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Sulfur and Nitrogen Co-Doped Graphene for Metal-Free Catalytic Oxidation Reactions

机译:硫和氮共掺杂石墨烯用于无金属催化氧化反应

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摘要

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.
机译:硫和氮共掺杂的还原氧化石墨烯(rGO)是通过一种简便的方法合成的,在过氧化单硫酸盐(PMS)的无金属活化过程中,苯酚的催化氧化具有显着增强的活性。基于一阶动力学模型,SN共掺杂rGO(SNG)的表观反应速率常数为0.043 +/- 0.002 min(-1),是其的86.6、22.8、19.7和4.5倍。分别位于氧化石墨烯(GO),rGO,S掺杂的rGO(S-rGO)和N掺杂的rGO(N-rGO)上。多种表征技术和密度泛函理论计算被用于研究硫和氮共掺杂的协同效应。在最佳硫负载下共掺杂rGO可以有效打破碳系统的惰性,激活sp(2)杂化的碳晶格,并促进电子从共价石墨烯薄板上转移以进行PMS激活。此外,电子顺磁共振(EPR)光谱和经典猝灭测试均用于研究SNG样品上用于酚催化氧化的反应性自由基的产生和演化。这项研究提出了一种新型的无金属催化剂,用于绿色修复水中的有机污染物。

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