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纳米结构草酸铜的沉淀:亚结构与生长机制

Precipitation of nanostructured copper oxalate: substructure and growth mechanism.

作者信息

Soare L Cristina, Bowen Paul, Lemaitre Jacques, Hofmann Heinrich

机构信息

Powder Technology Laboratory, Institute of Materials, Ecole Polytechnique Fédérale de Lausanne, CH-1015 Lausanne, Switzerland.

出版信息

J Phys Chem B. 2006 Sep 14;110(36):17763-71. doi: 10.1021/jp0606816.

Abstract

The possibility of controlling materials properties by tailoring their substructure at the nanometer scale is a current topic of great interest. To do so, a fundamental understanding of the growth mechanism is of key importance and an analytical challenge as nanostructured materials are often produced by precipitation methods at high supersaturations where formation kinetics are fast. The current study focuses on the precipitation of copper oxalate, which has been previously shown to produce self-assembled ordered nanostructured particles with the promise of being able to tailor this nanometer substructure. In the current study we investigate in detail the growth mechanism and kinetics of precipitation by using in-situ particle size measurement or by stopping the reaction at various stages and using ex-situ methods. Combining the ex-situ methods of high-resolution scanning electron microscopy, transmission electron microscopy, and X-ray powder diffraction along with the in-situ methods, we were able to follow the growth process from 2 min to 2 weeks. The results in the 2-30 min period lead to the proposal of a core-shell growth model with a poorly ordered core and a well-structured shell of nanosized crystallites (50-70 nm), adding support to the brick-by-brick model previously proposed for this phase of particle growth. Particle evolution over long periods up to 2 weeks show a ripening which produces lens-shaped particles that eliminate the "high" surface energy faces observed in the earlier stages of growth. A more complete growth mechanism for copper oxalate precipitation at moderate supersaturations is proposed similar to recent findings for other self-assembled nanostructured particles.

摘要

通过在纳米尺度上调整材料的亚结构来控制其性能的可能性是当前一个备受关注的话题。要做到这一点,对生长机制的基本理解至关重要,同时也是一项分析挑战,因为纳米结构材料通常是通过在高过饱和度下的沉淀方法制备的,此时形成动力学很快。当前的研究聚焦于草酸铜的沉淀,此前已表明其能产生自组装的有序纳米结构颗粒,有望对这种纳米亚结构进行调整。在当前研究中,我们通过原位粒度测量,或在不同阶段停止反应并采用非原位方法,详细研究了沉淀的生长机制和动力学。结合高分辨率扫描电子显微镜、透射电子显微镜和X射线粉末衍射的非原位方法以及原位方法,我们能够跟踪从2分钟到2周的生长过程。在2 - 30分钟期间的结果促使我们提出了一个核壳生长模型,其核心无序,外壳由纳米尺寸的微晶(50 - 70纳米)构成且结构良好,这为先前针对该颗粒生长阶段提出的逐砖模型提供了支持。长达2周的长时间内颗粒的演化显示出一种熟化现象,产生了透镜状颗粒,消除了在生长早期观察到的“高”表面能面。我们提出了一种在中等过饱和度下草酸铜沉淀的更完整生长机制,类似于最近对其他自组装纳米结构颗粒的研究发现。

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