光催化
异质结
材料科学
甲基橙
罗丹明B
化学工程
纳米颗粒
X射线光电子能谱
光降解
可见光谱
光电流
光化学
纳米技术
化学
光电子学
催化作用
有机化学
工程类
作者
Tingting Cheng,Huajing Gao,Guorong Liu,Zhongsheng Pu,Shifa Wang,Zao Yi,Xianwen Wu,Hua Yang
标识
DOI:10.1016/j.colsurfa.2021.127918
摘要
Herein we have assembled CdS nanoparticles onto the surface of Bi4Ti3O1 (BTO) hierarchical microspheres to construct core-shell BTO/CdS heterojunction photocatalysts. The as-prepared samples are systematically analyzed by various methods (e.g., XRD, SEM, TEM, XPS, UV–vis DR spectroscopy and FTIR spectroscopy), confirming the formation of core-shell structured BTO/CdS composites. Photocurrent response and EIS analyses demonstrate that enhanced separation of photogenerated electron-hole pairs is realized in the BTO/CdS heterojunctions. Simulated-sunlight driving photodegradation of methylene blue (MB) reveals that the optimal composite sample 20%BTO/CdS is endowed with a photocatalytic activity about 1.6 and 3.3 times higher than that of bare CdS and BTO, respectively. Moreover, the 20%BTO/CdS heterojunction photocatalyst also exhibits excellent photocatalytic elimination of methyl orange (MO)/rhodamine B (RhB)/MB mixture dyes, ciprofloxacin (CIP), sulfamethoxazole (SMX), tetrabromobisphenol A (TBBPA) and Cr(VI) ions. The enhanced photocatalytic mechanism of the BTO/CdS heterojunction photocatalysts was discussed based on a Z-scheme carrier transfer process.
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