Please use this identifier to cite or link to this item:
|Scopus||Web of Science®||Altmetric|
|Title:||Nanodiamonds in sp2/sp3 configuration for radical to nonradical oxidation: core-shell layer dependence|
|Citation:||Applied Catalysis B: Environmental, 2018; 222:176-181|
|Xiaoguang Duan, Zhimin Ao, Huayang Zhang, Martin Saunders, Hongqi Sun, Zongping Shao, Shaobin Wang|
|Abstract:||Nanocarbons in molecular configurations of sp2/sp3 present versatile structural and electronic properties, exhibiting a complexity in the structure-activity chemistry. In this work, we employed detonation nanodiamonds constructed as a characteristic core/shell structure in the sp2/sp3 configuration to demonstrate the intrinsic correlation between the structure and catalysis. Annealed detonation nanodiamonds were found to show a superb activity for catalytic peroxymonosulfate activation and organic oxidation. A synergistic effect of charge transport was discovered at the interface to construct an electron-enriched carbon surface that further promoted the catalytic activity evidenced by the density functional theory (DFT) calculations. More importantly, both experimental results and theoretical predictions revealed that the catalytic oxidation via peroxymonosulfate (PMS) activation was intimately dependent on the proportion of graphitic carbon layer in the sp2/sp3 configurations. The increase of graphitic layers on nanodiamonds would alter the PMS activation from a radical-based reaction to a nonradical pathway for catalytic oxidation. The novel catalytic properties of tunable oxidative potentials from carbocatalysis may simulate fascinating prospects for environmental catalysis and organic synthesis.|
|Keywords:||Nanodiamond; carbocatalysis; peroxymonosulfate, nonradical; DFT|
|Rights:||© 2017 Elsevier B.V. All rights reserved.|
|Appears in Collections:||Chemical Engineering publications|
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.