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水分散性二氧化钛纳米晶体的分子动力学和颗粒形成的原位研究。

In situ investigation of molecular kinetics and particle formation of water-dispersible titania nanocrystals.

作者信息

Garnweitner G, Grote C

机构信息

TU Braunschweig, Institute for Particle Technology, Volkmaroder Str. 5, 38104, Braunschweig, Germany.

出版信息

Phys Chem Chem Phys. 2009 May 21;11(19):3767-74. doi: 10.1039/b821973g. Epub 2009 Apr 2.

Abstract

Metal oxide nanoparticles can be fabricated under high control via nonaqueous sol-gel synthesis. This route has been shown to lead to highly crystalline, uniform nanostructures, which explains the high and growing interest it is receiving. The underlying mechanisms are, however, so far only rudimentarily understood on a molecular scale. Here, we applied in situ FTIR spectroscopy and other techniques to monitor the nonaqueous synthesis of titania nanoparticles that can be easily stabilised in polar solvents and thus, possess high potential for application. A special focus is put on the kinetics of the organic condensation mechanisms enabling the reaction of the precursor to the inorganic nanoparticles. By comparing these kinetics to the process of nanoparticle formation monitored via complementary methods such as TEM and dynamic light scattering, a detailed insight into the principles and mechanisms of nanoparticle formation via the nonaqueous sol-gel synthesis is achieved.

摘要

金属氧化物纳米颗粒可以通过非水溶胶 - 凝胶合成法在高度可控的条件下制备。已表明该方法可得到高度结晶、均匀的纳米结构,这解释了它正受到的高度且不断增长的关注。然而,到目前为止,其潜在机制在分子尺度上仅得到初步理解。在此,我们应用原位傅里叶变换红外光谱法和其他技术来监测二氧化钛纳米颗粒的非水合成,该纳米颗粒可轻松稳定在极性溶剂中,因此具有很高的应用潜力。特别关注的是有机缩合机制的动力学,它使前驱体与无机纳米颗粒发生反应。通过将这些动力学与通过诸如透射电子显微镜(TEM)和动态光散射等互补方法监测的纳米颗粒形成过程进行比较,深入了解了通过非水溶胶 - 凝胶合成法形成纳米颗粒的原理和机制。

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