Ackerbauer, S.-V., Senyshyn, A., Borrmann, H., Burkhardt, U., Ormeci, A., Rosner, H., Schnelle, W., Gamza, Monika, Gumeniuk, R., Ramlau, R., Bischoff, E., Schuster, J. C., Weitzer, F., Leithe-Jasper, A., Tjeng, L. H. and Grin, Yu. (2012) Structural Transformation with “Negative Volume Expansion”: Chemical Bonding and Physical Behavior of TiGePt. Chemistry - A European Journal, 18 (20). pp. 6272-6283. ISSN 09476539
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Official URL: http://dx.doi.org/10.1002/chem.201102401
The synthesis and a joint experimental and theoretical study of the crystal structure and physical properties of the new ternary intermetallic compound TiGePt are presented. Upon heating, TiGePt exhibits an unusual structural phase transition with a huge volume contraction of about 10 %. The transformation is characterized by a strong change in the physical properties, in particular, by an insulator–metal transition. At temperatures below 885 °C TiGePt crystallizes in the cubic MgAgAs (half-Heusler) type (LT phase, space group Fequation image3m, a=5.9349(2) Å). At elevated temperatures, the crystal structure of TiGePt transforms into the TiNiSi structure type (HT phase, space group Pnma, a=6.38134(9) Å, b=3.89081(5) Å, c=7.5034(1) Å). The reversible, temperature-dependent structural transition was investigated by in-situ neutron powder diffraction and dilatometry measurements. The insulator–metal transition, indicated by resistivity measurements, is in accord with band structure calculations yielding a gap of about 0.9 eV for the LT phase and a metallic HT phase. Detailed analysis of the chemical bonding in both modifications revealed an essential change of the Ti–Pt and Ti–Ge interactions as the origin of the dramatic changes in the physical properties.
|Schools:||Faculty of Science and Technology > School of Physical Sciences and Computing|
|Deposited By:||Paul Harrison|
|Deposited On:||07 Oct 2015 08:56|
|Last Modified:||15 Mar 2017 10:41|
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