Cyrille Galven, Marie-Pierre Crosnier-Lopez, Françoise Le Berre
{"title":"Li2TeO4: Structural characterization and ionic conductivity measurements of a new tellurate","authors":"Cyrille Galven, Marie-Pierre Crosnier-Lopez, Françoise Le Berre","doi":"10.1016/j.jssc.2024.125170","DOIUrl":null,"url":null,"abstract":"<div><div>A new tellurate Li<sub>2</sub>TeO<sub>4</sub> (Li<sub>2</sub>TeO<sub>4</sub>-LT) was synthesized via a conventional solid-state route from specific precursors, LiOH.H<sub>2</sub>O and H<sub>6</sub>TeO<sub>6</sub>. The cell, initially identified as tetragonal from X-ray powder diffraction at room temperature, was finally found to be orthorhombic thanks to thermal X-ray powder diffraction. The space group, <em>Pbcn</em>, was determined with the help of electron diffraction while the structure was obtained from neutron powder diffraction (a = 5.0106(3), b = 11.5369(8) and c = 5.0057(4) Å. As the tellurate β-Na<sub>2</sub>TeO<sub>4</sub>, its structure is built from TeO<sub>6</sub> octahedra sharing edges forming thus infinite chains [TeO<sub>4</sub>]<sub>n</sub><sup>2n−</sup> parallel to the <em>c</em> axis. These chains are separated from each other by Li<sup>+</sup> ions in octahedral coordination. Contrary to β-Na<sub>2</sub>TeO<sub>4</sub><sup>,</sup> Li<sub>2</sub>TeO<sub>4</sub>-LT does not capture CO<sub>2</sub> and presents a modest ionic conduction (300 °C, T = 1.8 10<sup>−8</sup> S cm<sup>−1</sup>), lower than the tetragonal Li<sub>2</sub>TeO<sub>4</sub> variety (300 °C, ≈10<sup>−6</sup> S.cm-<sup>1</sup>). In addition, a complete solid solution Na<sub>2-x</sub>Li<sub>x</sub>TeO<sub>4</sub> was evidenced.</div></div>","PeriodicalId":378,"journal":{"name":"Journal of Solid State Chemistry","volume":"344 ","pages":"Article 125170"},"PeriodicalIF":3.5000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Solid State Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022459624006248","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/12/25 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
Abstract
A new tellurate Li2TeO4 (Li2TeO4-LT) was synthesized via a conventional solid-state route from specific precursors, LiOH.H2O and H6TeO6. The cell, initially identified as tetragonal from X-ray powder diffraction at room temperature, was finally found to be orthorhombic thanks to thermal X-ray powder diffraction. The space group, Pbcn, was determined with the help of electron diffraction while the structure was obtained from neutron powder diffraction (a = 5.0106(3), b = 11.5369(8) and c = 5.0057(4) Å. As the tellurate β-Na2TeO4, its structure is built from TeO6 octahedra sharing edges forming thus infinite chains [TeO4]n2n− parallel to the c axis. These chains are separated from each other by Li+ ions in octahedral coordination. Contrary to β-Na2TeO4, Li2TeO4-LT does not capture CO2 and presents a modest ionic conduction (300 °C, T = 1.8 10−8 S cm−1), lower than the tetragonal Li2TeO4 variety (300 °C, ≈10−6 S.cm-1). In addition, a complete solid solution Na2-xLixTeO4 was evidenced.
以特定的前驱物LiOH为原料,通过传统的固态途径合成了新型碲酸盐Li2TeO4 (Li2TeO4- lt)。H2O和H6TeO6。在室温下通过x射线粉末衍射初步鉴定为四边形,最终通过热x射线粉末衍射发现为正交晶型。通过电子衍射确定了空间群Pbcn,通过中子粉末衍射获得了结构(a = 5.0106(3), b = 11.5369(8), c = 5.0057(4) Å)。作为碲酸盐β-Na2TeO4,它的结构是由TeO6八面体组成的,它们共享边缘,形成平行于c轴的无限链[TeO4]n2n−。这些链在八面体配位中由Li+离子相互分离。与β-Na2TeO4相反,Li2TeO4- lt不捕获二氧化碳,并表现出适度的离子传导(300°C, T = 1.8 10−8 S cm-1),低于四边形Li2TeO4品种(300°C,≈10−6 S cm-1)。此外,还得到了完整的Na2-xLixTeO4固溶体。
期刊介绍:
Covering major developments in the field of solid state chemistry and related areas such as ceramics and amorphous materials, the Journal of Solid State Chemistry features studies of chemical, structural, thermodynamic, electronic, magnetic, and optical properties and processes in solids.