Solid-state electrolyte and solid-state battery containing same
A solid-state electrolyte and battery technology, which is applied in the manufacture of electrolyte batteries, non-aqueous electrolyte batteries, solid electrolytes, etc. It can solve the problems that all solid-state lithium-ion batteries cannot be assembled, affect the electrochemical performance of solid-state lithium batteries, and lithium ions cannot pass smoothly, etc. problem, to achieve the effect of solving poor interface contact, reducing transmission impedance, and improving interface performance
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Embodiment 1
[0083] Preparation of crown ethers COFs-1:
[0084] S1: In a glove box filled with argon, the LLZTO (Li 6.75 La 3 Zr 1.75 Ta 0.25 o 12 ) the surface of the electrolyte, and then use anhydrous tetrahydrofuran solvent to wash off the residual impurities on the surface of the electrolyte;
[0085] S2: Place the clean LLZTO electrolyte treated in step S1 in a reaction flask containing 0.024 mmol 1,3,6,8-tetrakis-(p-aminophenyl)-pyrene and 10 mL o-dichlorobenzene solution, and Stir at 50°C for 1 hour;
[0086] S3: Add 0.024mmol of B to the above solution 18 C 6 And 0.1mL 6M acetic acid solution, and continue to stir and react at 50°C for 24h;
[0087] S4: The unreacted residue was washed away with anhydrous tetrahydrofuran, and heated at 50° C. for 1 h to remove the residual solvent. ;
[0088] S5: Add a crystallization transition solvent consisting of 13.5 mL of o-dichlorobenzene and 1.5 mL of n-butanol to the COF@LLZTO material prepared in step S4, and simultaneously ad...
Embodiment 2
[0093] Preparation of crown ethers COFs-2:
[0094] S1: In a glove box filled with argon, the LLZTO (Li 6.75 La 3 Zr 1.75 Ta 0.25 o 12 ) the surface of the electrolyte, and then use anhydrous tetrahydrofuran solvent to wash away possible residual impurities on the surface of the electrolyte;
[0095] S2: Place the clean LLZTO electrolyte treated in step S1 in a reaction flask containing 0.024 mmol 1,3,6,8-tetrakis-(p-aminophenyl)-pyrene and 10 mL o-dichlorobenzene solution, and Stir at ℃ for 1 h;
[0096] S3: Add 0.024mmol of B to the above solution 24 C 8 And 0.1mL 6M acetic acid solution, and continue to stir and react at 50°C for 24h;
[0097] S4: wash off the unreacted residue with anhydrous tetrahydrofuran, and heat at 50° C. for 1 h to remove the residual solvent;
[0098] S5: Add a crystallization transition solvent consisting of 13.5 mL of o-dichlorobenzene and 1.5 mL of n-butanol to the COF@LLZTO material prepared in step S4, and simultaneously add 1.5 mL of ...
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