Cai Chenxin, Mirkin Michael V
Department of Chemistry and Biochemistry, Queens College-CUNY, Flushing, NY 11367, USA.
J Am Chem Soc. 2006 Jan 11;128(1):171-9. doi: 10.1021/ja055091k.
Rapid kinetics of electron transfer (ET) reactions across the interface between water and 1,2-dichloroethane were measured by steady-state voltammetry at nanopipet electrodes (50- to 400-nm orifice radius). The origins of previously reported imperfect voltammetric responses of ET reactions at micropipets were investigated. Several new experimental systems were explored, and two of them yielded high-quality voltammograms suitable for kinetic experiments. The determined standard rate constants were compared to those measured previously at polarized and nonpolarized liquid/liquid interfaces. The effect of the interfacial dimensions on the magnitude of the apparent ET rate constant is discussed. A new approach to ET kinetic measurements based on the use of the scanning electrochemical microscope with a nanopipet tip and a metallic substrate has been developed and employed to check the validity of determined kinetic parameters.
通过纳米吸管电极(孔半径为50至400纳米)上的稳态伏安法测量了电子转移(ET)反应在水和1,2 - 二氯乙烷界面间的快速动力学。研究了先前报道的微吸管处ET反应伏安响应不理想的原因。探索了几个新的实验系统,其中两个产生了适用于动力学实验的高质量伏安图。将测定的标准速率常数与先前在极化和非极化液/液界面处测量的速率常数进行了比较。讨论了界面尺寸对表观ET速率常数大小的影响。基于使用带有纳米吸管尖端和金属基底的扫描电化学显微镜,开发了一种新的ET动力学测量方法,并用于检验所测定动力学参数的有效性。