Efficient hydrogen isotope separation utilizing photocatalytic capability

IF 10.7 2区 材料科学 Q1 CHEMISTRY, PHYSICAL Journal of Materials Chemistry A Pub Date : 2024-11-12 DOI:10.1039/d4ta07355j
Linzhen Wu, Sifan Zeng, Weiwei Wang, Shengtai Zhang, Hongbo Li, Xiaosong Zhou
{"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}
引用次数: 0

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 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.

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
利用光催化能力高效分离氢同位素
开发高效、低能的氢同位素分离技术是当前核聚变发展对燃料循环和氘氚废水处理的关键要求之一。由于氢同位素的物理和化学性质几乎完全相同,因此快速产生 H2 是选择性光催化氢同位素分离的重要挑战。我们报告了一种基于 N-O-C3N4 光催化的有效氢同位素分离策略。通过同时掺杂氮和氧,g-C3N4 催化剂的微观结构和能带结构得到显著优化,从而提高了催化活性。H2O 和 D2O 之间固有的流态差异以及 H-O 和 D-O 之间结合能的差异为氢同位素的分离提供了机会。在可见光条件下,N-O-C3N4 催化剂的产氢速率为 7.439 mmol g-1 h-1,氢/二氧分离因子约为 6.44。光催化策略的反应条件温和,对环境友好,这项研究工作为开发高效先进的同位素分离系统提供了参考。
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
Journal of Materials Chemistry A
Journal of Materials Chemistry A CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
19.50
自引率
5.00%
发文量
1892
审稿时长
1.5 months
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.
期刊最新文献
Manipulating defects simultaneously boosts the crystal stability and the electrochemical reversibility toward long-life aqueous zinc ion batteries Light-induced degradation of methylammonium tin iodide absorber layers High-voltage Symmetric Supercapacitors Developed by Engineering DyFeO3 Electrodes and Aqueous Electrolytes Advancing High Capacity 3D VO2(B) Cathodes for Improved Zinc-ion Battery Performance High-temperature oxidation behavior of transition metal complex concentrated alloys (TM-CCAs): a comprehensive review
×
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