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Publications in Scientific Journals:

I. Zeiringer, N. Melnychenko-Koblyuk, A. Grytsiv, E. Bauer, G. Giester, P. Rogl:
"Phase Equilibria, Crystal Chemistry and Physical Properties of Au-Ba-Ge Clathrates";
Journal Of Phase Equilibria And Diffusion, 32 (2011), 115 - 127.



English abstract:
In the Au-Ba-Ge system the clathrate type I solid solution, Ba8Au x Ge46−x−y □ y , extends at 800 C from binary Ba8Ge43□3 (□ is a vacancy) to Ba8Au6Ge40. For the clathrate phase (1 ≤ x ≤ 6) cubic primitive symmetry (space group Pm3n) was confirmed by x-ray powder diffraction assisted by x-ray single crystal analyses of Ba8Au4.6Ge40.3□1.1. The lattice parameters of the solid solution show an almost linear increase with increasing gold content. Site preference from x-ray refinement shows that gold atoms preferably occupy the 6d site in random mixture with Ge and vacancies, which vanish at the solubility limit. Clathrate type ΙX (Ba6Ge25 type) has a maximum solubility of 2.7 at.% gold at 800 C. Phase equlilibria at 800 C are characterized by four ternary phases in the investigated region up to 33.3 at.% barium. The homogeneity range of Ba(Au1−x Ge x )2 (AlB2-type) and BaAu1+x Ge3−x has been established: Ba(Au1−x Ge x )2 extends from BaAu0.5Ge1.5 to BaAu0.9Ge1.1 and BaAu1+x Ge3−x from BaAu1.1Ge2.9 (BaNiSn3-type) to BaAu2.7Ge1.3 (Ce(Ni,Sb)4-type). The crystal structures of two phases in the gold-rich part have been determined from single crystal x-ray data and were found to form new structure types: BaAu3Ge with BaAu3Ge-type (space group P4/nmm, a = 0.6459(2), c = 0.5487(2) nm) and BaAu5+x Ge2−x (x = 0, BaAu5Si2-type, space group Pnma, a = 0.8981(2), b = 0.7106(2) and c = 1.0363(2) nm), the latter revealing with increasing gold content a closely related derivative structure type (BaAu5.3Ge1.7, a=aBaAu5Si2b=bBaAu5Si2c=2cBaAu5Si2). Transport properties and particularly the thermoelectric behavior were studied for Ba8Au6Ge40.


"Official" electronic version of the publication (accessed through its Digital Object Identifier - DOI)
http://dx.doi.org/10.1007/s11669-011-9852-7


Created from the Publication Database of the Vienna University of Technology.