光催化
罗丹明B
石墨氮化碳
X射线光电子能谱
单线态氧
降级(电信)
化学需氧量
氯
核化学
材料科学
兴奋剂
化学
光化学
化学工程
催化作用
氧气
废水
有机化学
环境工程
电信
光电子学
计算机科学
工程类
作者
Jing Zhang,Lixia Wang,Yang Li,Yuhong Huang,Renguo Song,Cheng Chen,Qian Luo,Ruiqi Zhai,Yuanlong Meng,Peixin Zhang,Qiang Ma,Y. Zhang
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2025-04-25
卷期号:30 (9): 1910-1910
标识
DOI:10.3390/molecules30091910
摘要
The increasing global demand for clean water is driving the development of advanced wastewater treatment technologies. Graphitic carbon nitride (g-C3N4) has emerged as an efficient photocatalyst for degrading organic pollutants, such as synthetic dyes, due to its exceptional thermo-chemical stability. However, its application is limited by an insufficient specific surface area, low photocatalytic efficiency, and an unclear degradation mechanism. In this study, we aimed to enhance g-C3N4 by doping it with elemental chlorine, resulting in a series of Cl-C3N4 photocatalysts with varying doping ratios, prepared via thermal polymerization. The photocatalytic activity of g-C3N4 was assessed by measuring the degradation rate of RhB. A comprehensive characterization of the Cl-C3N4 composites was conducted using SEM, XRD, XPS, PL, DRS, BET, EPR, and electrochemical measurements. Our results indicated that the optimized 1:2 Cl-C3N4 photocatalyst exhibited exceptional performance, achieving 99.93% RhB removal within 80 min of irradiation. TOC mineralization reached 91.73% after 150 min, and 88.12% removal of antibiotics was maintained after four cycles, demonstrating the excellent stability of the 1:2 Cl-C3N4 photocatalyst. Mechanistic investigations revealed that superoxide radicals (·O2−) and singlet oxygen (1O2) were the primary reactive oxygen species responsible for the degradation of RhB in the chlorine-doped g-C3N4 photocatalytic system.
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