Cu7Bi6S10Cl5 - Mobile copper(I) cations inside dendritic channels of a rigid framework

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Contributors

Abstract

The melting reaction of copper, CuCl, sulfur, and Bi2S 3 yields black, shiny needles of the sulfide chloride Cu 7Bi6S10Cl5. The compound decomposes peritectically above 639(5) K. Cu-K-XANES data confirm the oxidation state +I of Cu. Cu7Bi6SiCl5 crystallizes in the monoclinic space group C2/m with a = 2878.3(9) pm, b = 396.59(9) pm, c = 1156.5(4) pm, and β = 111.55(3)° at T = 293(2) K. Three sulfur and four chlorine anions coordinate each of the threeindependent bismuth cations in the shape of mono-capped trigonal prisms. The [BiS3Cl4] polyhedra share edges and faces resulting in furrowed layers parallel (2̄01). Localized as well as disordered copper cations occupy trigonal or tetrahedral voids in the packing of anions. The Joint Probability Density Function (JPDF) reveals branched and unbranched continuous pathways along [010], which are available for cation conduction.

Details

Original languageEnglish
Pages (from-to)1860-1864
Number of pages5
JournalZeitschrift fur Anorganische und Allgemeine Chemie
Volume636
Issue number9-10
Publication statusPublished - Sept 2010
Peer-reviewedYes

External IDs

ORCID /0000-0002-2391-6025/work/159171906

Keywords

ASJC Scopus subject areas

Keywords

  • Bismuth, Cation mobility, Copper, Covalent polyhedra networks, One-dimensional ionic conductors