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Finding Order in Disorder: The Highly Disordered Lithium Oxonitridophosphate Double Salt Li8+x P3 O10-x N1+x (x=1.4(5)).
Schneider, Stefanie; Kreiner, Sandra T; Balzat, Lucas G; Lotsch, Bettina V; Schnick, Wolfgang.
Afiliação
  • Schneider S; Department of Chemistry, University of Munich (LMU), Butenandtstraße 5-13 (D), 81377, Munich, Germany.
  • Kreiner ST; Department of Chemistry, University of Munich (LMU), Butenandtstraße 5-13 (D), 81377, Munich, Germany.
  • Balzat LG; Department of Chemistry, University of Munich (LMU), Butenandtstraße 5-13 (D), 81377, Munich, Germany.
  • Lotsch BV; Max Planck Institute for Solid State Research, Department of Nanochemistry, Heisenbergstraße 1 (D), 70569, Stuttgart, Germany.
  • Schnick W; Department of Chemistry, University of Munich (LMU), Butenandtstraße 5-13 (D), 81377, Munich, Germany.
Chemistry ; 29(55): e202301986, 2023 Oct 02.
Article em En | MEDLINE | ID: mdl-37436099
ABSTRACT
The crystalline lithium oxonitridophosphate Li8+x P3 O10-x N1+x , was obtained in an ampoule synthesis from P3 N5 and Li2 O. The compound crystallizes in the triclinic space group P 1 - ${\mathrel{\mathop{{\rm { 1}}}\limits^{{\rm -}}}}$ with a=5.125(2), b=9.888(5), c=10.217(5) Å, α=70.30(2), ß=76.65(2), γ=77.89(2)°. Li8+x P3 O10-x N1+x is a double salt, the structure of which contains distinctive complex anion species, namely non-condensed P(O,N)4 tetrahedra, and P(O,N)7 double tetrahedra connected by one N atom. Additionally, there is mixed occupation of O/N positions, which enables further anionic species by variation of O/N occupancies. To characterize these motifs in detail, complementary analytical methods were applied. The double tetrahedron exhibits significant disorder in single-crystal X-ray diffraction. Furthermore, the title compound is a Li+ ion conductor with a total ionic conductivity of 1.2×10-7  S cm-1 at 25 °C, and a corresponding total activation energy of 0.47(2) eV.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article