Department of Chemical Engineering, Tianjin University, Tianjin, 300350, China.
Chemistry and Chemical Engineering Guangdong Laboratory, Shantou, 515031, China.
Adv Sci (Weinh). 2021 Nov;8(22):e2101824. doi: 10.1002/advs.202101824. Epub 2021 Oct 12.
Fenton-like reactions with persulfates as the oxidants have attracted increasing attentions for the remediation of emerging antibiotic pollutions. However, developing effective activators with outstanding activities and long-term stabilities remains a great challenge in these reactions. Herein, a novel activator is successfully synthesized with single iron atoms anchored on porous N-doped carbon (Fe-N-PC) by a facile chemical vapor deposition (CVD) method. The single Fe atoms are coordinated with four N atoms according to the XANES, and the Fe-N -PC shows enhanced activity for the activation of peroxymonosulfate (PMS) to degrade sulfamethoxazole (SMX). The experiments and density functional theory (DFT) calculations reveal that the introduction of single Fe atoms will regulate the main active sites from graphite N into Fe-N , thus could enhance the stability and tune the PMS activation pathway from non-radical into radical dominated process. In addition, the N atoms connected with single Fe atoms in the Fe-N -C structure can be used to enhance the adsorption of organic molecules on these materials. Therefore, the Fe-N -C here has dual roles for antibiotics adsorption and PMS activation. The CVD synthesized Fe-N -C shows enhanced performance in persulfates based Fenton-like reactions, thus has great potential in the environmental remediation field.
芬顿样反应以过硫酸盐作为氧化剂,因其在新兴抗生素污染修复方面的应用而受到越来越多的关注。然而,在这些反应中开发具有高活性和长期稳定性的有效活化剂仍然是一个巨大的挑战。本研究通过简便的化学气相沉积(CVD)法成功合成了一种新型的活化剂,即单原子铁锚定在多孔氮掺杂碳(Fe-N-PC)上。根据 XANES 结果,单原子铁与四个氮原子配位,Fe-N-PC 对过一硫酸盐(PMS)的活化活性增强,可用于降解磺胺甲恶唑(SMX)。实验和密度泛函理论(DFT)计算表明,单原子铁的引入将调节主要活性位点从石墨 N 转化为 Fe-N ,从而增强稳定性并调节 PMS 活化途径从非自由基向自由基为主的过程。此外,在 Fe-N-C 结构中与单原子铁相连的氮原子可以增强这些材料对有机分子的吸附。因此,这里的 Fe-N-C 对抗生素吸附和 PMS 活化具有双重作用。CVD 合成的 Fe-N-C 在基于过硫酸盐的芬顿样反应中表现出增强的性能,因此在环境修复领域具有很大的应用潜力。