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首页> 外文期刊>Electrochimica Acta >Passive oxide film characterisation on Al-Cr-Fe and Al-Cu-Fe-Cr complex metallic alloys in neutral to alkaline electrolytes by photo- and electrochemical methods
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Passive oxide film characterisation on Al-Cr-Fe and Al-Cu-Fe-Cr complex metallic alloys in neutral to alkaline electrolytes by photo- and electrochemical methods

机译:用光电化学方法对中性到碱性电解质中的Al-Cr-Fe和Al-Cu-Fe-Cr复合金属合金进行钝化氧化膜表征

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摘要

The formation, chemical composition and especially electrochemical reactivity of the passive oxide formed on the Al_(64.2)Cr_(27.2)Fe_(8.1) (at. %) and Al_(66.9)Cu_(11.6)Fe_(11.6)Cr_(10.6) (at. %) complex metallic alloys (CMAs) were investigated in borate buffer electrolyte of pH8.4 and 0.1 M Na_2SO_4 electrolyte of pH 12. Open Circuit Potential evolution, potentiodynamic and potentiostatic anodic polarisation as well as electrochemical impedance measurements revealed high stability of the investigated materials in the alkaline domain relevant to cathodic areas. The high stability of these phases is attributed to the presence of a passive oxyhydroxide layer consisting of thin chromium oxyhydroxide as outermost layer and an inner aluminium oxyhydroxide layer close to the metal/oxide interface as found by XPS. The semiconducting properties characterised by means of photoelectrochemistry reveal further that the bandgap of the passive oxide on the CMAs corresponds to a less hydrated situation (closer to alumina) compared to the one grown on pure Al, thus supporting the higher stability of the CMAs phases.
机译:在Al_(64.2)Cr_(27.2)Fe_(8.1)(at。%)和Al_(66.9)Cu_(11.6)Fe_(11.6)Cr_(10.6)上形成的钝化氧化物的形成,化学组成,尤其是电化学反应性(at。%)复杂金属合金(CMAs)在pH8.4的硼酸盐缓冲电解质和pH 12的0.1 M Na_2SO_4电解质中进行了研究。开路电势的演变,恒电位和恒电位的阳极极化以及电化学阻抗测量显示出高稳定性。在与阴极区域有关的碱性范围内研究的材料。这些相的高稳定性归因于存在由羟基氧化铬作为最外层的钝化羟基氧化物层和靠近XPS所发现的靠近金属/氧化物界面的内部羟基氧化铝铝层。通过光电化学表征的半导体性质进一步表明,与在纯Al上生长的氧化物相比,CMA上的被动氧化物的带隙对应于较少水合的情况(更接近氧化铝),因此支持了CMAs相的更高稳定性。

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