Department of Chemistry, University of Munich (LMU) , Butenandtstr. 5-13, 81377 Munich, Germany.
Institute for Mineralogy, Crystallography and Materials Science, Faculty of Chemistry and Mineralogy, Leipzig University , Scharnhorststr. 20, 04275 Leipzig, Germany.
J Am Chem Soc. 2017 Sep 13;139(36):12724-12735. doi: 10.1021/jacs.7b07075. Epub 2017 Sep 5.
Thorough investigation of nitridophosphates has rapidly accelerated through development of new synthesis strategies. Here we used the recently developed high-pressure metathesis to prepare the first rare-earth metal nitridophosphate, CeLiPN, with a high degree of condensation >1/2. CeLiPN consists of an unprecedented hexagonal framework of PN tetrahedra and exhibits blue luminescence peaking at 455 nm. Transmission electron microscopy (TEM) revealed two intergrown domains with slight structural and compositional variations. One domain type shows extremely weak superstructure phenomena revealed by atomic-resolution scanning TEM (STEM) and single-crystal diffraction using synchrotron radiation. The corresponding superstructure involves a modulated displacement of Ce atoms in channels of tetrahedra 6-rings. The displacement model was refined in a supercell as well as in an equivalent commensurate (3 + 2)-dimensional description in superspace group P6(α, β, 0)0(-α - β, α, 0)0. In the second domain type, STEM revealed disordered vacancies of the same Ce atoms that were modulated in the first domain type, leading to sum formula CeLiPNO (x ≈ 0.72) of the average structure. The examination of these structural intricacies may indicate the detection limit of synchrotron diffraction and TEM. We discuss the occurrence of either Ce displacements or Ce vacancies that induce the incorporation of O as necessary stabilization of the crystal structure.
通过开发新的合成策略,对氮磷化合物的深入研究迅速加速。在这里,我们使用最近开发的高压复分解反应来制备第一个具有高缩合度 (>1/2)的稀土金属氮磷化合物 CeLiPN。CeLiPN 由前所未有的 PN 四面体六方骨架组成,并表现出峰值为 455nm 的蓝色发光。透射电子显微镜 (TEM) 显示了两种共生的畴,它们在结构和组成上略有变化。一种畴类型表现出极其微弱的超结构现象,这是由原子分辨扫描 TEM (STEM) 和使用同步辐射的单晶衍射揭示的。相应的超结构涉及 Ce 原子在四面体 6-环通道中的调制位移。位移模型在超胞中以及在超空间群 P6(α, β, 0)0(-α - β, α, 0)0 中的等效协调 (3 + 2)-维描述中进行了细化。在第二种畴类型中,STEM 揭示了相同的 Ce 原子的无序空位,这些空位在第一种畴类型中发生了调制,导致平均结构的 CeLiPNO (x ≈ 0.72) 化学式。这些结构复杂性的研究可能表明同步辐射衍射和 TEM 的检测极限。我们讨论了 Ce 位移或 Ce 空位的发生,这是晶体结构必要的稳定化所必需的。