Crystal material, preparation method of crystal material, and application of crystal material as non-linear optical crystal
A crystal material and crystal structure technology, applied in nonlinear optics, polycrystalline material growth, optics, etc., can solve the problems that cannot be applied in the middle and far infrared range, low laser damage threshold, strong two-photon absorption, etc., and achieve excellent Infrared nonlinear optical performance, nonlinear optical performance improvement, and the effect of simple steps
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Embodiment 1
[0047] The preparation of embodiment 1 powder crystal sample
[0048] Mix A source, Ge source, and Q source evenly, place them in a quartz reaction tube, and evacuate to 10 -4 Pa and use a hydrogen-oxygen flame to melt and seal the quartz reaction tube. Put the quartz reaction tube into the muffle furnace, heat it to the solid solution temperature, and keep it for a period of time. Then the temperature was lowered to 300° C. at a rate of 5° C. / hour, then the heating was stopped, cooled to room temperature naturally, washed with distilled water, and dried to obtain a powder crystal sample of the crystal material.
[0049] The sample number, raw material type, flux type and dosage, solid melting temperature and holding time are shown in Table 1.
[0050] Table 1
[0051]
Embodiment 2
[0052] The preparation of embodiment 2 single crystal sample
[0053] Raw material types and proportioning are the same as each sample in Example 1, and the raw materials are evenly ground and placed in a quartz reaction tube, and vacuumed to 10 -4 Pa and use a hydrogen-oxygen flame to melt and seal the quartz reaction tube. Put the quartz reaction tube into a high-temperature furnace, heat it to 650°C, keep it for 5 hours, then raise the temperature to 950°C and keep it for 24 hours, then cool it down to 300°C at a speed of no more than 5°C / hour, then stop heating and let it cool naturally to room temperature, washed with distilled water, and dried to obtain a single crystal sample of the crystal material (with a particle size between 0.05 mm and 2 mm). Using PII-1 # ~PII-4 # , PIII-1 # ~PIII-4 # The single crystal samples prepared by the ratio of raw materials are correspondingly recorded as SII-1 # ~SII-4 # , SIII-1 # ~SIII-4 # . As per sample PII-1 # The single ...
Embodiment 3
[0054] The structural characterization of embodiment 3 sample
[0055] Sample PII-1 # ~PII-4 # , PIII-1 # ~PIII-4 # and sample SII-1 # ~SII-4 # , SIII-1 # ~SIII-4 # X-ray powder diffraction phase analysis (XRD) after grinding was carried out on MiniFlex II X-ray diffractometer of Rigaku Company, Cu target, Kα radiation source (λ=0.154184nm). The results show that the samples prepared in Examples 1 and 2 are samples with high purity and high crystallinity.
[0056] Among them, PII-1 # ~PII-4 # , PIII-1 # ~PIII-4 # respectively with sample SII-1 # ~SII-4 # , SIII-1 # ~SIII-4 # Have the same powder XRD spectrum. That is, the position and shape of the diffraction peaks are the same, and the relative peak intensity fluctuates within ±5%. Description Sample PII-1 # ~PII-4 # , PIII-1 # ~PIII-4 # respectively with sample SII-1 # ~SII-4 # , SIII-1 # ~SIII-4 # correspond to the same crystal structure.
[0057] Sample SII-1 # ~SII-4 # , SIII-1 # ~SIII-4 # Th...
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