Institute of Intelligent Machines, Hefei Institutes of Physical Science, Chinese Academy of Sciences , Hefei 230031, China.
Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Sciences , Chongqing 400714, China.
Anal Chem. 2016 Aug 16;88(16):8145-51. doi: 10.1021/acs.analchem.6b01884. Epub 2016 Jul 25.
The design and application of liquid interfacial plasmonic platform is still in its infancy but is an exciting topic in tunable optical devices, sensors, and catalysis. Here, we developed an interfacial surface-enhanced Raman scattering (SERS) platform through the large-scale self-assembly of gold nanoparticle (GNP) arrays at the cyclohexane (CYH)/water interface for detecting trace drug molecules in the urine of humans. The molecules extracted by the CYH phase from a urine sample were directly localized into the self-organized plasmonic hotspots, yielded excellent Raman enhancement, and realized the substrate-free interfacial SERS detection. Synchrotron radiation small-angle X-ray scattering (SR-SAXS) experiments reveals a good uniformity of approximately 2-3 nm interparticle distance in the GNP arrays. SERS colocalization experiments demonstrated that amphetamine molecules of different concentration levels could be loaded into the interfacial GNP arrays and realized the coassembly together with nanoparticles at the liquid/liquid interface. Interfacial GNP arrays with dynamic nanogaps in liquid interfacial structure can make surrounding molecules easily diffuse into the nanogaps. In contrast, the fixed GNP arrays on Si wafer were more irregular, such as multilayer stack, random aggregates, and voids, during the drying process. When the drugs directly participate in the self-assembly process, it becomes easier for analytes diffusing into the nanogaps of GNP arrays, produces a concentration effect, and amplified the SERS sensitivity. This feature also enables molecules to be adsorbed evenly in the arrays and makes a more uniform distribution of both the analytes and GNPs in the liquid interface and realizes the significant increase in signal reproducibility. Interfacial SERS produced a standard deviation of 12.5% at 1001 cm(-1) peak of methamphetamine (MAMP) molecules under the concentration of 1 ppm, implying a good reproducibility. Moreover, dual-analyte detection at organic and aqueous phases was also realized and confirmed a good capability for analytes detection by liquid interfacial SERS platform, which promises nonengineering detection of analytes dissolved in often-inaccessible environments.
液体界面等离子体平台的设计和应用仍处于起步阶段,但它是可调谐光学器件、传感器和催化领域中一个令人兴奋的课题。在这里,我们通过在环己烷(CYH)/水界面上大规模自组装金纳米颗粒(GNP)阵列,开发了一种界面表面增强拉曼散射(SERS)平台,用于检测人体尿液中的痕量药物分子。通过 CYH 相从尿液样本中提取的分子被直接定位到自组织等离子体热点中,产生了极好的拉曼增强,并实现了无基底的界面 SERS 检测。同步辐射小角 X 射线散射(SR-SAXS)实验表明,GNP 阵列中的颗粒间距离约为 2-3nm,具有良好的均匀性。SERS 共定位实验表明,不同浓度水平的安非他命分子可以负载到界面 GNP 阵列中,并与液体/液体界面上的纳米粒子一起实现共组装。液体界面结构中具有动态纳米间隙的界面 GNP 阵列可以使周围的分子容易扩散到纳米间隙中。相比之下,在干燥过程中,硅片上的固定 GNP 阵列更不规则,例如多层堆叠、随机聚集和空隙。当药物直接参与自组装过程时,分析物更容易扩散到 GNP 阵列的纳米间隙中,产生浓度效应,并放大 SERS 灵敏度。该特性还使分子能够均匀地吸附在阵列中,并使液体界面中的分析物和 GNP 更均匀地分布,从而显著提高信号重现性。界面 SERS 在 1ppm 浓度下, methamphetamine(MAMP)分子在 1001cm(-1)峰处的标准偏差为 12.5%,表明重现性良好。此外,还实现了有机相和水相的双分析物检测,并通过液体界面 SERS 平台证实了对分析物检测的良好能力,这有望实现对通常难以进入的环境中溶解的分析物的非工程检测。