Wu Ying, Liang Gang, Li Wen-Bin, Zhong Xiao-Feng, Zhang Yang-Yang, Ye Jia-Wen, Yang Tao, Mo Zong-Wen, Chen Xiao-Ming
School of Environmental and Chemical Engineering, Jiangmen Key Laboratory of Synthetic Chemistry and Cleaner Production, Wuyi University Jiangmen Guangdong 529020 China
MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, GBRCE for Functional Molecular Engineering, School of Chemistry, IGCME, Sun Yat-Sen University Guangzhou 510275 China.
Chem Sci. 2024 May 16;15(25):9733-9741. doi: 10.1039/d4sc02850c. eCollection 2024 Jun 26.
Highly efficient degradation of antibiotics is a huge challenge due to the extremely stable molecules and the potential for biological resistance. However, conventional degradation methods are limited to lower degradation rate, higher energy consumption and secondary pollution. Herein, we report a new Cu-based metal-organic framework (MOF), featuring classical planar trinuclear [Cu(µ-O)] clusters within the pores. The presence of the rich open metal sites and the large pore ratio, as well as the high catalytic activity of Cu ions, are conducive to boosting the degradation of various antibiotics (>95%) under the activation of peroxymonosulfate. Remarkably, this is the first MOF to achieve such exceptional catalytic performance under neutral and even alkaline conditions, which exceeds those of most reported materials. Mechanism investigation demonstrates that multiple active species were produced and promoted the degradation synergistically during the advanced oxidation processes.
由于抗生素分子极其稳定且存在生物抗性的可能性,高效降解抗生素是一项巨大挑战。然而,传统降解方法存在降解速率较低、能耗较高以及二次污染等局限。在此,我们报道了一种新型的铜基金属有机框架材料(MOF),其孔道内具有经典的平面三核[Cu(µ-O)]簇。丰富的开放金属位点、较大的孔隙率以及铜离子的高催化活性,有利于在过一硫酸盐的活化作用下促进各种抗生素的降解(>95%)。值得注意的是,这是首例在中性甚至碱性条件下实现如此优异催化性能的MOF,其性能超过了大多数已报道的材料。机理研究表明,在高级氧化过程中产生了多种活性物种并协同促进了降解。