Er3+和Yb3+掺杂α-LiNH4SO4多型材料的结构和热稳定性

N. Sabalisck, C. Guzmán-Afonso, C. González-Silgo, M. Torres, J. Pasán, J. del-Castillo, D. Ramos-Hernández, A. Hernández-Suárez, L. Mestres
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引用次数: 4

摘要

为了阐明硫酸锂家族中的多态性,LiREx(NH4)1−xSO4(0.5≤x≤4.0 mol%,标称值;RE = Er3+, Yb3+和Dy3+)晶体在298 ~ 313 K的水溶液中缓慢蒸发生长。样品的掺杂使我们获得了LiNH4SO4 (LAS)的α和β两种多晶形式。利用单晶x射线衍射(XRD)测定了两种新的α-多型化合物的晶体结构,分别命名为α1-和α2-LAS。它们具有相同的空间群P21/c,它们的晶格参数之间有如下关系:a2 =−c1, b2 =−b1, c2 =−2a1−c1。为了评价新α-多型材料的稳定性,我们在190→575→190 K的循环温度范围内对单晶和多晶样品进行了热分析、x射线衍射和介电光谱分析。实验结果表明,α-多型在较宽的温度范围内是稳定的,并且在500 K以上表现出不可逆的向准电β相转变。此外,α-和β-多型的比较研究表明,两种多型结构都有一个共同的轴,可能存在共生,促进了它们的共存,并促进了重构的α→β转变。这种共生生长与在240 ~ 260 K之间检测到的α-习性晶体的小异常有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Structures and thermal stability of the α-LiNH4SO4 polytypes doped with Er3+ and Yb3+
In order to clarify the polymorphism in the lithium sulfate family, LiREx(NH4)1 − xSO4 (0.5 ≤ x ≤ 4.0 mol%, nominal value; RE = Er3+, Yb3+ and Dy3+) crystals were grown from aqueous solution by slow evaporation between 298 and 313 K. The doping of the samples allowed us to obtain two polymorphic forms, α and β, of LiNH4SO4 (LAS). By means of X-ray diffraction (XRD) in single crystals, we determined the crystal structures of two new α-polytypes, which we have named α1- and α2-LAS. They present the same space group P21/c and the following relation among their lattice parameters: a2 = −c1, b2 = −b1, c2 = −2a1 − c1. In order to evaluate the stability of the new α-polytypes, we performed thermal analysis, X-ray diffraction and dielectric spectroscopy on single crystals and polycrystalline samples over the cyclic temperature range: 190 → 575  → 190 K. The results obtained by all the techniques used in this study demonstrate that α-polytypes are stable across a wide range of temperatures and they show an irreversible phase transition to the paraelectric β-phase above 500 K. In addition, a comparative study of α- and β-polytypes shows that both polymorphic structures have a common axis, with a possible intergrowth that facilitates their coexistence and promotes the reconstructive α → β transition. This intergrowth was related to small anomalies detected between 240 and 260 K, in crystals with an α-habit.
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