Ag@Fe3O4 Core-Shell Surface-Enhanced Raman Scattering Probe for Trace Arsenate Detection

被引:10
作者
Sun, Hang [1 ]
Zeng, Shan [1 ]
Shang, Yinxing [1 ]
He, Qinrong [1 ]
机构
[1] Jilin Univ, Coll Biol & Agr Engn, Key Lab Bion Engn, Minist Educ, Changchun 130022, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
Core-Shell; Drinking Water; Heavy Metals; Fe3O4; Trace Detection; ONE-STEP SYNTHESIS; SERS; NANOPARTICLES; SPECTROSCOPY; NANOSTRUCTURES; REMOVAL; WATER; IDENTIFICATION; RESONANCE; BACTERIA;
D O I
10.1166/jnn.2018.13962
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Developing an effective and reliable method for trace arsenic (As) detection is a prerequisite for improving the safety of drinking water. In this paper, we designed and prepared Ag@Fe3O4 coreshell nanoparticles (NPs), which were then used as Surface-Enhanced Raman Scattering (SERS) probe for trace arsenate (As(V)) detection. The Ag@Fe3O4 core-shell NPs were prepared by in situ growth of Fe3O4 NPs on the surface of AgNPs, which can effectively combine the strong adsorption ability of Fe3O4 nanoshells to As(V) with high SERS activity of Ag nanocores to decrease the detection limit. By use of Ag@Fe3O4 core-shell NPs for As(V) detection, the detection limit can be as low as 10 mu g/L, and a good linear relationship between the SERS intensity of As(V) and their concentrations in the range from 10 to 500 mu g/L was achieved. Furthermore, Ag@Fe3O4 core-shell NPs could be regenerated through desorption of As(V) from Fe3O4 nanoshells in NaOH solution, and then used for recyclic SERS detection. Therefore, it has been demonstrated for the first time that multifunctional Ag@Fe3O4 core-shell SERS probe could be applied to realize the highly sensitive and reversible detection of As(V).
引用
收藏
页码:1097 / 1102
页数:6
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