Perovskite-like intermediate gel, preparation and method for preparing electronic skin by using perovskite-like intermediate gel
An electronic skin and perovskite technology, applied in thermometers using electrical/magnetic components directly sensitive to heat, using electrical devices, using electromagnetic means, etc., can solve the problems of single sensing function of electronic skin, complex integration process, and electrical conductivity. There are few types of materials, etc., to achieve the effect of simple process, rich sources, and widening selection types.
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specific Embodiment approach 1
[0027] Specific embodiment 1: The perovskite-like intermediate gel of this embodiment is prepared from 200-400 mg of organic halide amine or organic halide amidine, 400-800 mg of tin halide, 1-3 ml of γ-butyrolactone and 0.5-2 ml of toluene into; the organic halide amine is RNH 3 X, or RC(NH 2 ) 2 X, wherein R is an alkyl group, X is Cl, Br or I; the organohalogenated amidine is CH(NH 2 ) 2 X(FAX), wherein R is an alkyl group, X is Cl, Br or I; the tin halide is SnCl 4 , SnBr 4 or SnI 4 .
[0028] In this embodiment, FA is formamidine.
specific Embodiment approach 2
[0029]Specific embodiment 2: The difference between this embodiment and specific embodiment 1 is that the perovskite-like intermediate gel is composed of 260-380 mg organic halide amine, 450-700 mg tin halide, 1.2-2.8 ml γ-butyrolactone and Prepared from 0.8-1.8ml of toluene. Others are the same as in the first embodiment.
specific Embodiment approach 3
[0030] Specific embodiment three: the preparation method of the perovskite-like intermediate gel in this embodiment is realized according to the following steps:
[0031] 200-400 mg of organic amine halides or organic halide amidines, and 400-800 mg of tin halides are ultrasonically dissolved in 1-3 ml of γ-butyrolactone in sequence, then stirred at room temperature for 12 hours, and then placed in toluene atmosphere for 2-5 days to obtain Black gel, that is, the preparation of the perovskite-like intermediate gel is completed; wherein the organic halide amine is RNH 3 X, or RC(NH 2 ) 2 X, wherein R is an alkyl group, X is Cl, Br or I; the organohalogenated amidine is CH(NH 2 ) 2 X(FAX), wherein R is an alkyl group, X is Cl, Br or I; the tin halide is SnCl 4 , SnBr 4 or SnI 4 .
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