Li Xiaoling, Xu Weiqing, Jia Huiying, Wang Xu, Zhao Bing, Li Bofu, Ozaki Yukihiro
Key Laboratory for Supermolecular Structure and Materials of Ministry of Education, Jilin University, Changchun 130023, People's Republic of China.
Appl Spectrosc. 2004 Jan;58(1):26-32. doi: 10.1366/000370204322729432.
A new surface-enhanced Raman scattering (SERS) active substrate has been developed based on our previous study. Small silver nanoparticles on a quartz slide can be enlarged by using a mixture of commercially available reagents called Silver Enhancer and Initiator. The optical properties and characteristics of the new substrate have been investigated by ultraviolet-visible (UV-Vis) spectroscopy and atomic force microscopy (AFM). The results indicate that the small silver nanoparticles grow and some silver aggregates emerge on the quartz slide after the slide is immersed into the Silver Enhancer and Initiator Mixture (SEIM). The average diameter of the silver nanoparticles on the substrate becomes approximately double after the immersion into SEIM for 20 s. 1,4-bis[2-(4-pyridyl)ethenyl]-benzene (BPENB) was used as a Raman probe to evaluate the enhancement ability of the new silver substrate. It has been found that the SERS intensity can be increased about 10 times by using the substrate treated by SEIM compared with that without being treated by SEIM. Interestingly enough, the SERS enhancement increases with time. This may be due to the reorganization of silver nanoparticles on the quartz surface. The new substrate can remain active for more than 90 days. The adsorption mode of BPENB on the new substrate and the dependence of the BPENB configurations on the concentration of BPENB in methanol solution have also been investigated by SERS or UV-Vis spectroscopy. The SERS spectra of a self-assembled monolayer (SAM) BPENB film adsorbed on a silver substrate treated by SEIM show that BPENB molecules are chemically absorbed through the Ag-N bond. Consequently, a nearly perpendicular orientation of BPENB on the silver surface is proposed. The SERS spectra of BPENB SAMs on the new substrates fabricated from methanol solutions with different concentrations are compared. The concentration dependence of the SERS spectra reveals that the BPENB molecules are adsorbed on the silver film as monomers when the film is prepared from the solution with a lower concentration (<4 x 10(-6) M) and as aggregates when it is prepared from the solution with a higher concentration (>1 x 10(-5) M).
基于我们之前的研究,开发了一种新型表面增强拉曼散射(SERS)活性基底。石英载玻片上的小银纳米颗粒可以通过使用称为银增强剂和引发剂的市售试剂混合物来放大。通过紫外可见(UV-Vis)光谱和原子力显微镜(AFM)研究了新型基底的光学性质和特征。结果表明,将载玻片浸入银增强剂和引发剂混合物(SEIM)后,石英载玻片上的小银纳米颗粒会生长并出现一些银聚集体。浸入SEIM 20秒后,基底上银纳米颗粒的平均直径大约变为原来的两倍。使用1,4-双[2-(4-吡啶基)乙烯基]-苯(BPENB)作为拉曼探针来评估新型银基底的增强能力。已经发现,与未用SEIM处理的基底相比,使用经SEIM处理的基底时,SERS强度可以提高约10倍。有趣的是,SERS增强随时间增加。这可能是由于银纳米颗粒在石英表面的重新排列。新型基底可以保持活性超过90天。还通过SERS或UV-Vis光谱研究了BPENB在新型基底上的吸附模式以及BPENB构型对甲醇溶液中BPENB浓度的依赖性。吸附在经SEIM处理的银基底上的自组装单分子层(SAM)BPENB膜的SERS光谱表明,BPENB分子通过Ag-N键化学吸附。因此,提出BPENB在银表面上几乎垂直取向。比较了由不同浓度甲醇溶液制备的新型基底上BPENB SAM的SERS光谱。SERS光谱的浓度依赖性表明,当从较低浓度(<4×10(-6) M)的溶液制备膜时,BPENB分子以单体形式吸附在银膜上,而当从较高浓度(>1×10(-5) M)的溶液制备膜时,BPENB分子以聚集体形式吸附。