Alagurasu Arunkumar, Behera Satyabrat, Yang Joon-Mo, Kim Dai-Sik, Namgung Seon
Department of Physics, Ulsan National Institute of Science and Technology, Ulsan 44919, Republic of Korea.
Department of Biomedical Engineering, Ulsan National Institute of Science and Technology, Ulsan 44919, Republic of Korea.
Biosensors (Basel). 2025 Jun 9;15(6):369. doi: 10.3390/bios15060369.
Sub-wavelength metallic nanostructures allow the squeezing of light within nanoscale regions, called plasmonic hotspots. Squeezed near-field light has been demonstrated to detect, modulate, and generate light in more effective ways. The enhanced electric field in the plasmonic hotspots are also utilized for identifying molecular fingerprints in a more sensitive manner, i.e., surface-enhanced Raman spectroscopy (SERS). SERS is a versatile tool used to characterize chemicals and biomolecules with the advantages of label-free detection, specificity, and high sensitivity compared to fluorescence and colorimetric sensing methods. With its practical and diverse applications such as biomedical sensing, the evaluation of SERS on diverse nano-structure platforms and materials is highly in demand. Nanogap structures are promising SERS platforms which can be fabricated over a large area with uniform nanoscale gap size. Here, we demonstrate the fabrication of large-area metal-insulator-metal nanogap structures with different metals (i.e., Au and Ag) and analyze material dependence on SERS. While both nanometer-sized gap structures exhibit a large enhancement factor for Raman spectroscopy, Ag-based structures exhibit 58- and 15-times-larger enhancement factors for bottom and top plasmonic hotspots, respectively. The enhanced detection on a silver nanogap platform is attributed to enhanced electric field in the gap, as confirmed by simulation. Our findings provide not only a way to better understand SERS in different metallic nano platforms but also insights for designing highly sensitive nanoscale chemical and biomedical sensors.
亚波长金属纳米结构能够将光压缩在称为等离激元热点的纳米级区域内。已证明压缩后的近场光能够以更有效的方式检测、调制和产生光。等离激元热点中增强的电场还被用于以更灵敏的方式识别分子指纹,即表面增强拉曼光谱(SERS)。与荧光和比色传感方法相比,SERS是一种用于表征化学物质和生物分子的通用工具,具有无需标记检测、特异性和高灵敏度等优点。鉴于其在生物医学传感等实际且多样应用,对不同纳米结构平台和材料上的SERS进行评估的需求非常高。纳米间隙结构是很有前景的SERS平台,能够大面积制造出具有均匀纳米级间隙尺寸的结构。在此,我们展示了用不同金属(即金和银)制造大面积金属-绝缘体-金属纳米间隙结构,并分析了材料对SERS的依赖性。虽然这两种纳米级间隙结构对拉曼光谱都表现出很大的增强因子,但基于银的结构对底部和顶部等离激元热点的增强因子分别大58倍和15倍。正如模拟所证实的,在银纳米间隙平台上增强的检测归因于间隙中增强的电场。我们的研究结果不仅提供了一种更好地理解不同金属纳米平台中SERS的方法,还为设计高灵敏度纳米级化学和生物医学传感器提供了思路。