High-pressure high-temperature synthesis of novel binary and ternary nitride phases of group 4 and 14 elements

Dzivenko, D. A. ; Horvath-Bordon, E. ; Zerr, A. ; Miehe, G. ; Kroll, P. ; Boehler, R. ; McMillan, P. F. ; Riedel, R. :
High-pressure high-temperature synthesis of novel binary and ternary nitride phases of group 4 and 14 elements.
[Online-Edition: http://dx.doi.org/10.1088/1742-6596/121/6/062003]
In: Journal of Physics: Conference Series, 121 (6) 062003. ISSN 1742-6596
[Artikel] , (2008)

Offizielle URL: http://dx.doi.org/10.1088/1742-6596/121/6/062003

Kurzbeschreibung (Abstract)

Our recent experiments on high-pressure high-temperature synthesis of novel ternary nitrides of group 4 and 14 elements are presented. Dense carbon nitride imide, C2N2(NH), was synthesized for the first time in a laser heated diamond anvil cell (LH-DAC) at pressures above 27 GPa and temperatures around 2000 K. Based on results of the electron diffraction-, EELS-and SIMS-measurements combined with theoretical calculations the structure of this new C-N-H phase was suggested to be of the defect-wurtzite type. Farther, macroscopic amounts of a new oxynitride of zirconium having cubic Th3P4-type structure, c-Zr2.86(N0.88O0.12)4, were synthesized at high pressures and temperatures using a multi-anvil apparatus. Earlier this structure was observed for binary nitrides of zirconium(IV) and hafnium(IV) synthesized in microscopic amounts in a LH-DAC. The lattice parameter of c-Zr2.86(N0.88O0.12)4 was found to be a0 = 6.7549(1) Å which is slightly larger than that of c-Zr3N4. Isotropic bulk and shear moduli of c-Zr2.86(N0.88O0.12)4 of B0 = 219 GPa and G0 = 96 GPa, respectively, were determined from the compression and nanoindentation measurements. The Vickers microhardness, HV(1), of the porous (about 30 vol. %) sample of c-Zr2.86(N0.88O0.12)4 was measured to be 12 GPa, similar to that of single crystal δ-ZrN.

Typ des Eintrags:	Artikel
Erschienen:	2008
Autor(en):	Dzivenko, D. A. ; Horvath-Bordon, E. ; Zerr, A. ; Miehe, G. ; Kroll, P. ; Boehler, R. ; McMillan, P. F. ; Riedel, R.
Titel:	High-pressure high-temperature synthesis of novel binary and ternary nitride phases of group 4 and 14 elements
Sprache:	Englisch
Kurzbeschreibung (Abstract):	Our recent experiments on high-pressure high-temperature synthesis of novel ternary nitrides of group 4 and 14 elements are presented. Dense carbon nitride imide, C2N2(NH), was synthesized for the first time in a laser heated diamond anvil cell (LH-DAC) at pressures above 27 GPa and temperatures around 2000 K. Based on results of the electron diffraction-, EELS-and SIMS-measurements combined with theoretical calculations the structure of this new C-N-H phase was suggested to be of the defect-wurtzite type. Farther, macroscopic amounts of a new oxynitride of zirconium having cubic Th3P4-type structure, c-Zr2.86(N0.88O0.12)4, were synthesized at high pressures and temperatures using a multi-anvil apparatus. Earlier this structure was observed for binary nitrides of zirconium(IV) and hafnium(IV) synthesized in microscopic amounts in a LH-DAC. The lattice parameter of c-Zr2.86(N0.88O0.12)4 was found to be a0 = 6.7549(1) Å which is slightly larger than that of c-Zr3N4. Isotropic bulk and shear moduli of c-Zr2.86(N0.88O0.12)4 of B0 = 219 GPa and G0 = 96 GPa, respectively, were determined from the compression and nanoindentation measurements. The Vickers microhardness, HV(1), of the porous (about 30 vol. %) sample of c-Zr2.86(N0.88O0.12)4 was measured to be 12 GPa, similar to that of single crystal δ-ZrN.
Titel der Zeitschrift, Zeitung oder Schriftenreihe:	Journal of Physics: Conference Series
Band:	121
(Heft-)Nummer:	6
Verlag:	IOP Publishing
Fachbereich(e)/-gebiet(e):	11 Fachbereich Material- und Geowissenschaften > Materialwissenschaft > Fachgebiet Disperse Feststoffe 11 Fachbereich Material- und Geowissenschaften > Materialwissenschaft 11 Fachbereich Material- und Geowissenschaften
Hinterlegungsdatum:	16 Apr 2012 08:14
Offizielle URL:	http://dx.doi.org/10.1088/1742-6596/121/6/062003
ID-Nummer:	doi:10.1088/1742-6596/121/6/062003
Sponsoren:	We acknowledge financial supports of the Deutsche Forschungsgemeinschaft (Bonn, Germany), We acknowledge financial supports of the Fonds der Chemischen Industrie (Frankfurt, Germany),, We acknowledge financial supports of the Heisenberg-Fellowship program (Germany),, We acknowledge financial supports of the Adolf-Messer-Foundation (Germany), We acknowledge financial supports of the Engineering and Physical Science Research Council (UK)
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