Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/139337
Title: Single cobalt atoms anchored on porous N-doped graphene with dual reaction sites for efficient Fenton-like catalysis
Authors: Li, Xuning
Huang, Xiang
Xi, Shibo
Miao, Shu
Ding, Jie
Cai, Weizheng
Liu, Song
Yang, Xiaoli
Yang, Hongbin
Gao, Jiajian
Wang, Junhu
Huang, Yanqiang
Zhang, Tao
Liu, Bin
Keywords: Engineering::Chemical engineering
Issue Date: 2018
Source: Li, X., Huang, X., Xi, S., Miao, S., Ding, J., Cai, W., . . . Liu, B. (2018). Single cobalt atoms anchored on porous N-doped graphene with dual reaction sites for efficient Fenton-like catalysis. Journal of the American Chemical Society, 140(39), 12469-12475. doi:10.1021/jacs.8b05992
Journal: Journal of the American Chemical Society
Abstract: The Fenton-like process presents one of the most promising strategies to generate reactive oxygen-containing radicals to deal with the ever-growing environmental pollution. However, developing improved catalysts with adequate activity and stability is still a long-term goal for practical application. Herein, we demonstrate single cobalt atoms anchored on porous N-doped graphene with dual reaction sites as highly reactive and stable Fenton-like catalysts for efficient catalytic oxidation of recalcitrant organics via activation of peroxymonosulfate (PMS). Our experiments and density functional theory (DFT) calculations show that the CoN4 site with a single Co atom serves as the active site with optimal binding energy for PMS activation, while the adjacent pyrrolic N site adsorbs organic molecules. The dual reaction sites greatly reduce the migration distance of the active singlet oxygen produced from PMS activation and thus improve the Fenton-like catalytic performance.
URI: https://hdl.handle.net/10356/139337
ISSN: 0002-7863
DOI: 10.1021/jacs.8b05992
Schools: School of Chemical and Biomedical Engineering 
Rights: © 2018 American Chemical Society. All rights reserved.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SCBE Journal Articles

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