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基于巯基苯并噻唑 II 修饰的金纳米粒子的比色和表面增强拉曼散射双信号传感器用于 Hg2+检测。

A colorimetric and surface-enhanced Raman scattering dual-signal sensor for Hg2+ based on Bismuthiol II-capped gold nanoparticles.

机构信息

Key Laboratory of Colloid and Interface Chemistry, Ministry of Education, Department of Chemistry, Shandong University, Jinan 250100, China.

出版信息

Anal Chim Acta. 2012 Apr 20;723:88-93. doi: 10.1016/j.aca.2012.02.031. Epub 2012 Feb 24.

Abstract

The addition of Bismuthiol II to the gold nanoparticles (AuNPs) solution led to the aggregation of AuNPs with a color change from red to blue. As a result, hot spots were formed and strong surface-enhanced Raman scattering (SERS) signal of Bismuthiol II was observed. However, the Bismuthiol II-induced aggregation of AuNPs could be reversed by Hg(2+) in the system, accompanied by a remarkable color change from blue to red. As evidenced by UV-vis and SERS spectroscopy, the variation in absorption band and SERS intensity was strongly dependent on the concentration of Hg(2+), suggesting a colorimetric and SERS dual-signal sensor for Hg(2+). The sensor had a high sensitivity, low detection limits of 2nM and 30nM could be achieved by UV-vis spectroscopy and by SERS spectroscopy, respectively. Other environmentally relevant metal ions did not interfere with the detection of Hg(2+). The method was successfully applied to detect Hg(2+) in water samples. It was simple, rapid and cost-effective without any modifying or labeling procedure.

摘要

将双硫腙添加到金纳米粒子 (AuNPs) 溶液中导致 AuNPs 聚集,颜色从红色变为蓝色。结果形成了热点,并且观察到双硫腙的强表面增强拉曼散射 (SERS) 信号。然而,系统中的 Hg(2+) 可以使 AuNPs 的双硫腙诱导聚集逆转,同时伴随着颜色从蓝色变为红色的明显变化。紫外可见光谱和 SERS 光谱证明,吸收带和 SERS 强度的变化强烈依赖于 Hg(2+) 的浓度,这表明该传感器是一种用于检测 Hg(2+) 的比色和 SERS 双信号传感器。该传感器具有高灵敏度,通过紫外可见光谱和 SERS 光谱分别可以达到 2nM 和 30nM 的低检测限。其他环境相关的金属离子不会干扰 Hg(2+) 的检测。该方法成功应用于水样中 Hg(2+) 的检测。该方法简单、快速且具有成本效益,无需任何修饰或标记过程。

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