Characterization of carboxylic acid-terminated self-assembled monolayers by electrochemical impedance spectroscopy and scanning electrochemical microscopy

被引:35
作者
Sanders, Wesley [2 ]
Vargas, Ricardo [2 ]
Anderson, Mark R. [1 ]
机构
[1] Univ Colorado, Dept Chem, Denver, CO 80217 USA
[2] Virginia Polytech Inst & State Univ, Dept Chem, Blacksburg, VA 24060 USA
关键词
D O I
10.1021/la704059q
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrochemical impedance spectroscopy (EIS) and scanning electrochemical microscopy (SECM) are used to monitor changes in the ionization of monolayers of 11-mercaptoundecanoic acid. When using an anionic redox probe, Fe(CN)(6)(-4), the charge-transfer resistance of the 11-mercaptoundecanoic acid monolayer-modified interface increases in a sigmoidal fashion as the solution is made basic. The opposite effect is observed when using a cationic redox probe. The inflection points of these two titration curves, however, differ when using the different redox probes. This result is taken as being characteristic of the influence that applied potential has on the ionization of the monolayer. The role of substrate potential on the ionization of the monolayer is further investigated by SECA The SECM measurement monitors the concentration of Ru(NH3)(6)(+3) as the potential of the substrate is varied about the potential of zero charge. For monolayers of 11-mercaptoundecanoic acid in solutions buffered near the pK(a) of the terminal carboxylic acid, potential excursions positive of the PZC cause an increase in the concentration of Ru(NH3)(6)(+3) local to the interface, and potential excursions negative of the PZC cause a decrease in the local concentration of Ru(NH3)(6)(+3). Similar experiments conducted with an interface modified with 11-undecanethiol had no impact on the local concentration of Ru(NH3)(6)(+3). These results are interpreted in terms of the influence that applied potential has on the pH of the solution local to the interface and the impact that this has on the ionization of the monolayer.
引用
收藏
页码:6133 / 6139
页数:7
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