e-/h+) pair recombination rate and the increase of its charge separation respectively. The superoxide radical anions (•O2–) and hydroxyl radicals (•OH) played a prominent role in the photocatalytic MB dye degradation process by efficient GTO2 PCs.
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