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Surface Modification On Silver Nanoparticles For Enhancing Vapor Selectivity Of Localized Surface Plasmon Resonance Sensors

机译:银纳米粒子的表面改性,以提高局部表面等离子体共振传感器的蒸汽选择性。

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This study focuses on localized surface plasmon resonance (LSPR) sensors employing silver nanoparticles that were surface functionalized with various thiolate self-assembled monolayers (SAM) to provide chemical selectivity for detection of volatile organic compounds (VOCs). Changes in the LSPR spectrum of silver nanoparticles were measured as the response signal. One unmodified and three surface-modified nanoparticle LSPR sensors generated distinguishable patterns for tested organic vapors with different functional groups. The sensor responses were rapid and reversible for all tested vapors. The detection limits of the LSPR sensor were as low as 18-30 ppm for heptanone, depending on the surface modification of Ag nanoparticles. SAM modification not only altered chemical affinity of the surface, but also moderately improved the detection limit without lengthening the response time. Surface modification using thiolates with refractive indices higher than condensed VOC neither reduced nor reversed the sensor response. Mechanisms for this phenomenon are also discussed.
机译:这项研究的重点是采用银纳米颗粒的局部表面等离子体激元共振(LSPR)传感器,这些纳米颗粒已通过各种硫醇盐自组装单分子层(SAM)进行了表面功能化,从而为检测挥发性有机化合物(VOC)提供了化学选择性。测量银纳米粒子的LSPR光谱变化作为响应信号。一种未经修饰的和三种经表面修饰的纳米LSPR传感器为具有不同官能团的受试有机蒸气生成了可区分的图案。对于所有测试的蒸汽,传感器响应迅速且可逆。 LSPR传感器对庚酮的检测限低至18-30 ppm,这取决于Ag纳米颗粒的表面改性。 SAM改性不仅改变了表面的化学亲和力,而且在不延长响应时间的情况下适度提高了检测限。使用折射率高于缩合VOC的硫醇盐进行表面修饰既不会降低也不会逆转传感器响应。还讨论了这种现象的机制。

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