光降解
激进的
过硫酸盐
光催化
双酚A
催化作用
降级(电信)
材料科学
可见光谱
量子点
光化学
异质结
猝灭(荧光)
复合数
化学工程
化学
纳米技术
荧光
复合材料
光电子学
有机化学
光学
工程类
计算机科学
环氧树脂
电信
物理
作者
He Jiang,Yan Zhong,Kaixun Tian,Haoliang Pang,Yaoyao Hao
标识
DOI:10.1016/j.apsusc.2021.151902
摘要
A novel nitrogen- and sulfur-doped carbon quantum dot-modified MIL-101(Fe) (N,S:CQD/MIL-101(Fe)) heterojunction for visible light-induced activation of persulfate (PS) for bisphenol A (BPA) degradation was studied. The photocatalytic performance of BPA degradation was remarkably promoted by the composite material under the simultaneous action of PS and visible light irradiation. BPA photodegradation (100%) was achieved over 60 min with 0.4 g/L of the N,S:CQD/MIL-101(Fe) composite and 3 mM PS at natural pH. The degradation kinetics rate constants (k) approached 3.6 times higher than that of MIL-101(Fe). The enhanced performance in BPA degradation can be ascribed to the interfacial transference of photoinduced electrons from N,S:CQD to MIL-101(Fe), leading to the valid separation of electron-hole pairs and greatly accelerating PS activation to generate highly reactive SO4•−. Both holes (h+), sulfate radicals (SO4•−), superoxide radicals (•O2−), and hydroxyl radicals (•OH) contributed to BPA degradation according to radical quenching experiments. N,S:CQD/MIL-101(Fe) also exhibited great reusability and excellent catalytic performance after four consecutive cycles of use. This work provides valid organic contaminant degradation under the dual action of visible light and PS with a novel perspective on the fabrication of heterojunction photocatalysts ground on Fe-based MOFs.
科研通智能强力驱动
Strongly Powered by AbleSci AI