协同增强过氧化氢的生成:在可见光下用 MXene 和金纳米粒子修饰的 WO3 光催化剂

IF 4.4 3区 化学 Q2 CHEMISTRY, PHYSICAL
Xiaoyu Sun , Teruhisa Ohno
{"title":"协同增强过氧化氢的生成:在可见光下用 MXene 和金纳米粒子修饰的 WO3 光催化剂","authors":"Xiaoyu Sun ,&nbsp;Teruhisa Ohno","doi":"10.1039/d4cy00443d","DOIUrl":null,"url":null,"abstract":"<div><p>A novel composite material composed of WO<sub>3</sub>, Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> MXene, and Au for the photocatalytic formation of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) is introduced here. Through optimization, the ideal MXene and Au concentrations were determined to be both 0.5%. And after loading Au and MXene the amount of H<sub>2</sub>O<sub>2</sub> generated increases to 7.52 mg L<sup>−1</sup> at pH 3, which is a remarkable 21.5-fold increase. Quenching experiments unequivocally revealed identified ·O<sub>2</sub><sup>−</sup> as the predominant intermediate product, indicating a two-stage, single-electron indirect mechanism. Enhanced effectiveness for H<sub>2</sub>O<sub>2</sub> synthesis is ascribed to the synergistic impact of Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> MXene and gold, enhancing charge transfer efficiency while impeding the recombination of these electron–hole pairs.</p></div>","PeriodicalId":66,"journal":{"name":"Catalysis Science & Technology","volume":null,"pages":null},"PeriodicalIF":4.4000,"publicationDate":"2024-06-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synergistic enhancement of hydrogen peroxide generation: WO3 photocatalyst modified with MXene and Au nanoparticles under visible light†\",\"authors\":\"Xiaoyu Sun ,&nbsp;Teruhisa Ohno\",\"doi\":\"10.1039/d4cy00443d\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>A novel composite material composed of WO<sub>3</sub>, Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> MXene, and Au for the photocatalytic formation of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) is introduced here. Through optimization, the ideal MXene and Au concentrations were determined to be both 0.5%. And after loading Au and MXene the amount of H<sub>2</sub>O<sub>2</sub> generated increases to 7.52 mg L<sup>−1</sup> at pH 3, which is a remarkable 21.5-fold increase. Quenching experiments unequivocally revealed identified ·O<sub>2</sub><sup>−</sup> as the predominant intermediate product, indicating a two-stage, single-electron indirect mechanism. Enhanced effectiveness for H<sub>2</sub>O<sub>2</sub> synthesis is ascribed to the synergistic impact of Ti<sub>3</sub>C<sub>2</sub>T<sub>x</sub> MXene and gold, enhancing charge transfer efficiency while impeding the recombination of these electron–hole pairs.</p></div>\",\"PeriodicalId\":66,\"journal\":{\"name\":\"Catalysis Science & Technology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.4000,\"publicationDate\":\"2024-06-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Catalysis Science & Technology\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S2044475324002922\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Science & Technology","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2044475324002922","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

摘要

本文介绍了一种由 WO3、Ti3C2Tx MXene 和金组成的新型复合材料,用于光催化形成过氧化氢(H2O2)。通过优化,确定理想的 MXene 和 Au 浓度均为 0.5%。加入金和 MXene 后,在 pH 值为 3 时产生的 H2O2 量增至 7.52 mg L-1,显著增加了 21.5 倍。淬火实验明确显示-O2-是主要的中间产物,表明这是一种两阶段、单电子间接机制。Ti3C2Tx MXene 和金的协同作用提高了 H2O2 的合成效率,在提高电荷转移效率的同时阻碍了这些电子-空穴对的重组。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synergistic enhancement of hydrogen peroxide generation: WO3 photocatalyst modified with MXene and Au nanoparticles under visible light†

Synergistic enhancement of hydrogen peroxide generation: WO3 photocatalyst modified with MXene and Au nanoparticles under visible light†

Synergistic enhancement of hydrogen peroxide generation: WO3 photocatalyst modified with MXene and Au nanoparticles under visible light†

A novel composite material composed of WO3, Ti3C2Tx MXene, and Au for the photocatalytic formation of hydrogen peroxide (H2O2) is introduced here. Through optimization, the ideal MXene and Au concentrations were determined to be both 0.5%. And after loading Au and MXene the amount of H2O2 generated increases to 7.52 mg L−1 at pH 3, which is a remarkable 21.5-fold increase. Quenching experiments unequivocally revealed identified ·O2 as the predominant intermediate product, indicating a two-stage, single-electron indirect mechanism. Enhanced effectiveness for H2O2 synthesis is ascribed to the synergistic impact of Ti3C2Tx MXene and gold, enhancing charge transfer efficiency while impeding the recombination of these electron–hole pairs.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Catalysis Science & Technology
Catalysis Science & Technology CHEMISTRY, PHYSICAL-
CiteScore
8.70
自引率
6.00%
发文量
587
审稿时长
1.5 months
期刊介绍: A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis. Editor-in-chief: Bert Weckhuysen Impact factor: 5.0 Time to first decision (peer reviewed only): 31 days
×
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