کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
4907906 | 1426582 | 2017 | 9 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Reprint of “Analytical theoretical approach to the transient and steady state voltammetric response of reaction mechanisms. Linear diffusion and reaction layers at micro- and submicroelectrodes of arbitrary geometry” Reprint of “Analytical theoretical approach to the transient and steady state voltammetric response of reaction mechanisms. Linear diffusion and reaction layers at micro- and submicroelectrodes of arbitrary geometry”](/preview/png/4907906.png)
- A general solving strategy for reaction mechanisms at any interface geometry is proposed.
- The approach is based on appropriate definitions of linear reaction and diffusion layers.
- δr, G and δG are defined by electrode geometry and formally identical for any reaction scheme.
- Accurate equations for the current-potential response at microelectrodes are obtained.
- Steady-state and total chemical equilibrium responses can be derived as limit cases.
A powerful theoretical approach to solve electrochemical reaction-diffusion problems with fast homogeneous kinetics is applied to obtain expressions for the transient current-potential-time response of a number of reaction mechanisms at microelectrodes of very different shapes, also applicable to ion transfer processes at liquid | liquid microinterfaces. The steady state response can be obtained as a limit when the characteristic dimension of the microelectrode tends to zero. Also, expressions under total chemical equilibrium conditions are derived when the linear reaction layer vanishes. The physico-chemical principles are based on suitable definitions of the so-called linear diffusion and reaction layers, which take into account the influence of the geometry of the diffusion field. The results presented fall within the so-called “kinetic steady state” and “diffusive-kinetic steady state” approaches and also give insight into the magnitude and extent of the perturbation of the chemical equilibrium conditions near the electrode surface as a consequence of the charge transfer process.
Journal: Journal of Electroanalytical Chemistry - Volume 793, 15 May 2017, Pages 104-112