排序方式: 共有29条查询结果,搜索用时 15 毫秒
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EXAFS研究Fe-Cu系二元金属的Fe和Cu配位环境随球磨时间及组成的变化情况,结果表明机械合金化方法能扩展Fe和Cu金属的固溶范围并形成纳米尺寸的非平衡亚稳态合金晶粒,Fe80Cu20(160b)中Cn的K吸收谱和RSF出现bcc结构的特征,其Fe-Cu的合金晶粒为bcc结构;Fe60Cu40(160k)中Cu和Fe的RSF都为fcc结构,其合金晶粒的结构与Fe80Cu20的不同,为fcc结构,但合金晶粒中未形成均匀分散的Fe-Cu合金相是Cu略富积于核,Fe偏析于表面的亚稳态结构。 相似文献
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An inter-component epitaxial strain-induced PbTiOa metastable phase is observed in a PbTiO3-GoFe2O4 epitaxial composite film, corresponding to the dielectric anomaly reported previously. High-resolution synchrotron radiation X-ray diffraction and first principles calculation demonstrate the coexistence of different PbTi03 phases, even a possible morphotropie phase boundary in the film, elucidating the underlying microscopic rneehanism of the formation of Pb TiO3 metastable phase. This sheds light on the design and manipulation of electromechanical properties of epitaxial films, through the strain engineering. 相似文献
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利用水热合成法制备了一系列不同晶化时间的核壳结构双功能催化剂[CuO-ZnO-Al2O3]/[HZSM-5],通过X射线衍射(XRD)、扫描电镜(SEM)和能量分散谱(EDS)对催化剂结构进行了表征,并考察了核壳催化剂CO2加氢直接合成二甲醚的反应性能。结果表明,通过水热合成法可在甲醇合成催化剂CuO-ZnO-Al2O3表面包覆一层完整的HZSM-5分子筛膜,形成核壳结构,并且调节晶化时间可以控制分子筛晶粒尺寸及膜厚。与物理混合法制备的传统双功能催化剂相比,核壳结构催化剂合成二甲醚的选择性显著提高,其中晶化时间为3d的催化剂反应性能最为理想,CO2转化率为38.9%,二甲醚选择性达到77.0%。 相似文献
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Activated carbon supported Mo-based catalysts were prepared and reduced under different activation atmospheres, including pure H2, syngas (H2/CO=2/1), and pure CO. The catalysts structures were characterized by X-ray diffraction, X-ray absorption fine structure, and in situ diffuse reflectance infrared Fourier transform spectroscopy. The catalytic performance for the higher alcohol synthesis from syngas was tested. The pure H2 treatment showed a high reduction capacity. The presence of a large amount of metallic Co0. and low valence state Moφ+ (0<φ<2) on the surface suggested a super activity for the CO dissociation and hydrogenation, which promoted hydrocarbons formation and reduced the alcohol selectivity. In contrast, the pure CO-reduced catalyst had a low reduction degree. The Mo and Co species at the catalyst mainly existed in the form of Mo4+ and Co2+. The syngas-reduced catalyst showed the highest activity and selectivity for the higher alcohols synthesis. We suggest that the syngas treatment had an appropriate reduction capacity that is between those of pure H2 and pure CO and led to the coexistence of multivalent Co species as well as the enrichment of Moδ+ on the catalyst''s surface. The synergistic effects between these active species provided a better cooperativity and equilibrium between the CO dissociation, hydrogenation and CO insertion and thus contributed beneficially to the formation of higher alcohols. 相似文献
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In this paper, the X-ray diffraction profiles of multilayer with uncorrelated rough interfaces are directly simulated using kinematic theory of X-ray diffraction. The result shows that the decrease of the reflective intensity caused by the interracial roughness is more severe than that caused by random fluctuation of period of the same degree, and the decrease of the reflective intensity of high order Bragg deffraction is more rapid than that of low order ones. So it is very important to reduce the interracial roughness in the deposition and in the annealing of multilayer films. 相似文献
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本文通过简单的水热法制备了一种CdO-CdS一维纳米棒阵列,并系统地研究了材料的结构、形貌及其光电化学性质和产氢活性. 所得纳米棒为直径100至200 nm的六方柱. 通过优化煅烧温度和时间得到了该实验条件下光电催化性能最优的样品. 在0 V vs. Ag/AgCl偏压下,CdO-CdS光电流密度为6.5 mA/cm2,光电催化产氢活性为240 μmol·cm-2·h-1,几乎是纯CdS的2倍. 该体系的光电催化性能超过了许多已报道的相似体系. 根据材料结构和光电化学性能表征结果,提出了直接z型光催化机理,该机理可以很好地解释光致载流子的高分离效率和优异的氧化还原性能. 相似文献