Napruszewska Bogna D, Walczyk Anna, Duraczyńska Dorota, Kryściak-Czerwenka Joanna, Karcz Robert, Gaweł Adam, Nowak Paweł, Serwicka Ewa M
Jerzy Haber Institute of Catalysis and Surface Chemistry, Polish Academy of Sciences, Niezapominajek 8, 30-239 Krakow, Poland.
Faculty of Chemistry, Jagiellonian University Krakow, Gronostajowa 2, 30-387 Krakow, Poland.
Nanomaterials (Basel). 2024 Jun 30;14(13):1130. doi: 10.3390/nano14131130.
Titania nanoparticles (NPs) find wide application in photocatalysis, photovoltaics, gas sensing, lithium batteries, etc. One of the most important synthetic challenges is maintaining control over the polymorph composition of the prepared nanomaterial. In the present work, TiO NPs corresponding to anatase, rutile, or an anatase/rutile/brookite mixture were obtained at 80 °C by an inverse microemulsion method in a ternary system of water/cetyltrimethylammonium bromide/1-hexanol in a weight ratio of 17:28:55. The only synthesis variables were the preparation of the aqueous component and the nature of the Ti precursor (Ti(IV) ethoxide, isopropoxide, butoxide, or chloride). The materials were characterized with X-ray diffraction, scanning/transmission electron microscopy, N adsorption-desorption isotherms, FTIR and Raman vibrational spectroscopies, and diffuse reflectance spectroscopy. The synthesis products differed significantly not only in phase composition, but also in crystallinity, textural properties, and adsorption properties towards water. All TiO NPs were active in the photocatalytic decomposition of rhodamine B, a model dye pollutant of wastewater streams. The mixed-phase anatase/rutile/brookite nanopowders obtained from alkoxy precursors showed the best photocatalytic performance, comparable to or better than the P25 reference. The exceptionally high photoactivity was attributed to the advantageous electronic effects known to accompany multiphase titania composition, namely high specific surface area and strong surface hydration. Among the single-phase materials, anatase samples showed better photoactivity than rutile ones, and this effect was associated, primarily, with the much higher specific surface area of anatase photocatalysts.
二氧化钛纳米颗粒(NPs)在光催化、光伏、气体传感、锂电池等领域有着广泛应用。最重要的合成挑战之一是如何控制所制备纳米材料的多晶型组成。在本工作中,通过反相微乳液法,在水/十六烷基三甲基溴化铵/1 - 己醇重量比为17:28:55的三元体系中,于80℃制得了对应锐钛矿型、金红石型或锐钛矿/金红石/板钛矿混合物的TiO NPs。唯一的合成变量是水相组分的制备以及钛前驱体(四乙基钛、异丙醇钛、丁醇钛或氯化钛)的性质。通过X射线衍射、扫描/透射电子显微镜、N吸附 - 脱附等温线、傅里叶变换红外光谱和拉曼振动光谱以及漫反射光谱对材料进行了表征。合成产物不仅在相组成上有显著差异,在结晶度、织构性质以及对水的吸附性质方面也存在差异。所有TiO NPs对罗丹明B(一种废水中的典型染料污染物)的光催化分解均具有活性。由烷氧基前驱体制得的锐钛矿/金红石/板钛矿混合相纳米粉末表现出最佳的光催化性能,与P25参考样品相当或更优。这种异常高的光活性归因于多相二氧化钛组成所伴随的有利电子效应,即高比表面积和强表面水合作用。在单相材料中,锐钛矿样品的光活性优于金红石样品,这种效应主要与锐钛矿光催化剂高得多的比表面积有关。