Abstract
We present a strategy for enhancing Li+ conduction in block copolymer electrolytes by introducing trace amounts of Li salts into polystyrene-b-poly(ethylene oxide) (PS-b-PEO), wherein Li+ ions preferentially coordinate with the -OH end groups of the PEO chains, resulting in the formation of double primitive cubic (Im3̅m) structures. Compared with TFSI- anions in Li salts, smaller anions (PF6- and BF4-) could facilitate ion localization more effectively, expanding the salt concentration range for developing stable Im3̅m structures. The Im3̅m structures formed in PS-b-PEOs doped with LiBF4 at r = 0.013-0.02 (r ≡ [Li+]/[EO]) exhibited ionic conductivities several times higher than those doped at the conventional level (e.g., r = 0.06). The corresponding morphology factors were more than eight times higher than those of the lamellar-forming electrolytes. Notably, the activation energy value for Li+ conduction in PS-b-PEO with one Li+ ion per entire PEO chain was only 0.012 eV (by Vogel-Fulcher-Tammann), indicating that Li+ transport was less dependent on polymer relaxation. Furthermore, modifying the PEO chain ends with three -PO3H2 groups further strengthened the Li+-mediated end-end interactions and significantly extended the salt concentration range to form Im3̅m structures. In contrast, increasing the number of -OH end groups (such as diols and triols) had minimal effect on stabilizing the network morphologies.
Published Version
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