Department of Chemistry, Seoul National University, Seoul 151-742, Korea.
Analyst. 2012 Apr 21;137(8):1930-6. doi: 10.1039/c2an16044g. Epub 2012 Mar 7.
Organic isocyanide adsorbed on a noble metal nanostructure can be used as a platform for a volatile organic compound (VOC) sensor operating via surface-enhanced Raman scattering (SERS). This is possible since the NC stretching band of organic isocyanides such as 2,6-dimethylphenylisocyanide (2,6-DMPI) is very susceptible to the surface potential of Au onto which 2,6-DMPI is assembled. The surface potential of Au nanoparticles is even subject to change by VOCs, which can be easily monitored by the SERS of 2,6-DMPI. Thereby, under the flow of CCl(4) vapor at a partial pressure of 12.8 kPa, for instance, the NC stretching band is blue-shifted by up to 20 cm(-1) within 30 s, corresponding to a potential change of +0.56 V. Conversely, under the flow of butylamine at 12.8 kPa, the NC stretching band is red-shifted, instead of being blue-shifted, by as much as 12 cm(-1). At lower partial pressures, even a blue- or red-shift of 1 cm(-1) was reproducibly measured at a partial pressure of 125 mPa, corresponding to 6.5 ppm for CCl(4), suggesting that the present detection limit is superior to the results obtained via other techniques, especially those operating based on gold nanoparticles and aggregates.
有机异氰酸酯吸附在贵金属纳米结构上可用作通过表面增强拉曼散射 (SERS) 操作的挥发性有机化合物 (VOC) 传感器的平台。这是因为有机异氰化物(如 2,6-二甲基苯异氰酸酯(2,6-DMPI))的 NC 伸缩带对其组装在其上的 Au 的表面电势非常敏感。甚至 Au 纳米颗粒的表面电势也会受到 VOC 的变化的影响,而这可以通过 2,6-DMPI 的 SERS 很容易地监测到。因此,例如,在 12.8 kPa 的分压下,在 CCl(4)蒸气的流动下,NC 伸缩带在 30 秒内蓝移高达 20 cm(-1),对应于+0.56 V 的电势变化。相反,在 12.8 kPa 的正丁胺流动下,NC 伸缩带红移,而不是蓝移,多达 12 cm(-1)。在较低的分压下,即使在 125 mPa 的分压下,也可重复测量到 1 cm(-1)的蓝移或红移,对应于 CCl(4)的 6.5 ppm,表明本检测限优于通过其他技术获得的结果,特别是基于金纳米颗粒和聚集体操作的那些技术。