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

杂原子 过氧化氢 化学 石墨烯 光化学 催化作用 电化学 电子转移 密度泛函理论 氧化物 硫黄 氧化还原 无机化学 有机化学 材料科学 纳米技术 物理化学 计算化学 戒指(化学) 电极
作者
Yiming Sun,Peng Zhou,Minglu Sun,Yuchen Zhang,Xiao Wang,Chenying Zhou,Yang Liu,Chuan-Shu He,Bo Lai
出处
期刊:ACS Catalysis [American Chemical Society]
卷期号:14 (9): 6525-6534 被引量:50
标识
DOI:10.1021/acscatal.4c00048
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 (R2 = 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 π 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═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.
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