| Home > Publications database > Crystal structure and high-pressure stability of hydrothermally grown LiKTmF$_{5}$ > print |
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| 024 | 7 | _ | |a 10.1016/j.solidstatesciences.2014.11.002 |2 doi |
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| 024 | 7 | _ | |a 1873-3085 |2 ISSN |
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| 100 | 1 | _ | |a Grzechnik, Andrzej |0 P:(DE-HGF)0 |b 0 |e Corresponding Author |
| 245 | _ | _ | |a Crystal structure and high-pressure stability of hydrothermally grown LiKTmF$_{5}$ |
| 260 | _ | _ | |a Amsterdam [u.a.] |c 2015 |b Elsevier |
| 336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1428932466_30908 |2 PUB:(DE-HGF) |
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| 520 | _ | _ | |a Single crystals of LiKTmF5 were grown hydrothermally. Its crystal structure was studied with single-crystal X-ray diffraction to 8.6 GPa. The material is monoclinic (P21/c, Z = 4) and does not undergo any phase transition in the pressure range studied here. The analysis of its pseudosymmetry with respect to the minimal k-supergroup C2/m reveals that the deviations of the individual atoms from the respective higher symmetrical positions in C2/m are increasing on compression, i.e., due to the reduction of the unit-cell volume. Such a behaviour is the opposite of the effect of incorporation of various M cations in the LiKMF5 materials (M:Y and rare earths) at atmospheric conditions, since LiKYbF5 and LiKLuF5 with the smallest unit cells crystallize in space group C2/m, while LiLYF5 with a larger unit cell has P21/c symmetry. |
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| 773 | _ | _ | |a 10.1016/j.solidstatesciences.2014.11.002 |g Vol. 39, p. 40 - 44 |0 PERI:(DE-600)2035101-X |p 40 - 44 |t Solid state sciences |v 39 |y 2015 |x 1293-2558 |
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