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使用原位电化学扫描透射电子显微镜(ec-S/TEM)设备进行定量电化学测量。

Quantitative electrochemical measurements using in situ ec-S/TEM devices.

作者信息

Unocic Raymond R, Sacci Robert L, Brown Gilbert M, Veith Gabriel M, Dudney Nancy J, More Karren L, Walden Franklin S, Gardiner Daniel S, Damiano John, Nackashi David P

机构信息

1 Oak Ridge National Laboratory, Center for Nanophase Materials Sciences, Oak Ridge, TN 37831, USA.

2 Oak Ridge National Laboratory, Materials Science and Technology Division, Oak Ridge, TN 37831, USA.

出版信息

Microsc Microanal. 2014 Apr;20(2):452-61. doi: 10.1017/S1431927614000166. Epub 2014 Mar 11.

Abstract

Insight into dynamic electrochemical processes can be obtained with in situ electrochemical-scanning/transmission electron microscopy (ec-S/TEM), a technique that utilizes microfluidic electrochemical cells to characterize electrochemical processes with S/TEM imaging, diffraction, or spectroscopy. The microfluidic electrochemical cell is composed of microfabricated devices with glassy carbon and platinum microband electrodes in a three-electrode cell configuration. To establish the validity of this method for quantitative in situ electrochemistry research, cyclic voltammetry (CV), choronoamperometry (CA), and electrochemical impedance spectroscopy (EIS) were performed using a standard one electron transfer redox couple [Fe(CN)6]3-/4--based electrolyte. Established relationships of the electrode geometry and microfluidic conditions were fitted with CV and chronoamperometic measurements of analyte diffusion coefficients and were found to agree with well-accepted values that are on the order of 10-5 cm2/s. Influence of the electron beam on electrochemical measurements was found to be negligible during CV scans where the current profile varied only within a few nA with the electron beam on and off, which is well within the hysteresis between multiple CV scans. The combination of experimental results provides a validation that quantitative electrochemistry experiments can be performed with these small-scale microfluidic electrochemical cells provided that accurate geometrical electrode configurations, diffusion boundary layers, and microfluidic conditions are accounted for.

摘要

通过原位电化学扫描/透射电子显微镜(ec-S/TEM)可以深入了解动态电化学过程,该技术利用微流控电化学池,通过S/TEM成像、衍射或光谱来表征电化学过程。微流控电化学池由微加工装置组成,在三电极池配置中具有玻碳和铂微带电极。为了确定该方法在定量原位电化学研究中的有效性,使用基于标准单电子转移氧化还原对[Fe(CN)6]3-/4-的电解质进行循环伏安法(CV)、计时电流法(CA)和电化学阻抗谱(EIS)。通过CV和计时电流法测量分析物扩散系数,拟合了电极几何形状和微流控条件之间已建立的关系,发现与公认的约10-5 cm2/s量级的值一致。在CV扫描期间,发现电子束对电化学测量的影响可以忽略不计,在电子束开启和关闭时,电流分布仅在几纳安范围内变化,这完全在多次CV扫描之间的滞后范围内。实验结果的结合提供了一个验证,即只要考虑准确的几何电极配置、扩散边界层和微流控条件,就可以使用这些小型微流控电化学池进行定量电化学实验。

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