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Oxygen-induced inhibition of noble metal silicide formation: implications for electrode/barrier structures used with perovskite materials

机译:氧诱导的贵金属硅化物形成的抑制:对钙钛矿材料使用的电极/阻挡层结构的影响

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We describe how the inhibitory effect of ambient oxygen on silicide formation may be exploited in designing noble metal electrode structures suitable for perovskite-based memory devices. Reactions of Pt and Ir films with substrates of silicon and tungsten silicide (WSi_(2.8)/Si) were examined after anneals in atmospheric pressure ambients of oxygen or nitrogen at temperatures of 640 deg C for various initial noble metal film thicknesses. Metal/silicon reactions and phase formation were studied by Rutherford Backscattering Spectroscopy, X-ray diffraction, and electrical resistance measurements. While annealing in nitrogen resulted in complete noble metal silicidation in the all samples, some Pt and most to all of the Ir remained after equivalent anneals in oxygen. Oxygen exhibited a greater inhibitory effect on silicidation in thin Ir samples, where no silicide formation was observed. The consistent presence of unreacted noble metal M after oxygen annealing is attributed to the formation of an oxygen-containing M-O-Si barrier which interferes with the silicidation reaction. Qualitative through-film resistance measurements indicate that these in-situ formed M-O-Si barrier layers can be at least moderately conductive, a prerequisite for their possible use as a replacement for deposited barrier materials.
机译:我们描述了如何在设计适用于钙钛矿型存储设备的贵金属电极结构中利用环境氧对硅化物形成的抑制作用。在氧气或氮气的大气压环境中,在640摄氏度的温度下,对各种初始贵金属膜厚度进行退火后,检查了Pt和Ir膜与硅和硅化钨(WSi_(2.8)/ Si)衬底的反应。通过卢瑟福背散射光谱,X射线衍射和电阻测量研究了金属/硅的反应和相的形成。尽管在氮气中退火导致所有样品中的贵金属完全硅化,但在氧气中进行等效退火后,仍保留了一些Pt和大部分(直到全部)Ir。氧气对稀薄的Ir样品中的硅化作用表现出更大的抑制作用,在该样品中未观察到硅化物的形成。氧退火后未反应的贵金属M的一致存在是由于形成了含硅的M-O-Si势垒,它会干扰硅化反应。定性的穿过膜的电阻测量表明,这些原位形成的M-O-Si势垒层可以至少具有中等导电性,这是它们可能用作沉积的势垒材料的替代的前提条件。

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