化学
光催化
降级(电信)
金属有机骨架
配体(生物化学)
罗丹明B
亚甲蓝
孔雀绿
光化学
催化作用
有机化学
受体
吸附
计算机科学
生物化学
电信
作者
Jianbo Huang,Lin Yin,Tian‐Cai Yue,Lulu Wang,Duo‐Zhi Wang
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2024-04-04
卷期号:63 (15): 6928-6937
被引量:51
标识
DOI:10.1021/acs.inorgchem.4c00372
摘要
Four Co(II)-based metal-organic frameworks (MOFs) were constructed by a mixed ligand strategy under solvothermal conditions. The controllable modification of the bridging groups in the secondary building units was realized by changing the anions in MOFs 1-3. The MOF 4 with 3D framework structure was obtained by regulating the solvent ratio following the synthesis process of MOF 3. Furthermore, the MOFs 1-4 exhibited efficient photocatalytic activity for the degradation of malachite green (MG) dye without any photosensitizer or cocatalyst under a low-energy light source, the decolorization ratio of MG all reached more than 96.0% within 60 min, and maximal degradation was obtained to be 99.4% (MOF 4). The recycling experiments showed that the degradation rate of MG was still higher than 91% after 10 cycles. In the MOF 4 as representation, the photocatalytic process was explored systematically. The possible mechanism of catalytic degradation was discussed, which proved the existence of efficient oxidation active factors (•O2-, •OH, and h+). The possible intermediates and degradation pathways were investigated based on high-performance liquid chromatography tandem mass spectrometry. Additionally, MOFs 1-4 also exhibited excellent photocatalytic activity for the degradation of methylene blue, methyl violet, rhodamine B, and basic red 9.
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