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Materials Research

versão impressa ISSN 1516-1439

Mat. Res. v.6 n.3 São Carlos abr./jun. 2003

http://dx.doi.org/10.1590/S1516-14392003000300008 

Effect of viscosity and temperature on the microstructure of BBT thin films

 

 

Gustavo Carneiro da Costa; Alexandre Zirpoli Simões*; Gisele Gasparotto; Maria Aparecida Zaghette; Biljana Stojanovic; Mario Cilense; José Arana Varela

Chemistry Institute, Universidade Estadual Paulista, UNESP 14801-970 Araraquara - SP, Brazil

 

 


ABSTRACT

Thin films of BBT were deposited on silicate and Pt/Ti /SiO2 (111) substrates by spin- coating from the polymeric precursor method (Pechini process). The obtained films were characterized by optical microscopy, X-ray diffraction and atomic force microscopy. The influence of viscosity on the morphology of BBT thin films as well as the influence of temperature on crystallization, morphology and properties of BBTare discussed. Surface roughness and crystallization of these films are strongly dependent on the annealing conditions.

Keywords: BBT, thermal treatment, viscosity


 

 

1. Introduction

In recent years, ferroelectric thin films have attracted much attention for use in nonvolatile applications. High dielectric constant materials are being explored for the next generation of high-density dynamic random-access memory (DRAM) applications because the thickness limit of oxide/nitride is about to be reached. The so-called Aurivillius compounds were discovered in the late 40's1-3, and their basic structural and ferroelectric properties were studied in the early 60's4. The crystal structure of BaBi2Ta2O9, consists of Bi2O2 layers and perovskite-type BaTa2O7 units with double TaO6 octahedral layers. The Aurivillius family of bismuth layered structure compounds, which were first reported 50 years ago, can be described by the general formula (Bi2O2)2+ (Am-1BmO3m+1 )2-, where A = Ba, Pb, Sr, Bi, K or Na; m = 2, 4, or 5 and B = Ti, Nb, Ta1-3, 5-10. Spontaneous polarization in these types of materials is an effect of a combination of both, the displacement of the B cations and a tilting of the BO6 octaedra6. The Curie temperature, Tc, is 210 °C and 110 °C for B = Nb and Ta, respectively. Either BaBi2Nb2O9 or BaBi2Ta2O9 exhibits a broad temperature dependent phase transition5. These materials may be good candidates for nonvolati1e or volati1e memory applications7,8. Currently, PbZrxTi1-xO3 (PZT) is considered a most promising material for ferroelectric random access memory (FRAM) applications. However, one of the major disadvantages in using PZT films for FRAM applications is its high dielectric constant. Additionally, PZT films are known to suffer from significant polarization loss with increasing switching cycles (fatigue) on Pt electrodes. In contrast, bismuth layered structure ferroelectric oxides such as SrBi2Ta2O9-SrBi 2Nb2O9 solid solutions exhibit a low dielectric constant (~300 at 10 kHz), almost no fatigue on Pt electrodes, and very low leakage currents (~10-8 A/cm2 at 100 kV/cm)7,8,10. On the other hand, the properties of the above named materials are strongly influenced by the preparation method.

The polymeric precursors method, among other chemical methods, is well-known in the area of processing thin films for a number of virtues: easier composition control, better homogeneity, low processing temperature (compatible with Si processing), easier fabrication of large area thin films, and low cost9. An intrinsic problem of the solution-based methods is the large volume change that takes place when the liquid solution transforms into the thin solid inorganic oxide film. This volume change can cause cracking in the film during the pyrolysis and sintering process. In general, the appearance of cracks is lower in thinner films. The main reason for this is that in the thinner coatings the adhesion on the interface film-substrate is higher and lateral shrinkage of film is suppressed. When the critical value for thickness of films is reached, the cracks can not be avoided. To obtain crack-free films one has to control the characteristic parameters of the solution, such as: viscosity and ionic concentration, substrate-film adhesion, heating conditions, atmosphere, substrate and withdrawal speed. The differences between thermal expansion coefficients of the film and the substrate also have influenced a role in the process of cracking11. Moreover, the use of clean room processing is advisable in order to avoid cracks and atmosphere contamination. In general, the choice of substrate depends on the intended application. To investigate the integration of BBT materials in ferroelectric random access memory (FRAM), a platinum coated silicon substrate is used8.

This paper describes the preparation of BBT thin films by the polymeric precursors method (so-called Pechini method) and their structural characterization in terms of phase formation, morphology and chemical composition. The BBT films obtained from polymeric precursors are amorphous and post annealing in oxygen atmosphere is necessary. The main objective of this work was to verify the effect of viscosity and temperature on the microstructure of BBT thin films.

 

2. Experimental Procedure

Barium carbonate (BaCO3 - Mallinckrodt - 99.9%), bismuth oxide (Bi2O3 - Baker Analyzed- 99.6%) and tantalum ethoxide (Ta(OC2H5)5 - Alpha-aesar - 99.999%) were used as purchased without further purification. The precursor solutions of barium, bismuth and tantalum were prepared by adding the raw materials into ethylene glycol and citric acid with heating and stirring at 90 °C. The viscosity of the solution was adjusted from 20 to 100 cPs by addition of water using a Brookfield viscosimeter. In order to investigated the influence of viscosity on the microstructure of BBT thin films, the precursor was deposited on glass substrates with 3 layers and annealed at 550 °C for 1 h in oxygen atmosphere. To verify the influence of temperature on the crystallization and microstructure of BBT films, platinum coated silicon was used as a substrate. The 5-layer films were prepared annealing each individual layer. The spinning speed used was 5000 rpm and the films were treated in temperatures ranging from 700 to 800 °C for 2 h. The heating rate was 1 °C/min up to 300 °C and 5 °C/min from 300 °C to 700-800 °C. Phase analysis of the films was performed at room temperature by X-ray diffraction using a Bragg-Brentano diffractometer (Rigaku 20-2000) and CuKa radiation. Atomic force microscopy (AFM - Multi-mode Nanoscope IIIa) was used to obtain a three-dimensional image reconstruction of the sample surface. These images allow for an accurate analysis of the sample surface and the quantification of very important parameters such as grain size and roughness. The thickness of the annealed films was studied using scanning electron microscopy (SEM - Topcon SM-300) observing the transversal section of films. Each value of the thickness obtained by SEM represents an average value of three measurements.

 

3. Results and Discussion

As mentioned above, it is well-known that the control of viscosity, heating condition, thickness and spinning rate, as well as the differences in the thermal expansion coefficients of film and substrate, are very important factors to be considered in the preparation of thin films. In order to investigate the influence of viscosity on the microstructure of BBT thin films, specimens with 20, 40, 80 and 100 cPs were evaluated. The surface characteristics of the films deposited on silicate substrates with 3 layers and annealed at 550 °C for 1 h in oxygen atmosphere were analyzed by optical microscopy, Fig. 1. In order to determine the convenient viscosity to obtain crack-free films the three-layered film was used since the deposition of more layers even for low viscosities usually leads to surface defects.

 

 

Crack-free thin films were obtained and the topographic morphology was homogeneous for the films deposited with viscosity of 20 cPs. On the other hand, for the same conditions of spinning rate and heating rate but for higher viscosities, Fig. 1b-d, various kinds of crack morphologies were observed. For the films deposited with 40 cPs, only some islands of microcracks were present (Fig. 1b). The films obtained with viscosity of 80 cPs have the surface covered with long straight lines of cracks (Fig. 1c). Differently, for the films obtained with viscosity of 100 cPs, short straight lines of cracks were observed (Fig. 1d). These results suggest that the amount of material deposited on the substrate surface influences the microstructure. This study shows that low viscosities are more convenient for the preparation of BBT films with good morphologic characteristics and free of cracks.

Figure 2 shows the dependence of thickness as a function of viscosity for BBT thin films annealed at 550 °C for 1 h in oxygen atmosphere. As discussed previously, for films deposited with viscosities higher than 20 cPs, the appearance of cracks was noticed. This means that the decomposition of organic material in the case of films with higher thickness causes cracks on the surface of substrate. This is not observed for films prepared from solutions with low viscosities because the amount of organic material in the substrate surface is smaller and the appearance of cracks on the film surface was avoided. Bearing in mind that the films prepared with viscosity of 20 cPs showed homogeneous and crack-free surface the influence of temperature on the microstructure of these films was investigated.

 

 

It is important to control the thickness of the layer due to its strong influence on the grain size, dielectric and ferroelectric properties. It was observed that for thinner films interfacial ``dead layers'' could appear at the interface between films and substrate. These layers possess poor dielectric properties, influencing the performance of the device12. These ``dead layers'' are originated from oxygen interdiffusion, chemical reaction, or structural defects at the interfaces and their effect could be suppressed with thickness of films higher than 200 nm. Such thickness could be obtained by multi-layer depositions. To obtain films with thickness higher than 200 nm it was necessary to deposit 5-layer on the platinum-coated silicon substrate.

The X-ray diffraction data for the films with 5 layers deposited on (111) platinum-coated silicon substrates and annealed from 700 to 800 °C for 2 h, are shown in Fig. 3. The main peaks of the BaBi2Ta2O9 crystalline phase were observed after annealing in this temperature range. The characteristic peak for (111) platinum-coated silicon substrates at 2q = 40° is identified in Fig. 3. The increase of temperature improves crystallinity of the BBT phase. The XRD pattern clearly indicates the presence of a small amount of secondary phase (Bi2Pt)at 2q = 32.3° for film treated at 800 °C for 2 h. This phase is originated from an interface reaction between the platinum and bismuth. The measured pattern evidences that the specimen is polycrystalline.

 

 

The average grain size and roughness determined from surface analyses by AFM are shown in Table 1 and in Fig. 4. Due to the higher ionic mobility during the sintering process, the grain growth and densification of the material were observed when the sintering temperature was increased from 700 to 800 °C. Thus, the grain growth is occurring preferentially on the z direction, perpendicular to the substrate surface and, as a consequence, the roughness of film surface increased when the annealing temperature was enhanced from 700 to 800 °C. Therefore, the distance from the substrate base to the top of the grain increases with the grain growth, promoting an increase of the roughness (Fig. 4).

 

 

 

 

4. Conclusions

The best morphologic characteristics were obtained for BBT films deposited from a solution with viscosity of 20 cPs. BBT thin films without preferential orientation and with good crystallinity were obtained on platinum-coated silicon substrates. The roughness increases with the annealing temperature due to the preferential grain growth along the z direction. The annealing temperature influenced on grain growth due to the higher ionic mobility during the sintering process. Crack-free BBT films without secondary phases with surface roughness from 10 to 15 nm can be obtained up to thickness of 400 nm.

 

Acknowledgements

The authors acknowledge the Brazilian agencies CNPq, CAPES and FAPESP for financial support of this work.

 

References

1. Aurivillius, B. Ark. Kemi, v. 1, p. 463, 1949.        [ Links ]

2. Aurivillius, B. Ark. Kemi, v. 1, p. 499, 1949.        [ Links ]

3. Aurivillius, B. Ark. Kemi, v. 2, p. 519, 1950.        [ Links ]

4. Subbarao, E.C. J. Phys. Chem. Solids, v. 23, p. 665, 1962.         [ Links ]

5. Smolenskii, G.A.; Isupov, V.A.; Agranovskaya, A.I. Fiz. Tverd. Tela, v. 3, p. 895, 1961.        [ Links ]

6. Wachsmuth, B.; Zshech, E.; Thomas, N.W.; Brodie, S.G.; Gurman, S.J.; Baker, S.; Bayliss, S.C. Phys. Status Solidi A, v. 135, n. 1, p. 59, 1993.        [ Links ]

7. Araujo. C.Paz de, Cuchiaro, J.D.; McMillan, L.D.; Scott, M.C.; Scott, J.F. Nature, v. 374, p. 627, 1995.        [ Links ]

8. Foschini, C.R.; Joshi, P.C.; Varela, J.A.; Desu, S.B. J. Mater. Res, v. 14, n. 5, p. 1860, 1999.        [ Links ]

9. Paulin Filho, P.I.; Foschini, C.R.; Varela, J.A.; Suchicital, C.T.A. Acta Microscópica, v. 8, Supp. A, 1999.        [ Links ]

10. Desu, S.B.; Vijay, D.P. Mater Sci. Eng, v. B32, p. 83, 1995.        [ Links ]

11. Brinker, C.J.; Hurd, A.J.; Schunk, P.R.; Frye, G.C.; Asley, C.S. J. Non Cryst. Solids, v. 424, p. 147, 1992.        [ Links ]

12. Raymond , M.V.; Smyth, D.M. J. Phys. Chem. Solids, v. 57, p. 1507, 1996.        [ Links ]

 

 

Received: October 18, 2002
Revised: April 13, 2003
Trabalho apresentado no 1º Congresso da Sociedade Brasileira em Materiais, Rio de Janeiro, Julho de 2002.

 

 

*e-mail: alezipo@yahoo.com