Adsorbed nitric oxide on iron(110)

C. Klauber, B.G. Baker
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引用次数: 2

Abstract

The adsorption of nitric oxide on an Fe(110) single crystal at temperatures 90–350 K has been investigated by HeI UPS and by Auger spectroscopy. Four adsorption states are detected in UPS depending on the substrate temperature. Molecular absorption states, α1 at 90–110 K and α2 at 110–170 K are observed. The α2 state is preceded by some NO dissociation. A β adsorption state exists over a very wide temperature range of 170–290 K. It consists of NO chemisorbed amidst atomic N and O from the initial dissociation. Nitric oxide was found to initially dissociate at all substrate temperatures above 110 K. The extent of dissociation increased with temperature, being complete at above 300 K (d state). No measurable molecular NO was found to exist above 330 K. The lower temperature adsorption states are shown to undergo an irreversible conversion to the next highest temperature state upon heating the substrate: α1→α2→β→d.

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在铁上吸附一氧化氮(110)
用HeI UPS和俄歇光谱研究了90 ~ 350k温度下Fe(110)单晶对一氧化氮的吸附。根据衬底温度,UPS中检测到四种吸附状态。观察到90 ~ 110 K下α1和110 ~ 170 K下α2的分子吸收态。α2状态发生前有一定程度的NO解离。β吸附态存在于170 ~ 290 K的极宽温度范围内。它由氮原子和氧原子从初始解离中化学吸收的一氧化氮组成。发现一氧化氮在110 K以上的所有底物温度下都能初始解离。解离程度随温度升高而增加,在300 K以上解离完全(d态)。在330k以上没有发现可测量的No分子。温度较低的吸附态在加热底物后发生α1→α2→β→d的不可逆转化。
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