Temperature-driven growth of uranyl-organic frameworks for efficient photocatalytic CO2 reduction†

IF 6.4 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR Inorganic Chemistry Frontiers Pub Date : 2025-02-28 DOI:10.1039/D5QI00141B
Lu-Yao Wang, Guang Che, Ya-Ru Gong, Wei-Ting Yang, Yuan Lin, Jiao-Rong Liu, Shu-Yu Chen, Meng-Dan Xiao, Xu-Dong Tian and Zhong-Min Su
{"title":"Temperature-driven growth of uranyl-organic frameworks for efficient photocatalytic CO2 reduction†","authors":"Lu-Yao Wang, Guang Che, Ya-Ru Gong, Wei-Ting Yang, Yuan Lin, Jiao-Rong Liu, Shu-Yu Chen, Meng-Dan Xiao, Xu-Dong Tian and Zhong-Min Su","doi":"10.1039/D5QI00141B","DOIUrl":null,"url":null,"abstract":"<p >The design of efficient photocatalysts to convert CO<small><sub>2</sub></small> into CO and other high-value-added chemicals is an effective strategy for solving environmental issues and the energy crisis. Herein, a uranyl-organic framework (UOF) photocatalyst, HNU-94, with uranyl ions as catalytically active centers was designed and prepared by a simple solvothermal method for photocatalytic CO<small><sub>2</sub></small> reduction. Particularly, the reaction temperature has an obvious influence on the morphology, which is further reflected in the photocatalytic performance of HNU-94. The morphology of HNU-94 evolves from strip to cluster to flower-like when the temperature rises from 80 °C to 120 °C. The sample obtained at 120 °C can reduce CO<small><sub>2</sub></small> to CO under visible light, and the yield reaches 2.57 mmol g<small><sup>−1</sup></small> after 2 h, which is significantly higher than that of HNU-94 obtained at 80 °C (0.53 mmol g<small><sup>−1</sup></small>). The study demonstrates the efficient photocatalytic activity of uranyl ions for reducing CO<small><sub>2</sub></small> and provides an effective method for the logical design of UOF catalysts.</p>","PeriodicalId":79,"journal":{"name":"Inorganic Chemistry Frontiers","volume":" 8","pages":" 3262-3269"},"PeriodicalIF":6.4000,"publicationDate":"2025-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/qi/d5qi00141b","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0

Abstract

The design of efficient photocatalysts to convert CO2 into CO and other high-value-added chemicals is an effective strategy for solving environmental issues and the energy crisis. Herein, a uranyl-organic framework (UOF) photocatalyst, HNU-94, with uranyl ions as catalytically active centers was designed and prepared by a simple solvothermal method for photocatalytic CO2 reduction. Particularly, the reaction temperature has an obvious influence on the morphology, which is further reflected in the photocatalytic performance of HNU-94. The morphology of HNU-94 evolves from strip to cluster to flower-like when the temperature rises from 80 °C to 120 °C. The sample obtained at 120 °C can reduce CO2 to CO under visible light, and the yield reaches 2.57 mmol g−1 after 2 h, which is significantly higher than that of HNU-94 obtained at 80 °C (0.53 mmol g−1). The study demonstrates the efficient photocatalytic activity of uranyl ions for reducing CO2 and provides an effective method for the logical design of UOF catalysts.

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
用于高效光催化二氧化碳还原的铀酰有机框架的温度驱动生长
设计将CO2转化为CO和其他高附加值化学品的高效光催化剂是解决环境问题和能源危机的有效策略。本文设计并制备了以铀酰离子为催化活性中心的铀酰-有机骨架(UOF)光催化剂HNU-94,采用简单的溶剂热法进行光催化CO2还原。特别是反应温度对形貌有明显的影响,这进一步体现在HNU-94的光催化性能上。当温度从80℃升高到120℃时,HNU-94的形态由条状到簇状再到花状。120℃下得到的样品可以在可见光下将CO2还原为CO, 2 h后的产率达到2.57 mmol g-1,显著高于80℃下得到的HNU-94 (0.53 mmol g-1)。该研究证明了铀酰离子对还原CO2的高效光催化活性,为UOF催化剂的逻辑设计提供了有效的方法。
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
Inorganic Chemistry Frontiers
Inorganic Chemistry Frontiers CHEMISTRY, INORGANIC & NUCLEAR-
CiteScore
10.40
自引率
7.10%
发文量
587
审稿时长
1.2 months
期刊介绍: The international, high quality journal for interdisciplinary research between inorganic chemistry and related subjects
期刊最新文献
An in situ reconstructed CuOx–BTA heterointerface enables stable and selective nitrate electroreduction to ammonia Tuning Guest Cations to Liberate Pore Space for Efficient C4 Hydrocarbon Separation Research Progress on Self-Discharge Mechanisms and Mitigation Strategies of Aqueous Zinc-Ion Batteries Local symmetry engineering and Judd–Ofelt decoupling in SrLaInO4:Eu3+ for high-purity red emission toward advanced solid-state lighting Ba 2+ Co-doping Enhances Phase Purity and Enables Narrow-Band Green Emission in Sr 5/6 Li 17/6 Al 7/6 O 4 :Eu 2+ Phosphor for Backlight Display Applications
×
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:604180095
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