{"title":"使用铀配位聚合物进行过氧化氢的持久光合作用:激子解离与氢汲取。","authors":"Mengnan Yuan, Lisha Jiang, Jinlu Li, Zhenyu Li, Jianxin Song, Xuemin Wang, Zuju Ma, Yanlong Wang, Wei Liu","doi":"10.1021/acs.inorgchem.4c03947","DOIUrl":null,"url":null,"abstract":"<p><p>The photosynthesis of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>), involving water oxidation and oxygen reduction, is crucial for optimizing light utilization. Here, a previously synthesized one-dimensional chain-like semiconductive uranyl coordination polymer (NDC-UCP) was used for the efficient overall photosynthetic reaction of H<sub>2</sub>O<sub>2</sub> and its photocatalytic mechanism was systematically investigated. The excellent stability of NDC-UCP enables continuous H<sub>2</sub>O<sub>2</sub> production for up to 96 h. Its unique hydrogen extraction capability enhances the photocatalytic performance, achieving a H<sub>2</sub>O<sub>2</sub> production rate of 283.80 μmol g<sup>-1</sup> h<sup>-1</sup>. Two mechanisms for H<sub>2</sub>O<sub>2</sub> generation were revealed: efficient electron-hole separation in NDC-UCP facilitates a two-step one-electron oxygen reduction and direct water oxidation, while hydrogen abstraction of UO<sub>2</sub><sup>2+</sup> generates hydroxyl (·OH) and hydroperoxyl radicals (HO<sub>2</sub><sup>·</sup>), enhancing H<sub>2</sub>O<sub>2</sub> photosynthesis. This study highlights the potential of uranyl coordination polymers in H<sub>2</sub>O<sub>2</sub> production and their synergistic exciton dissociation and hydrogen abstraction functionalities in photocatalytic redox reactions.</p>","PeriodicalId":40,"journal":{"name":"Inorganic Chemistry","volume":" ","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2024-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Durable Photosynthesis of Hydrogen Peroxide Using a Uranyl Coordination Polymer: Exciton Dissociation and Hydrogen Abstraction.\",\"authors\":\"Mengnan Yuan, Lisha Jiang, Jinlu Li, Zhenyu Li, Jianxin Song, Xuemin Wang, Zuju Ma, Yanlong Wang, Wei Liu\",\"doi\":\"10.1021/acs.inorgchem.4c03947\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The photosynthesis of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>), involving water oxidation and oxygen reduction, is crucial for optimizing light utilization. Here, a previously synthesized one-dimensional chain-like semiconductive uranyl coordination polymer (NDC-UCP) was used for the efficient overall photosynthetic reaction of H<sub>2</sub>O<sub>2</sub> and its photocatalytic mechanism was systematically investigated. The excellent stability of NDC-UCP enables continuous H<sub>2</sub>O<sub>2</sub> production for up to 96 h. Its unique hydrogen extraction capability enhances the photocatalytic performance, achieving a H<sub>2</sub>O<sub>2</sub> production rate of 283.80 μmol g<sup>-1</sup> h<sup>-1</sup>. Two mechanisms for H<sub>2</sub>O<sub>2</sub> generation were revealed: efficient electron-hole separation in NDC-UCP facilitates a two-step one-electron oxygen reduction and direct water oxidation, while hydrogen abstraction of UO<sub>2</sub><sup>2+</sup> generates hydroxyl (·OH) and hydroperoxyl radicals (HO<sub>2</sub><sup>·</sup>), enhancing H<sub>2</sub>O<sub>2</sub> photosynthesis. This study highlights the potential of uranyl coordination polymers in H<sub>2</sub>O<sub>2</sub> production and their synergistic exciton dissociation and hydrogen abstraction functionalities in photocatalytic redox reactions.</p>\",\"PeriodicalId\":40,\"journal\":{\"name\":\"Inorganic Chemistry\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2024-11-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Inorganic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.inorgchem.4c03947\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.inorgchem.4c03947","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Durable Photosynthesis of Hydrogen Peroxide Using a Uranyl Coordination Polymer: Exciton Dissociation and Hydrogen Abstraction.
The photosynthesis of hydrogen peroxide (H2O2), involving water oxidation and oxygen reduction, is crucial for optimizing light utilization. Here, a previously synthesized one-dimensional chain-like semiconductive uranyl coordination polymer (NDC-UCP) was used for the efficient overall photosynthetic reaction of H2O2 and its photocatalytic mechanism was systematically investigated. The excellent stability of NDC-UCP enables continuous H2O2 production for up to 96 h. Its unique hydrogen extraction capability enhances the photocatalytic performance, achieving a H2O2 production rate of 283.80 μmol g-1 h-1. Two mechanisms for H2O2 generation were revealed: efficient electron-hole separation in NDC-UCP facilitates a two-step one-electron oxygen reduction and direct water oxidation, while hydrogen abstraction of UO22+ generates hydroxyl (·OH) and hydroperoxyl radicals (HO2·), enhancing H2O2 photosynthesis. This study highlights the potential of uranyl coordination polymers in H2O2 production and their synergistic exciton dissociation and hydrogen abstraction functionalities in photocatalytic redox reactions.
期刊介绍:
Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.