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以高温烧结三聚氰胺制得的CNH化合物为C、N源,与分析纯单质硼粉以一定比例混合,在5.0~5.5 GPa、1 400~1 500 ℃高温高压条件下,经化学反应合成了六角硼碳氮(h-BCN)晶体。用傅立叶变换红外光谱(FTIR)和X射线光电子能谱(XPS)对产物进行了表征,结果表明,得到了含碳量较高的六方结构B0.18C0.66N0.16化合物,成分接近于BC4N,硼、碳、氮是以原子化合的形式存在;XRD分析确定该合成产物具有六角网状结构;SEM测量结果表明,B-C-N晶体具有片状六角形貌,尺寸在1 μm左右。 相似文献
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Cubic boron nitride is synthesized by the reaction of Li3N and B203 under high pressure and high temperature (4.0-5.0 GPa, 1350-1500℃). The minimum pressure of cBN formation is 4.0 GPa. The present condition of cBN formation is clearly lower than the eutectic temperature of Li3BN2 and BN in the Li3N-hBN system (5.5 GPa, 1610℃). The content of cBN in the sample increases, while the content of hBN decreases with the temperature and pressure. The maximum conversion rate (5.0 GPa, 1500℃) is about 34%, which is higher than that in the hBN-Li3N system. The cBN crystals are octahedral or tetrahedral in shape and approximately 20 μm in diameter. 相似文献
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Cubic boron nitride (c-BN) films were deposited on highly-oriented (111) bulk c-BN crystal by using the rf magnetron sputtering method. The growth films are characterized by micro-Raman spectroscopy (μ-RS) and scanning electron microscopy (SEM), The results show that the high crystallization electron transparent c-BN films in thickness of about 10μm are obtained, Island and step growth models are clearly shown. 相似文献
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以高温烧结三聚氰胺制得的CNH化合物为C、N源,与分析纯单质硼粉以一定比例混合,在5.0~5.5 GPa、1 400~1 500℃高温高压条件下,经化学反应合成了六角硼碳氮(h-BCN)晶体。用傅立叶变换红外光谱(FTIR)和X射线光电子能谱(XPS)对产物进行了表征,结果表明,得到了含碳量较高的六方结构B0.18C0.66N0.16化合物,成分接近于BC4N,硼、碳、氮是以原子化合的形式存在;XRD分析确定该合成产物具有六角网状结构;SEM测量结果表明,B-C-N晶体具有片状六角形貌,尺寸在1μm左右。 相似文献
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Chemical Synthesis and Characterization of Flaky h-BCN at High Pressure and High Temperature 下载免费PDF全文
Hexagonal boron carbonitrogen (h-BCN) compound is synthesized from a mixture of boron powder and CNH compound prepared by pyrolysis of melamine (CaH6N6) under high temperature (1400-1500℃) and high pressure (5.0-5.5 GPa). X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy and Raman spec- troscopy are used to determine the chemical composition and bonds of the product. The results show that the product has composition of B0.18C0.64N0.16 (near BC4N) and atomic-level hybrid. X-ray diffraction analysis indicates that the powder has a hexagonal network structure. Scanning and transmission electron microscopy results suggest that h-BCN compound morphology is mainly flaky in width about 1 μm and thickness 200nm. 相似文献
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