Flexible and low-cost poly(ethylene oxide) (PEO)-based electrolytes are promising for all-solid-state Li-metal batteries because of their compatibility with a metallic lithium anode. However, the low room-temperature Li-ion conductivity of PEO solid electrolytes and severe lithium-dendrite growth limit their application in high-energy Li-metal batteries. Here we prepared a PEO/perovskite Li 3/8 Sr 7/16 Ta 3/4 Zr 1/4 O 3 composite electrolyte with a Li-ion conductivity of 5.4 × 10 −5 and 3.5 × 10 −4 S cm −1 at 25 and 45 °C, respectively; the strong interaction between the F − of TFSI − (bis-trifluoromethanesulfonimide) and the surface Ta 5+ of the perovskite improves the Li-ion transport at the PEO/perovskite interface. A symmetric Li/composite electrolyte/Li cell shows an excellent cyclability at a high current density up to 0.6 mA cm −2 . A solid electrolyte interphase layer formed in situ between the metallic lithium anode and the composite electrolyte suppresses lithium-dendrite formation and growth. All-solid-state Li|LiFePO 4 and high-voltage Li|LiNi 0.8 Mn 0.1 Co 0.1 O 2 batteries with the composite electrolyte have an impressive performance with high Coulombic efficiencies, small overpotentials, and good cycling stability. 
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                            Solid Electrolytes for Li−S Batteries: Solid Solutions of Poly(ethylene oxide) with LixPON- and LixSiPON-Based Polymers
                        
                    
    
            We report here efforts to synthesize free-standing, dry polymer electrolytes that exhibit superior ionic conductivities at ambient for Li−S batteries. Co-dissolution of poly(ethylene oxide) (PEO) (Mn 900k) with LixPON and LixSiPON polymer systems at a ratio of approximately 3:2 followed by casting provides transparent, solid-solution films 25−50 μm thick, lowering PEO crystallinity, and providing measured impedance values of 0.1−2.8 × 10−3 S/cm at ambient. These values are much higher than simple PEO/Li+ salt systems. These solid-solution polymer electrolytes (PEs) are (1) thermally stable to 100 °C; (2) offer activation energies of 0.2−0.5 eV; (3) suppress dendrite formation; and (4) enable the use of lithium anodes at current densities as high as 3.5 mAh/cm2. Galvanostatic cycling of SPAN/PEs/Li cell (SPAN = sulfurized, carbonized polyacrylonitrile) shows discharge capacities of 1000 mAh/gsulfur at 0.25C and 800 mAh/gsulfur at 1C with high coulumbic efficiency over 100 cycles. 
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                            - Award ID(s):
- 1926199
- PAR ID:
- 10357014
- Date Published:
- Journal Name:
- ACS applied materials interfaces
- Volume:
- 12
- ISSN:
- 1944-8252
- Page Range / eLocation ID:
- 30353-30364
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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