吸附
分析物
拉曼散射
苯
分子
硝基苯
表面改性
拉曼光谱
金属有机骨架
甲苯
微晶
材料科学
化学
金属
等离子体子
纳米技术
化学工程
光化学
无机化学
有机化学
物理化学
光电子学
结晶学
光学
催化作用
工程类
物理
作者
Lauren E. Kreno,Nathan G. Greeneltch,Omar K. Farha,Joseph T. Hupp,Richard P. Van Duyne
出处
期刊:Analyst
[Royal Society of Chemistry]
日期:2014-06-05
卷期号:139 (16): 4073-4073
被引量:131
摘要
The potential for discriminating between analytes by their unique vibrational signature makes surface-enhanced Raman scattering (SERS) extremely interesting for chemical detection. However, for molecules that weakly adsorb to non-functionalized plasmonic materials, detection by SERS remains a key challenge. Here we present an approach to SERS-based detection where a polycrystalline metal-organic framework (MOF) film is used to recruit a range of structurally similar volatile organic compounds for detection by SERS. MOF films were grown on the surface of Ag "films-over-nanospheres" (FONs), which have previously been shown to enhance Raman signals of surface adsorbates by a factor of 10(7). Upon exposing the MOF-coated FON to benzene, toluene, nitrobenzene, or 2,6-di-tert-butylpyridine, the MOF film traps the vapors at the FON surface, allowing the unique Raman spectrum of each vapor to be recorded. By contrast, these analytes do not adsorb to a bare FON surface and thus cannot be detected by conventional SERS substrates. Pyridine was also tested as a Ag-adsorbing control analyte. Concentration dependence and time resolved measurements provide evidence for the hypothesis that the vapors are reversibly adsorbed on the surfaces of MOF nanocrystals exposed at grain boundaries. This represents a generalized approach for confining aromatic molecules through interactions with the MOF surface, which can be applied for future SERS-based sensors.
科研通智能强力驱动
Strongly Powered by AbleSci AI