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基于多金属氧酸盐的结晶材料作为一种高灵敏度电化学传感器用于痕量 Cr(vi)的检测。

Polyoxometalate-based crystalline materials as a highly sensitive electrochemical sensor for detecting trace Cr(vi).

机构信息

Hebei Key Laboratory of Organic Functional Molecules, National Demonstration Center for Experimental Chemistry Education, College of Chemistry and Material Science, Hebei Normal University, Shijiazhuang, Hebei 050024, People's Republic of China.

出版信息

Dalton Trans. 2020 Apr 7;49(14):4570-4577. doi: 10.1039/d0dt00446d.

Abstract

It is crucial to find a convenient and sensitive method for quantitative determination of heavy metal chromium(vi) ions. Developing crystalline materials coupled with polyoxometalates as an electrochemical sensor is a promising approach to address the above issues. Here we reported two reductive polyoxometalate-based crystalline compounds with the formula of (H2bpp)2[Na4Fe(H2O)7][Fe(P4Mo6O31H6)2]·2H2O (1) and (H2bpp)6(bpp)2[Fe(P4Mo6O31H8)2]2·13H2O (2) (bpp = 1,3-bi(4-pyridyl)propane). Structural analysis indicated that both two compounds were composed of inorganic polyanionic clusters and organic protonated bpp cations. The difference lies in the arrangement mode of the inorganic moiety: crystal 1 shows a unique three-dimensional (3-D) inorganic porous skeleton, while crystal 2 consists of isolated 0-D polyanionic clusters. When used as electrochemical sensors in the determination of trace Cr(vi), crystal 1 shows a broad linearity range (2-2610 μM) with a low limit of detection (LOD) of 0.174 μM (9 ppb), which is superior to that of compound 2 (a LOD of 0.33 μM) and meets the standard of Cr(vi) in drinking water set by the WHO (less than 0.962 μM or 50 ppb). Importantly, crystal 1 showed benign selectivity to Cr(vi) in the presence of various heavy metal ions and good reproducibility in a real water sample, which prove its strong anti-interference ability. In addition, experimental results showed that the spatial arrangement of polyanionic clusters could affect the final electrochemical behavior of crystalline materials. This work provides some insights into the design of cost-effective POM-based electrochemical sensors at the molecular level.

摘要

找到一种方便且灵敏的方法来定量测定重金属六价铬离子至关重要。开发与多金属氧酸盐结合的结晶材料作为电化学传感器是解决上述问题的一种很有前途的方法。在这里,我们报道了两种基于还原多金属氧酸盐的结晶化合物,其化学式为(H2bpp)2[Na4Fe(H2O)7][Fe(P4Mo6O31H6)2]·2H2O(1)和(H2bpp)6(bpp)2[Fe(P4Mo6O31H8)2]2·13H2O(2)(bpp = 1,3-双(4-吡啶基)丙烷)。结构分析表明,这两种化合物都由无机多阴离子簇和有机质子化的 bpp 阳离子组成。不同之处在于无机部分的排列方式:晶体 1 显示出独特的三维(3-D)无机多孔骨架,而晶体 2 由孤立的 0-D 多阴离子簇组成。当用作痕量 Cr(vi)测定的电化学传感器时,晶体 1 显示出较宽的线性范围(2-2610 μM),检测限(LOD)低至 0.174 μM(9 ppb),优于化合物 2(LOD 为 0.33 μM),符合世界卫生组织(WHO)规定的饮用水中 Cr(vi)标准(小于 0.962 μM 或 50 ppb)。重要的是,在存在各种重金属离子的情况下,晶体 1 对 Cr(vi)表现出良好的选择性,并且在实际水样中具有良好的重现性,这证明了其强大的抗干扰能力。此外,实验结果表明,多阴离子簇的空间排列会影响结晶材料的最终电化学行为。这项工作为在分子水平上设计具有成本效益的基于 POM 的电化学传感器提供了一些见解。

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