Abstract Chloroaluminate ionic liquids are commonly used electrolytes in rechargeable aluminum batteries due to their ability to reversibly electrodeposit aluminum at room temperature. Progress in aluminum batteries is currently hindered by the limited electrochemical stability, corrosivity, and moisture sensitivity of these ionic liquids. Here, a solid polymer electrolyte based on 1‐ethyl‐3‐methylimidazolium chloride‐aluminum chloride, polyethylene oxide, and fumed silica is developed, exhibiting increased electrochemical stability over the ionic liquid while maintaining a high ionic conductivity of ≈13 mS cm−1. In aluminum–graphite cells, the solid polymer electrolytes enable charging to 2.8 V, achieving a maximum specific capacity of 194 mA h g−1at 66 mA g−1. Long‐term cycling at 2.7 V showed a reversible capacity of 123 mA h g−1at 360 mA g−1and 98.4% coulombic efficiency after 1000 cycles. Solid‐state nuclear magnetic resonance spectroscopy measurements reveal the formation of five‐coordinate aluminum species that crosslink the polymer network to enable a high ionic liquid loading in the solid electrolyte. This study provides new insights into the molecular‐level design and understanding of polymer electrolytes for high‐capacity aluminum batteries with extended potential limits. 
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                            Molecular-level environments of intercalated chloroaluminate anions in rechargeable aluminum-graphite batteries revealed by solid-state NMR spectroscopy
                        
                    
    
            Rechargeable aluminum–graphite batteries are an emerging energy storage technology with great promise: they exhibit high rate performance, cyclability, and a discharge potential of approximately 2 V, while both electrodes are globally abundant, low cost, and inherently safe. The batteries use chloroaluminate-containing electrolytes and store charge in the graphite electrodes when molecular AlCl 4 − anions electrochemically intercalate within them. However, much remains to be understood regarding the ion intercalation mechanism, in part due to challenges associated with characterizing the chloroaluminate anions themselves. Here, we use solid-state 27 Al nuclear magnetic resonance (NMR) spectroscopy to probe the molecular-level electronic and magnetic environments of intercalated chloroaluminate anions at different states-of-charge. The results reveal broad 27 Al NMR signals associated with intercalated AlCl 4 − anions, reflecting high extents of local disorder. The intercalated anions experience a diversity of local environments, many of which are far from the ideal crystalline-like structures often depicted in graphite staging models. Density functional theory (DFT) calculations of the total 27 Al isotropic shifts enable the contributions of chemical shift, ring-current effects, and electric quadrupolar interactions to be disentangled quantitatively. In combination, the solid-state NMR and DFT results reveal the molecular geometries and environments of intercalated AlCl 4 − anions and capture the significant disorder present in intercalated graphite battery electrodes. 
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                            - Award ID(s):
- 1706926
- PAR ID:
- 10232494
- Date Published:
- Journal Name:
- Journal of Materials Chemistry A
- Volume:
- 8
- Issue:
- 31
- ISSN:
- 2050-7488
- Page Range / eLocation ID:
- 16006 to 16017
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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