{"title":"利用光催化能力高效分离氢同位素","authors":"Linzhen Wu, Sifan Zeng, Weiwei Wang, Shengtai Zhang, Hongbo Li, Xiaosong Zhou","doi":"10.1039/d4ta07355j","DOIUrl":null,"url":null,"abstract":"Developing efficient and low-energy hydrogen isotope separation technology is one of the key requirements for fuel cycle and deuterium tritium wastewater treatment in the current development of nuclear fusion. Due to the almost identical physical and chemical properties of hydrogen isotopes, the rapid production of H<small><sub>2</sub></small> is an important challenge for selective photocatalytic hydrogen isotope separation. We report an effective strategy for hydrogen isotope separation based on N–O–C<small><sub>3</sub></small>N<small><sub>4</sub></small> photocatalysis. By simultaneously doping nitrogen and oxygen, the microstructure and band structure of the g-C<small><sub>3</sub></small>N<small><sub>4</sub></small> catalyst were significantly optimized, resulting in improved catalytic activity. The inherent differences in flow states between H<small><sub>2</sub></small>O and D<small><sub>2</sub></small>O, as well as the differences in binding energy between H–O and D–O, provide opportunities for the separation of hydrogen isotopes. The hydrogen production rate of the N–O–C<small><sub>3</sub></small>N<small><sub>4</sub></small> catalyst under visible light conditions is 7.439 mmol g<small><sup>−1</sup></small> h<small><sup>−1</sup></small> and the H/D separation factor is about 6.44. The photocatalytic strategy has mild and environmentally friendly reaction conditions, and this research work provides a reference for the development of efficient and advanced isotope separation systems.","PeriodicalId":82,"journal":{"name":"Journal of Materials Chemistry A","volume":"10 1","pages":""},"PeriodicalIF":10.7000,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Efficient hydrogen isotope separation utilizing photocatalytic capability\",\"authors\":\"Linzhen Wu, Sifan Zeng, Weiwei Wang, Shengtai Zhang, Hongbo Li, Xiaosong Zhou\",\"doi\":\"10.1039/d4ta07355j\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Developing efficient and low-energy hydrogen isotope separation technology is one of the key requirements for fuel cycle and deuterium tritium wastewater treatment in the current development of nuclear fusion. Due to the almost identical physical and chemical properties of hydrogen isotopes, the rapid production of H<small><sub>2</sub></small> is an important challenge for selective photocatalytic hydrogen isotope separation. We report an effective strategy for hydrogen isotope separation based on N–O–C<small><sub>3</sub></small>N<small><sub>4</sub></small> photocatalysis. By simultaneously doping nitrogen and oxygen, the microstructure and band structure of the g-C<small><sub>3</sub></small>N<small><sub>4</sub></small> catalyst were significantly optimized, resulting in improved catalytic activity. The inherent differences in flow states between H<small><sub>2</sub></small>O and D<small><sub>2</sub></small>O, as well as the differences in binding energy between H–O and D–O, provide opportunities for the separation of hydrogen isotopes. The hydrogen production rate of the N–O–C<small><sub>3</sub></small>N<small><sub>4</sub></small> catalyst under visible light conditions is 7.439 mmol g<small><sup>−1</sup></small> h<small><sup>−1</sup></small> and the H/D separation factor is about 6.44. The photocatalytic strategy has mild and environmentally friendly reaction conditions, and this research work provides a reference for the development of efficient and advanced isotope separation systems.\",\"PeriodicalId\":82,\"journal\":{\"name\":\"Journal of Materials Chemistry A\",\"volume\":\"10 1\",\"pages\":\"\"},\"PeriodicalIF\":10.7000,\"publicationDate\":\"2024-11-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Materials Chemistry A\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1039/d4ta07355j\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Materials Chemistry A","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1039/d4ta07355j","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Developing efficient and low-energy hydrogen isotope separation technology is one of the key requirements for fuel cycle and deuterium tritium wastewater treatment in the current development of nuclear fusion. Due to the almost identical physical and chemical properties of hydrogen isotopes, the rapid production of H2 is an important challenge for selective photocatalytic hydrogen isotope separation. We report an effective strategy for hydrogen isotope separation based on N–O–C3N4 photocatalysis. By simultaneously doping nitrogen and oxygen, the microstructure and band structure of the g-C3N4 catalyst were significantly optimized, resulting in improved catalytic activity. The inherent differences in flow states between H2O and D2O, as well as the differences in binding energy between H–O and D–O, provide opportunities for the separation of hydrogen isotopes. The hydrogen production rate of the N–O–C3N4 catalyst under visible light conditions is 7.439 mmol g−1 h−1 and the H/D separation factor is about 6.44. The photocatalytic strategy has mild and environmentally friendly reaction conditions, and this research work provides a reference for the development of efficient and advanced isotope separation systems.
期刊介绍:
The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.