Birefringent crystal for UV-visible band, powder and preparation methods thereof
A technology of birefringent crystals and wavelength bands, applied in the field of birefringent crystals and their preparation, cyanurate birefringent crystals and their powder preparation, can solve the problems of small size, inconvenient use, small birefringence, etc., and achieve fast speed Effect
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Embodiment 1
[0020] Embodiment 1, adopt high-temperature solid phase reaction method to prepare Ba 2 (C 3 N 3 o 3 ) CNO crystals:
[0021] Weigh 0.208 g of anhydrous BaCl 2 and 0.203 g of anhydrous KOCN (i.e. BaCl 2 : KOCN=1mmol: 2.5mmol), after mixing evenly, put it into a quartz ampoule of Φ16mm×200mm, and vacuumize the ampoule to 10 -3 Pa is melted and sealed, put into a muffle furnace, and heated to 700K within 5 hours, and after 24 hours of heat preservation, the furnace is closed and cooled to room temperature naturally, and the product is washed with ethanol to obtain Ba 3 (C 3 N 3 o 3 ) 2 Pure phase powder. After that, Ba will be obtained 3 (C 3 N 3 o 3 ) 2 The pure phase powder is placed in a quartz ampoule and the ampoule is evacuated to 10 -3 Pa was melted and sealed, put into a muffle furnace, heated to 893K within 5 hours and kept for 24h, then slowly cooled to 423K at a rate of 3K / h, and finally closed the furnace and naturally cooled to room temperature to ob...
Embodiment 2
[0022] Embodiment 2, adopt high temperature solid state reaction method to synthesize Ba 2 (C 3 N 3 o3 )CNO powder:
[0023] Weigh 3.536 grams of anhydrous BaCl 2 and 2.754 grams of anhydrous KOCN (molar ratio = 1:2), placed in the quartz ampoule of Φ16mm × 200mm after mixing, the ampoule was evacuated to 10 -3 Pa and melted and sealed, put it into a muffle furnace, raised the temperature to 873K at a rate of 40K / h, kept the temperature for 72 hours, and then slowly cooled to room temperature at a rate of 3K / h, and took out the sample after cooling; After the sample is ground, the product can be obtained by washing and filtering with ethanol, and the product is confirmed by X-ray diffraction as follows: figure 2 As shown, it is indeed powdery Ba 2 (C 3 N 3 o 3 ) CNO crystals.
[0024] The preparation method of the invention has the advantages of being simple, easy to implement, reliable and the like, and the obtained product has good uniformity and high purity.
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