Z-scheme FeOOH/g-C3N4 nanosheets promoted PDS activation for efficient tetracycline degradation under visible light

被引:0
|
作者
Li, Yongqi [1 ]
Qu, Chao [1 ]
Ye, Qing [1 ]
Meng, Fanwei [1 ]
Yang, Decai [1 ]
Wang, Lanyang [1 ]
机构
[1] Beijing Univ Technol, Coll Environm Sci & Engn, Dept Environm Sci, Key Lab Beijing Reg Air Pollut Control, Beijing 100124, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Photocatalysis; PDS activation; Graphitic carbon nitride; FeOOH; Tetracycline; CARBON NITRIDE; OXIDATION; REMOVAL; HETEROJUNCTION; ANTIBIOTICS; PERFORMANCE; ADSORPTION; MECHANISM;
D O I
10.1016/j.jece.2024.113791
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Recently, photocatalysis combined peroxydisulfate (PDS) activation as a novel advanced oxidation processes (AOPs) was applied to remove pharmaceuticals and personal care products (PPCPs) in waterbody. Under visible light irradiation, photocatalysts, such as graphitic carbon nitride (g-C3N4, CN), could generated holes and electrons for both organic oxidation and PDS activation. However, it exhibits the drawbacks of low organics removal rate, high electron-hole recombination rate and low activation efficiency of PDS. In this study, amorphous iron oxyhydroxide (FeOOH) was intercalated into the surface of the g-C3N4 nanosheets (CNNS) to form a Z-scheme heterojunction to solve these problems. Electrochemical impedance spectroscopy (EIS) and photoluminescence spectrum (PL) tests proved the enhancement of the charge separation and migration capability of FeOOH/CNNS. The density functional theory (DFT) supported the constructive role of the Z-type heterojunction between FeOOH and CNNS in promoting photocarrier transfer and facilitating more effective PDS activation reactions. The removal rate of tetracycline (TC) achieved 98.8 % within 80 min by FeOOH/CNNS coupled PDS under visible light (FeOOH/CNNS-PDS/Vis) system. Finally, electron spin resonance (ESR) approved the pivotal role of (OH)-O-center dot, SO4 center dot-, and O-center dot(2)- during the process.
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页数:11
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