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Effect of polymerizing on lithium-ion transport in electrolyte
The effect of polymerizing 1,3-dioxolane (DOL) on the transport properties of the lithium (Li) ions in electrolytes from liquid to gel has been studied. After polymerization, liquid DOL electrolytes (LDOLEs) can form poly(1,3-dioxolane) (PDOL)-based electrolytes (PDOLEs), a gel polymer electrolyte w...
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Published in: | Ionics 2023-02, Vol.29 (2), p.591-601 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The effect of polymerizing 1,3-dioxolane (DOL) on the transport properties of the lithium (Li) ions in electrolytes from liquid to gel has been studied. After polymerization, liquid DOL electrolytes (LDOLEs) can form poly(1,3-dioxolane) (PDOL)-based electrolytes (PDOLEs), a gel polymer electrolyte with DOL as self-plasticizer. The chemical environment of Li
+
ions is investigated with
7
Li nuclear magnetic resonance (NMR) and Raman spectrum. Compared with LDOLEs, the
7
Li NMR peaks of PDOLEs show upfield shift and increased full width at half-maximum, indicating more substantial shielding effect and larger Li
+
solvates. The diffusion coefficients of Li
+
ions (
D
Li
+
) are determined with pulsed field gradient NMR. The
D
Li
+
in PDOLEs decreases about two orders of magnitude than that in LDOLEs. Larger activation enthalpy is needed for PDOLEs than LDOLEs to change the coordination state of Li
+
ions due to the necessity of cooperative movement of several chain segments. The effect of bis(trifluoromethane)sulfonimide lithium salt concentration on the
D
Li
+
is mainly ascribed to the change of mixing entropy (Δ
S
). In PDOLEs, the Δ
S
caused by the concentration variation has a more significant influence on the
D
Li
+
than that in LDOLEs. |
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ISSN: | 0947-7047 1862-0760 |
DOI: | 10.1007/s11581-022-04839-2 |