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用于超高灵敏分子拉曼检测的可控 MXene 纳米片/Au 纳米结构体系

Controllable MXene nano-sheet/Au nanostructure architectures for the ultra-sensitive molecule Raman detection.

机构信息

School of Optical and Electronic Information and Wuhan National Laboratory of Optoelectronics, Huazhong University of Science and Technology, Wuhan, Hubei 430074, China.

出版信息

Nanoscale. 2019 Nov 28;11(46):22230-22236. doi: 10.1039/c9nr08340e.

DOI:10.1039/c9nr08340e
PMID:31735944
Abstract

Surface-enhanced Raman scattering (SERS) spectroscopy aims to augment the relatively weak molecular vibrations based on electromagnetic enhancement (EE) and chemical enhancement (CE) mechanisms, and offers a potential way for material identification, even up to the single-molecule level, under atmospheric conditions. We have subtly combined the advantages of EE and CE, and propose new MXene (Ti3C2TX) nano-sheet/Au nanostructure architectures to break through the limitations of the Raman detection with long-time stability. The MXene nanosheets with excellent biocompatibility can effectively prevent structural distortion from the interaction with the Au NSs, and can also guarantee a high enhancement effect owing to the spatially extended electromagnetic field distribution and electron injection into the molecules. The self-assembled Au nanostructures are aggregated based on the Volmer-Weber growth model, and the electromagnetic field distribution radically evolves depending on the morphologies of the resultant Au nanostructures, leading to a drastic compensation for the limited EE of the MXene nano-sheets. Consequently, the intensified Raman vibrational signals of R6G molecules lead to a high enhancement factor of 2.9 × 107, even at an ultra-low concentration of 10-10 M. Similarly, the Raman signals of the methylene blue (MB) and crystal violet (CV) molecules can also be detected at low concentrations below 10-8 M, manifesting universal applications of the MXene/Au architectures for ultra-sensitive molecular detection under atmospheric conditions.

摘要

表面增强拉曼散射(SERS)光谱旨在基于电磁增强(EE)和化学增强(CE)机制增强相对较弱的分子振动,并提供一种潜在的方法来进行材料识别,甚至在大气条件下达到单分子水平。我们巧妙地结合了 EE 和 CE 的优点,并提出了新的 MXene(Ti3C2TX)纳米片/Au 纳米结构架构,以突破具有长期稳定性的拉曼检测的限制。具有优异生物相容性的 MXene 纳米片可以有效地防止与 Au NSs 相互作用引起的结构变形,并且由于空间扩展的电磁场分布和电子注入到分子中,也可以保证高增强效果。自组装的 Au 纳米结构基于 Volmer-Weber 生长模型聚集,并且电磁场分布根据所得 Au 纳米结构的形态发生剧烈演变,从而对 MXene 纳米片的有限 EE 进行了剧烈补偿。因此,R6G 分子的增强拉曼振动信号导致高增强因子为 2.9×107,即使在 10-10 M 的超低浓度下也是如此。同样,亚甲基蓝(MB)和结晶紫(CV)分子的拉曼信号也可以在 10-8 M 以下的低浓度下检测到,表明 MXene/Au 架构在大气条件下对超灵敏分子检测具有普遍适用性。

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