Morphological and kinetic studies on hexagonal tungstates

被引:51
作者
Michailovski, Alexej
Kiebach, Ragnar
Bensch, Wolfgang
Grunwaldt, Jan-Dierk
Baiker, Alfons
Komarneni, Sridhar
Patzke, Greta R. [1 ]
机构
[1] ETH, Inorgan Chem Lab, CH-8093 Zurich, Switzerland
[2] Univ Kiel, Inst Inorgan Chem, D-24098 Kiel, Germany
[3] ETH, Inst Chem & Bioengn, CH-8093 Zurich, Switzerland
[4] Penn State Univ, Mat Res Lab 205, University Pk, PA 16802 USA
关键词
D O I
10.1021/cm061020o
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Formation of nanostructured hexagonal alkali tungstates (HTBs) from ammonium metatungstate (AMT) and alkali chlorides has been investigated by a combined strategy encompassing in situ spectroscopic techniques and hydrothermal synthetic studies. They demonstrate how the morphology of the HTBs can be tuned by the straightforward hydrothermal reaction of ammonium metatungstate with the choice of appropriate alkali chlorides. The resulting particle shapes vary from highly anisotropic fibers to multilevel assemblies of hierarchically grown nanorods. Microwave-hydrothermal techniques have further expanded this morphological spectrum. Next, the growth process of alkali HTBs was explored for selected cases by combination of in situ EXAFS and EDXRD investigations. They both show that nucleation starts after a certain induction time and is strongly dependent on the concentration. Though the individual kinetics of alkali HTB formation differ slightly from each other, all alkali cations have a nucleation-controlled growth mechanism in common.
引用
收藏
页码:185 / 197
页数:13
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