期刊
JOURNAL OF CHEMICAL PHYSICS
卷 157, 期 23, 页码 -出版社
AIP Publishing
DOI: 10.1063/5.0129255
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- Wolfgang Sprengel (Institute of Materials Physics, TU Graz)
The positronium chemistry of a Fe2+/3+ solution was studied using a novel approach of positronium electrochemistry. The oxidation and reduction reactions were precisely monitored by positron lifetime, and the asymmetric behavior of positron lifetime variation with applied potential was explained by the influence of Fe3+ on positronium formation and annihilation. This study highlights the potential application of positronium electrochemistry for in situ studies of iron-based redox-flow battery electrolytes.
The positronium chemistry of a Fe2+/3+ solution is studied under full electrochemical control. For this novel approach to positronium electrochemistry, a suitable cell setup is used, which allows simultaneously both electrochemical measurements and positron annihilation spectroscopy. For the Fe2+/3+ redox couple, positronium serves as an ideally suited atomic probe owing to the rather different positronium chemistry of Fe2+ (spin conversion) and Fe3+ (total positronium inhibition and oxidation). This enabled the precise in situ monitoring of oxidation and reduction by means of positron lifetime upon slow cycling voltammetry or galvanostatic charging. The variation of the mean positron lifetime with the Fe2+/3+ concentration ratio could be quantitatively described by a reaction rate model for positronium formation and annihilation. An asymmetric behavior of the variation of the mean positron lifetime with applied potential, as compared to the simultaneously recorded symmetric current-potential curve, could be explained by the stronger influence of Fe3+ on the characteristics of positronium formation and annihilation. The highly reversible galvanostatic charging behavior monitored by positron lifetime underlines the attractive application potentials of positronium electrochemistry for in situ studies of iron-based redox-flow battery electrolytes. (c) 2022 Author(s).
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