光催化
光降解
介电谱
光电流
异质结
材料科学
X射线光电子能谱
光致发光
电子顺磁共振
降级(电信)
光化学
化学
催化作用
电化学
光电子学
化学工程
电极
核磁共振
生物化学
物理化学
电子工程
物理
工程类
作者
Xiaomeng Gu,Taijie Chen,Jian Lei,Yang Yang,Xiuzhen Zheng,Sujuan Zhang,Qian Zhu,Xianliang Fu,Sugang Meng,Shifu Chen
出处
期刊:Chinese Journal of Catalysis
[China Science Publishing & Media Ltd.]
日期:2022-01-01
卷期号:43 (10): 2569-2580
被引量:32
标识
DOI:10.1016/s1872-2067(22)64142-1
摘要
To realize the high-efficiency photodegradation of antibiotics, a novel S-scheme heterojunction photocatalyst g-C3N4/Bi8(CrO4)O11 was proposed and successfully prepared in this work. The 10% g-C3N4/Bi8(CrO4)O11 heterojunction exhibits the highest degradation rate of norfloxacin (NOR) and bisphenol A (BPA). The degradation rate of NOR on 10% g-C3N4/Bi8(CrO4)O11 is about 1.38 and 2.33 times higher than that of pure Bi8(CrO4)O11 and g-C3N4, respectively. Further, the degradation rate of BPA over 10% g-C3N4/Bi8(CrO4)O11 heterojunction is bout 1.35 and 9.11 times higher than that of pure Bi8(CrO4)O11 and g-C3N4, respectively. The formation of S-scheme heterojunction facilitates the separation of photogenerated electron-hole pairs and reduces the recombination of charge carriers, which was confirmed by photocurrent, electrochemical impedance spectroscopy, steady-state and time-resolved transient photoluminescence spectrum, etc. The in-situ X-ray photoelectron spectroscopy, radical trapping experiments and electron paramagnetic resonance results demonstrate that the charge transfer is in accord with S-scheme mechanism.
科研通智能强力驱动
Strongly Powered by AbleSci AI