Barium strontium titanate (Ba 0.8 Sr 0.2 TiO 3 ) films with good ferroelectricity have been obtained by a developed sol-gel processing, using a 0.05-M spin-on solution. X-ray diffraction and Raman spectroscopy investigations showed that the Ba 0.8 Sr 0.2 TiO 3 film exhibited a tetragonal structure at room temperature. Field-emission scanning electron microscopy measurements revealed that large columnar grains with the size of 100 to 200 nm in the film were formed from the highly dilute spin-on solution with layerby-layer homoepitaxy. Electrical measurements for the prepared Ba 0.8 Sr 0.2 TiO 3 film showed a remnant polarization of 3.5 µC/cm 2 , a coercive field of 53 kV/cm, two distinctive phase transitions, lower dissipation factor, and good insulating properties. These results indicate the sol-gel-derived Ba 0.8 Sr 0.2 TiO 3 film from a 0.05-M solution is suitable for uncooled infrared detector applications. 77.80.Dj; 81.20.Fw; 77.84.Dy Barium strontium titanate (BST) is currently one of the most interesting ferroelectric materials due to its high dielectric constant and composition-dependent Curie temperature (from 30 to 400 K). The latter property makes an excellent infrared response obtainable at room temperature. In recent years, BST films have attracted much attention for their potential device applications such as advanced dynamic random access memories (DRAM) and uncooled infrared detectors [1,2]. Many film growth techniques such as rf-magnetron sputtering, laser ablation, metalorganic chemical vapor deposition [3][4][5], and sol-gel process [6-10] have been employed to fabricate BST films. Compared to other deposition methods, the sol-gel process offers some advantages, such as homogeneity, stoichiometry control, and the ability to coat large and complex area substrates. However, the sol-gel-derived BST films always fail to display pronounced ferroelectric hysteresis loops [6][7][8][9][10]. This makes the sol-gel-derived BST thin films unsuitable for uncooled infrared detector applications. There are several possible reasons for the disappearance or suppression of ferroelectricity of the sol-gel-derived BST films. (i) The critical size for the existence of ferroelectricity of BaTiO 3 (≈ 120 nm [11]) is much larger than that of PbTiO 3 (≈ 7 nm [12]). Tahan et al.
PACS:[6] deposited BST films of various compositions by the sol-gel method from a 0.75-M solution, the grain size of the films ranged from 20 to 50 nm, and no ferroelectricity was present. Similar results were shown in [7][8][9][10]. (ii) The sol-gel deposition of BaTiO 3 films commonly results in polycrystalline, granular films with grain diameters of lower than 70 nm due to random nucleation in the pyrolyzed gel films [10]. This is in contrast to Pb(Ti, Zr)O 3 films, which can easily be grown by the solgel method into a columnar or epitaxial structure, because of heterogeneous nucleation from a nanocrystalline pyrochlore phase into the perovskite phase at the substrate [13]. (iii) The tetragonality (c/a) of BST films decreases with the incr...