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Structural, Morphological, Optical, and Room Temperature Magnetic Characterization on Pure and Sm-Doped ZnO Nanoparticles

机译:纯和SM掺杂ZnO纳米粒子上的结构,形态,光学和室温磁性表征

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Nano crystalline Zn_(1-x)Sm_xO, (0.00 ≤ x ≤ 0.10), were prepared by wet chemical coprecipitation method. The effect of samarium doping on the structural, morphological, optical, and magnetic properties of ZnO nanoparticles was examined by X-ray powder diffraction (XRD), Transmission electron microscopy (TEM), Fourier-transform infrared spectroscopy (FTIR), Ultravioletvisible spectroscopy (UV) and M-H magnetic hysteresis. XRD analysis showed the hexagonal wurtzite structure of ZnO. The absence of Sm_2O_3 as separate phase may be attributed to the complete dissolving of samarium in ZnO lattice. The lattice parameters (a and c) of Zn_(1-x)Sm_xO were calculated and they fluctuated with the increase of Sm doping which indicated that the structure of ZnO was perturbed by the doping of Sm. The crystallite size was computed for all the samples using Debye- Scherrer’s method. The crystallite size decreased with the increase of Sm doping. TEM micrographs revealed that the size and the shape of the ZnO nanocomposites were changed by modifying the doping level of samarium. FTIR analysis spectrum confirmed the formation of ZnO phase and revealed a peak shift between pure and Sm-doped ZnO. The band gap energy and Urbach energy were calculated for Zn_(1-x)Sm_xO, (0.00 ≤ x ≤ 0.10). The band energy gaps of pure and Sm doped ZnO samples are in the range 2.6–2.98 eV. M-H hysteresis inspection, at room temperature, showed that the pure ZnO exhibited a ferromagnetic behavior incorporated with diamagnetic and paramagnetic contributions. Ferromagnetic behavior was reduced for the doped samples with x = 0 01 and x = 0 04. The samples with x = 0 02 and 0.06 ≤ x ≤ 0.10 tend to be superparamagnetic. The saturation magnetization (M_s), the coercivity (H_c), and the retentivity (M_r) were recorded for Zn_(1-x)Sm_xO, (0.00 ≤ x ≤ 0.10).
机译:纳米结晶Zn_(1-X)Sm_xO(0.00≤x≤0.10),通过湿化学共沉淀法制制备。通过X射线粉末衍射(XRD),透射电子显微镜(TEM),傅里叶变换红外光谱(FTIR),紫外等光谱(FTIR)检查钐纳米粒子对结构,形态,光学和磁性的影响ZnO纳米粒子的结构,形态学,光学和磁性性能( UV)和MH磁滞。 XRD分析显示ZnO的六边形湿度结构。没有SM_2O_3作为单独的相位可以归因于ZnO格子中的钐的完全溶解。计算Zn_(1-x)SM_XO的晶格参数(A和C),它们随着SM掺杂的增加而波动,表明ZnO的结构被SM的掺杂扰动。使用Debye-Scherrer的方法计算所有样品的微晶尺寸。随着SM掺杂的增加,微晶尺寸降低。 TEM显微照片显示通过改变钐的掺杂水平来改变ZnO纳米复合材料的尺寸和形状。 FTIR分析光谱证实了ZnO相的形成,并揭示了纯和SM掺杂ZnO之间的峰值。为Zn_(1-x)SM_XO计算带隙能量和URBACH能量,(0.00≤x≤0.10)。纯和SM掺杂ZnO样品的带能差距在2.6-2.98eV的范围内。在室温下,M-H滞后检测表明,纯ZnO表现出与钻石和顺磁贡献的铁磁性行为。掺杂样品的掺杂样品具有X = 0 01和X = 0 04的铁磁性行为。具有X = 0 02和0.06≤x≤0.10的样品往往是超顺磁性的。饱和磁化强度(M_S),矫顽力(H_C)和保持性(M_R)被记录为Zn_(1-x)Sm_xo,(0.00≤x≤0.10)。

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