Enhanced Photocatalytic Production of Hydrogen Peroxide by Covalent Triazine Frameworks with Stepwise Electron Transfer

IF 11.3 1区 化学 Q1 CHEMISTRY, PHYSICAL ACS Catalysis Pub Date : 2024-11-15 DOI:10.1021/acscatal.4c05328
Hao Zhang, Wenxin Wei, Kai Chi, Yong Zheng, Xin Ying Kong, Liqun Ye, Yan Zhao, Kai A. I. Zhang
{"title":"Enhanced Photocatalytic Production of Hydrogen Peroxide by Covalent Triazine Frameworks with Stepwise Electron Transfer","authors":"Hao Zhang, Wenxin Wei, Kai Chi, Yong Zheng, Xin Ying Kong, Liqun Ye, Yan Zhao, Kai A. I. Zhang","doi":"10.1021/acscatal.4c05328","DOIUrl":null,"url":null,"abstract":"The photosynthesis of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) from pure water and oxygen using metal-free photocatalysts offers a renewable approach to convert solar energy to storable chemical energy. However, the efficiency of H<sub>2</sub>O<sub>2</sub> photosynthesis is often hindered by the rapid recombination of photogenerated charge carriers. Herein, we present an elegantly designed covalent triazine framework (CTF) photocatalyst, denoted as Ace-asy-CTF, with a stepwise electron transfer pathway for the highly efficient photosynthesis of H<sub>2</sub>O<sub>2</sub>. Notably, Ace-asy-CTF possesses localized excited-state charge distribution and stepwise electron transfer that is created by the weakly conjugated acetenyl units in the asymmetric frameworks, as revealed by transient spectroscopies and further supported by theoretical calculations. Meanwhile, the introduced acetenyl units also serve as active sites for the oxygen reduction reaction (ORR). The simultaneously enhanced stepwise charge transfer and two-step 2e<sup>–</sup> ORR in Ace-asy-CTF result in an excellent H<sub>2</sub>O<sub>2</sub> yield of 2594 μmol g<sup>–1</sup> h<sup>–1</sup>, directly produced from oxygen and pure water without requiring any sacrificial reagents. This work paves the way for the development of next-generation metal-free catalysts, providing a feasible benchmark for the highly efficient and stable photosynthesis of H<sub>2</sub>O<sub>2</sub>.","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":"25 1","pages":""},"PeriodicalIF":11.3000,"publicationDate":"2024-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Catalysis ","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acscatal.4c05328","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

The photosynthesis of hydrogen peroxide (H2O2) from pure water and oxygen using metal-free photocatalysts offers a renewable approach to convert solar energy to storable chemical energy. However, the efficiency of H2O2 photosynthesis is often hindered by the rapid recombination of photogenerated charge carriers. Herein, we present an elegantly designed covalent triazine framework (CTF) photocatalyst, denoted as Ace-asy-CTF, with a stepwise electron transfer pathway for the highly efficient photosynthesis of H2O2. Notably, Ace-asy-CTF possesses localized excited-state charge distribution and stepwise electron transfer that is created by the weakly conjugated acetenyl units in the asymmetric frameworks, as revealed by transient spectroscopies and further supported by theoretical calculations. Meanwhile, the introduced acetenyl units also serve as active sites for the oxygen reduction reaction (ORR). The simultaneously enhanced stepwise charge transfer and two-step 2e ORR in Ace-asy-CTF result in an excellent H2O2 yield of 2594 μmol g–1 h–1, directly produced from oxygen and pure water without requiring any sacrificial reagents. This work paves the way for the development of next-generation metal-free catalysts, providing a feasible benchmark for the highly efficient and stable photosynthesis of H2O2.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
通过共价三嗪框架分步电子转移增强过氧化氢的光催化生产
利用无金属光催化剂从纯水和氧气中产生过氧化氢(H2O2)的光合作用提供了一种将太阳能转化为可储存化学能的可再生方法。然而,H2O2 光合作用的效率往往受到光生电荷载流子快速重组的阻碍。在此,我们提出了一种设计优雅的共价三嗪框架(CTF)光催化剂,命名为 Ace-asy-CTF,它具有逐步电子传递途径,可实现 H2O2 的高效光合作用。值得注意的是,Ace-asy-CTF 具有局部激发态电荷分布和阶跃式电子转移,这是由不对称框架中的弱共轭乙炔基单元产生的,瞬态光谱揭示了这一点,理论计算也进一步证实了这一点。同时,引入的乙炔基单元也是氧还原反应(ORR)的活性位点。Ace-asy-CTF 中同时增强的分步电荷转移和两步 2e- ORR 使 H2O2 产率达到 2594 μmol g-1 h-1,而且无需任何牺牲试剂就能直接从氧气和纯水中产生。这项工作为开发下一代无金属催化剂铺平了道路,为 H2O2 的高效稳定光合作用提供了可行的基准。
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 去求助
来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
期刊最新文献
Ancestral Sequence Reconstruction Meets Machine Learning: Ene Reductase Thermostabilization Yields Enzymes with Improved Reactivity Profiles Exploring the Mechanism of Biomimetic Arene Hydroxylation: When a Diiron Metal Center Meets a Sulfur-Containing Ligand {TiO2/TiO2(B)} Quantum Dot Hybrids: A Comprehensible Route toward High-Performance [>0.1 mol gr–1 h–1] Photocatalytic H2 Production from H2O Geometrically Constrained Cofacial Bi-Titanium Olefin Polymerization Catalysts: Tuning and Enhancing Comonomer Incorporation Density Expanding the Reaction Network of Ethylene Epoxidation on Partially Oxidized Silver Catalysts
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1