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基于模式识别的等离子体激元间隙纳米结构的定向组装用于单分子 SERS。

Pattern Recognition Directed Assembly of Plasmonic Gap Nanostructures for Single-Molecule SERS.

机构信息

Key Laboratory for Organic Electronics and Information Displays (KLOEID) & Jiangsu Key Laboratory for Biosensors, Institute of Advanced Materials (IAM), National Synergetic Innovation Center for Advanced Materials (SICAM), Nanjing University of Posts and Telecommunications, 9 Wenyuan Road, Nanjing 210023, People's Republic of China.

School of Chemistry and Chemical Engineering, Frontiers Science Center for Transformative Molecules and National Center for Translational Medicine, Shanghai Jiao Tong University, Shanghai 200240, People's Republic of China.

出版信息

ACS Nano. 2022 Sep 27;16(9):14622-14631. doi: 10.1021/acsnano.2c05150. Epub 2022 Sep 9.

Abstract

Gold nanocubes (AuNCs) with tunable localized surface plasmon resonance properties are good candidates for plasmonic gap nanostructures (PGNs) with hot spots (areas with intense electric field localization). Nevertheless, it remains challenging to create shape-controllable nanogaps between AuNCs. Herein, we report a DNA origami directed pattern recognition strategy to assemble AuNCs into PGNs. By tuning the position and number of capture strands on the DNA origami template, different geometrical configurations of PGNs with nanometer-precise and shape-controllable gaps are created. The localized field enhancement in these gaps can generate hot spots that are in accordance with finite difference time domain simulations. Benefiting from the single Raman probe molecule precisely anchored at these nanogaps, the dramatic enhanced electromagnetic fields localized in hot spots arouse stronger single-molecule SERS (SM-SERS) signals. This method can be utilized in the design of ultrahigh-sensitivity photonic devices with tailored optical properties and SERS-based applications.

摘要

具有可调谐局域表面等离激元共振特性的金纳米立方体(AuNCs)是等离子体激元间隙纳米结构(PGNs)的理想候选材料,这些结构具有热点(电场高度局域化的区域)。然而,在 AuNCs 之间制造形状可控的纳米间隙仍然具有挑战性。在此,我们报告了一种 DNA 折纸定向模式识别策略,用于将 AuNCs 组装成 PGNs。通过调整 DNA 折纸模板上捕获链的位置和数量,可以创建具有纳米精度和形状可控间隙的不同几何构型的 PGNs。这些间隙中的局域场增强可以产生热点,与有限差分时域模拟结果一致。得益于精确固定在这些纳米间隙中的单个拉曼探针分子,局域在热点中的剧烈增强电磁场引起更强的单分子拉曼光谱(SM-SERS)信号。这种方法可用于设计具有定制光学性能的超高灵敏度光子器件和基于 SERS 的应用。

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