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首页> 外文期刊>Surface Science >The growth of protective ultra-thin alumina layers on γ-TiAl(111) intermetallic single-crystal surfaces
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The growth of protective ultra-thin alumina layers on γ-TiAl(111) intermetallic single-crystal surfaces

机译:γ-TiAl(111)金属间单晶表面上保护性超薄氧化铝层的生长

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An XPS and AES study of the early stages of oxidation of γ-TiAl(111) surfaces at 650℃ under 1.0x 10~(-7)-1.0 x 10~(-6) mbar O_2 is reported. The data evidence a first regime of oxidation characterized by the growth of a pure alumina layer followed by a second regime of simultaneous oxidation of both alloying elements. In the first regime, continuous alumina layers from ~0.4 to ~1.5 nm thick have been observed by angle-resolved XPS. The composition of the metallic phase underneath the growing oxide is modified by a depletion of Al and the injection of Al vacancies in the metal during the growth of the transient alumina formed at 650℃. The onset of Ti oxidation was repeatedly observed for a critical concentration in the modified region of the alloy underneath the alumina layer: Ti_(75±2)Al_(25±2) (Ti_(50)Al_(17±2)V(Al)_(33±2)), showing that decreasing the number of Ti-Al bonds in the modified intermetallic region increases the activity of Ti up to a critical point where its oxidation at the oxide/metal interface becomes competitive with that of Al. The growth of Ti~(3+) and Ti~(4+) oxide particles observed above the alumina layer by angle-resolved XPS indicates the transport of titanium cations trough the alumina layer and their subsequent reaction with oxygen at the outer gas/oxide interface. Improving structural ordering in the intermetallic phase slows down the growth kinetics of the alumina layer and the related Al-depletion of the substrate, and increases the resistance of the alloy to the subsequent oxidation of Ti. This is assigned to two combined effects: a slower diffusion of Al in the better ordered metallic phase and the growth of less defective alumina layers allowing to slow down the ionic transport through the oxide. Highly stable and corrosion resistant alloy surfaces covered by a 0.4 nm thick alumina layer have been obtained by slowly oxidizing the alloy at lower partial pressure (< 5.0 x 10~(-10) mbar O_2).
机译:报道了在1.0x 10〜(-7)-1.0 x 10〜(-6)mbar O_2下650℃下γ-TiAl(111)表面在650℃氧化早期的XPS和AES研究。数据证明了以纯氧化铝层生长为特征的第一氧化方式,然后是两种合金元素同时氧化的第二方式。在第一种方法中,通过角度分辨XPS观察到了厚度在〜0.4至〜1.5 nm之间的连续氧化铝层。在650℃形成的过渡氧化铝的生长过程中,生长的氧化物下的金属相的组成通过铝的耗尽和金属中铝的注入来改变。在氧化铝层下面的合金改性区域中的临界浓度下反复观察到Ti氧化的开始:Ti_(75±2)Al_(25±2)(Ti_(50)Al_(17±2)V(Al )_(33±2)),表明减少修饰金属间区域中的Ti-Al键数可将Ti的活性提高到一个临界点,在该临界点处,其在氧化物/金属界面的氧化变得与Al的竞争。通过角度分辨XPS在氧化铝层上方观察到的Ti〜(3+)和Ti〜(4+)氧化物颗粒的生长表明钛阳离子通过氧化铝层的迁移以及它们随后与外部气体/氧化物处的氧反应接口。金属间相中改善的结构有序性减慢了氧化铝层的生长动力学以及基底的相关Al消耗,并且增加了合金对随后的Ti氧化的抵抗力。这归因于两种综合效果:铝在有序金属相中的扩散较慢,缺陷氧化铝层的生长较少,从而减慢了离子通过氧化物的传输。通过在较低的分压(<5.0 x 10〜(-10)mbar O_2)下缓慢氧化合金,已获得了覆盖有0.4 nm厚氧化铝层的高度稳定且耐腐蚀的合金表面。

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