Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/128297
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Type: Journal article
Title: High-performance porous graphene from synergetic nitrogen doping and physical activation for advanced nonradical oxidation
Author: Wu, D.
Song, W.
Chen, L.
Duan, X.
Xia, Q.
Fan, X.
Li, Y.
Zhang, F.
Peng, W.
Wang, S.
Citation: Journal of Hazardous Materials, 2020; 381:121010-1-121010-10
Publisher: Elsevier
Issue Date: 2020
ISSN: 0304-3894
1873-3336
Statement of
Responsibility: 
Di Wu, Weiyu Song, Lulu Chen, Xiaoguang Duan, Qing Xia, Xiaobin Fan, Yang Li, Fengbao Zhang, Wenchao Peng, Shaobin Wang
Abstract: Porous nitrogen-doped reduced graphene oxide (NRGO) is successfully synthesized from graphene oxide via the combination of CO₂ activation and nitrogen doping with ammonia. The performances of the carbon materials are evaluated by catalytic activation of perroxymonosulfate (PMS) for phenol degradation. The effect of the treatment sequence of CO₂ activation and nitrogen doping on the catalytic activity of the derived product is investigated. The material obtained by CO₂ activation-nitrogen doping (P-NRGO) shows better activity than the one obtained from nitrogen doping-CO₂ activation (N-PRGO). The activation mechanisms are also investigated by radical scavenging test, and the P-NRGO/PMS system is unveiled to rely on the nonradical oxidation pathway. The turnover frequencies (TOFs) of these RGOs are also calculated, and the P-NRGO has the largest TOF of 58.39. Based on the analysis of synthesis method and catalytic activity, it is proposed that new catalytic sites are generated on P-NRGO. Density functional theory (DFT) calculations also illustrated that the most reactive sites are the structure vacancies with two nitrogen atoms, which is consistent with the results. The conclusion in this study provides new insights into the synergistic effect of N-doping and structural defects of carbon materials and the induced nonradical pathway in advanced oxidation.
Keywords: Graphene; nitrogen doping; activation by CO₂; catalytic oxidation; new active sites
Rights: © 2019 Elsevier B.V. All rights reserved.
RMID: 0030133663
DOI: 10.1016/j.jhazmat.2019.121010
Appears in Collections:Chemical Engineering publications

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