微流控
粒子(生态学)
化学
拉曼光谱
纳米技术
拉曼散射
等离子体子
纳米颗粒
表面增强拉曼光谱
检出限
分析化学(期刊)
光电子学
材料科学
光学
色谱法
海洋学
地质学
物理
作者
Danyang Liu,Chuanyu Liu,Yuan Yuan,Xin Zhang,Yingzhou Huang,Sheng Yan
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2021-07-26
卷期号:93 (30): 10672-10678
被引量:23
标识
DOI:10.1021/acs.analchem.1c02139
摘要
For its ultrahigh sensitivity, the microfluidic system combined with surface-enhanced Raman spectroscopy (SERS) becomes one of the most interesting topics in integrated online monitoring related fields. In previous reports, the commonest surface plasmon-enhanced substrates in microfluidics consist of immobilized metal nanostructures on the channel surface to overcome the disturbance of Brownian motion. In this work, a hybrid optoplasmonic microfluidic conveyer is developed, in which the movable, highly ordered optoplasmonic particles are delivered to the detection spot for SERS detection. Here, the optoplasmonic particle is the SiO2 microsphere with in situ photochemical reduced Ag nanoparticles on the surface. Because of the converged light at the SiO2 microsphere surface, the SERS spectra collected at this optoplasmonic particle in the channel exhibit excellent performance, which is confirmed by the simulated electric field distribution. In addition, the experimental data also demonstrate that the quantitative analysis is achieved at 1 nM in this optoplasmonic microfluidic conveyer. Furthermore, the used optoplasmonic particle can be ejected from the microfluidic channel by modulating the velocity of injected fluid such that the new optoplasmonic particle will be delivered to the detection spot for repeatable SERS detection in the same channel. The dynamic process of optoplasmonic particle transport is investigated in this microconveyer, and the built theoretical model to predict the particle release is highly identical with the experimental data. These data point out that our hybrid optoplasmonic microfluidic conveyer has repeatable enhanced substrates with the high SERS sensitivity to overcome the cross-contamination of different target molecules in repeatable detection.
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