| Home > Publications database > Order–disorder transition in the (1−x)Li $_{2}$ TiO $_{3}$ –xMgO system (0 ≤ x ≤ 0.5) > print |
| 001 | 201679 | ||
| 005 | 20240619092030.0 | ||
| 024 | 7 | _ | |a 10.1039/C1RA00677K |2 doi |
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| 100 | 1 | _ | |a Leu, Lii-Cherng |0 P:(DE-HGF)0 |b 0 |e Corresponding Author |
| 245 | _ | _ | |a Order–disorder transition in the (1−x)Li $_{2}$ TiO $_{3}$ –xMgO system (0 ≤ x ≤ 0.5) |
| 260 | _ | _ | |a London |c 2012 |b RSC Publishing |
| 336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1435555626_10718 |2 PUB:(DE-HGF) |
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| 520 | _ | _ | |a The order–disorder phase transition of magnesium lithium titanate solid–solution (1−x)Li2TiO3–xMgO (0 ≤ x ≤ 0.5) ceramics prepared by conventional solid-state processing has been examined. The phase and structural analysis was carried out using electron diffraction, neutron diffraction and high-resolution transmission electron microscopy. Both electron and neutron diffraction results revealed the onset of an order-to-disorder transition at 0.3 < x < 0.4. Superlattice reflections found in certain regions of x = 0.2 samples and most areas of x = 0.3 samples were caused by a twin structure stabilized by Mg incorporation. Rietveld refinements of neutron diffraction data suggested a random distribution of Mg on the Li 4e sites and equal distribution of Mg on the two Ti 4e sites for x ≤ 0.3. As the Mg content continues to increase, the crystal symmetry transforms from monoclinic to cubic rocksalt. Consequently, the cation ordering on the 8f and 4d sites of the C2/c structure became corrupted and turned into short-range ordering on the 4a sites of a cubic structure with Image ID:c1ra00677k-t1.gif symmetry, resulting in diffuse scattering in electron diffraction patterns. |
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| 700 | 1 | _ | |a Bian, Jianjiang |0 P:(DE-HGF)0 |b 1 |
| 700 | 1 | _ | |a Gout, Delphine |0 P:(DE-HGF)0 |b 2 |
| 700 | 1 | _ | |a Letourneau, Steve |0 P:(DE-HGF)0 |b 3 |
| 700 | 1 | _ | |a Ubic, Rick |0 P:(DE-HGF)0 |b 4 |
| 773 | _ | _ | |a 10.1039/C1RA00677K |g Vol. 2, no. 4, p. 1598 - 1604 |0 PERI:(DE-600)2623224-8 |n 4 |p 1598 - 1604 |t RSC Advances |v 2 |y 2012 |x 2046-2069 |
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