On the formation of an interface amorphous layer in nanostructured ferroelectric Ba0.8Sr0.2TiO3 thin films integrated on Pt-Si and its effect on the electrical properties

被引:12
|
作者
Silva, J. P. B. [1 ]
Sekhar, K. C. [1 ]
Rodrigues, S. A. S. [1 ]
Pereira, M. [1 ]
Parisini, A. [2 ]
Alves, E. [3 ]
Barradas, N. P. [3 ]
Gomes, M. J. M. [1 ]
机构
[1] Univ Minho, Ctr Phys, P-4710057 Braga, Portugal
[2] CNR IMM Sez Bologna, I-40129 Bologna, Italy
[3] Inst Super Tecn, IST ITN, P-2686953 Sacavem, Portugal
关键词
Pulsed laser deposition; BaTiO3 and titanates; Dielectric properties; Interfacial amorphous layer; PULSED-LASER DEPOSITION; RUTHERFORD BACKSCATTERING SPECTRA; DIELECTRIC-PROPERTIES; DEAD-LAYER; SOL-GEL; THICKNESS; CAPACITORS; CRYSTALLIZATION; DEPENDENCE; CONSTANT;
D O I
10.1016/j.apsusc.2012.11.161
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
The thin films of Ba0.8Sr0.2TiO3 (BST) investigated in this work were produced by pulsed laser deposition at different pulse-repetition frequencies (PRFs). First measurements by X-ray diffraction suggested a crystalline nature of the deposited films. However, scanning transmission electron microscopy and transmission electron microscopy images have revealed that a BST amorphous layer of considerable thickness is formed at the interface between the film and the Pt layer in the films deposited at 10 Hz. Moreover, energy-dispersive X-ray spectroscopy shows that the composition of the BST layer is the same in both the amorphous and the crystalline phases whereas Rutherford backscattering spectrometry measurements have revealed a stoichiometry of the films identical to that of the target. A new interpretation is proposed to explain the formation of this amorphous layer, based on the PRF used during the deposition. Finally, measurements of dielectric and electric properties were performed on as-grown and annealed samples. The results of these measurements are explained by a model, where a low-permittivity amorphous layer is connected in series with the crystalline BST layer. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:136 / 141
页数:6
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