4.7 Article

Ionic Mott-Schottky formalism allows the assessment of mobile ion concentrations in Li+-conducting solid electrolytes

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出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jelechem.2022.116750

关键词

Li-ion conductors; Mobile Li-ion concentration; Space charge layer; Solid electrolytes; Solid-state ionics

资金

  1. Bavarian Ministry of Economic Affairs, Regional Development and Energy

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Li+-conducting solid electrolytes have attracted researchers' attention due to the development of efficient all-solid-state batteries. In this study, we propose a Mott-Schottky-based analysis to calculate the concentration of mobile Li+ in a lithium-conducting glass-ceramic. By using the space charge layer capacitances obtained from electrochemical impedance data, we can gain insights into the conductivity and temperature dependencies in ion conductors.
Li+-conducting solid electrolytes have been in the focus of researchers for the last decade thanks to the recent efforts to develop efficient all-solid-state batteries. While material scientists discovered new compounds with unprecedented Li+ conductivities, surprisingly often, a fundamental question remains: What fraction of the total lithium-ions inside the solid electrolyte is mobile and thus contributes to the conductivity? In this work, we propose an approach, which can be considered as a Mott-Schottky-based analysis applied to an ionically conducting system, to calculate the concentration of mobile Li+ in a lithium-conducting glass-ceramic. We use the space charge layer (SCL) capacitances obtained from the electrochemical impedance data recorded at different bias potentials and temperatures as the input. We demonstrate that the space charge layer in the ionic conductors can be formally described similarly to the SCLs formed in semiconductors in contact with, e.g., liquid electrolytes. This analysis makes it possible to provide deeper insights into the mechanisms of conductivity and its temperature dependencies in the SCL in ion conductors and, in general, help to uncover the nature of the mobility of Li-ions in various Li+-conducting electrolytes.

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