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Oxidation of Ni(Pt)Si by molecular vs. atomic oxygen

机译:分子氧与原子氧氧化Ni(Pt)Si

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X-ray photoelectron spectroscopy (XPS) has been used to characterize the oxidation of a clean Ni(Pt)Si surface under two distinct conditions: exposure to a mixed flux of atomic and molecular oxygen (O + O_2; P_(O+O2) =5 × 10~(-6)Torr) and pure molecular oxygen (O_2: P_(O_2) =10~(-5)Torr) at ambient temperatures. Formation of the clean, stoichiometric (nickel monosilicide) phase under vacuum conditions results in the formation of a surface layer enriched in PtSi. Oxidation of this surface in the presence of atomic oxygen initially results in formation of a silicon oxide overlayer. At higher exposures, kinetically limited oxidation of Pt results in Pt silicate formation. No passivation of oxygen uptake of the sample is observed for total O + O_2 exposure <8 x 104 L, at which point the average oxide/silicate overlayer thickness is 23 (3) A (uncertainty in the last digit in parentheses). In contrast, exposure of the clean Ni(Pt)Si surface to molecular oxygen only (maximum exposure: 5 × 10~5 L) results in slow growth of a silicon oxide overlayer, without silicate formation, and eventual passivation at a total average oxide thickness of 8(1) A, compared to a oxide average thickness of 17(2) A (no silicate formation) for the as-received sample (i.e., exposed to ambient.) The aggressive silicon oxidation by atomic oxygen, results in Ni-rich silicide formation in the substrate and the kinetically limited oxidation of the Pt.
机译:X射线光电子能谱(XPS)已用于表征两种不同条件下纯净Ni(Pt)Si表面的氧化:暴露于原子和分子氧的混合通量(O + O_2; P_(O + O2) = 5×10〜(-6)Torr)和纯分子氧(O_2:P_(O_2)= 10〜(-5)Torr)。在真空条件下形成清洁的化学计量(单硅化镍)相会导致形成富含PtSi的表面层。在存在原子氧的情况下对该表面的氧化最初导致形成氧化硅覆盖层。在较高的暴露量下,Pt的动力学受限氧化导致形成Pt硅酸盐。对于总的O + O_2暴露量<8 x 104 L,没有观察到样品的氧吸收钝化,此时平均氧化物/硅酸盐覆盖层平均厚度为23(3)A(括号中最后一位的不确定性)。相反,仅将干净的Ni(Pt)Si表面暴露于分子氧中(最大暴露量:5×10〜5 L)会导致氧化硅覆盖层的缓慢生长,而不会形成硅酸盐,并且最终会在总平均氧化物上被钝化样品原样(即暴露于环境中)的平均氧化物厚度为8(1)A,而氧化物的平均厚度为17(2)A(无硅酸盐形成)。基质中富硅化物形成和Pt的动力学受限氧化。

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