Chowdhury Joydeep, Ghosh Manash
Department of Physics, Sammilani Mahavidyalaya, Baghajatin Station, EM Bypass, Kolkata 700 075, India.
J Colloid Interface Sci. 2004 Sep 1;277(1):121-7. doi: 10.1016/j.jcis.2004.04.030.
Surface-enhanced Raman scattering (SERS) of 2-benzoylpyridine (2-BP) adsorbed on silver hydrosols has been investigated. It has been observed that with a small change in the adsorbate concentration, the SER spectra of 2-BP show significant change in their features, indicating different orientational changes of the different part of the flexible molecule on the colloidal silver surface with adsorbate concentration. The time dependence of the SER spectra of the molecule has been explained in terms of aggregation of colloidal silver particles and co-adsorption and replacement kinetics of the adsorbed solute and solvent molecules on the silver surface. The broad long-wavelength band in the absorption spectra of the silver sol due to solute-induced coagulation of colloidal silver particles is found to be red-shifted with the increase in adsorbate concentration. The surface-enhanced Raman excitation profiles indicate that the resonance of the Raman excitation radiation with the new aggregation band contributes more to the SERS intensity than that with the original sol band.
研究了吸附在水合银溶胶上的2-苯甲酰基吡啶(2-BP)的表面增强拉曼散射(SERS)。已观察到,随着吸附质浓度的微小变化,2-BP的SERS光谱在特征上显示出显著变化,这表明柔性分子的不同部分在胶体银表面上随吸附质浓度发生了不同的取向变化。分子的SERS光谱的时间依赖性已根据胶体银颗粒的聚集以及吸附溶质和溶剂分子在银表面上的共吸附和置换动力学进行了解释。发现由于溶质诱导的胶体银颗粒凝聚,银溶胶吸收光谱中的宽长波带随着吸附质浓度的增加而发生红移。表面增强拉曼激发谱表明,拉曼激发辐射与新的聚集带的共振对SERS强度的贡献比对原始溶胶带的共振更大。