Efficient Charge Transfer of p-n Heterojunction UiO-66-NH2/CuFe2O4 Composite for Photocatalytic Hydrogen Production

IF 3.8 3区 化学 Q2 CHEMISTRY, PHYSICAL
Catalysts Pub Date : 2024-05-24 DOI:10.3390/catal14060341
M. Shanmugam, Nithish Agamendran, Karthikeyan Sekar
{"title":"Efficient Charge Transfer of p-n Heterojunction UiO-66-NH2/CuFe2O4 Composite for Photocatalytic Hydrogen Production","authors":"M. Shanmugam, Nithish Agamendran, Karthikeyan Sekar","doi":"10.3390/catal14060341","DOIUrl":null,"url":null,"abstract":"Using a p-n heterojunction is one of the efficient methods to increase charge transfer in photocatalysis applications. So, herein, p-type UiO-66 (NH2) and n-type CuFe2O4 (CFO) are used to form an effective p-n heterojunction. Due to their poor charge separation in their pristine form, both UiO-66 (NH2) and CFO materials cannot produce hydrogen; however, the composite p-n heterojunction formed between these materials makes fast charge separation and so hydrogen is efficiently produced. The optimized catalyst UCFO 25% produces a maximum of 62.5 µmol/g/h hydrogen in an aqueous methanol solution. The formation of a p-n heterojunction is confirmed by Mott–Schottky analysis and optical properties, crystallinity and the local atomic environment of the material was analyzed by various analytical tools like UV-Vis spectroscopy, XRD, and XANES.","PeriodicalId":9794,"journal":{"name":"Catalysts","volume":null,"pages":null},"PeriodicalIF":3.8000,"publicationDate":"2024-05-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysts","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.3390/catal14060341","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

Using a p-n heterojunction is one of the efficient methods to increase charge transfer in photocatalysis applications. So, herein, p-type UiO-66 (NH2) and n-type CuFe2O4 (CFO) are used to form an effective p-n heterojunction. Due to their poor charge separation in their pristine form, both UiO-66 (NH2) and CFO materials cannot produce hydrogen; however, the composite p-n heterojunction formed between these materials makes fast charge separation and so hydrogen is efficiently produced. The optimized catalyst UCFO 25% produces a maximum of 62.5 µmol/g/h hydrogen in an aqueous methanol solution. The formation of a p-n heterojunction is confirmed by Mott–Schottky analysis and optical properties, crystallinity and the local atomic environment of the material was analyzed by various analytical tools like UV-Vis spectroscopy, XRD, and XANES.
用于光催化制氢的 p-n 异质结 UiO-66-NH2/CuFe2O4 复合材料的高效电荷转移
在光催化应用中,使用 p-n 异质结是增加电荷转移的有效方法之一。因此,本文使用 p 型 UiO-66 (NH2) 和 n 型 CuFe2O4 (CFO) 形成有效的 p-n 异质结。由于原始形式的 UiO-66 (NH2) 和 CFO 材料的电荷分离能力较差,因此不能产生氢气;但是,这些材料之间形成的复合 p-n 异质结可以快速分离电荷,因此可以高效地产生氢气。经过优化的催化剂 UCFO 25% 在甲醇水溶液中最多可产生 62.5 µmol/g/h 的氢气。Mott-Schottky 分析证实了 p-n 异质结的形成,紫外可见光谱、XRD 和 XANES 等各种分析工具分析了材料的光学特性、结晶度和局部原子环境。
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
Catalysts
Catalysts CHEMISTRY, PHYSICAL-
CiteScore
6.80
自引率
7.70%
发文量
1330
审稿时长
3 months
期刊介绍: Catalysts (ISSN 2073-4344) is an international open access journal of catalysts and catalyzed reactions. Catalysts publishes reviews, regular research papers (articles) and short communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
×
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