八面体
结晶学
化学
晶体结构
氮化物
单晶
红外光谱学
粉末衍射
X射线晶体学
作者
Lucien Eisenburger,Philipp Strobel,Peter J. Schmidt,Thomas Bräuniger,Jonathan Wright,Eleanor Lawrence Bright,Carlotta Giacobbe,Oliver Oeckler,Wolfgang Schnick
标识
DOI:10.1002/ange.202114902
摘要
We present the first nitridic analogs of micas, namely AESi3P4N10(NH)2 (AE=Mg, Mg0.94Ca0.06, Ca, Sr), which were synthesized under high-pressure high-temperature conditions at 1400 °C and 8 GPa from the refractory nitrides P3N5 and Si3N4, the respective alkaline earth amides, implementing NH4F as a mineralizer. The crystal structure was elucidated by single-crystal diffraction with microfocused synchrotron radiation, energy-dispersive X-ray spectroscopic (EDX) mapping with atomic resolution, powder X-ray diffraction, and solid-state NMR. The structures consist of typical tetrahedra–octahedra–tetrahedra (T-O-T) layers with P occupying T and Si occupying O layers, realizing the rare motif of sixfold coordinated silicon atoms in nitrides. The presence of H, as an imide group forming the SiN4(NH)2 octahedra, is confirmed by SCXRD, MAS-NMR, and IR spectroscopy. Eu2+-doped samples show tunable narrow-band emission from deep blue to cyan (451–492 nm).
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