Anionic uranyl oxyfluorides as a bifunctional platform for highly selective ion-exchange and photocatalytic degradation of organic dyes
文献类型:期刊论文
作者 | Yue, ZH; Lin, J; Silver, MA; Han, L; Li, XY; Zhou, J; Guo, XJ; Bao, HL; Huang, YY; Wang, JQ |
刊名 | DALTON TRANSACTIONS
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出版日期 | 2018 |
卷号 | 47期号:42页码:- |
关键词 | VARIABLE DIMENSIONALITY CATIONIC DYES CRYSTAL TRANSFORMATION HYDROTHERMAL SYNTHESIS LAYERED MATERIAL HIGH-CAPACITY URANIUM FRAMEWORK TOPOLOGY SYSTEM |
ISSN号 | 1477-9226 |
DOI | 10.1039/c8dt02309c |
文献子类 | 期刊论文 |
英文摘要 | Uranium is unique owing not only to its intriguing physiochemical properties, but also to the diverse coordination chemistry that uranyl adopts and bonding that enables rich and unpredictable topologies of uranium-bearing materials. Six anionic uranium oxyfluorides with various dimensionalities, including a 3D framework (MeUF), four 2D lamellar structures (EtUF-1, PrUF, BuUF-1, and BuUF-2), and a 1D chained topology (EtUF-2), have been rationally constructed by employing tetra-alkyl ammonium ions as structure-directing agents. By combining the tunable interlayer distance of the lamellar structures with the photooxygenation properties of uranyl ions, a bifunctional platform for highly selective ion-exchange and photocatalytic degradation over organic dyes has been developed. Specifically, BuUF-2 can efficiently capture 94.5% methylene blue (MB+) within 24 h from solution with remarkable selectivity related to both the size and the charge of organic dyes. Such size- and charge-dependent selectivity toward organic dyes has been documented for MOFs, but is rare for 2D lamellar materials. Furthermore, the removal of MB+ can be largely accelerated under UV radiation (e.g. 84.7% for BuUF-2 within 1 h) due to the photocatalytic activities of EtUF-1, EtUF-2, PrUF, and BuUF-2. |
语种 | 英语 |
源URL | [http://ir.sinap.ac.cn/handle/331007/30844] ![]() |
专题 | 上海应用物理研究所_中科院上海应用物理研究所2011-2017年 |
作者单位 | 1.Univ Chinese Acad Sci, 19 A Yuquan Rd, Beijing 100049, Peoples R China 2.Soochow Univ, Sch Radiol & Interdisciplinary Sci RAD X, 199 Renai Rd, Suzhou 215123, Peoples R China 3.Soochow Univ, Collaborat Innovat Ctr Radiat Med Jiangsu Higher, 199 Renai Rd, Suzhou 215123, Peoples R China 4.Chinese Acad Sci, Shanghai Inst Appl Phys, 2019 Jia Luo Rd, Shanghai 201800, Peoples R China 5.Chinese Acad Sci, Shanghai Synchrotron Radiat Facil, Shanghai Inst Appl Phys, 239 Zhangheng Rd, Shanghai 201204, Peoples R China |
推荐引用方式 GB/T 7714 | Yue, ZH,Lin, J,Silver, MA,et al. Anionic uranyl oxyfluorides as a bifunctional platform for highly selective ion-exchange and photocatalytic degradation of organic dyes[J]. DALTON TRANSACTIONS,2018,47(42):-. |
APA | Yue, ZH.,Lin, J.,Silver, MA.,Han, L.,Li, XY.,...&Wang, JQ.(2018).Anionic uranyl oxyfluorides as a bifunctional platform for highly selective ion-exchange and photocatalytic degradation of organic dyes.DALTON TRANSACTIONS,47(42),-. |
MLA | Yue, ZH,et al."Anionic uranyl oxyfluorides as a bifunctional platform for highly selective ion-exchange and photocatalytic degradation of organic dyes".DALTON TRANSACTIONS 47.42(2018):-. |
入库方式: OAI收割
来源:上海应用物理研究所
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