Electron transfer at self-assembled monolayers measured by scanning electrochemical microscopy

被引:183
作者
Liu, B
Bard, AJ [1 ]
Mirkin, MV
Creager, SE
机构
[1] Univ Texas, Dept Chem & Biochem, Austin, TX 78712 USA
[2] CUNY Queens Coll, Dept Chem & Biochem, Flushing, NY 11367 USA
[3] Clemson Univ, Dept Chem, Clemson, SC 29634 USA
关键词
D O I
10.1021/ja038611p
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
New approaches have been developed for measuring the rates of electron transfer (ET) across self-assembled molecular monolayers by scanning electrochemical microscopy (SECM). The developed models can be used to independently measure the rates of ET mediated by monolayer-attached redox moieties and direct ET through the film as well as the rate of a bimolecular ET reaction between the attached and dissolved redox species. By using a high concentration of redox mediator in solution, very fast heterogeneous (10(8) s(-1)) and bimolecular (10(11) Mol(-1) cm(3) s(-1)) ET rate constants can be measured. The ET rate constants measured for ferrocene/alkanethiol on gold were in agreement with previously published data. The rates of bimolecular heterogeneous electron transfer between the monolayer-bound ferrocene and water-soluble redox species were measured. SECM was also used to measure the rate of ET through nonelectroactive alkanethiol molecules between substrate gold electrodes and a redox probe (Ru(NH3)(6)(3+)) freely diffusing in the solution, yielding a tunneling decay constant, beta, of 1.0 per methylene group.
引用
收藏
页码:1485 / 1492
页数:8
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