Teng Yuanjie, Li Xin, Chen Yingxin, Zhong Yi, Xu Pei, Shan Shengyan, Gunasekaran Sundaram
State Key Laboratory Breeding Base of Green Chemistry-Synthesis Technology, College of Chemical Engineering, Zhejiang University of Technology, Hangzhou, 310032, China.
Hangzhou Wahaha Technology Co., Ltd., Hangzhou, 310009, China.
Mikrochim Acta. 2024 Oct 30;191(11):719. doi: 10.1007/s00604-024-06800-8.
The uneven distribution of hotspots and the challenges associated with precise analyte localization within these hotspots present significant hurdles in the field of surface-enhanced Raman scattering (SERS). Here, at the water-oil interface, gold nanoparticles (AuNPs) interconnected by cucurbiturils[8] (CB[8]) with sub-nanometer gaps (AuNPs:CB[8]) were organized into plasmonic arrays. This arrangement was engineered to generate highly efficient hotspots. The CB[8] molecules, serving a dual role, not only facilitated the assembly of AuNPs with sub-nanometer (~ 1 nm) gaps to create intense plasmonic hotspots but also acted as molecular traps, enabling the precise localization of molecules within these hotspots. By comparing the enhancement effect of probe molecule on Au nanofilm, AuNPs:CB[8] colloids, and AuNPs:CB[8] nanofilm, it was found that the SERS intensity of the E1 characteristic peak in AuNPs:CB[8] nanofilm is five times higher than that on Au nanofilm, and more than 10 times higher than that of AuNPs:CB[8] colloids. The gaps are also accessible to different electronegativite molecules, such as estrone, p-aminoazobenzene, or methylene blue, which are captured at the plasmonic hotspots by the interaction of CB[8]. The method was employed for the practical detection of artificial antioxidant butylated hydroxyanisole (BHA), which has a weak Raman scattering cross-section, by coupling it with a reaction to enhance its SERS effect. The detection limit of BHA in soybean oil sample is 5.89 × 10 mol/L, with the recovery range 85.1-115%. In conclusion, this hot-spot design and molecular capture approach will offer a highly effective method for detecting weak Raman scattering cross-section molecules and holds great promise for practical applications in the future.
热点的不均匀分布以及在这些热点内精确分析物定位所面临的挑战,在表面增强拉曼散射(SERS)领域构成了重大障碍。在此,在水油界面处,由具有亚纳米间隙的葫芦脲[8](CB[8])相互连接的金纳米颗粒(AuNP)被组装成等离子体阵列(AuNP:CB[8])。这种排列方式旨在产生高效的热点。CB[8]分子起到双重作用,不仅促进了具有亚纳米(约1纳米)间隙的AuNP组装,以形成强烈的等离子体热点,还充当分子陷阱,使分子能够精确地定位在这些热点内。通过比较探针分子对金纳米膜、AuNP:CB[8]胶体和AuNP:CB[8]纳米膜的增强效果,发现AuNP:CB[8]纳米膜中E1特征峰的SERS强度比金纳米膜上的高五倍,比AuNP:CB[8]胶体的高十多倍。不同电负性的分子,如雌酮、对氨基偶氮苯或亚甲基蓝,也能够进入这些间隙,并通过CB[8]的相互作用被捕获在等离子体热点处。该方法通过与增强其SERS效应的反应相结合,用于实际检测具有弱拉曼散射截面的人工合成抗氧化剂丁基羟基茴香醚(BHA)。大豆油样品中BHA的检测限为5.89×10⁻⁸mol/L,回收率范围为85.1 - 115%。总之,这种热点设计和分子捕获方法将为检测弱拉曼散射截面分子提供一种高效的方法,并在未来的实际应用中具有广阔的前景。