Abstract
Solid polymer electrolytes (SPEs) are promising candidates for solid-state lithium-ion batteries. Potentially, they can be used with lithium metal anodes and high-voltage cathodes, provided that their electrochemical stability is sufficient. Thus far, the oxidative stability has largely been asserted based on results obtained with sweep voltammetry, which are often determined and reliant on arbitrary assessments that are highly dependent on the experimental conditions and do not take the interaction between the electrolyte and the electrode material into account. In this study, alternative techniques are introduced to address the pitfalls of sweep voltammetry for determining the oxidative stability of SPEs. Staircase voltammetry involves static conditions and eliminates the kinetic aspects of sweep voltammetry, and coupled with impedance spectroscopy provides information of changes in resistance and interphase layer formation. Synthetic charge–discharge profile voltammetry applies the real voltage profile of the active material of interest. The added effect of the electrode active material is investigated with a cut-off increase cell cycling method where the upper cut-off voltage during galvanostatic cycling is gradually increased. The feasibility of these techniques has been tested with both poly(ethylene oxide) and poly(trimethylene carbonate) combined with LiTFSI, thereby showing the applicability for several categories of SPEs.
Highlights
Going Beyond Sweep Voltammetry: Alternative Approaches in Search of the Elusive Electrochemical Stability of Polymer Electrolytes
This may lead to impossibly large electrochemical stability windows (ESWs) being suggested from, e.g., HOMO and LUMO levels obtained from density functional theory (DFT) calculations.[2,8]
The aim of this study is to determine whether it is possible to unambiguously and reliably determine electrochemical stability limits for solid polymer electrolytes (SPEs). To answer this question and to illustrate the utilized techniques, we have measured the anodic stability of two model SPEs—poly(ethylene oxide) (PEO):lithium bis(trifluoromethanesulfonyl)imide salt (LiTFSI) and poly(trimethylene carbonate) (PTMC):LiTFSI, each with 22 wt% salt—in an attempt to determine which of these electrolytes exhibits the highest oxidation stability
Summary
Going Beyond Sweep Voltammetry: Alternative Approaches in Search of the Elusive Electrochemical Stability of Polymer Electrolytes. Solid polymer electrolytes (SPEs) constitute promising alternatives because of their wettability and adhesion to the electrodes, reduced flammability, scalability in production and being potentially low-cost.[1,2] Compatibility with lithium metal anodes and an inherent ability to resist dendrite growth are often cited as motivational factors and have been widely studied for SPEbased batteries.[3,4,5,6] Improved electrochemical stability compared to liquid electrolytes is commonly cited as a motivation for solidstate electrolytes, but it is not clear whether this criterion is met.
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