Amiri Amir, Ravi Manu Jyothi, Huang Siao-Han, Janda Donald C, Amemiya Shigeru
Department of Chemistry, University of Pittsburgh, 219 Parkman Avenue, Pittsburgh, Pennsylvania, 15260, United States.
Sens Actuators B Chem. 2024 May 1;406. doi: 10.1016/j.snb.2024.135440. Epub 2024 Feb 3.
A nanogap cell involves two working electrodes separated by a nanometer-wide solution to enable unprecedented electrochemical measurements. The powerful nanogap measurements, however, can be seriously interfered with by resistive coupling between the two electrodes to yield erroneous current responses. Herein, we employ the nanogap cell based on double carbon-fiber microelectrodes to suppress resistive coupling for the assessment of intrinsic current responses. Specifically, we modify a commercial bipotentiostat to compensate the Ohmic potential drop shared by the two electrodes through the common current pathway with a fixed resistance in the solution. Resistive coupling through both non-Faradaic and Faradaic processes is suppressed to eliminate erroneous current responses. Our approach is applied to investigate the mechanism of dopamine oxidation at carbon-fiber microelectrodes as important electrochemical sensors for the crucial neurotransmitter. Resistive coupling is suppressed to manifest the intrinsic current responses based on the oxidation of both adsorbed and non-adsorbed forms of dopamine to the respective forms of dopamine--quinone. The simultaneous dual oxidation pathways are observed for the first time and can be mediated through either non-concerted or concerted mechanisms of adsorption-coupled electron transfer. The two mechanisms are not discriminated for the two-electron oxidation of dopamine because it can not be determined whether the intermediate, dopamine semi-quinone, is adsorbed on the electrode surface. Significantly, our approach will be useful to manifest intrinsic current responses without resistive coupling for nanogaps and microgaps, which are too narrow to eliminate the common solution resistance by optimizing the position of a reference electrode.
纳米间隙电池包含两个工作电极,它们由纳米级宽度的溶液隔开,以实现前所未有的电化学测量。然而,强大的纳米间隙测量可能会受到两个电极之间的电阻耦合严重干扰,从而产生错误的电流响应。在此,我们采用基于双碳纤维微电极的纳米间隙电池来抑制电阻耦合,以评估固有电流响应。具体而言,我们对商用双恒电位仪进行了改进,通过溶液中具有固定电阻的公共电流路径来补偿两个电极共享的欧姆电位降。通过非法拉第和法拉第过程的电阻耦合均被抑制,以消除错误的电流响应。我们的方法被应用于研究碳纤维微电极上多巴胺氧化的机制,碳纤维微电极是用于这种关键神经递质的重要电化学传感器。电阻耦合被抑制,以显示基于多巴胺吸附和非吸附形式分别氧化为多巴胺醌形式的固有电流响应。首次观察到同时存在的双氧化途径,并且可以通过吸附耦合电子转移的非协同或协同机制介导。对于多巴胺的双电子氧化,这两种机制无法区分,因为无法确定中间体多巴胺半醌是否吸附在电极表面。重要的是,我们的方法将有助于在纳米间隙和微间隙中显示无电阻耦合的固有电流响应,这些间隙太窄,无法通过优化参比电极的位置来消除公共溶液电阻。