Yun Jungheum, Lee Haemi, Mun ChaeWon, Jahng Junghoon, Morrison William A, Nowak Derek B, Song Jung-Hwan, Lim Dong-Kwon, Bae Tae-Sung, Kim Hyung Min, Kim Nam Hoon, Nam Sang Hwan, Kim Jongwoo, Seo Min-Kyo, Kim Dong-Ho, Park Sung-Gyu, Suh Yung Doug
Advanced Functional Thin Films Department, Korea Institute of Materials Science (KIMS) Changwon 51508 Republic of Korea
Research Center for Convergence NanoRaman Technology, Korea Research Institute of Chemical Technology (KRICT) Daejeon 34114 Republic of Korea
RSC Adv. 2018 Feb 8;8(12):6444-6451. doi: 10.1039/c7ra13322g. eCollection 2018 Feb 6.
Developing a sensor that identifies and quantifies trace amounts of analyte molecules is crucially important for widespread applications, especially in the areas of chemical and biological detection. By non-invasively identifying the vibrational signatures of the target molecules, surface-enhanced Raman scattering (SERS) has been widely employed as a tool for molecular detection. Here, we report on the reproducible fabrication of wafer-scale dense SERS arrays and single-nanogap level near-field imaging of these dense arrays under ambient conditions. Plasmonic nanogaps densely populated the spaces among globular Ag nanoparticles with an areal density of 120 particles per μm upon application of a nanolithography-free simple process consisting of the Ar plasma treatment of a polyethylene terephthalate substrate and subsequent Ag sputter deposition. The compact nanogaps produced a high SERS enhancement factor of 3.3 × 10 and homogeneous (coefficient of variation of 8.1%) SERS response. The local near fields at these nanogaps were visualized using photo-induced force microscopy that simultaneously enabled near-field excitation and near-field force detection under ambient conditions. A high spatial resolution of 3.1 nm was achieved. Taken together, the generation of a large-area SERS array with dense plasmonic nanogaps and the subsequent single-nanogap level characterization of the local near field have profound implications in the nanoplasmonic imaging and sensing applications.
开发一种能够识别和量化痕量分析物分子的传感器对于广泛的应用至关重要,特别是在化学和生物检测领域。通过非侵入性地识别目标分子的振动特征,表面增强拉曼散射(SERS)已被广泛用作分子检测工具。在此,我们报告了在环境条件下晶圆级密集SERS阵列的可重复制造以及这些密集阵列的单纳米间隙级近场成像。通过对聚对苯二甲酸乙二醇酯基板进行氩等离子体处理并随后进行银溅射沉积的无纳米光刻简单工艺,等离子体纳米间隙密集地填充在球形银纳米颗粒之间的空间中,面密度为每微米120个颗粒。紧凑的纳米间隙产生了3.3×10的高SERS增强因子和均匀的(变异系数为8.1%)SERS响应。利用光诱导力显微镜对这些纳米间隙处的局部近场进行了可视化,该显微镜能够在环境条件下同时实现近场激发和近场力检测。实现了3.1nm的高空间分辨率。综上所述,具有密集等离子体纳米间隙的大面积SERS阵列的产生以及随后对局部近场的单纳米间隙级表征在纳米等离子体成像和传感应用中具有深远意义。