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一步快速合成用于抗坏血酸电化学传感的Ni(CHS)纳米簇

One-step rapid synthesis of Ni(CHS) nanoclusters for electrochemical sensing of ascorbic acid.

作者信息

Zhuang Zhihua, Chen Wei

机构信息

State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, Jilin, China.

出版信息

Analyst. 2020 Apr 7;145(7):2621-2630. doi: 10.1039/c9an01947b. Epub 2020 Jan 29.

DOI:10.1039/c9an01947b
PMID:31993586
Abstract

Metal nanoclusters (NCs) are highly desirable as active catalysts due to their highly active surface atoms. Among the reported metal clusters, nickel nanoclusters (Ni NCs) have been less well developed than others, such as gold, silver and copper. Herein a simple method is developed to synthesize atomically precise Ni clusters with the molecular formular of Ni(CHS). Moreover, the single crystal of the Ni(CHS) cluster is also obtained. The composition, morphology and optical properties of the prepared Ni clusters are characterized by X-ray crystallography, XPS, XRD, SEM, HRTEM, FTIR and UV-Vis spectroscopy. The Ni cluster is composed of six nickel atoms that form a hexagonal ring with an exterior 1-dodecanethiol shell, resembling a double crown. Meanwhile, the Ni NCs can be self-assembled into nanosheets due to their uniform size. It was found that the Ni(CHS) clusters loaded on carbon black exhibit higher electrocatalytic activity than Ni nanoparticles towards ascorbic acid (AA) oxidation. The Ni clusters show high sensing performance for AA with a wide linear range (1-3212 μM) and a low detection limit of 0.1 μM (S/N = 3). The significantly enhanced catalytic activity can be ascribed to the high fraction of surface Ni atoms with low coordination in the sub-nanometer clusters. The present work not only provides a straightforward method for synthesizing atomically precise metal clusters but also indicates that ultrasmall Ni clusters can be used as highly efficient catalysts for the electrochemical detection of AA.

摘要

金属纳米团簇(NCs)因其具有高活性的表面原子而作为活性催化剂备受青睐。在已报道的金属团簇中,镍纳米团簇(Ni NCs)的发展不如金、银和铜等其他金属团簇。在此,开发了一种简单的方法来合成分子式为Ni(CHS)的原子精确的镍团簇。此外,还获得了Ni(CHS)团簇的单晶。通过X射线晶体学、XPS、XRD、SEM、HRTEM、FTIR和UV-Vis光谱对制备的镍团簇的组成、形态和光学性质进行了表征。该镍团簇由六个镍原子组成,形成一个带有外部1-十二烷硫醇壳的六边形环,类似双冠。同时,由于其尺寸均匀,Ni NCs可以自组装成纳米片。研究发现,负载在炭黑上的Ni(CHS)团簇在抗坏血酸(AA)氧化方面比镍纳米颗粒表现出更高的电催化活性。镍团簇对AA具有高传感性能,线性范围宽(1-3212 μM),检测限低至0.1 μM(S/N = 3)。催化活性的显著增强可归因于亚纳米团簇中低配位表面镍原子的高比例。本工作不仅提供了一种合成原子精确金属团簇的直接方法,还表明超小镍团簇可作为用于AA电化学检测的高效催化剂。

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