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反钙钛矿的堆积设计:(Sr3-xBaxN)E体系,E = Bi,Sb

Stacking design of inverse perovskites: the systems (Sr3-xBaxN)E, E = Bi, Sb.

作者信息

Gäbler Frank, Niewa Rainer

机构信息

Max-Planck-Institut für Chemische Physik fester Stoffe, 01187 Dresden, Germany.

出版信息

Inorg Chem. 2007 Feb 5;46(3):859-65. doi: 10.1021/ic061863h.

Abstract

The first representatives of 4H (BaMnO3-type structure, P63/mmc, Z = 4) and 9R (BaMnO3-type structure, Rm, Z = 9) inverse Perovskite phases are presented. The phases are obtained within the solid solutions (Sr3-xBaxN)E with E = Bi, Sb. The crystal structures and homogeneity ranges were studied by combined X-ray and neutron diffraction as well as chemical analyses. The cubic Perovskite phase with Bi (Sb) is stable in the range of 0.00 < or = x < or = 0.90(5) (0.00 < or = x < or = 1.30(5)), the 4H variant is stable for 1.55(5) < or = x < or = 2.10(5) (1.85(5) < or = x < or = 2.45(5)), the 9R structure is stable for 2.50(2) < or = x < or = 2.55(2) (2.56(2) < or = x < or = 2.60(2)), and the 2H phase is stable for 2.75(5) < or = x < or = 3.00 (2.80(5) < or = x < or = 3.00). Ba occupies preferable sites in the hexagonal stacking of close packed layers of alkaline earth metal ions and E3-; Sr is mainly located in cubic stacked layers. The phase order upon going from cubic (Sr3N)E to 2H-type (Ba3N)E concomitant to the pronounced Sr/Ba partial order can, in general, be rationalized considering the Coulomb repulsion of nitride ions, as well as the size and charge density of the alkaline earth metal ions.

摘要

首次报道了4H(BaMnO₃型结构,P63/mmc,Z = 4)和9R(BaMnO₃型结构,Rm,Z = 9)反钙钛矿相的代表物。这些相是在固溶体(Sr₃₋ₓBaₓN)E(E = Bi、Sb)中获得的。通过结合X射线和中子衍射以及化学分析对晶体结构和均匀性范围进行了研究。含Bi(Sb)的立方钙钛矿相在0.00 ≤ x ≤ 0.90(5)(0.00 ≤ x ≤ 1.30(5))范围内稳定,4H变体在1.55(5) ≤ x ≤ 2.10(5)(1.85(5) ≤ x ≤ 2.45(5))范围内稳定,9R结构在2.50(2) ≤ x ≤ 2.55(2)(2.56(2) ≤ x ≤ 2.60(2))范围内稳定,2H相在2.75(5) ≤ x ≤ 3.00(2.80(5) ≤ x ≤ 3.00)范围内稳定。Ba在碱土金属离子和E³⁻的密堆积层的六方堆积中占据优先位置;Sr主要位于立方堆积层中。从立方相(Sr₃N)E到2H型(Ba₃N)E时伴随明显的Sr/Ba部分有序的相序,一般来说,考虑到氮化物离子的库仑排斥以及碱土金属离子的尺寸和电荷密度,可以得到合理的解释。

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