Abstract
Single-ion-conducting polymer electrolytes are attractive to use in lithium batteries as the transference number of the lithium cation approaches unity. This helps prevent concentration gradients across the electrolyte, which can result in dendrite formation. The addition of ceramic particles to polymer electrolytes at high loadings can increase the mechanical strength of the polymer, which can also help suppress dendrite formation. Here, a single-ion-conducting polymer electrolyte is blended with lithium-conducting oxide ceramic particles to make a composite electrolyte. This electrolyte is studied in comparison to a composite electrolyte containing freely dissolved lithium salt. It is found that the addition of ceramic particles to the single-ion-conducting polymer can result in increased cation dissociation and consequent increased ionic conductivity. The electrolytes are cycled in lithium symmetrical cells, and it is found that the ceramic-containing electrolytes show increased interfacial stability with the lithium metal compared to the pristine polymer electrolytes. Our findings shed light on how to optimize the polymer host chemistry to form composite electrolytes that can meet the challenging requirements to stabilize the lithium metal anode.
Original language | English |
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Pages (from-to) | 8871-8881 |
Number of pages | 11 |
Journal | ACS Applied Energy Materials |
Volume | 3 |
Issue number | 9 |
DOIs | |
State | Published - Sep 28 2020 |
Funding
This research was primarily sponsored by the U.S. Department of Energy (DOE), Office of Energy Efficiency and Renewable Energy for the Vehicle Technologies Office’s Advanced Battery Materials Research Program (Tien Duong, Program Manager). This research was supported in part by an appointment to the Oak Ridge National Laboratory ASTRO Program, sponsored by the U.S. Department of Energy and administered by the Oak Ridge Institute for Science and Education. DMA experiments were conducted at the Oak Ridge National Laboratory’s Center for Nanophase Materials Sciences (CNMS), which is a DOE Office of Science user facility. The LLTO synthesis was supported by National Science Foundation DMR-1608398. J.L.S. gratefully acknowledges financial support from the NSF via award DMR-1706370 for the synthesis of the monomer.
Funders | Funder number |
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Office of Energy Efficiency and Renewable Energy for the Vehicle Technologies Office | |
National Science Foundation | 1706370, DMR-1706370, DMR-1608398 |
U.S. Department of Energy | |
Oak Ridge Institute for Science and Education |
Keywords
- battery
- ceramic
- composite
- electrolyte
- lithium
- polymer
- single-ion conducting