Single-crystal micro/nanostructures and thin films of lamellar molybdenum oxide by solid-state pyrolysis of organometallic derivatives of a cyclotriphosphazene

被引:34
作者
Diaz, Carlos [4 ]
Lavayen, Vladimir [3 ]
O'Dwyer, Colm [1 ,2 ]
机构
[1] Univ Limerick, Dept Phys, Limerick, Ireland
[2] Univ Limerick, Mat & Surface Sci Inst, Limerick, Ireland
[3] Univ Tecn Federico Santa Maria, Dept Fis, Valparaiso 2390123, Chile
[4] Univ Chile, Fac Ciencias, Dept Quim, Santiago, Chile
关键词
Nanostructures; Metal oxides; Organometallic synthesis; Pyrolysis; Battery materials; Intercalation; CHEVREL PHASES; MOO3; METAL; DISPERSION; PRECURSORS; ALPHA-MOO3; NANOBELTS; TRIOXIDE; FRICTION; NITRILE;
D O I
10.1016/j.jssc.2010.05.006
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The solid-state pyrolysis of organometallic derivatives of a cyclotriphosphazene is demonstrated to be a new, simple and versatile solid-state templating method for obtaining single-crystal micro- and nanocrystals of transition and valve metal oxides. The technique, when applied to Mo-containing organometallics N3P3[OC6H4CH2CN center dot Mo(CO)(5)](6) and N3P3[OC6H4CH2CN center dot Mo(CO)(4) py](6), results in stand-alone and surface-deposited lamellar MoO3 single crystals, as determined by electron and atomic force microscopies and X-ray diffraction. The size and morphology of the resulting crystals can be tuned by the composition of the precursor. X-ray photoelectron and infrared spectroscopies indicate that the deposition of highly lamellar MoO3 directly on an oxidized (400 nm SiO2) surface or (100) single-crystal silicon surfaces yields a layered uniphasic single-crystal film formed by cluster diffusion on the surface during pyrolysis of the metal-carbonyl derivatives. For MoO3 in its layered form, this provides a new route to an important intercalation material for high energy density battery materials. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:1595 / 1603
页数:9
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