Sensor Research Unit, Department of Chemistry, Faculty of Science, Chulalongkorn University, Bangkok 10240, Thailand.
Anal Chem. 2011 May 15;83(10):3655-62. doi: 10.1021/ac200743j. Epub 2011 Apr 26.
In this report, we propose a novel technique for the determination of the concentrations of iodide and thiocyanate by surface-enhanced Raman scattering (SERS) of starch-reduced gold nanoparticles. Starch-reduced gold nanoparticles show an intrinsic Raman peak at 2125 cm(-1) due to the -C≡C- stretching mode of a synthesized byproduct. Because of the high adsorptivity of iodide on a gold surface, the intensity of the SERS peak at 2125 cm(-1) decreases with an increase in the iodide concentration. Thiocyanate also strongly adsorbs on a gold surface, and a new peak appears at around 2100 cm(-1), attributed to the -C≡N stretching vibration in a SERS spectrum of starch-reduced gold nanoparticles. These two peaks were successfully used to determine the iodide and thiocyanate concentrations separately, even in their mixture system. The detection limit of this technique for iodide is 0.01 μM with a measurement range of 0.01-2.0 μM, while the detection limit of this technique for thiocyanate is 0.05 μM with a measurement range of 0.05-50 μM. This technique is highly selective for iodide and thiocyanate ions without interference from other coexisting anions such as other halides, carbonate, and sulfate.
在本报告中,我们提出了一种通过淀粉还原金纳米粒子的表面增强拉曼散射(SERS)来测定碘化物和硫氰酸盐浓度的新方法。淀粉还原金纳米粒子由于合成副产物的 -C≡C- 伸缩模式在 2125cm-1 处表现出固有拉曼峰。由于碘化物在金表面的高吸附性,2125cm-1 处的 SERS 峰强度随碘化物浓度的增加而降低。硫氰酸盐也强烈地吸附在金表面上,在大约 2100cm-1 处出现新的峰,归因于 SERS 光谱中淀粉还原金纳米粒子的 -C≡N 伸缩振动。这两个峰可成功地用于分别测定碘化物和硫氰酸盐的浓度,即使在它们的混合体系中也是如此。该技术对碘化物的检测限为 0.01μM,测量范围为 0.01-2.0μM,而对硫氰酸盐的检测限为 0.05μM,测量范围为 0.05-50μM。该技术对碘化物和硫氰酸盐离子具有高度选择性,不受其他共存阴离子(如其他卤化物、碳酸盐和硫酸盐)的干扰。