School of Basic Medical Science, Xinxiang Medical University, Xinxiang 453003, China.
Shanghai Key Laboratory of Magnetic Resonance, School of Physics and Electronic Science, East China Normal University, Shanghai 200241, China.
J Colloid Interface Sci. 2022 Nov;625:466-478. doi: 10.1016/j.jcis.2022.06.057. Epub 2022 Jun 14.
In this work, CoO/g-CN catalyst with highly efficient adsorption and degradation of antibiotics was developed based on the combination of three-dimensional (3D) porous morphological controls of g-CN and the loading of CoO quantum dots (CoO QDs). It was discovered that the catalyst can effectively activate peroxymonosulfate (PMS) through a non-photochemical path, and a high tetracycline elimination rate of 99.7% can be achieved within 18 min. The characterization and density functional theory calculation results demonstrated that the porous 3D structure can not only promote the substrate adsorption reaction but also provide large surface area and countless exposed active sites for catalytic reaction. The introduction of CoO QDs lowered activation energy barrier and lead to high energy of PMS adsorption. More efficient charge migration between the catalyst and PMS further accelerated PMS activation. Thus, leading to the excellent catalytic performance. In addition, non-free radical mediated degradation mechanism of catalytic activity was also proposed. This work provides a scheme for designing novel and efficient PMS activators for the removal of abusive antibiotics from aqueous environments.
在这项工作中,通过将 g-CN 的三维(3D)多孔形态控制与 CoO 量子点(CoO QDs)的负载相结合,开发出了一种对抗生素具有高效吸附和降解能力的 CoO/g-CN 催化剂。研究发现,该催化剂可以通过非光化学途径有效激活过一硫酸盐(PMS),在 18 分钟内即可实现高达 99.7%的四环素消除率。通过对其进行表征和密度泛函理论计算,结果表明多孔 3D 结构不仅可以促进底物吸附反应,而且还为催化反应提供了大的表面积和无数暴露的活性位点。CoO QDs 的引入降低了活化能垒,从而提高了 PMS 的吸附能。催化剂和 PMS 之间更有效的电荷迁移进一步加速了 PMS 的活化。因此,表现出了优异的催化性能。此外,还提出了非自由基介导的催化活性降解机制。这项工作为设计新型高效 PMS 活化剂以去除水环境中滥用的抗生素提供了一种方案。