Metal organic framework laden poly(ethylene oxide) based composite electrolytes for all-solid-state Li-S and Li-metal polymer batteries
In this work, the possibility of employing aluminium terephthalic acid metal organic framework (Al-TPA-MOF)-laden composite polymer membranes as electrolyte for all-solid-state lithium-sulfur (Li-S) and lithium-metal (Li-metal) polymer batteries is explored. The prepared composite polymer electrolyt...
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Veröffentlicht in: | Electrochimica acta 2018-09, Vol.285, p.355-364 |
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Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | In this work, the possibility of employing aluminium terephthalic acid metal organic framework (Al-TPA-MOF)-laden composite polymer membranes as electrolyte for all-solid-state lithium-sulfur (Li-S) and lithium-metal (Li-metal) polymer batteries is explored. The prepared composite polymer electrolytes (CPEs) based on a poly(ethylene oxide) (PEO) network with lithium bis(trifluoromethane)sulfonimide (LiTFSI) and Al-TPA-MOF are mechanically robust and thermally stable up to 270 °C, and provide appreciable ionic conductivity in the order of 0.1 mS cm−1 at 60 °C. The enhanced compatibility of CPEs with the lithium metal anode is attributed to the scavenging effect of Al-TPA-MOF. Laboratory scale all-solid-state Li-S and Li-metal polymer cells are assembled, which deliver specific capacities exceeding 800 and 130 mAh g−1, respectively, and a stable performance upon prolonged cycling even at 60 °C, which is superior to earlier reports on similar systems.
•MOF-laden composite polymer electrolyte (CPE) is proposed for Li-S and Li-metal batteries.•CPE are based on PEO, LiTFSI and Al terephthalic acid MOF (Al-TPA-MOF).•CPE are thermally stable up to >300 °C, with ionic conductivity up to 0.1 mS cm−1 at 60 °C.•Enhanced compatibility with Li metal is attributed to the scavenging effect of Al-TPA-MOF.•Stable cycling in Li-S and Li-metal polymer cells is obtained at 60 °C. |
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ISSN: | 0013-4686 1873-3859 |
DOI: | 10.1016/j.electacta.2018.08.012 |