Charge transport in lithium peroxide: Relevance for rechargeable metal-air batteries
Maxwell D. Radin, Donald J. Siegel

TL;DR
This study uses first-principles calculations to analyze charge transport mechanisms in lithium peroxide, revealing the roles of defects and polarons, and discussing implications for rechargeable metal-air batteries.
Contribution
It provides a detailed theoretical analysis of charge carriers and defect chemistry in Li2O2, highlighting the limited bulk conductivity and proposing a two-stage charging process.
Findings
Charge transport involves both ionic and polaronic contributions.
Bulk Li2O2 is insulating with charge transport occurring at high potentials.
Limited charge transport impacts discharge and recharge efficiency.
Abstract
The mechanisms and efficiency of charge transport in lithium peroxide (Li2O2) are key factors in understanding the performance of non-aqueous Li-air batteries. Towards revealing these mechanisms, here we use first-principles calculations to predict the concentrations and mobilities of charge carriers and intrinsic defects in Li2O2 as a function of cell voltage. Our calculations reveal that changes in the charge state of O2 dimers controls the defect chemistry and conductivity of Li2O2. Negative lithium vacancies (missing Li+) and small hole polarons are identified as the dominant charge carriers. The electronic conductivity associated with polaron hopping (5 x 10-20 S/cm) is comparable to the ionic conductivity arising from the migration of Li-ions (4 x 10-19 S/cm), suggesting that charge transport in Li2O2 occurs through a mixture of ionic and polaronic contributions. These data…
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