Enhanced sodium ion mobility in sodium tellurosilicates and crystal structures of Na4SiTe4 and Na10Si2Te9 with isolated [SiTe4]<SUP>4-</SUP> tetrahedra and isolated Te<SUP>2-</SUP> anions

Kamm, Franziska and Pielnhofer, Florian and Schlosser, Marc and Pfitzner, Arno (2024) Enhanced sodium ion mobility in sodium tellurosilicates and crystal structures of Na4SiTe4 and Na10Si2Te9 with isolated [SiTe4]<SUP>4-</SUP> tetrahedra and isolated Te<SUP>2-</SUP> anions. DALTON TRANSACTIONS, 53 (37). pp. 15630-15637. ISSN 1477-9226, 1477-9234

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Abstract

The sodium tellurosilicates Na4SiTe4, Na10Si2Te9, Na6Si2Te6 and Na8Si4Te10 were synthesized by ball milling and subsequent high temperature solid state reactions and analyzed by electrochemical impedance spectroscopy. All compounds show moderate to remarkable sodium ion conductivities. The crystal structures of the novel materials Na4SiTe4 and Na10Si2Te9 were determined by X-ray diffraction. Both compounds represent new structure types with isolated SiTe4 tetrahedra. The crystal structure of Na10Si2Te9 exhibits a single telluride anion besides two SiTe4 tetrahedra. Na4SiTe4 crystallizes in the cubic space group Pa (3) over bar (no. 205) with lattice parameters a = 13.0312(1) angstrom and V = 2212.84(2) angstrom(3). Na10Si2Te9 crystallizes in the orthorhombic space group Pna2(1) (no. 33) with lattice parameters a = 12.8235(7) angstrom, b = 14.8398(8) angstrom, c = 12.9530(7) angstrom and V = 2464.9(2) angstrom(3). The presence of two different anionic units makes this compound stand out from other alkali chalcogenotetrelates. The electronic structure of all compounds was investigated by density functional theory, revealing their semiconducting behaviour.

Item Type: Article
Uncontrolled Keywords: LITHIUM; CONDUCTIVITY; ELECTROLYTES; ALPHA;
Subjects: 500 Science > 540 Chemistry & allied sciences
Divisions: Chemistry and Pharmacy > Institut für Anorganische Chemie > Chair Prof. Dr. Arno Pfitzner
Depositing User: Dr. Gernot Deinzer
Date Deposited: 17 Jul 2025 07:12
Last Modified: 17 Jul 2025 07:12
URI: https://pred.uni-regensburg.de/id/eprint/63539

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