银溶胶上AMT分子吸附行为的SERS表征  

SERS for adsorption behavior of AMT molecule at the silver colloid

作　　者：朱璇[1] 纪佳华[1] 马晓玲[1] 宋巍[1] 段国萍[1] 孙一平[1] 阮玲玲[1] 杨海峰[1] 

机构地区：[1]上海师范大学生命与环境科学学院,上海200234

出　　处：《上海师范大学学报（自然科学版）》2008年第5期493-498,共6页Journal of Shanghai Normal University(Natural Sciences)

基　　金：上海市自然科学基金(06JC14094);上海市教委重点基金(06ZZ18);湖南大学化学生物传感与化学计量学国家重点实验室开放基金(2006012)

摘　　要：利用表面增强拉曼散射(SERS)光谱,考察AMT浓度对于其在银纳米粒子上吸附取向的影响.SERS实验结果表明:AMT分子以巯基和噻重氮环上的2个硫原子作为吸附位点,浓度为10-3M时,AMT以斜立的方式吸附于银溶胶表面;浓度为10-4M时,AMT分子中噻唑环更垂直于银表面;当浓度为10-5M时,AMT分子中则以较为平躺的方式吸附于银溶胶表面.Surface - enhanced Raman scattering （SERS） Spectroscopy was employed to examine the adsorption behavior of 2 - amino - 5 - mercapto - 1, 3, 4 - thiadiazole （AMT） at the silver colloid. Both the concentration and the time strongly affect adsorption fashion of AMT. At relatively high concentration （1.0 ×10^-3M）, AMT molecules were adsorbed at the silver colloid surface in a titled orientation through two sulfur atoms of mercapto and thiadiazole ring. While at relatively low concentration （ 1.0 × 10^-4M） , AMT molecules were adsorbed via a model perperdieular to surface. At extremely low concentration （ 1.0 × 10^-5 M）, AMT molecules tended to he on the the silver surface in a flat mode of ring.

关 键 词：表面增强拉曼光谱 银溶胶 AMT 

分 类 号：O647.3[理学—物理化学]