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首页> 外文期刊>Surface Science >High Resolution X-ray Photoelectron Spectroscopy Study On Initial Oxidation Of 4h-sic(0001)-(3~(1/2) × 3~(1/2))r30° Surface
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High Resolution X-ray Photoelectron Spectroscopy Study On Initial Oxidation Of 4h-sic(0001)-(3~(1/2) × 3~(1/2))r30° Surface

机译:4h-sic(0001)-(3〜(1/2)×3〜(1/2))r30°表面初始氧化的高分辨率X射线光电子能谱研究

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摘要

An initial oxidation dynamics of 4H-SiC(0001)-(3~(1/2) × 3~(1/2))R30° surface has been studied using high resolution X-ray photoelectron spectroscopy and supersonic molecular beams. Clean 4H-SiC(0001)-(3~(1/2) × 3~(1/2))R30° surface was exposed to oxygen molecules with translational energy of 0.5 eV at 300 K. In the first step of initial oxidation, oxygen molecules are immediately dissociated and atomic oxygens are inserted into Si-Si back bonds to form stable oxide species. At this stage, drastic increase in growth rate of stable oxide species by heating molecular beam source to 1400 K was found. We concluded that this increase in growth rate of stable oxide is mainly caused by molecular vibrational excitation. It suggests that the dissociation barrier is located in the exit channel on potential energy hypersurface. A meta-stable molecular oxygen species was found to be adsorbed on a Si-adatom that has two oxygen atoms inserted into the back bonds. The adsorption of the metastable species is neither enhanced nor suppressed by molecular vibrational excitation.
机译:利用高分辨率X射线光电子能谱和超声分子束研究了4H-SiC(0001)-(3〜(1/2)×3〜(1/2))R30°表面的初始氧化动力学。清洁的4H-SiC(0001)-(3〜(1/2)×3〜(1/2))R30°表面在300 K下暴露于转换能量为0.5 eV的氧分子中。在初始氧化的第一步然后,氧分子立即解离,原子氧被插入Si-Si背键中,形成稳定的氧化物。在此阶段,发现通过将分子束源加热到1400 K,可以大幅增加稳定氧化物的生长速率。我们得出的结论是,稳定氧化物生长速率的增加主要是由分子振动激发引起的。这表明解离势垒位于势能超表面上的出口通道中。发现亚稳态分子氧物质吸附在具有两个氧原子插入背键的硅原子上。分子振动激发既不增强也不抑制对亚稳态物质的吸附。

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