Curing time-controllable solid-state electrolyte and preparation method thereof
A solid electrolyte and curing time technology, applied in electrolytic capacitors, circuits, capacitors, etc., can solve the problems of uncontrollable curing time, heating, and inconvenient assembly of dye-sensitized solar cells, and achieve the effect of improving photoelectric conversion efficiency
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[0029] The above-mentioned preparation method of a solid electrolyte with controllable curing time comprises the steps of:
[0030] A, iodized salt, iodine and additive are dissolved with organic solvent, make the I of iodized salt - The molar concentration is 0.1-1 mol / L, the I of iodine 3 - The molar concentration is 0.01-0.1 mol / liter, the concentration of the additive is 0.1-1.0 mol / liter, and its organic solvent is 1,4-butyrolactone, N-methylpyrrolidone, ethylene carbonate, propylene carbonate, acetonitrile, One or a combination of two or more of 3-methoxypropionitrile, dimethyl carbonate or diethyl carbonate, after dissolving to obtain a liquid electrolyte;
[0031] B. Dehydrate the polyol used at 110°C-120°C and vacuum pressure of 0.13KPa for about 2 hours. When the temperature is lowered to 70°C to 80°C, add a certain proportion of liquid electrolyte, stir and mix evenly, add the measured polyisocyanate dropwise, and continue to stir and mix evenly. The mass ratio ...
Embodiment 1
[0044] Dissolve 75g of sodium iodide, 12.69g of iodine, 3.96g of pyridine, 6.76g of 4-tert-butylpyridine with 500mL of 1-methyl-2-pyrrolidone to obtain a liquid electrolyte, and its I of sodium iodide - The molar concentration is 0.5 mol / L, the I of iodine 3 - The molar concentration of 4-tert-butylpyridine is 0.05 mole / liter, the molar concentration of pyridine is 0.5 mole / liter, and the molar concentration of 4-tert-butylpyridine is 0.1 mole / liter; the polyethylene glycol (molecular weight is 10000) of weighing 20g is placed in the flask , at 110°C to 120°C, under a vacuum pressure of 0.13KPa, dehydrate for about 2 hours. When the temperature is lowered to 70°C to 80°C, nitrogen gas is introduced, 200g of the prepared liquid electrolyte is added, stirred and mixed evenly, 3.5g of toluene diisocyanate (TDI) is added dropwise, and stirred and mixed evenly, to obtain a polyurethane solid electrolyte precursor solution, which is flow state. Will be in 5×10 -4 mol L -1 Bipyr...
Embodiment 2
[0046] Dissolve 66.83g of lithium iodide, 12.68g of iodine, and 0.79g of pyridine in 500mL of 1,4-butyrolactone to obtain a liquid electrolyte. The I of lithium iodide - The molar concentration is 0.5 mol / L, the I of iodine 3 - The molar concentration of pyridine is 0.05 mol / liter, and the molar concentration of pyridine is 0.1 mol / liter; The polyethylene glycol (molecular weight is 4000) 10.0g, hydroxyl-terminated propylene oxide-dimethylsiloxane-epoxy 4g of propane block copolymer (molecular weight: 6000) was dehydrated for about 2 hours at 120°C and vacuum pressure of 0.13KPa. When the temperature was lowered to 80°C, nitrogen gas was introduced, 180g of the prepared liquid electrolyte was added, 8.7g of toluene diisocyanate TDI was added dropwise, and the stirring and mixing was continued to obtain the polyurethane solid electrolyte precursor solution, which was in a flowing state. Will be in 5×10 -4 mol L -1 Bipyridyl ruthenium dye RuL 2 (NCS) 2 : Nanocrystalline po...
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