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首页> 外文期刊>Physical Review, B. Condensed Matter >SYNTHESIS OF EPITAXIAL TERNARY CO1-XFEXSI2 SILICIDES WITH CSCL- AND CAF2-TYPE CUBIC STRUCTURES ON SI(111) BY CODEPOSITION TECHNIQUES
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SYNTHESIS OF EPITAXIAL TERNARY CO1-XFEXSI2 SILICIDES WITH CSCL- AND CAF2-TYPE CUBIC STRUCTURES ON SI(111) BY CODEPOSITION TECHNIQUES

机译:通过共沉积技术在SI(111)上合成具有CSCL和CAF2型立方结构的环​​氧三元CO1-XFEXSI2硅化物

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We have grown ternary Co1-xFexSi2 silicide films, about 100 Angstrom thick, by codeposition onto Si(111) held at room temperature in the whole composition range 0 less than or equal to x less than or equal to 1. Low-energy electron diffraction, inelastic medium-energy electron diffraction, x-ray diffraction, x-ray photoelectron diffraction, and photoemission spectroscopy techniques are used to investigate the atomic and electronic structure of these ternary silicides, It is found that the as-deposited films are metallic and adopt an ordered cubic structure of CsCl type with essentially random vacancies, except in Go-rich films (x less than or equal to 0.25) where a tendency toward an ordered vacancy arrangement of the CaF2 type is already visible. Upon annealing at 650 degrees C, these silicides are found to be metastable, but phase separation does not take place. Fe-rich (x greater than or equal to 0.85) films invariably convert into a semiconducting phase with a structure similar to the orthorhombic beta-FeSi2 one. Yet, most interestingly, the cubic structure is preserved for x less than or equal to 0.85, i.e., stabilized when the Co content exceeds about 15%. X-ray diffraction reveals that these phases exhibit partial CaF2 long-range order. The order parameter is close to zero for x=0.85 and increases rapidly with increasing Co content. The data indicate that Fe does not merely substitute for Co atoms in a perfect CaF2-type CoSi2 structure. Several of the Fe and possibly Co atoms preferentially occupy the interstitial octahedral sites of this latter structure even for x less than or equal to 0.50, while for x greater than or equal to 0.75 a local environment essentially similar to that in defected CsCl-type structure is observed for both Fe and Co sites. [References: 33]
机译:通过共沉积到室温下组成的Si(111)上,在整个组成范围内0小于或等于x小于或等于1的情况下,我们已经生长了约100埃厚的三元Co1-xFexSi2硅化物薄膜。 ,非弹性中能电子衍射,x射线衍射,x射线光电子衍射和光发射光谱技术研究了这些三元硅化物的原子和电子结构,发现沉积的膜是金属的,并采用CsCl类型的有序立方结构具有基本上随机的空位,但富Go膜(x小于或等于0.25)中CaF2类型的有序空位排列的趋势已经可见。在650℃下退火时,发现这些硅化物是亚稳态的,但是没有发生相分离。富铁(x大于或等于0.85)膜始终转变为半导体相,其结构类似于正交晶β-FeSi2膜。然而,最令人感兴趣的是,立方结构被保留x小于或等于0.85,即,当Co含量超过约15%时稳定。 X射线衍射表明,这些相表现出部分CaF2的长程有序。对于x = 0.85,阶参数接近于零,并且随着Co含量的增加而迅速增加。数据表明,Fe不仅可以完美地替代CaF2型CoSi2结构中的Co原子。甚至对于x小于或等于0.50而言,几个Fe原子和可能的Co原子仍优先占据后一种结构的间隙八面体位点,而对于x大于或等于0.75而言,局部环境基本上类似于缺陷CsCl型结构中的局部环境。在Fe和Co位点都观察到。 [参考:33]

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