High resolution x ray diffraction study of phase and domain structures and thermally induced phase transformations in PZN (4 5 9)%PT 3

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High resolution x ray diffraction study of phase and domain structures and thermally induced phase transformations in PZN (4 5 9)%PT 3

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Figure 5.10 (002) RSM taken from the as-polished surface of annealed PZN-4.5%PT, showing the smeared contour lines over the area in the lower 2θ sides of the main (002)R peak despite after annealing at 600 °C for h. The intensity contours are on log scale. 71 (a) PZN-7%PT As-polished surface (c) PZN-8%PT As-polished surface (e) PZN-9%PT As-polished surface Figure 5.11 (b) PZN-7%PT Fractured surface (d) PZN-8%PT Fractured surface (f) PZN-9%PT Fractured surface (a), (c) and (e) (002) RSMs taken from the as-polished surface of PZN-7%PT, PZN-8%PT and PZN-9%PT after annealing at 257 °C for h, respectively. (b), (d) and (f) same as (a), (c) and (e) but taken from the fractured surface. The intensity contours are on log scale. 72 The smeared contour lines over an area of the ω-2θ plane at the lower 2θ side of the main (002)R peak in the (002) RSM (Figure 5.10) indicates that the diffraction effects associated with the polishing processes down to µm remain despite annealing to high temperature. The HR-XRD (002) RSMs were also performed on polished-and-annealed (at 257 °C for h) PZN-7%PT, PZN-8%PT, and PZN-9%PT single crystals. The results are provided in Figures 5.11(a), (c), and (e). To expose the bulk material, the same samples were later fractured into two halves and were again x-rayed. The results are shown in Figures 5.11(b), (d), and (f). The polished-and-annealed bulk PZN-PT single crystals were found to cover with a deformed layer even after heating to above TC, giving rise to smear effect in the x-ray diffraction patterns (Figures 5.11a, c, and e). As a result, the polished surface can hardly reveal any useful structural information of the crystals hence unsuitable for x-ray diffraction studies. It should be emphasized that distinct diffraction peaks were obtained from the fractured surface (Figures 5.11b, d, and f), suggesting that the fractured surface are relatively strain-free bulk structure which are more suitable for x-ray diffraction study. 5.3.2 Electrical resistance 73 The effect of room-temperature poling on the stability of the deformed surface layer was also investigated. Figure 5.12 shows the XRD profiles when a dc E-field of increasing strength was applied to the as-polished sample. This figure shows that the lower 2θ peak is no longer present after the poling field was increased to 1.5 kV/mm. Thus, an appropriate poling can eliminate most of the deformed surface layer. However, such a poling treatment should be carried out with care to avoid a non-R phase or overpoling phenomenon as a result of E-field induced phase transformation in relaxor single crystals [1, 16, 90, 91]. A different result was obtained when poling was applied on annealed samples instead. As shown in Figure 5.13, the lower 2θ peak persisted in the annealed samples even after poling to high fields (up to 1.5 kV/mm). The annealing treatment thus helps stabilize the deformed surface layer such that it becomes more resistant to the poling treatment. 5.4 (a) Summary of main observations The cause for the occurrence of the extremely broad lower 2θ peak adjacent to the main (002)R peak in standard XRD profiles of (001)-orientated PZN-PT single crystals has been examined. This diffraction arises from a surface layer produced by mechanical polishing during the sample preparation stage. 74 Intensity (arb. units) (a) 0.2 kV/mm R (b) 0.7 kV/mm R (c) 1.5 kV/mm R 42 43 44 45 2θ Figure 5.12 Effect of increasing poling field on the lower 2θ peak for as-polished samples without any prior annealing. Note that the lower 2θ peak is largely eliminated after poling to 1.5 kV/mm. Sample thickness is 1mm. 75 Intensity (arb. units) (a) 0.2 kV/mm R (b) 0.7 kV/mm R (c) 1.5 kV/mm R 42 43 44 45 2θ Figure 5.13 Same as Figure 5.12 but for sample annealed at 600 °C for h prior poling treatment. Note the persistence of the lower 2θ peak after poling to 1.5 kV/mm at room condition. Sample thickness is 1mm. 76 (b) High-resolution synchrotron RSMs revealed that this surface layer consisted of highly distorted R phase owing to the soft elastic constants of R. The distorted R phases are microscopic in size, of a wide range of lattice parameters and are stressed in intense compression in the plane of the polished surface. (c) Under the PLM, the surface layer may exhibit parallel domain patterns when the polishing was performed in a given direction but was relatively featureless except regions of slight birefringence when the polishing direction was uncoordinated. (d) This polishing-induced surface layer was fairly resistant to annealing but could be largely eliminated by poling to 0.7-1.5 kV/mm at room temperature. After annealing, it became resistant to poling such that the lower 2θ peak persisted even after poling at 1.5 kV/mm. (e) The present work showed that the diffractions arose from polished surface pertained to surface phase while those from the fractured surface represented the bulk phase. The fractured surfaces are relatively strain-free surface which are suitable for x-ray diffraction study of bulk structure in relaxor ferroelectric single crystals. 77 . R phase owing to the soft elastic constants of R. The distorted R phases are microscopic in size, of a wide range of lattice parameters and are stressed in intense compression in the plane of. poling treatment. 5. 4 Summary of main observations (a) The cause for the occurrence of the extremely broad lower 2θ peak adjacent to the main (002) R peak in standard XRD profiles of (001)-orientated. polishing processes down to 1 µm remain despite annealing to high temperature. The HR-XRD (002) RSMs were also performed on polished -and- annealed (at 257 °C for 1 h) PZN- 7%PT, PZN- 8%PT, and PZN- 9%PT

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