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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Zhang, Fuxiang
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Publications (7/7 displayed)
- 2019Thermal stability and irradiation response of nanocrystalline CoCrCuFeNi high-entropy alloycitations
- 2018A(2)TiO(5) (A = Dy, Gd, Er, Yb) at High Pressure
- 2018Radiation-induced disorder in compressed lanthanide zirconates
- 2015Response of Gd2Ti2O7 and La2Ti2O7 to swift-heavy ion irradiation and annealingcitations
- 2014Swift heavy ion irradiation-induced amorphization of La2Ti2O7citations
- 2014Swift heavy ion irradiation-induced amorphization of $La_2Ti_2O_7$citations
- 2012Swift heavy ion-induced amorphization of $CaZrO_{3}$ perovskitecitations
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article
Swift heavy ion irradiation-induced amorphization of La2Ti2O7
Abstract
<p>Polycrystalline La<sub>2</sub>Ti<sub>2</sub>O<sub>7</sub> powders have been irradiated with 2.0 GeV <sup>181</sup>Ta ions up to a fluence of 1 × 10<sup>13</sup> ions/cm<sup>2</sup>. Radiation-induced structural modifications were analyzed using synchrotron-based X-ray diffraction (XRD), small angle X-ray scattering (SAXS), Raman spectroscopy and transmission electron microscopy (TEM). An increase in the amorphous fraction as a function of fluence was revealed by XRD and Raman analyses and is evidenced by the reduction in intensity of the sharp Bragg maxima from the crystalline regions. Concurrently, diffraction maxima and vibrational absorption bands broaden with the increasing amorphous fraction. The cross-section for the crystalline-to-amorphous transformation (ion tracks) was determined by quantitative analysis of XRD patterns yielding a track diameter of d = 7.2 ± 0.9 nm. Slightly larger track diameters were obtained directly from TEM images (d = 10.6 ± 0.8 nm) and SAXS analysis (d = 10.6 ± 0.3 nm). High-resolution TEM images revealed that single tracks are entirely amorphous without any outer crystalline, disordered shell as found in pyrochlore oxides of the same stoichiometry. The large ratio of ionic radii of the A- and B-site cations (r<sub>A</sub>/r<sub>B</sub> = 1.94) means that disordering over the A- and B-sites is energetically unfavorable.</p>