Rechargeable Ca batteries offer the advantages of high energy density, low cost, and earth-abundant constituents, presenting a viable alternative to lithium-ion batteries. However, using polymer electrolytes in practical Ca batteries is not often reported, despite its potential to prevent leakage and preserve battery flexibility. Herein, a Ca(BH)-based gel-polymer electrolyte (GPE) is prepared from Ca(BH) and poly(tetrahydrofuran) (pTHF) and tested its performance in Ca batteries. The electrolyte demonstrates excellent stability against Ca-metal anodes and high ionic conductivity. The results of infrared spectroscopy and H and B NMR indicate that the terminal ─OH groups of pTHF reacted with BH anions to form B─H─(pTHF) moieties, achieving cross-linking and solidification. Cyclic voltammetry measurements indicate the occurrence of reversible Ca plating/stripping. To improve the performance at high current densities, the GPE is supplemented with LiBH to achieve a lower overpotential in the Ca plating/stripping process. An all-solid-state Ca-metal battery with a dual-cation (Ca and Li) GPE, a Ca-metal anode, and a LiTiO cathode sustained >200 cycles, confirming their feasibility. The results pave the way for further developing lithium salt-free Ca batteries by developing electrolyte salts with high oxidation stability and optimal electrochemical properties.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11434029 | PMC |
http://dx.doi.org/10.1002/advs.202308318 | DOI Listing |
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