Hao Zhang, Wenxin Wei, Kai Chi, Yong Zheng, Xin Ying Kong, Liqun Ye, Yan Zhao, Kai A. I. Zhang
{"title":"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","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":"{\"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}","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}
Enhanced Photocatalytic Production of Hydrogen Peroxide by Covalent Triazine Frameworks with Stepwise Electron Transfer
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.
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.