Method for improving stability of composite solid electrolyte
A technology of solid electrolyte and enhanced compounding, which is applied in the direction of circuits, electrical components, secondary batteries, etc., can solve problems such as damage to electrolyte stability, aggregation of inorganic solid electrolyte particles, etc. The effect of reunion
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Embodiment 1
[0026] Dry 60g polyethylene oxide (PEO) at 50°C for 18h, LiTi 2 (PO 4 ) 3 and carbon black (Super P) were dried at 120°C for 18h, while the zeolite was heat-treated at 300°C for 24h. The above raw materials were mixed according to the mass ratio of polymer solid electrolyte, inorganic solid electrolyte, carbon black (Super P) and mineral material at 1:2.2:0.02:0.1, and uniformly dispersed in a ball mill for 3 hours. Finally, a composite solid electrolyte membrane with a film thickness of about 1 μm was made from the raw materials by a blending hot pressing method at 120°C.
Embodiment 2
[0028] Dry 60g polyethylene oxide (PEO) at 50°C for 18h, LiTi 2 (PO 4 ) 3 and carbon black (Super P) were dried at 120°C for 18h, while attapulgite was heat-treated at 300°C for 24h. The above raw materials were mixed according to the mass ratio of polymer solid electrolyte, inorganic solid electrolyte, carbon black (Super P) and mineral material at 1:2.2:0.02:0.1, and uniformly dispersed in a ball mill for 3 hours. Finally, a composite solid electrolyte membrane with a film thickness of about 1 μm was made from the raw materials by a blending hot pressing method at 120°C.
Embodiment 3
[0030] Dry 60g polyethylene oxide (PEO) at 50°C for 18h, LiTi 2 (PO 4 ) 3 and carbon black (Super P) were dried at 120°C for 18h, while sepiolite was heat-treated at 300°C for 24h. The above raw materials were mixed according to the mass ratio of polymer solid electrolyte, inorganic solid electrolyte, carbon black (Super P) and mineral material at 1:2.2:0.02:0.1, and uniformly dispersed in a ball mill for 3 hours. Finally, a composite solid electrolyte membrane with a film thickness of about 1 μm was made from the raw materials by a blending hot pressing method at 120°C.
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