Yujie Li , Wenhao Liu , Fang Duan , Shengrong Yan , Yanyan Ren , Haiping Liu , Shuanglong Lu , Mingliang Du , Xin Chen , Jun Wang
{"title":"一种具有可逆互变异构结构的亲水邻菲罗啉共价有机聚合物,用于促进光催化过氧化氢的生产","authors":"Yujie Li , Wenhao Liu , Fang Duan , Shengrong Yan , Yanyan Ren , Haiping Liu , Shuanglong Lu , Mingliang Du , Xin Chen , Jun Wang","doi":"10.1039/d4cy01158a","DOIUrl":null,"url":null,"abstract":"<div><div>Photocatalytic production of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) from solar energy, oxygen and water is an environmentally friendly and sustainable approach. However, the efficiency is highly restricted by the limited light absorption, charge separation and oxygen capture of the active centers. In this study, a novel hydrophilic <em>o</em>-phenanthroline-based covalent organic polymer (COP) with a reversible iminol-to-ketoenamine tautomeric structure was successfully prepared through the Schiff base reaction. The highly conjugated structure significantly enhances its visible light absorption and accelerates the separation and migration of photogenerated charges. Furthermore, the <em>o</em>-phenanthroline linker facilitates the adsorption and activation of oxygen molecules, and the hydrophilicity is highly advantageous for the rapid photocatalytic reactions. Therefore, the as-prepared COP exhibits excellent photocatalytic H<sub>2</sub>O<sub>2</sub> production performance (814 μmol g<sup>−1</sup> h<sup>−1</sup>) without the addition of any cocatalysts or sacrificial agents. This work provides a new example for the design of photocatalysts based on covalent organic polymers towards H<sub>2</sub>O<sub>2</sub> production.</div></div>","PeriodicalId":66,"journal":{"name":"Catalysis Science & Technology","volume":"15 2","pages":"Pages 448-456"},"PeriodicalIF":4.4000,"publicationDate":"2024-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A hydrophilic o-phenanthroline-based covalent organic polymer with a reversible tautomeric structure for boosting photocatalytic hydrogen peroxide production†\",\"authors\":\"Yujie Li , Wenhao Liu , Fang Duan , Shengrong Yan , Yanyan Ren , Haiping Liu , Shuanglong Lu , Mingliang Du , Xin Chen , Jun Wang\",\"doi\":\"10.1039/d4cy01158a\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Photocatalytic production of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) from solar energy, oxygen and water is an environmentally friendly and sustainable approach. However, the efficiency is highly restricted by the limited light absorption, charge separation and oxygen capture of the active centers. In this study, a novel hydrophilic <em>o</em>-phenanthroline-based covalent organic polymer (COP) with a reversible iminol-to-ketoenamine tautomeric structure was successfully prepared through the Schiff base reaction. The highly conjugated structure significantly enhances its visible light absorption and accelerates the separation and migration of photogenerated charges. Furthermore, the <em>o</em>-phenanthroline linker facilitates the adsorption and activation of oxygen molecules, and the hydrophilicity is highly advantageous for the rapid photocatalytic reactions. Therefore, the as-prepared COP exhibits excellent photocatalytic H<sub>2</sub>O<sub>2</sub> production performance (814 μmol g<sup>−1</sup> h<sup>−1</sup>) without the addition of any cocatalysts or sacrificial agents. This work provides a new example for the design of photocatalysts based on covalent organic polymers towards H<sub>2</sub>O<sub>2</sub> production.</div></div>\",\"PeriodicalId\":66,\"journal\":{\"name\":\"Catalysis Science & Technology\",\"volume\":\"15 2\",\"pages\":\"Pages 448-456\"},\"PeriodicalIF\":4.4000,\"publicationDate\":\"2024-12-02\",\"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/S2044475324006488\",\"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/S2044475324006488","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
A hydrophilic o-phenanthroline-based covalent organic polymer with a reversible tautomeric structure for boosting photocatalytic hydrogen peroxide production†
Photocatalytic production of hydrogen peroxide (H2O2) from solar energy, oxygen and water is an environmentally friendly and sustainable approach. However, the efficiency is highly restricted by the limited light absorption, charge separation and oxygen capture of the active centers. In this study, a novel hydrophilic o-phenanthroline-based covalent organic polymer (COP) with a reversible iminol-to-ketoenamine tautomeric structure was successfully prepared through the Schiff base reaction. The highly conjugated structure significantly enhances its visible light absorption and accelerates the separation and migration of photogenerated charges. Furthermore, the o-phenanthroline linker facilitates the adsorption and activation of oxygen molecules, and the hydrophilicity is highly advantageous for the rapid photocatalytic reactions. Therefore, the as-prepared COP exhibits excellent photocatalytic H2O2 production performance (814 μmol g−1 h−1) without the addition of any cocatalysts or sacrificial agents. This work provides a new example for the design of photocatalysts based on covalent organic polymers towards H2O2 production.
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