Jarosz Magdalena, Zaraska Leszek, Kozieł Marcin, Simka Wojciech, Sulka Grzegorz D
Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30387 Krakow, Poland.
Faculty of Chemistry, Silesian University of Technology, B. Krzywoustego 6, 44100 Gliwice, Poland.
Nanomaterials (Basel). 2020 Dec 30;11(1):68. doi: 10.3390/nano11010068.
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 NHF and 1.11 M HO. 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 (D) and interpore distance (D) 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 D and D 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 E 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 E 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.
众所周知,材料的结构和组成在表面发生的过程中起着重要作用。在本文中,详细研究了通过施加不同的阳极氧化参数在Ti15Mo上电化学生长的纳米结构氧化层的表面形貌。Ti15Mo合金的一步阳极氧化在室温下于含有0.11 M NHF和1.11 M HO的乙二醇基电解液中进行。测试了不同的阳极氧化时间(5至60分钟)和施加电位(40 - 100 V),并分别通过扫描电子显微镜(SEM)、能量色散X射线光谱仪(EDS)和X射线衍射仪(XRD)监测表面形貌、元素含量和晶体结构。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貌包含覆盖纳米管结构的纳米多孔外层。此外,此类层的孔径(D)和孔间距(D)呈现出与纯钛阳极氧化时不同的趋势。特别是,在一定电位范围内,观察到随着电位增加D和D均减小。然而,无论使用何种阳极氧化条件,氧化层的元素含量保持相似,钼含量约为15 wt.%。最后,证实了阳极氧化层的非晶性质,并从漫反射紫外 - 可见光谱确定了它们的光学带隙。发现通过改变阳极氧化电位,E在一定程度上是可调的。然而,在400°C空气中进一步热处理导致形成锐钛矿相,并伴随着E的显著降低。因此,我们相信所呈现的结果将极大地有助于理解具有可调性能的纳米结构功能氧化层的阳极形成,这些氧化层可应用于各个领域。