College of Science and Technology, Nihon University, 1-8-14 Kanda Surugadai, Chiyoda-ku, Tokyo 101-8308, Japan.
Photochem Photobiol Sci. 2014 Jan;13(1):82-91. doi: 10.1039/c3pp50281c. Epub 2013 Nov 13.
Fabrication of dense two-dimensional assemblies consisting of gold(core)-silver(shell) nanoparticles and the resulting peculiar surface-enhanced Raman scattering (SERS) activity are reported. The assemblies were prepared via assembly at air-toluene interfaces by drop-casting toluene solutions containing the nanoparticles protected with octadecylamine molecules onto glass plates. This simple process, which does not require special apparatus or significant fabrication time, leads to uniform assemblies over vast areas (~34 cm(2)). In the SERS measurements, the high spatial reproducibility of the SERS signals from p-aminothiophenol adsorbed on the assemblies over vast areas demonstrates that this method is useful for the quantitative investigation of SERS mechanisms. Under 532 nm laser excitation, the difference in the enhancement factors of the SERS signals at the a1 mode between assemblies consisting of gold, silver, and core-shell nanoparticles can be explained by the degree of overlap of the excitation wavelength with their plasmon coupling modes. In contrast, under 785 nm excitation, even though the plasmon band of the core-shell nanoparticle assemblies does not significantly overlap with the excitation wavelength as compared with that of gold nanoparticle assemblies, the enhancement factor from the core-shell nanoparticle assemblies was stronger than those from the gold nanoparticle assemblies. Therefore, we have demonstrated that the gold(core)-silver(shell) nanoparticle assemblies are excellent SERS active materials, which have strong electromagnetic mechanism (EM) as well as chemical mechanism (CM) effects due to the silver shells.
本文报道了由金(核)-银(壳)纳米粒子组成的密集二维组装体的制备及其独特的表面增强拉曼散射(SERS)活性。该组装体是通过在空气-甲苯界面处通过滴铸甲苯溶液来制备的,该溶液中含有被十八胺分子保护的纳米粒子,并将其滴铸在玻璃片上。这种简单的过程不需要特殊的仪器或大量的制造时间,可在大面积(约 34cm²)上得到均匀的组装体。在 SERS 测量中,从吸附在组装体上的对氨基苯硫酚获得的 SERS 信号在大面积上具有很高的空间重现性,这表明该方法可用于定量研究 SERS 机制。在 532nm 激光激发下,金、银和核壳纳米粒子组装体的 a1 模式 SERS 信号的增强因子之间的差异可以用激发波长与它们的等离子体耦合模式的重叠程度来解释。相比之下,在 785nm 激发下,尽管与金纳米粒子组装体相比,核壳纳米粒子组装体的等离子体带与激发波长没有明显重叠,但核壳纳米粒子组装体的增强因子要强于金纳米粒子组装体的增强因子。因此,我们已经证明,金(核)-银(壳)纳米粒子组装体是出色的 SERS 活性材料,由于银壳的存在,它们具有强烈的电磁机制(EM)和化学机制(CM)效应。