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
光电流
靛蓝胭脂红
光化学
纳米技术
核化学
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI