Department of Chemical Engineering, Curtin University, GPO Box U1987, WA, 6845, Australia.
Department of Imaging and Applied Physics, Curtin University, GPO Box U1987, WA, 6845, Australia.
Small. 2015 Jul 1;11(25):3036-44. doi: 10.1002/smll.201403715. Epub 2015 Mar 18.
Sulfur and nitrogen co-doped reduced graphene oxide (rGO) is synthesized by a facile method and demonstrated remarkably enhanced activities in metal-free activation of peroxymonosulfate (PMS) for catalytic oxidation of phenol. Based on first-order kinetic model, S-N co-doped rGO (SNG) presents an apparent reaction rate constant of 0.043 ± 0.002 min(-1) , which is 86.6, 22.8, 19.7, and 4.5-fold as high as that over graphene oxide (GO), rGO, S-doped rGO (S-rGO), and N-doped rGO (N-rGO), respectively. A variety of characterization techniques and density functional theory calculations are employed to investigate the synergistic effect of sulfur and nitrogen co-doping. Co-doping of rGO at an optimal sulfur loading can effectively break the inertness of carbon systems, activate the sp(2) -hybridized carbon lattice and facilitate the electron transfer from covalent graphene sheets for PMS activation. Moreover, both electron paramagnetic resonance (EPR) spectroscopy and classical quenching tests are employed to investigate the generation and evolution of reactive radicals on the SNG sample for phenol catalytic oxidation. This study presents a novel metal-free catalyst for green remediation of organic pollutants in water.
硫氮共掺杂还原氧化石墨烯(rGO)通过简便的方法合成,并在过一硫酸盐(PMS)无金属活化中表现出显著增强的催化氧化苯酚的活性。基于一级反应动力学模型,S-N 共掺杂 rGO(SNG)的表观反应速率常数为 0.043±0.002 min(-1),分别是氧化石墨烯(GO)、rGO、S 掺杂 rGO(S-rGO)和 N 掺杂 rGO(N-rGO)的 86.6、22.8、19.7 和 4.5 倍。采用多种表征技术和密度泛函理论计算研究了硫和氮共掺杂的协同效应。在最佳硫负载下共掺杂 rGO 可以有效地打破碳体系的惰性,激活 sp(2)杂化碳晶格,并促进从共价石墨烯片的电子转移以活化 PMS。此外,还采用电子顺磁共振(EPR)光谱和经典猝灭实验研究了 SNG 样品中用于催化氧化苯酚的活性自由基的生成和演变。本研究提供了一种用于水中有机污染物绿色修复的新型无金属催化剂。