A kind of lead halide hybrid material and preparation method thereof
A lead chloride and lead bromide technology, applied in the field of fluorescent emitters, can solve the problems of poor luminous stability, instability, and reduced luminous intensity, and achieve high luminous performance and high stability.
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Embodiment 1
[0040] Weigh 0.11g of lead chloride and 0.0344g of trans-1,4-cyclohexanedicarboxylic acid into a 15ml autoclave, add 10ml of a mixed solvent of N,N-dimethylformamide and ethanol, and then add 0.2ml of perchloric acid, followed by ultrasonication for half an hour to make it evenly mixed, then put it into an oven, heat up to 120°C at a rate of 15°C / hour, and react for 72 hours. After the reaction, cool down the system at a rate of 15°C / hour Speed to 20°C, transfer the flaky colorless crystals to a beaker, wash with ethanol three times, and then dry in a constant temperature oven at 60°C.
[0041] The properties of the material obtained in this embodiment are no flaky crystals. Confirmed by single crystal X-ray diffraction characterization, the frame connection structure of the material is as follows: figure 1 As shown, it can be seen that the material possesses a highly distorted two-dimensional lead chloride inorganic layer.
[0042] Material [Pb 2 Cl 2 2+ ][ - o 2 C(C...
Embodiment 2
[0047] Weigh 0.278g of lead chloride and 0.172g of trans-1,4-cyclohexanedicarboxylic acid into a 50ml autoclave, add 20ml of a mixed solvent of N,N-dimethylformamide and ethanol, and then add 200μl perchloric acid, followed by ultrasound for half an hour to make it evenly mixed, then put it in an oven, raise the temperature to 120°C, and react for 72 hours. The flaky colorless crystals were transferred to a beaker, washed three times with ethanol, and then dried in a constant temperature oven at 60°C. The properties of the material obtained in this example are colorless flaky crystals.
Embodiment 3
[0049] Weigh 0.278g of lead chloride and 0.344g of trans-1,4-cyclohexanedicarboxylic acid into a 50ml autoclave, add 30ml of a mixed solvent of N,N-dimethylformamide and ethanol, and then add 200μl perchloric acid, followed by ultrasound for half an hour to make it evenly mixed, then put it in an oven, raise the temperature to 120°C, and react for 72 hours. The flaky colorless crystals were transferred to a beaker, washed three times with ethanol, and then dried in a constant temperature oven at 60°C. The properties of the material obtained in this example are colorless flaky crystals.
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