Nanostructured composites with precipitated silica – Ni crystallites coated by char with carbonized starch

V. Gun'ko, B. Charmas, J. Skubiszewska-Zięba
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Abstract

Hybrid carbons/metals/metal (metalloid) oxides composites could be effective adsorbents for low– and high–molecular weight compounds, polar and nonpolar, gaseous and liquid. The presence of metal nanocrystallites and carbon nanostructures could provide catalytic properties in redox reactions. For more effective use of hybrid composites, their morphological, structural, textural, and adsorption characteristics should be appropriate for target applications and, therefore, well controlled. Therefore, the aim of this study was to synthesize carbon/metal/silica nanostructured composites with varied content of metal (Ni) to control the mentioned characteristics. Precipitated silica Sipernat 50 was selected as a substrate. Potato starch was used as a carbon precursor. Nickel nitrate (Ni(NO3)2·6H2O) of varied amounts was used as a precursor of Ni nanoparticles reduced upon the starch carbonization. After the starch carbonization and Ni reduction, a set of C/Ni/silica samples was studied using atomic force microscopy, X–ray diffraction, X–ray fluorescence spectroscopy, nitrogen and p-nitrophenol adsorption, thermogravimetry, and Raman spectroscopy. The presence of nickel phase results in the formation of smaller but denser packed char nanoparticles. Estimation of possible contribution of pores accessible for nitrogen molecules in silica globules and outer surface of carbon/Ni particles suggests that the carbon phase is porous that provides a significant part of the specific surface area of the composites. Amorphous silica and char phases are characterized by the presence of certain nuclei of radius (R) < 1 nm and 2 nm < R < 10 nm estimated from the XRD patterns using full peak profile analysis with a self–consistent regularization procedure. Ni crystallites are of several sizes, since particle size distributions include two–three peaks in the range of 3–13 nm in radius. The Raman spectra show that the main changes with increasing Ni content are characteristic to sp3 carbon structures (D line) in contrast to the sp2 structures (G line). The pore size distributions (both differential and incremental) demonstrate complex changes in a broad size range due to increasing Ni content in composites. As a whole, changes in the Ni content in nanostructured C/Ni/silica composites allow one to control the morphological, structural, and textural characteristics of the whole materials.
碳化淀粉炭包覆沉淀二氧化硅-镍晶纳米复合材料
杂化碳/金属/金属(类金属)氧化物复合材料可作为低分子量和高分子量化合物、极性和非极性、气体和液体的有效吸附剂。金属纳米晶和碳纳米结构的存在可以为氧化还原反应提供催化性能。为了更有效地利用杂化复合材料,它们的形态、结构、质地和吸附特性应该适合目标应用,因此,要很好地控制。因此,本研究的目的是合成不同金属(Ni)含量的碳/金属/二氧化硅纳米结构复合材料,以控制上述特性。选择沉淀二氧化硅sipernat50作为底物。马铃薯淀粉被用作碳前体。采用不同量的硝酸镍(Ni(NO3)2·6H2O)作为淀粉炭化后还原的纳米镍的前驱体。采用原子力显微镜、x射线衍射、x射线荧光光谱、氮和对硝基苯酚吸附、热重、拉曼光谱等方法对淀粉碳化、Ni还原后的C/Ni/silica样品进行了研究。镍相的存在导致形成更小但更致密的堆积炭纳米颗粒。对二氧化硅球和碳/Ni颗粒外表面氮分子可接近的孔隙的可能贡献的估计表明,碳相是多孔的,提供了复合材料比表面积的重要部分。采用自一致正则化方法对XRD谱图进行全峰谱分析,发现非晶态二氧化硅和炭相存在半径(R) < 1 nm和2 nm < R < 10 nm的核。Ni晶有多种尺寸,因为粒度分布包括2 - 3个半径在3-13 nm范围内的峰。拉曼光谱表明,随着Ni含量的增加,sp3碳结构(D线)的变化明显,而sp2碳结构(G线)的变化明显。由于复合材料中Ni含量的增加,孔隙尺寸分布(包括差异和增量)在广泛的尺寸范围内表现出复杂的变化。总的来说,纳米结构C/Ni/二氧化硅复合材料中Ni含量的变化使人们能够控制整个材料的形态、结构和纹理特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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