石墨烯
催化作用
硫黄
氧化物
电子顺磁共振
材料科学
无机化学
金属
激进的
化学工程
光化学
化学
纳米技术
有机化学
冶金
工程类
物理
核磁共振
作者
Xiaoguang Duan,Kane M. O’Donnell,Hongqi Sun,Yuxian Wang,Shaobin Wang
出处
期刊:Small
[Wiley]
日期:2015-03-18
卷期号:11 (25): 3036-3044
被引量:692
标识
DOI:10.1002/smll.201403715
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.
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