Synergistic enhancement of visible light Photocatalysis: Tailoring dual Z-scheme Fe2O3/C3N4/NH2-MIL-125 ternary composites for organic pollutant degradation

IF 3.4 3区 化学 Q2 CHEMISTRY, PHYSICAL
Li-Heng Kao , Jun-Jie Liu , To-Yu Wang , Duo-Syuan Lin , Ying-Shuo Cheng , Chia-Hao Tseng , Kanit Manatura , Wei-Yu Chen , Kun-Yi Andrew Lin , Chao-Wei Huang
{"title":"Synergistic enhancement of visible light Photocatalysis: Tailoring dual Z-scheme Fe2O3/C3N4/NH2-MIL-125 ternary composites for organic pollutant degradation","authors":"Li-Heng Kao ,&nbsp;Jun-Jie Liu ,&nbsp;To-Yu Wang ,&nbsp;Duo-Syuan Lin ,&nbsp;Ying-Shuo Cheng ,&nbsp;Chia-Hao Tseng ,&nbsp;Kanit Manatura ,&nbsp;Wei-Yu Chen ,&nbsp;Kun-Yi Andrew Lin ,&nbsp;Chao-Wei Huang","doi":"10.1016/j.catcom.2024.106893","DOIUrl":null,"url":null,"abstract":"<div><p>In this study, Fe<sub>2</sub>O<sub>3</sub>/C<sub>3</sub>N<sub>4</sub>/NH<sub>2</sub>-MIL-125 ternary composite photocatalysts were synthesized. Their amino groups provided close bonding between these materials, facilitating the effective separation of electrons and holes. Besides, each component of Fe<sub>2</sub>O<sub>3</sub>/C<sub>3</sub>N<sub>4</sub>/NH<sub>2</sub>-MIL-125 plays a crucial role. NH<sub>2</sub>-MIL-125 provided a high surface area, C<sub>3</sub>N<sub>4</sub> contributed to the primary photocatalytic activity, and Fe<sub>2</sub>O<sub>3</sub> aided in enhancing light absorption, generating additional potential to produce hydroxyl radicals, thereby further enhancing photocatalytic activity. Moreover, the proportion of loaded Fe<sub>2</sub>O<sub>3</sub> and C<sub>3</sub>N<sub>4</sub> in the ternary material was investigated. It was found that Fe<sub>2</sub>O<sub>3</sub>/C<sub>3</sub>N<sub>4</sub>/NH<sub>2</sub>-MIL-125 with a 1:1 ratio of Fe<sub>2</sub>O<sub>3</sub> and C<sub>3</sub>N<sub>4</sub> (FeCN1:1/NM125) exhibited excellent photocatalytic performance, in which RhB degradation reached 100% under visible light irradiation, conforming to first-order kinetics analysis with a reaction rate constant k of 0.0164 min<sup>−1</sup>. Its efficiency was twice that of the binary catalyst C<sub>3</sub>N<sub>4</sub>/NH<sub>2</sub>-MIL-125 or Fe<sub>2</sub>O<sub>3</sub>/NH<sub>2</sub>-MIL-125, seven times that of the pristine catalyst C<sub>3</sub>N<sub>4</sub>, and ten times that of the pristine catalyst NH<sub>2</sub>-MIL-125. Scavenger experiments showed that the degradation efficiencies were 52.57%, 55.51%, and 63.41%, respectively, indicating that three active species, namely superoxide radicals, holes, and hydroxyl radicals, made significant contributions to photocatalysis.</p></div>","PeriodicalId":263,"journal":{"name":"Catalysis Communications","volume":null,"pages":null},"PeriodicalIF":3.4000,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1566736724000530/pdfft?md5=88a7045d6c20ae52271cd0fd7a71553a&pid=1-s2.0-S1566736724000530-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Communications","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1566736724000530","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

In this study, Fe2O3/C3N4/NH2-MIL-125 ternary composite photocatalysts were synthesized. Their amino groups provided close bonding between these materials, facilitating the effective separation of electrons and holes. Besides, each component of Fe2O3/C3N4/NH2-MIL-125 plays a crucial role. NH2-MIL-125 provided a high surface area, C3N4 contributed to the primary photocatalytic activity, and Fe2O3 aided in enhancing light absorption, generating additional potential to produce hydroxyl radicals, thereby further enhancing photocatalytic activity. Moreover, the proportion of loaded Fe2O3 and C3N4 in the ternary material was investigated. It was found that Fe2O3/C3N4/NH2-MIL-125 with a 1:1 ratio of Fe2O3 and C3N4 (FeCN1:1/NM125) exhibited excellent photocatalytic performance, in which RhB degradation reached 100% under visible light irradiation, conforming to first-order kinetics analysis with a reaction rate constant k of 0.0164 min−1. Its efficiency was twice that of the binary catalyst C3N4/NH2-MIL-125 or Fe2O3/NH2-MIL-125, seven times that of the pristine catalyst C3N4, and ten times that of the pristine catalyst NH2-MIL-125. Scavenger experiments showed that the degradation efficiencies were 52.57%, 55.51%, and 63.41%, respectively, indicating that three active species, namely superoxide radicals, holes, and hydroxyl radicals, made significant contributions to photocatalysis.

Abstract Image

可见光光催化的协同增强:定制用于有机污染物降解的双 Z 型 Fe2O3/C3N4/NH2-MIL-125 三元复合材料
本研究合成了 FeO/CN/NH-MIL-125 三元复合光催化剂。FeO/CN/NH-MIL-125是一种三元复合光催化剂,其氨基酸基团使这些材料之间紧密结合,从而促进了电子和空穴的有效分离。此外,FeO/CN/NH-MIL-125 中的每种成分都起着至关重要的作用。NH-MIL-125 提供了高比表面积,CN 促进了主要的光催化活性,而 FeO 则有助于增强光吸收,产生更多的羟基自由基,从而进一步提高光催化活性。此外,还研究了三元材料中负载的 FeO 和 CN 的比例。研究发现,FeO/CN/NH-MIL-125 中 FeO 和 CN 的比例为 1:1(FeCN1:1/NM125),具有优异的光催化性能,在可见光照射下,RhB 降解率达到 100%,符合一阶动力学分析,反应速率常数 k 为 0.0164 分钟。其效率是二元催化剂 CN/NH-MIL-125 或 FeO/NH-MIL-125 的两倍,原始催化剂 CN 的七倍,原始催化剂 NH-MIL-125 的十倍。清除剂实验表明,降解效率分别为 52.57%、55.51% 和 63.41%,这表明超氧自由基、空穴和羟基自由基这三种活性物种在光催化中做出了重要贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Catalysis Communications
Catalysis Communications 化学-物理化学
CiteScore
6.20
自引率
2.70%
发文量
183
审稿时长
46 days
期刊介绍: Catalysis Communications aims to provide rapid publication of significant, novel, and timely research results homogeneous, heterogeneous, and enzymatic catalysis.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信