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基于Tb功能化金属有机框架通过竞争性主客体配位对铀酰离子进行高灵敏度和高选择性检测

Highly Sensitive and Selective Detection of Uranyl Ions Based on a Tb-Functionalized MOF via Competitive Host-Guest Coordination.

作者信息

Xie Jian, Liang Jinpeng, Lei Ji, Xiao Yiheng, Luo Feng, Hu Baowei

机构信息

School of Life and Environmental Sciences, Shaoxing University, Shaoxing 312000, China.

School of Biology, Chemistry and Material Science, East China University of Technology, Nanchang, Jiangxi 344000, China.

出版信息

Inorg Chem. 2025 Feb 24;64(7):3616-3625. doi: 10.1021/acs.inorgchem.4c05586. Epub 2025 Feb 11.

Abstract

Owing to the rapid development of the nuclear industry, uranium has become a global environmental contaminant due to its radiotoxicity and chemotoxicity, posing significant threats to human health and ecological safety. Although various instrumental and chemical analytical methods have been developed for uranyl ion detection in aquatic environments, searching for new sensors with high stability, sensitivity, and selectivity remains a challenge. In this study, a luminescent Zr-based metal-organic framework (MOF), designated as Tb@UiO-66-(COOH), was successfully synthesized utilizing a postsynthetic exchange (PSE) method along with Tb ion doping for uranyl ion detection. Interestingly, the presence of UO ions causes a replacement of guest ions (Tb) in the sensor via a competitive host-guest interaction, leading to significant luminescence quenching. The attenuation of the luminescence intensity of Tb@UiO-66-(COOH) exhibits an excellent linear relationship with UO ion concentrations within a wide range of 0-2.52 μM. Notably, Tb@UiO-66-(COOH) demonstrates an unprecedentedly high detection sensitivity ( = 2.16 × 10 M) and an extremely low limit of detection (LOD) down to 8.03 nM (1.91 ppb) in deionized water. More importantly, Tb@UiO-66-(COOH) can achieve high selectivity and efficient detection performance, even in the presence of significant excesses of competing ions. The values of were determined to be 2.10 × 10 M in Xie'ao Lake water and 3.05 × 10 M in seawater; the values of LOD were determined to be 8.26 nM (1.96 ppb) in Xie'ao Lake water and 5.68 nM (1.35 ppb) in seawater. To the best of our knowledge, this is the first instance of introducing a competitive host-guest coordination strategy into a MOF-based chemical sensor to achieve high-performance uranyl ion detection. Hence, the present work offers a novel idea for building functional MOFs for uranyl ion detection in aqueous solutions.

摘要

由于核工业的快速发展,铀因其放射性毒性和化学毒性已成为一种全球环境污染物,对人类健康和生态安全构成重大威胁。尽管已经开发了各种仪器分析和化学分析方法用于检测水环境中的铀酰离子,但寻找具有高稳定性、灵敏度和选择性的新型传感器仍然是一项挑战。在本研究中,利用后合成交换(PSE)方法并掺杂Tb离子成功合成了一种发光的锆基金属有机框架(MOF),命名为Tb@UiO-66-(COOH),用于铀酰离子检测。有趣的是,UO离子的存在通过竞争性主客体相互作用导致传感器中的客体离子(Tb)被取代,从而导致显著的发光猝灭。在0 - 2.52 μM的宽范围内,Tb@UiO-66-(COOH)的发光强度衰减与UO离子浓度呈现出良好的线性关系。值得注意的是,Tb@UiO-66-(COOH)在去离子水中表现出前所未有的高检测灵敏度( = 2.16 × 10 M)和极低的检测限(LOD),低至8.03 nM(1.91 ppb)。更重要的是,即使在存在大量过量竞争离子的情况下,Tb@UiO-66-(COOH)也能实现高选择性和高效的检测性能。在谢岙湖水中测定的值为2.10 × 10 M,在海水中为3.05 × 10 M;在谢岙湖水中测定的LOD值为8.26 nM(1.96 ppb),在海水中为5.68 nM(1.35 ppb)。据我们所知,这是首次将竞争性主客体配位策略引入基于MOF的化学传感器以实现高性能铀酰离子检测。因此,本工作为构建用于水溶液中铀酰离子检测的功能性MOF提供了新思路。

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