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用于定向分子传感的超表面增强拉曼光谱(mSERS)。

Metasurface-Enhanced Raman Spectroscopy (mSERS) for Oriented Molecular Sensing.

作者信息

Zeng Yuan, Ananth Riddhi, Dill Tyler J, Rodarte Andrea, Rozin Matthew J, Bradshaw Nathan, Brown Eric R, Tao Andrea R

机构信息

Department of NanoEngineering, University of California, San Diego, 9500 Gilman Drive MC 0448, La Jolla, California 92093-0448, United States.

Materials Science and Engineering, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093, United States.

出版信息

ACS Appl Mater Interfaces. 2022 Jul 20;14(28):32598-32607. doi: 10.1021/acsami.2c01656. Epub 2022 Jul 11.

Abstract

Surface-enhanced Raman spectroscopy (SERS) is a widely used sensing technique for ultrasensitivity chemical sensing, biomedical detection, and environmental analysis. Because SERS signal is proportional to the fourth power of the local electric field, several SERS applications have focused on the design of plasmonic nanogaps to take advantage of the extremely strong near-field enhancement that results from plasmonic coupling, but few designs have focused on how SERS detection is affected by molecular orientation within these nanogaps. Here, we demonstrate a nanoparticle-on-metal metasurface designed for near-perfect optical absorption as a platform for Raman detection of highly oriented molecular analytes, including two-dimensional materials and aromatic molecules. This metasurface platform overcomes challenges in nanoparticle aggregation, which commonly leads to low or fluctuating Raman signals in other colloidal nanoparticle platforms. Our metasurface-enhanced Raman spectroscopy (mSERS) platform is based on a colloidal Langmuir-Schaefer deposition, with up to 32% surface coverage density of nanogaps across an entire sensor chip. In this work, we perform both simulations of the local electric field and experimental characterization of the mSERS signal obtained for oriented molecular layers. We then demonstrate this mSERS platform for the quantitative detection of the drinking-water toxin polybrominated diphenyl ether (BDE-15), with a limit of detection of 0.25 μM under 530 μW excitation. This detection limit is comparable to other SERS-based sensors operating at laser powers over 3 orders of magnitude higher, indicating the promise of our mSERS platform for nondestructive and low-level analyte detection.

摘要

表面增强拉曼光谱(SERS)是一种广泛应用于超灵敏化学传感、生物医学检测和环境分析的传感技术。由于SERS信号与局部电场的四次方成正比,因此一些SERS应用专注于等离子体纳米间隙的设计,以利用等离子体耦合产生的极强近场增强效应,但很少有设计关注这些纳米间隙内的分子取向如何影响SERS检测。在此,我们展示了一种设计用于近乎完美光吸收的金属超表面上的纳米颗粒,作为用于拉曼检测高度取向分子分析物(包括二维材料和芳香族分子)的平台。这种超表面平台克服了纳米颗粒聚集方面的挑战,而在其他胶体纳米颗粒平台中,纳米颗粒聚集通常会导致拉曼信号较低或波动。我们的超表面增强拉曼光谱(mSERS)平台基于胶体朗缪尔 - 谢弗沉积法,在整个传感器芯片上纳米间隙的表面覆盖密度高达32%。在这项工作中,我们对局部电场进行了模拟,并对取向分子层获得的mSERS信号进行了实验表征。然后,我们展示了这个mSERS平台用于定量检测饮用水毒素多溴二苯醚(BDE - 15),在530 μW激发下检测限为0.25 μM。这个检测限与其他基于SERS且激光功率高出3个数量级以上的传感器相当,这表明我们的mSERS平台在无损和低水平分析物检测方面具有潜力。

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