Han Xue, Mendes Sergio B
Department of Physics and Astronomy, University of Louisville.
Anal Sci. 2017;33(4):435-441. doi: 10.2116/analsci.33.435.
A novel methodology has been developed to determine electron-transfer rate in electrically driven redox reactions. Based on a widely adopted electrical circuit describing faradaic processes in an electrochemical cell, the approach uses a combination of impedance data from optical and electrical measurements that are simultaneously acquired in a spectroelectrochemical experiment. Once the consistency of our methodology was experimentally corroborated, it was put to practice for investigating electron-transfer rate of cytochrome c adsorbates at very low concentrations on an indium tin oxide electrode by using a highly sensitive, single-mode, electro-active, integrated optical waveguide platform. Different surface densities of redox species on the electrode interface and different ionic strengths in the electrolyte solution were studied. Higher surface densities and higher ionic strengths are shown to slow down the electron-transfer process between the redox molecules and the working electrode.
一种用于确定电驱动氧化还原反应中电子转移速率的新方法已被开发出来。基于描述电化学池中法拉第过程的广泛采用的电路,该方法使用了在光谱电化学实验中同时获取的光学和电学测量的阻抗数据的组合。一旦我们方法的一致性通过实验得到证实,就将其用于通过使用高度灵敏的单模电活性集成光波导平台来研究极低浓度下细胞色素c吸附物在氧化铟锡电极上的电子转移速率。研究了电极界面上氧化还原物种的不同表面密度以及电解质溶液中不同的离子强度。结果表明,较高的表面密度和较高的离子强度会减缓氧化还原分子与工作电极之间的电子转移过程。