电位滴定法
化学
离子载体
普鲁士蓝
电位传感器
膜
离子选择电极
电化学
无机化学
双功能
选择性
铵
离子
电极
有机化学
物理化学
生物化学
催化作用
作者
Longbin Xu,Lijie Zhong,Yitian Tang,Tingting Han,Siyi Liu,Zhonghui Sun,Yu Bao,Haoyu Wang,Ying He,Wei Wang,Shiyu Gan,Li Niu
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2022-07-15
卷期号:94 (29): 10487-10496
被引量:34
标识
DOI:10.1021/acs.analchem.2c01765
摘要
The determination of ammonium ions (NH4+) is of significance to environmental, agriculture, and human health. Potentiometric NH4+ sensors based on solid-contact ion selective electrodes (SC-ISEs) feature point-of-care testing and miniaturization. However, the state-of-the-art SC-ISEs of NH4+ during the past 20 years strongly rely on the organic ammonium ionophore-based ion selective membrane (ISM), typically by nonactin for the NH4+ recognition. Herein, we report a Prussian blue analogue of copper(II)-hexacyanoferrate (CuHCF) for an ISM-free potentiometric NH4+ sensor without using the ionophores. CuHCF works as a bifunctional transducer that could realize the ion-to-electron transduction and NH4+ recognition. CuHCF exhibits competitive analytical performances regarding traditional nonactin-based SC-ISEs of NH4+, particularly for the selectivity toward K+. The cost and preparation process have been remarkably reduced. The theoretical calculation combined with electrochemical tests further demonstrate that relatively easier intercalation of NH4+ into the lattices of CuHCF determines its selectivity. This work provides a concept of the ISM-free potentiometric NH4+ sensor beyond the nonactin ionophore through a CuHCF bifunctional transducer.
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