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Titania nanotubes prepared by rapid breakdown anodization for photocatalytic decolorization of organic dyes under UV and natural solar light

机译:通过快速击穿阳极氧化制备的二氧化钛纳米管用于在紫外线和自然光下对有机染料进行光催化脱色

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摘要

Titania nanotube (TNT) powder was prepared by rapid breakdown anodization (RBA) in a perchloric acid electrolyte. The photocatalytic efficiency of the as-prepared and powders annealed at temperatures between 250 and 550 °C was tested under UV and natural sunlight irradiation by decolorization of both anionic and cationic organic dyes, i.e., methyl orange (MO) and rhodamine B (RhB), as model pollutants. The tubular structure of the nanotubes was retained up to 250 °C, while at 350 °C and above, the nanotubes transformed into nanorods and nanoparticles. Depending on the annealing temperature, the TNTs consist of anatase, mixed anatase/brookite, or anatase/rutile phases. The bandgap of the as-prepared nanotubes is 3.04 eV, and it shifts towards the visible light region upon annealing. The X-ray photoelectron spectroscopy (XPS) results show the presence of titania and impurities including chlorine on the surface of the TNTs. The atomic ratio of Ti/O remains unchanged for the annealed TNTs, but the concentration of chlorine decreases with temperature. The photoluminescence (PL) indicate high electron-hole recombination for the as-prepared TNTs, probably due to the residual impurities, low crystallinity, and vacancies in the structure, while the highest photocurrent was observed for the TNT sample annealed at 450 °C. The TNTs induce a small degradation of the dyes under UV light; however, contrary to previous reports, complete decolorization of dyes is observed under sunlight. All TNT samples showed higher decolorization rates under sunlight irradiation than under UV light. The highest reaction rate for the TNT samples was obtained for the as-prepared TNT powder sample under sunlight using RhB (κ1 = 1.29 h−1). This is attributed to the bandgap, specific surface area and the crystal structure of the nanotubes. The as-prepared TNTs performed most efficiently for decolorization of RhB and outperformed the reference anatase powder under sunlight irradiation. This could be attributed to the abundance of reactive sites, higher specific surface area, and degradation mechanism of RhB. These RBA TNT photocatalyst powders demonstrate a more efficient use of the sunlight spectrum, making them viable for environmental remediation.Electronic supplementary materialThe online version of this article (10.1186/s11671-018-2591-5) contains supplementary material, which is available to authorized users.
机译:通过在高氯酸电解质中快速击穿阳极氧化(RBA)制备二氧化钛纳米管(TNT)粉末。在紫外线和自然阳光照射下,通过阴离子和阳离子有机染料,即甲基橙(MO)和若丹明B(RhB)的脱色,测试了制备的粉末和在250至550°C之间退火的粉末的光催化效率。 ,作为模型污染物。纳米管的管状结构可在高达250°C的温度下保留,而在350°C及更高温度下,纳米管会转变为纳米棒和纳米颗粒。取决于退火温度,TNT由锐钛矿,锐钛矿/板钛矿混合或锐钛矿/金红石相组成。制备好的纳米管的带隙为3.04eV,退火后它向可见光区域移动。 X射线光电子能谱(XPS)结果表明在TNT表面上存在二氧化钛和包括氯在内的杂质。对于退火的TNT,Ti / O的原子比保持不变,但是氯的浓度随温度降低。光致发光(PL)表明所制备的TNT具有高的电子-空穴复合性,这可能是由于残留杂质,低结晶度和结构中的空位所致,而在450°C退火的TNT样品中观察到了最高的光电流。 TNT在紫外光下会引起染料的少量降解。然而,与以前的报道相反,在阳光下观察到染料完全脱色。所有TNT样品在日光照射下均显示出比在紫外线下更高的脱色率。使用RhB(κ1= 1.29 h -1 )在阳光下获得的TNT粉末样品的TNT样品的最高反应速率。这归因于带隙,比表面积和纳米管的晶体结构。所制备的TNT对RhB的脱色效率最高,在阳光照射下性能优于参考锐钛矿粉末。这可能归因于大量的反应位,较高的比表面积和RhB的降解机理。这些RBA TNT光催化剂粉末展示了更有效地利用太阳光光谱,使其对环境修复具有可行性。电子补充材料本文的在线版本(10.1186 / s11671-018-2591-5)包含补充材料,可通过授权获得用户。

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