光催化
罗丹明B
吸附
亚甲蓝
金属有机骨架
材料科学
催化作用
猝灭(荧光)
复合数
化学工程
刚果红
核化学
无机化学
光化学
化学
有机化学
复合材料
荧光
量子力学
工程类
物理
作者
Chunfu Liu,Chenyu Zhu,Han Wang,Shenao Xie,Junyang Zhou,Hongjun Fang
标识
DOI:10.1016/j.jssc.2022.123582
摘要
Co-doped metal organic frameworks (MOFs) were fabricated by a facile route and applied to remove (tetracycline, congo red, methylene blue and rhodamine B) through integrated adsorption and photocatalysis. The assembled MOFs composite exhibited larger SBET (889 m2/g), broad light adsorption, and accelerated carrier kinetics, which helped to enhance adsorption and photocatalysis performance. Specifically, nearly 100% TC (40 mg/L) could be removed by the Co-MIL-10 within 12 min solar-light irradiation, significantly faster than that of solo MIL-53(Al) (82%) and CoAl-LDH (54%), separately. Furthermore the obtained rate constant (0.2064 min−1) was 4.8 times and 9.7 times greater than that of MIL-53(Al) and CoAl-LDH, respectively. The quenching/EPR characterization suggested that photo-generated h+/•O2−/•OH species were responsible for TC oxidation, of which h+ showed the great impact. Cycling experiments verified the robust stability of the MOFs catalyst. As well, an underlying photocatalytic mechanism of the current system was investigated in detail.
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