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Electrochemical Oxidation of Ti15Mo Alloy—The Impact of Anodization Parameters on Surface Morphology of Nanostructured Oxide Layers

机译:Ti15Mo合金的电化学氧化 - 阳极氧化参数对纳米结构氧化物层表面形态的影响

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摘要

It is well-known that the structure and composition of the material plays an important role in the processes occurring at the surface. In this paper, a surface morphology of nanostructured oxide layers electrochemically grown on Ti15Mo, tuned by applying different anodization parameters, was investigated in detail. The one-step anodization of Ti15Mo alloy was performed at room temperature in an ethylene glycol-based electrolyte containing 0.11 M NH4F and 1.11 M H2O. Different anodization times (ranging from 5 to 60 min) and applied potentials (40–100 V) were tested, and the surface morphology, elemental content, and crystalline structure were monitored by scanning electron microscopy (SEM), energy dispersive X-ray spectrometry (EDS), and X-ray diffractometry (XRD), respectively. The results showed that contrary to the multistep anodization of titanium foil, the surface morphology of anodic oxide obtained via the one-step process contains the nanoporous outer layer covering the nanotubular structure. What is more, the pore diameter (Dp) and interpore distance (Dint) of such layers exhibit different trends than those observed for anodization of pure titanium. In particular, at a certain potential range, a decrease in both Dp and Dint with increasing potential was observed. However, independently on the used anodization conditions, the elemental content of oxide layers remained similar, showing the amount of molybdenum at c.a. 15 wt.%. Finally, the amorphous nature of as-anodized layers was confirmed, and their optical band-gap was determined from the diffuse reflectance UV–Vis spectra. It was found that Eg is tunable to some extent by changing the anodizing potential. However, further thermal treatment in air at 400 °C resulted in the anatase phase formation that was accompanied by a significant Eg reduction. Therefore, we believe that the presented results will greatly contribute to the understanding of anodic formation of nanostructured functional oxide layers with tunable properties that can be applied in various fields.
机译:众所周知,材料的结构和组成在表面发生的过程中起重要作用。本文详细研究了通过施加不同阳极氧化参数的Ti15Mo上电化学生长的纳米结构氧化物层的表面形态。在含有0.11m NH 4 F和1.11m H 2 O的乙二醇基电解质中在室温下进行Ti15MO合金的一步阳极氧化。测试不同的阳极氧化次数(范围为5至60分钟)和施加电位(40-100V),通过扫描电子显微镜(SEM),能量分散X射线光谱法监测表面形态,元素含量和结晶结构(EDS)和X射线衍射测量(XRD)。结果表明,与钛箔的多步阳极氧化相反,通过一步法获得的阳极氧化物的表面形态含有覆盖纳米管结构的纳米多孔外层。更重要的是,孔径(DP)和中间距离(DINT)的这种层表现出不同于观察到纯钛的阳极氧化的趋势。特别地,在某个潜在范围内,观察到DP和DINT的降低。然而,在使用的阳极氧化条件下独立地,氧化物层的元素含量保持相似,显示在C.a的钼的量。 15重量%。%。最后,确认了AS-阳极氧化层的无定形性质,并从弥漫反射UV-Vis光谱确定它们的光学带状空间。发现例如通过改变阳极氧化潜力来某种程度上在一定程度上进行调谐。然而,在400℃下的空气中的进一步热处理导致锐钛矿相形成,其伴随着显着的例如还原。因此,我们认为,所提出的结果将极大地有助于了解纳米结构官能氧化物层的阳极形成,可在各种领域应用。

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