Hydrogen Peroxide as an Ideal Electron Donor for Long-Lasting Fenton Chemistry: Strong Enhancement of Fe(III) Activity by Heteroatom-Doped Nanocarbons

被引:23
作者
Sun, Yiming [1 ,2 ]
Zhou, Peng [1 ,2 ]
Sun, Minglu [1 ,2 ]
Zhang, Yuchen [1 ,2 ]
Wang, Xiao [1 ,2 ]
Zhou, Chenying [1 ,2 ]
Liu, Yang [1 ,2 ]
He, Chuanshu [1 ,2 ]
Lai, Bo [1 ,2 ]
机构
[1] Sichuan Univ, Coll Architecture & Environm, State Key Lab Hydraul & Mt River Engn, Chengdu 610065, Peoples R China
[2] Sichuan Univ, Sino German Ctr Water & Hlth Res, Chengdu 610041, Peoples R China
基金
中国国家自然科学基金;
关键词
carbon catalysis; Fenton oxidation; heteroatomdoping; Fe(III)/Fe(II) cycling; electrochemicalanalysis; OXYGEN REDUCTION REACTION; REDUCED GRAPHENE OXIDE; CATALYTIC OZONATION; REACTIVE RADICALS; BISPHENOL-A; CARBON; OXIDATION; WATER; EVOLUTION; PATHWAYS;
D O I
10.1021/acscatal.4c00048
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Heteroatom doping has been demonstrated to be an effective strategy to improve the catalytic activity of carbon materials. Herein, heteroatom-doped nanocarbons were found to be environmental protection cocatalysts for promoting Fenton oxidation. Nitrogen-doped reduced graphene oxide (N-rGO) exhibited better catalytic activity than sulfur-, boron-, and phosphorus-doped rGO for enhancing Fenton oxidation. Unlike classical electron sacrificial agents, H2O2 was employed as an electron donor to enhance Fenton oxidation during the catalysis of N-rGO. Electrochemical analysis and nitrogen molecular model tests indicated the oxidation potential of Fe(III) increased with improvement in the N atom content (R-2 = 0.97), revealing that the Fe atoms of FeOH2+ on the N-rGO surface are more likely to abstract electrons from H2O2. In addition, the delocalized pi electron is one of the active sites in N-rGO-boosted Fenton oxidation, and N-rGO could facilitate electron transfer from H2O2 to Fe(III) along the C-C/C & boxH;C structures due to the improvement of the conductivity ability and the oxidation potential of Fe(III). Moreover, density functional theory (DFT) calculations suggest that the pyrrole N species of N-rGO is the best catalytic activity site, resulting from the pyrrole N species with higher adsorption energy stretching the Fe-O bond of FeOH2+ to increase the activity of Fe(III) species. Therefore, the study findings provide insight into designing stable and efficient metal-free catalysts to enhance Fe(III) reactivity in overcoming the inherent drawbacks of the Fenton system.
引用
收藏
页码:6525 / 6534
页数:10
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