Details

Autor(en) / Beteiligte

• Römer, S. Rebecca
• Braun, Cordula
• Oeckler, Oliver
• Schmidt, Peter J.
• Kroll, Peter
• Schnick, Wolfgang

Titel

HP-Ca2Si5N8-A New High-Pressure Nitridosilicate: Synthesis, Structure, Luminescence, and DFT Calculations

Ist Teil von

• Chemistry : a European journal, 2008-09, Vol.14 (26), p.7892-7902

Ort / Verlag

Weinheim: WILEY-VCH Verlag

Erscheinungsjahr

2008

Quelle

Wiley Online Library - AutoHoldings Journals

Beschreibungen/Notizen

• HP‐Ca2Si5N8 was obtained by means of high‐pressure high‐temperature synthesis utilizing the multianvil technique (6 to 12 GPa, 900 to 1200 °C) starting from the ambient‐pressure phase Ca2Si5N8. HP‐Ca2Si5N8 crystallizes in the orthorhombic crystal system (Pbca (no. 61), a=1058.4(2), b=965.2(2), c=1366.3(3) pm, V=1395.7(7)×106 pm3, Z=8, R1=0.1191). The HP‐Ca2Si5N8 structure is built up by a three‐dimensional, highly condensed nitridosilicate framework with N[2] as well as N[3] bridging. Corrugated layers of corner‐sharing SiN4 tetrahedra are interconnected by further SiN4 units. The Ca2+ ions are situated between these layers with coordination numbers 6+1 and 7+1, respectively. HP‐Ca2Si5N8 as well as hypothetical orthorhombic o‐Ca2Si5N8 (isostructural to the ambient‐pressure modifications of Sr2Si5N8 and Ba2Si5N8) were studied as high‐pressure phases of Ca2Si5N8 up to 100 GPa by using density functional calculations. The transition pressure into HP‐Ca2Si5N8 was calculated to 1.7 GPa, whereas o‐Ca2Si5N8 will not be adopted as a high‐pressure phase. Two different decomposition pathways of Ca2Si5N8 (into Ca3N2 and Si3N4 or into CaSiN2 and Si3N4) and their pressure dependence were examined. It was found that a pressure‐induced decomposition of Ca2Si5N8 into CaSiN2 and Si3N4 is preferred and that Ca2Si5N8 is no longer thermodynamically stable under pressures exceeding 15 GPa. Luminescence investigations (excitation at 365 nm) of HP‐Ca2Si5N8:Eu2+ reveal a broadband emission peaking at 627 nm (FWHM=97 nm), similar to the ambient‐pressure phase Ca2Si5N8:Eu2+. Turn up the pressure: The synthesis of HP‐Ca2Si5N8 demonstrates that denser ternary nitridosilicates are accessible by high‐pressure methods (see picture). The experiments were paralleled by DFT calculations and the material properties of the new HP‐Ca2Si5N8 were examined.