Synthesis and crystal structure of novel Ruddlesden–Popper strontium niobium oxynitrides

G. Tobías , J. Oró-Solé , D. Beltrán-Porter , A. Fuertes
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引用次数: 14

Abstract

The family (SrO)(SrNbO2-xN)n is the first example of Ruddlesden-Popper strontium niobium oxynitrides and provides layered structures to obtain mixed valence niobium compounds with a variety of oxidation states and transport properties. We have prepared members with n=1 (Sr2NbO3N) and n=2 (Sr3Nb2O5N2) by solid state reaction of Nb2O5 and SrCO3 at 900–1050 °C under ammonia flow. These compounds crystallize in the I4/mmm space group and show a range of anionic stoichiometry that together with the N/O ratio determines the formal oxidation state for niobium and therefore the resultant physical properties. Samples of the n=1 member show mixed valence Nb5+/Nb4+ and are paramagnetic and very resistive at room temperature. This behavior may be understood by considering electron localization due to N/O disorder.

新型Ruddlesden-Popper锶铌氧氮化物的合成与晶体结构
家族(SrO)(SrNbO2-xN)n是Ruddlesden-Popper锶铌氧氮化物的第一个例子,并提供层状结构来获得具有各种氧化态和传输性质的混合价态铌化合物。用Nb2O5和SrCO3在900 ~ 1050℃的氨流条件下固相反应,制备了n=1 (Sr2NbO3N)和n=2 (Sr3Nb2O5N2)的构件。这些化合物在I4/mmm空间群中结晶,并显示出一系列阴离子化学计量,这些阴离子化学计量与N/O比一起决定了铌的形式氧化态,从而决定了最终的物理性质。n=1成员的样品表现出Nb5+/Nb4+的混合价态,在室温下具有顺磁性和高电阻性。这种行为可以通过考虑N/O无序引起的电子定位来理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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