吸附
分析物
表面增强拉曼光谱
化学
拉曼光谱
基质(水族馆)
分子
分子结合
纳米技术
材料科学
物理化学
有机化学
拉曼散射
海洋学
光学
物理
地质学
作者
Ali Ozhan Altun,Tiziana Bond,Wouter Pronk,Hyung Gyu Park
出处
期刊:Langmuir
[American Chemical Society]
日期:2017-06-25
卷期号:33 (28): 6999-7006
被引量:44
标识
DOI:10.1021/acs.langmuir.7b01186
摘要
Surface adsorption plays a critical role in a wide variety of fields from surface catalysis to molecular separation. Despite the importance, limited access to simultaneously sensitive and selective detection mechanisms has hampered the acquisition of comprehensive and versatile experimental data needed to understand the complex aspects of mixture adsorption, calling for a molecular detection method capable of obtaining the surface adsorption isotherms over a wide range of concentrations as well as distinguishing the competitive adsorption of different adsorbates. Here, we test surface-enhanced Raman spectroscopy (SERS) as an effective analysis tool of surface adsorption phenomena. Using a sensitive SERS substrate, we characterize the adsorption isotherms of chemical species of various binding energies. We obtained the isotherms for strongly binding species in a concentration range from subpicomolar to micromolar. A log-sigmoidal dependency of the SERS signals to the analyte concentration could be modeled by surface binding theories accurately using molecular dynamics simulations, thereby bringing out the potential capability of sensitive SERS for describing a single-compound adsorption process. SERS also enabled the determination of competitive adsorption isotherms from a multiple-compound solution for the first time. The successful demonstration of the sensitive and selective characterization of surface adsorption lends SERS adaptability to a cheap, facile, and effective solution for chemical analysis.
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