A novel scheme to improve the photo-Fenton performance of iron oxychloride by carbon: Three existent states and roles of carbon in the degradation of tetracycline in water

被引:10
作者
Wang, Lina [1 ]
Yang, Hanpei [1 ]
Yang, Yuankun [1 ]
He, Zuming [1 ]
机构
[1] Hohai Univ, Coll Environm, Key Lab Integrated Regulat & Resource Dev, Minist Educ, Nanjing 210098, Peoples R China
基金
中国国家自然科学基金;
关键词
FeOCl; Carbon; Existent state; Photo-Fenton; Isotropy; Fe (II); Fe(III) cycle; LIGHT PHOTOCATALYTIC ACTIVITY; CATALYST; REMOVAL; CONSTRUCTION; INSIGHTS; HYBRID; FEOCL; H2O2;
D O I
10.1016/j.jcis.2023.03.113
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
The photo-Fenton process is promising for sincerely treating contaminated water. In this work, carbon -decorated iron oxychloride (C-FeOCl) is synthesized as a photo-Fenton catalyst for removing tetracycline (TC) from water. Three actual states of carbon are identified and their different roles in enhancing photo -Fenton performance are revealed. All carbon on/in FeOCl, including graphite carbon, carbon dots and lattice carbon, enhance visible light adsorption. More importantly, a homogeneous graphite carbon on the outer surface of FeOCl accelerates the transportation-separation of photo-excited electrons along the horizontal direction of FeOCl. Meanwhile, the interlayered carbon dots offer a Fe-O-C bridge in helping the transportation-separation of photo-excited electrons along the vertical direction of FeOCl. In this way, C-FeOCl acquires isotropy in conduction electrons to ensure an efficient Fe(II)/Fe(III) cycle. These interlayered carbon dots extend the layer spacing (d) of FeOCl to about 1.10 nm, exposing the inter-nal iron centers. The lattice carbon significantly increases the amounts of coordinatively unsaturated iron sites (CUISs) in activating hydrogen peroxide (H2O2) to hydroxyl radical (.OH). Density functional theory (DFT) calculations confirm this activation on inner and external CUISs with a significantly low activation energy of about 0.33 eV.(c) 2023 Elsevier Inc. All rights reserved.
引用
收藏
页码:916 / 928
页数:13
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