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      Dead lithium: mass transport effects on voltage, capacity, and failure of lithium metal anodes

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          Abstract

          A mechanistic analysis of voltage shape changes in lithium metal anodes explains how dead lithium causes capacity fade and failure.

          Abstract

          Improvement of the performance of Li metal anodes is critical to enable high energy density rechargeable battery systems beyond Li-ion. However, a complete mechanistic understanding of electrode overpotential variations that occur during extended cycling of Li metal is lacking. Herein, we demonstrate that when using a Li metal electrode, the dynamic changes in voltage during extended cycles can be increasingly attributed to mass transport. It is shown that these mass transport effects arise as a result of dead Li accumulation at the Li metal electrode, which introduces a tortuous pathway for Li-ion transport. In Li–Li symmetric cells, mass transport effects cause the shape of the galvanostatic voltage response to change from “peaking” to “arcing”, along with an increase in total electrode overpotential. The continued accumulation of dead Li is also conclusively shown to directly cause capacity fade and rapid “failure” of Li–LCO full cells containing Li metal anodes. This work provides detailed insights into the coupled relationships between cycling, interphase morphology, mass transport and the overall cell performance. Furthermore, this work helps underscore the potential of Li–Li symmetric cells as a powerful analytical tool for understanding the effects of Li metal electrodes in full cell batteries.

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          Layered reduced graphene oxide with nanoscale interlayer gaps as a stable host for lithium metal anodes.

          Metallic lithium is a promising anode candidate for future high-energy-density lithium batteries. It is a light-weight material, and has the highest theoretical capacity (3,860 mAh g(-1)) and the lowest electrochemical potential of all candidates. There are, however, at least three major hurdles before lithium metal anodes can become a viable technology: uneven and dendritic lithium deposition, unstable solid electrolyte interphase and almost infinite relative dimension change during cycling. Previous research has tackled the first two issues, but the last is still mostly unsolved. Here we report a composite lithium metal anode that exhibits low dimension variation (∼20%) during cycling and good mechanical flexibility. The anode is composed of 7 wt% 'lithiophilic' layered reduced graphene oxide with nanoscale gaps that can host metallic lithium. The anode retains up to ∼3,390 mAh g(-1) of capacity, exhibits low overpotential (∼80 mV at 3 mA cm(-2)) and a flat voltage profile in a carbonate electrolyte. A full-cell battery with a LiCoO2 cathode shows good rate capability and flat voltage profiles.
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            Review of selected electrode–solution interactions which determine the performance of Li and Li ion batteries

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              Fluoroethylene Carbonate Additives to Render Uniform Li Deposits in Lithium Metal Batteries

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                Author and article information

                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                2017
                2017
                : 5
                : 23
                : 11671-11681
                Affiliations
                [1 ]Department of Materials Science and Engineering
                [2 ]University of Michigan
                [3 ]Ann Arbor
                [4 ]USA
                [5 ]Department of Mechanical Engineering
                Article
                10.1039/C7TA00371D
                629e4467-1445-4e68-ae5b-d7ef8b69fa35
                © 2017
                History

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