Covalent Organic Framework Encapsulating Layered Oxide Perovskite for Efficient Photosynthesis of H2O2

IF 24.4 1区 材料科学 Q1 CHEMISTRY, PHYSICAL
Yuan Teng, Jing Zhao, Zi‐Ming Ye, Chao‐Wen Tan, Ling‐Ling Ning, Yi‐Yang Zhou, Zhilian Wu, Dai‐Bin Kuang, Youji Li
{"title":"Covalent Organic Framework Encapsulating Layered Oxide Perovskite for Efficient Photosynthesis of H2O2","authors":"Yuan Teng, Jing Zhao, Zi‐Ming Ye, Chao‐Wen Tan, Ling‐Ling Ning, Yi‐Yang Zhou, Zhilian Wu, Dai‐Bin Kuang, Youji Li","doi":"10.1002/aenm.202404029","DOIUrl":null,"url":null,"abstract":"Driving efficient artificial photosynthesis of H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> is highly desirable in both academic and industrial fields. Here, a new core–shell Bi<jats:sub>3</jats:sub>TiNbO<jats:sub>9</jats:sub>@C<jats:sub>4</jats:sub>N heterojunction is constructed for efficient photocatalytic H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> production by in situ encapsulating an ultrathin layer of covalent organic framework material (C<jats:sub>4</jats:sub>N) on Aurivillius‐type Bi<jats:sub>3</jats:sub>TiNbO<jats:sub>9</jats:sub> microsheets. The porous C<jats:sub>4</jats:sub>N layer is found to enhance visible‐light absorption ability and facilitate the adsorption and activation of the reactants and intermediates. The hybrid heterojunction follows an S‐scheme charge transfer with the assistance of a strong internal electric field (IEF), which promotes the spatial separation of photogenerated carriers effectively and maintains their strong redox abilities. As a result, the optimized Bi<jats:sub>3</jats:sub>TiNbO<jats:sub>9</jats:sub>@C<jats:sub>4</jats:sub>N unveils a high H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> yield rate of 1.25(2) mmol g<jats:sup>−1</jats:sup> h<jats:sup>−1</jats:sup> in the absence of sacrificial agents and cocatalyst, 10.9 and 3.5 folds higher than those of pristine Bi<jats:sub>3</jats:sub>TiNbO<jats:sub>9</jats:sub> and C<jats:sub>4</jats:sub>N catalysts, respectively. This work provides an in situ encapsulating strategy to decorate covalent organic frameworks (COFs) on oxide perovskites for artificial photosynthesis of H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub>, which may stimulate the intensive investigation interests of functional materials/COFs heterojunction materials for various photocatalysis applications.","PeriodicalId":111,"journal":{"name":"Advanced Energy Materials","volume":"205 1","pages":""},"PeriodicalIF":24.4000,"publicationDate":"2024-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Energy Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/aenm.202404029","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Driving efficient artificial photosynthesis of H2O2 is highly desirable in both academic and industrial fields. Here, a new core–shell Bi3TiNbO9@C4N heterojunction is constructed for efficient photocatalytic H2O2 production by in situ encapsulating an ultrathin layer of covalent organic framework material (C4N) on Aurivillius‐type Bi3TiNbO9 microsheets. The porous C4N layer is found to enhance visible‐light absorption ability and facilitate the adsorption and activation of the reactants and intermediates. The hybrid heterojunction follows an S‐scheme charge transfer with the assistance of a strong internal electric field (IEF), which promotes the spatial separation of photogenerated carriers effectively and maintains their strong redox abilities. As a result, the optimized Bi3TiNbO9@C4N unveils a high H2O2 yield rate of 1.25(2) mmol g−1 h−1 in the absence of sacrificial agents and cocatalyst, 10.9 and 3.5 folds higher than those of pristine Bi3TiNbO9 and C4N catalysts, respectively. This work provides an in situ encapsulating strategy to decorate covalent organic frameworks (COFs) on oxide perovskites for artificial photosynthesis of H2O2, which may stimulate the intensive investigation interests of functional materials/COFs heterojunction materials for various photocatalysis applications.
求助全文
约1分钟内获得全文 求助全文
来源期刊
Advanced Energy Materials
Advanced Energy Materials CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
41.90
自引率
4.00%
发文量
889
审稿时长
1.4 months
期刊介绍: Established in 2011, Advanced Energy Materials is an international, interdisciplinary, English-language journal that focuses on materials used in energy harvesting, conversion, and storage. It is regarded as a top-quality journal alongside Advanced Materials, Advanced Functional Materials, and Small. With a 2022 Impact Factor of 27.8, Advanced Energy Materials is considered a prime source for the best energy-related research. The journal covers a wide range of topics in energy-related research, including organic and inorganic photovoltaics, batteries and supercapacitors, fuel cells, hydrogen generation and storage, thermoelectrics, water splitting and photocatalysis, solar fuels and thermosolar power, magnetocalorics, and piezoelectronics. The readership of Advanced Energy Materials includes materials scientists, chemists, physicists, and engineers in both academia and industry. The journal is indexed in various databases and collections, such as Advanced Technologies & Aerospace Database, FIZ Karlsruhe, INSPEC (IET), Science Citation Index Expanded, Technology Collection, and Web of Science, among others.
×
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