氧化亚氮与锗表面的相互作用

R.D Iyengar , A.C Zettlemoyer
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引用次数: 5

摘要

在10-300 torr和200-400°C的温度范围内,研究了氧化亚氮与n型和p型锗实际(氧化包覆)表面的相互作用。n型样品比p型样品更能促进分解。在所有研究的案例中,质谱仪都检测不到分解过程中产生的一丝氧气;显然,氧被吸收到进一步形成的氧化膜中。氧预处理降低了锗与氧化亚氮的相互作用程度。富集34%的15N14N16O的实验清楚地表明,分解机制主要是NO键断裂,释放一个氮分子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The interaction of nitrous oxide with germanium surfaces

The interaction of nitrous oxide with real (oxide-coated) surfaces of both n- and p-type germanium has been investigated in the range of 10–300 torr and 200–400°C. The n-type samples promoted greater decomposition than the p-type samples. In all cases studied, not a trace of oxygen resulting from the decomposition could be detected in a mass spectrometer; obviously, the oxygen was incorporated in further oxide film formation. Pretreatment of germanium with oxygen decreased the extent of its interaction with nitrous oxide.

Experiments with a 34% enriched 15N14N16O clearly showed that the decomposi tion mechanism primarily consists of the rupture of the NO bond to set a nitrogen molecule free.

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