Shiao Ming-Hua, Wu Tsunghsueh, Huang Hung Ji, Peng Ching-Yi, Lin Yung-Sheng, Lai Ting-Yu, Lin Yang-Wei
Taiwan Instrument Research Institute, National Applied Research Laboratories, Hsinchu 300092, Taiwan.
Department of Chemistry, University of Wisconsin-Platteville, 1 University Plaza, Platteville, WI 53818-3099, USA.
Nanomaterials (Basel). 2021 May 21;11(6):1359. doi: 10.3390/nano11061359.
Dendritic forest-like Ag nanostructures were deposited on a silicon wafer through fluoride-assisted galvanic replacement reaction (FAGRR) in aqueous AgNO and buffered oxide etchant. The prepared nanostructures were characterized using scanning electron microscopy, energy-dispersive X-ray spectroscopy, inductively coupled plasma-optical emission spectroscopy, a surface profiler (alpha step), and X-ray diffraction. Additionally, the dendritic forest-like Ag nanostructures were characterized using surface-enhanced Raman scattering (SERS) when a 4-mercaptobenzoic acid (4-MBA) monolayer was adsorbed on the Ag surface. The Ag nanostructures exhibited intense SERS signal from 4-MBA because of their rough surface, and this intense signal led to an intense local electromagnetic field upon electromagnetic excitation. The enhancement factor for 4-MBA molecules adsorbed on the Ag nanostructures was calculated to be 9.18 × 10. Furthermore, common Raman reporters such as rhodamine 6G, 4-aminothiolphenol, 5,5'-dithiobis-2-nitrobenzoic acid, and carboxyfluorescein (FAM) were characterized on these dendritic forest-like Ag nanostructures, leading to the development of an ultrasensitive SERS-based DNA sensor with a limit of detection of 33.5 nM of 15-mer oligonucleotide.
通过在硝酸银水溶液和缓冲氧化物蚀刻剂中进行氟化物辅助的电置换反应(FAGRR),将树枝状森林状银纳米结构沉积在硅片上。使用扫描电子显微镜、能量色散X射线光谱、电感耦合等离子体发射光谱、表面轮廓仪(α阶跃)和X射线衍射对制备的纳米结构进行表征。此外,当4-巯基苯甲酸(4-MBA)单层吸附在银表面时,使用表面增强拉曼散射(SERS)对树枝状森林状银纳米结构进行表征。由于银纳米结构表面粗糙,其对4-MBA表现出强烈的SERS信号,并且这种强烈信号在电磁激发时会导致强烈的局部电磁场。计算得出吸附在银纳米结构上的4-MBA分子的增强因子为9.18×10。此外,还对罗丹明6G、4-氨基硫酚、5,5'-二硫代双-2-硝基苯甲酸和羧基荧光素(FAM)等常见拉曼报告分子在这些树枝状森林状银纳米结构上进行了表征,从而开发出一种超灵敏的基于SERS的DNA传感器,其对15-mer寡核苷酸的检测限为33.5 nM。