退火处理对二氧化钛纳米管层行为的影响

Marie Siampiringue, C. Massard, E. Caudron, Y. Sibaud, M. Sarakha, K. Awitor
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引用次数: 2

摘要

在这项工作中,我们研究了退火处理对二氧化钛纳米管层行为的影响。热处理方案实际上是诱导稳定氧化层的关键参数,需要更好地理解。将钛箔在0.4 wt%的氢氟酸溶液中电化学阳极氧化20分钟,制备纳米管层,然后在空气中退火。原位x射线衍射分析,结合热重法,使我们对二氧化钛纳米管层的氧化行为有了一个深入的了解,与散装参考样品相比。在足够稳定的条件下,在700°C下进行12小时的结构研究,以跟踪时间对材料氧化的影响。原位XRD发现,在退火前30分钟,阳极氧化诱导的非晶态氧化层导致锐钛矿和金红石相同时生长,而大块样品氧化导致少量锐钛矿TiO2成核。与散装样品相比,阳极氧化产生的初始非晶态氧化层也是导致结晶延迟的原因。热重分析表明,阳极化样品和本体样品的质量增益呈抛物线形;这种动力学是由金红石外部保护层的形成引起的,如相关的原位XRD衍射图所示。我们记录到二氧化钛纳米管层表现出较低的平均质量增益,因为阳极氧化样品上存在初始无定形氧化层。原位XRD结果也提供了关于块体和纳米结构层在退火处理过程中子层行为的准确信息。锐钛矿晶体主要分布在氧化层-金属界面,金红石晶体主要分布在外界面。采用扫描电镜(SEM)对样品表面形貌进行了表征。为了考察退火后的TiO2纳米管层的光活性,研究了酸性橙7 (AO7)染料溶液和4-氯苯酚在365 nm紫外光照射下的降解。这种二氧化钛纳米管层表现出高效的光催化活性,分析结果证实了其他文献报道的4-氯苯酚的降解机理。
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Impact of Annealing Treatment on the Behaviour of Titanium Dioxide Nanotube Layers
In this work, we study the influence of the annealing treatment on the behaviour of titanium dioxide nanotube layers. The heat treatment protocol is actually the key parameter to induce stable oxide layers and needs to be better understood. Nanotube layers were prepared by electrochemical anodization of Ti foil in 0.4 wt% hydrofluoric acid solution during 20 minutes and then annealed in air atmosphere. In-situ X-ray diffraction analysis, coupled with thermogravimetry, gives us an inside on the oxidation behaviour of titanium dioxide nanotube layers compared to bulk reference samples. Structural studies were performed at 700°C for 12 h in order to follow the time consequences on the oxidation of the material, in sufficient stability conditions. In-situ XRD brought to light that the amorphous oxide layer induced by anodization is responsible for the simultaneous growths of anatase and rutile phase during the first 30 minutes of annealing while the bulk sample oxidation leads to the nucleation of a small amount of anatase TiO2. The initial amorphous oxide layer created by anodization is also responsible for the delay in crystallization compared to the bulk sample. Thermogravimetric analysis exhibits parabolic shape of the mass gain for both anodized and bulk sample; this kinetics is caused by the formation of a rutile external protective layer, as depicted by the associated in-situ XRD diffractograms. We recorded that titanium dioxide nanotube layers exhibit a lower mean mass gain than the bulk, because of the presence of an initial amorphous oxide layer on anodized samples. In-situ XRD results also provide accurate information concerning the sub-layers behavior during the annealing treatment for the bulk and nanostructured layer. Anatase crystallites are mainly localized at the interface oxide layer-metal and the rutile is at the external interface. Sample surface topography was characterized using scanning electron microscopy (SEM). As a probe of the photoactivity of the annealed TiO2 nanotube layers, degradation of an acid orange 7 (AO7) dye solution and 4-chlorophenol under UV irradiation (at 365 nm) were performed. Such titanium dioxide nanotube layers show an efficient photocatalytic activity and the analytical results confirm the degradation mechanism of the 4-chlorophenol reported elsewhere.
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