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首页> 外文期刊>Journal of Solid State Chemistry >Investigations of the crystallization mechanism of CrSb and CrSb _2 multilayered films using in-situ X-ray diffraction and in-situ X-ray reflectometry
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Investigations of the crystallization mechanism of CrSb and CrSb _2 multilayered films using in-situ X-ray diffraction and in-situ X-ray reflectometry

机译:原位X射线衍射和原位X射线反射法研究CrSb和CrSb_2多层膜的晶化机理

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Chromium and antimony multilayered films with variable elemental layer thickness were deposited on(1 0 0)-Si substrate cooled with liquid nitrogen. The stoichiometry of the films was adjusted to Cr:Sb=1:1 and 1:2. The thickness of Cr-Sb repeating units of these multifilms was varied between 11.4 and 102.5 ?. Satellite maxima in the X-ray reflectivity curves observed for films in the as-deposited state demonstrate an alternating stacking of the evaporated elements. The reactivity of the superlattice reactants was investigated with temperature dependent in-situ X-ray diffractometry and X-ray reflectometry. The crystallization temperature of CrSb depends on the double-layer thickness and is about 90 °C for a Cr:Sb ratio of 1:1 and double-layer thickness of 53.7 ? where nucleation and crystal formation occurs at the element interfaces, while for a thin double-layer thickness(11.4 ?)first interdiffusion of the elements occurs before crystallization starts, i.e., an amorphous intermediate is formed prior to crystallization of CrSb. A decomposition reaction into CrSb 2 occurs at about 230 °C, and up to about 575 °C, CrSb, CrSb 2 and amorphous Cr coexist. For the ratio Cr:Sb=1:2 and a thin double-layer thickness prior to crystallization of CrSb 2 nano-sized crystallites with a composition near CrSb 2 nucleate and grow. These crystallites are then successively transformed in long-range ordered crystals exhibiting a pronounced preferred orientation. For films with a thicker repeat unit first formation of CrSb is observed which then reacts with elemental Sb yielding crystalline CrSb 2. An activation energy for interdiffusion of Cr and Sb of about 1.8 eV is estimated for a film with Cr:Sb=1:1 exhibiting a double-layer thickness of about 53.7 ? and an energy for crystal growth of about 1.1 eV. For the film with the thinner double-layer thickness of 11.4 ? a lower value of the activation energy for interdiffusion is obtained. For CrSb 2 the energy for crystal growth is about 3.0 eV being significantly larger than for CrSb. Specific resistivity and Hall coefficient measurements were performed for crystalline CrSb and CrSb 2 films. The temperature-dependent resistivity measurement exhibits a metallic behavior for CrSb and semi-conducting properties for CrSb 2.
机译:在液氮冷却的(1 0 0)-Si衬底上沉积元素层厚度可变的铬和锑多层膜。将膜的化学计量调整为Cr:Sb = 1∶1和1∶2。这些多层膜的Cr-Sb重复单元的厚度在11.4和102.5Ω之间变化。在沉积状态下观察到的薄膜在X射线反射率曲线中的卫星最大值表明了蒸发元素的交替堆积。用依赖于温度的原位X射线衍射法和X射线反射法研究了超晶格反应物的反应性。 CrSb的结晶温度取决于双层厚度,对于Cr:Sb为1:1且双层厚度为53.7?的情况,其结晶温度约为90℃。其中在元素界面处发生成核和晶体形成,而对于薄的双层厚度(11.4Ω),在结晶开始之前首先发生元素的相互扩散,即,在CrSb结晶之前形成非晶态中间体。 CrSb 2的分解反应在约230°C发生,直至约575°C,CrSb,CrSb 2和无定形Cr共存。对于Cr∶Sb = 1∶2的比率和在结晶之前具有接近CrSb 2的组成的CrSb 2纳米晶粒的薄的双层厚度成核并生长。然后将这些微晶相继转变成具有明显优选取向的长程有序晶体。对于重复单元较厚的薄膜,首先观察到CrSb的形成,然后与元素Sb反应生成结晶的CrSb2。对于Cr:Sb = 1:1的薄膜,Cr和Sb相互扩散的活化能估计约为1.8 eV。双层厚度约为53.7?晶体生长的能量约为1.1 eV。双层厚度更薄的薄膜为11.4?获得较低的相互扩散活化能值。对于CrSb 2,晶体生长的能量约为3.0 eV,明显大于CrSb的能量。对晶体CrSb和CrSb 2薄膜进行了电阻率和霍尔系数测量。温度相关的电阻率测量结果表明CrSb具有金属性能,而CrSb 2具有半导体性能。

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