Structural properties of the titanium dioxide thin films grown by atomic layer deposition at various numbers of reaction cycles

被引:30
作者
Alekhin, A. P. [1 ]
Gudkova, S. A. [1 ]
Markeev, A. M. [1 ]
Mitiaev, A. S. [1 ]
Sigarev, A. A. [1 ]
Toknova, V. F. [1 ]
机构
[1] Moscow Inst Phys & Technol, Dept Gen Chem, Dolgoprudnyi 141700, Moscow Reg, Russia
关键词
Atomic layer deposition; Titanium ethoxide; Titanium methoxide; Titanium dioxide; TIO2; ISOPROPOXIDE; PRECURSOR; EPITAXY;
D O I
10.1016/j.apsusc.2010.06.061
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
A dependence of structural properties of TiO2 films grown on both Si-and Ti-substrates by atomic layer deposition (ALD) at the temperature range of 25-300 degrees C from titanium ethoxide and water on the number of reaction cycles N was investigated using Fourier-transform infrared (FTIR) spectroscopy and X-Ray diffraction (XRD). TiO2 films grown on both Si-and Ti-substrates revealed amorphous structure at low values of N < 400. However, an increase of N up to values 400-3600 resulted in the growth of polycrystalline TiO2 with structure of anatase on both types of substrates and according to XRD-measurements the sizes of crystallites rose with the increase of N. The maximum anatase crystallite size for TiO2 grown on Ti-substrate was found to be on similar to 35% lower in comparing with that for TiO2 grown on Si-substrate. A use of titanium methoxide as a Ti precursor with the ligand size smaller than in case of titanium ethoxide allowed to observe an influence of the ligand size on both the growth per cycle and structural properties of TiO2. The average growth per cycle of TiO2 deposited from titanium methoxide and water (0.052 +/- 0.01 nm/cycle) was essentially higher than that for TiO2 grown from titanium ethoxide and water (0.043 +/- 0.01 nm/cycle). Ligands of smaller sizes were found to promote the higher crystallinity of TiO2 in comparison with the case of using the titanium precursor with ligands of bigger sizes. Crown Copyright (C) 2010 Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:186 / 191
页数:6
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