首页> 外文期刊>Physica, E. Low-dimensional systems & nanostructures >A straightforward approach for the synthesis of nanostructured Y2O3 particles: Synthesis, morphology, microstructure and crystal imperfection
【24h】

A straightforward approach for the synthesis of nanostructured Y2O3 particles: Synthesis, morphology, microstructure and crystal imperfection

机译:用于合成纳米结构Y2O3颗粒的直接方法:合成,形态,微观结构和晶体缺陷

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

A facile and straightforward approach has been implemented for the synthesis of nanostructured Y2O3 particles via sol-gel method from yttrium nitrate solution. The individual effects of calcination temperature, precipitation-chelating agent and precursor concentration on microstructural parameters, crystal defects and morphology of Y2O3 were investigated in detail. The morphology of synthesized nanostructured Y2O3 particles was revealed by scanning electron microscopy (SEM). X-ray diffraction (XRD) and Williamson Hall analysis were used to find out how Y2O3 crystallite size, lattice strain-stress, dislocation density and morphology affect the sol-gel process parameters. Comparative studies for determining crystallite size of particles were carried out by Modified Debye-Scherer and Williamson Hall analysis. A more detailed microstructural analysis and investigation of crystallographic imperfections were conducted by Williamson- Hall (W-H) method. W-H analysis was carried out on Y2O3 particles with spherical shape and sponge morphology for the first time. Results reveal that as calcination temperature is increased from 700 degrees C to 900 degrees C, the crystallite size increases from 37.15 nm to 49.49 nm while lattice strain increases from 8.154 x 10(-4) to 8.696 x 10(-4). It is also found that, an increment in solution concentration from 0.1 mol/L to 0.2 mol/L results in crystallite size decrement from 47.27 nm to 44.37 nm. A further increment from 0.2 mol to 0.4 mol/L leads to crystallize size increase from 44.37 nm to 49.67 nm.
机译:通过来自硝酸钇溶液的溶胶 - 凝胶法合成纳米结构的Y2O3颗粒,实现了一种容易和直接的方法。详细研究了煅烧温度,沉淀 - 螯合剂和前体浓度对微结构参数,晶体缺陷和Y2O3形态的个体效果。通过扫描电子显微镜(SEM)揭示了合成的纳米结构Y2O3颗粒的形态。 X射线衍射(XRD)和Williamson霍尔分析用于了解Y2O3微晶尺寸,晶格应变应力,位错密度和形态学如何影响溶胶 - 凝胶工艺参数。通过改性的Debye-Scherer和WilliaMSON霍尔分析进行确定微晶尺寸的比较研究。通过WilliaMSOn-霍尔(W-H)方法进行了更详细的微观结构分析和对晶体缺陷的研究。 W-H分析在Y2O3颗粒上进行,第一次具有球形和海绵形态。结果表明,随着煅烧温度从700℃升高至900℃,晶格尺寸从37.15nm增加到49.49nm,而晶格应变从8.154×10(-4)增加到8.696×10(-4)。还发现,溶液浓度的增量从0.1mol / L至0.2mol / l导致从47.27nm至44​​.37nm的微晶尺寸减少。从0.2摩尔至0.4mol / L的进一步增量导致结晶尺寸从44.37nm增加到49.67nm。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号