光降解
异质结
材料科学
光催化
罗丹明B
X射线光电子能谱
光电流
甲基橙
光化学
化学工程
傅里叶变换红外光谱
催化作用
光电子学
化学
有机化学
工程类
作者
Tingting Cheng,Huajing Gao,Xiaofeng Sun,Tao Xian,Shifa Wang,Zao Yi,Guorong Liu,Xiangxian Wang,Hua Yang
标识
DOI:10.1016/j.apt.2021.01.039
摘要
Herein we have designed an excellent type of Z-scheme Ag2MoO4/Bi4Ti3O12 (AMO/BTO) heterojunction photocatalysts by immobilizing AMO particles onto rod-like BTO hierarchical architectures. The formation of Z-scheme AMO/BTO heterostructures was verified by various characterization techniques including XRD, UV–vis DR spectroscopy, SEM, TEM, XPS and FTIR spectroscopy. PL spectroscopy, photocurrent response and EIS analyses suggest that the creation of AMO/BTO heterojunctions is conducive to the efficient separation of photoexcited electron-hole pairs. The photocatalytic performances of the AMO/BTO composites were investigated by simulated-sunlight driving photodegradation of methylene blue (MB), tetrabromobisphenol A (TBBPA), tetracycline hydrochloride (TC), phenol and methyl orange (MO)/rhodamine B (RhB)/MB mixture solutions. It is demonstrated that the AMO/BTO heterojunction photocatalysts are endowed with excellent photodegradation performances much higher than that of bare AMO and BTO. For example, the photodegradation rate of MB by using 30 wt%AMO/BTO — confirmed to be the optimal composite sample — is about 17.0 and 14.7 times as high as that by using bare BTO and AMO, respectively. A Z-scheme electron transfer mechanism was proposed to elucidate the enhanced photodegradation performances of the AMO/BTO heterojunction photocatalysts.
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