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https://doi.org/10.1149/1945-7111/ad9fe3
Copy DOIPublication Date: Dec 16, 2024 | |
License type: CC BY-NC-ND 4.0 |
Abstract Some rate of oxidation and reduction side-reactions will inevitably coexist in most rechargeable batteries, contributing to reversible and irreversible self-discharge. While parasitic reduction traps electrons, parasitic oxidation donates electrons to the cell’s inventory and can lead to temporary capacity gain. This causes direct capacity measurements to be an unreliable source of information about the total extent of side-reactions occurring. The most widely used method to determine the rate of these two types of parasitic processes involves analyzing the slippage of endpoints Here, we argue that this approach could lead to inaccuracies when applied to certain systems, which includes Si electrodes in Li-ion batteries and hard carbon in Na-ion batteries. This inaccuracy originates from the smooth nature of the voltage profiles of these materials at low and high alkali-ion content, causing the termination of charge and discharge to be dictated by voltage changes at both the positive and negative electrodes. We analyze this issue in quantitative terms and propose equations that can provide true rates of parasitic processes from experimental endpoint slippage data. This work shows that, in battery science, well-established analytical approaches may not be directly transferrable to new electrode systems.
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