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Abstract
In this work, the use of atomic emission spectroelectrochemistry (AESEC) coupled to electrochemical impedance spectroscopy (EIS) is presented as a method of revealing dissolution mechanisms. To illustrate the method, the dissolution kinetics of Al cations from an Al-Zn pure phase (Zn-68 wt.% Al) was investigated in an alkaline solution. In the cathodic potential domain, a nearly direct formation of dissolved Al3+ was observed, while in the anodic potential domain the Al dissolution occurred by migration across a ZnO/Zn(OH)2 film. It was demonstrated that this methodology can be applied to a nonstationary system during a potentiostatic experiment for a lower Al content phase (Zn-22 wt.% Al). The nature of the charge transfer mechanisms depended on the applied potential and could be identified by comparing the direct current and alternating current faradaic yield using AESEC-EIS.
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1 Chimie ParisTech, PSL Research University, CNRS, Institut de Recherche Chimie Paris (IRCP), Paris, France (GRID:grid.4444.0) (ISNI:0000 0001 2112 9282); Department of Materials Science and Engineering, University of Virginia, Charlottesville, United States (GRID:grid.27755.32) (ISNI:0000 0000 9136 933X)
2 Sorbonne Université, CNRS, Laboratoire Interfaces et Systèmes Electrochimiques, LISE, Paris, France (GRID:grid.4444.0) (ISNI:0000 0001 2112 9282)
3 Chimie ParisTech, PSL Research University, CNRS, Institut de Recherche Chimie Paris (IRCP), Paris, France (GRID:grid.4444.0) (ISNI:0000 0001 2112 9282)