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Direct preparation of K0.5Na0.5NbO3 powders

机译:直接制备K0.5Na0.5NbO3粉末

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摘要

K0.5Na0.5NbO3 powders have been directly synthesized by an alternative solid-state method. Stoichimometric mixture of ammonium niobium oxalate and C4H4O6KNa· 4H2O were calcined in temperature range from 500 to 800 °C for 3 h. The precursor and calcination products were characterized with respect to stoichiometry, purity, crystalline structure, particle size and powder morphology using X-ray diffraction (XRD), X-ray fluorescence (XRF) spectrometer, scanning electron microscope (SEM), Fourier transform infrared (FTIR) spectra, thermogravimetric (TG) analysis, differential scanning calorimetry (DSC) and UV-Vis diffuse reflectance (UV-Vis) spectroscopy. XRD and XRF results reveal that stoichiometric K0.5Na0.5NbO3 powders could be synthesized by the method. The particle size is about 68 nm for the precursor calcined at 500 °C according to XRD data, which is in good agreement with SEM data. The average band gap energy is estimated to be 3.18 eV by UV-vis diffuse reflectance spectra.
机译:K0.5Na0.5NbO3粉末已通过另一种固态方法直接合成。草酸铌酸铵和C4H4O6KNa·4H2O的化学计量混合物在500至800°C的温度下煅烧3 h。使用X射线衍射(XRD),X射线荧光(XRF)光谱仪,扫描电子显微镜(SEM),傅里叶变换红外光谱仪对前体和煅烧产物的化学计量,纯度,晶体结构,粒度和粉末形态进行表征(FTIR)光谱,热重(TG)分析,差示扫描量热法(DSC)和UV-Vis漫反射光谱(UV-Vis)光谱。 XRD和XRF结果表明,该方法可以合成化学计量的K0.5Na0.5NbO3粉末。根据XRD数据,在500°C下煅烧的前体的粒径约为68 nm,这与SEM数据非常吻合。通过UV-vis漫反射光谱估计平均带隙能量为3.18eV。

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