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Time-Resolved in Situ Synchrotron X-ray Diffraction Studies of Type 1 Silicon Clathrate Formation

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Published
  • Peter T. Hutchins
  • Olivier Leynaud
  • Luke A. O'Dell
  • Mark E. Smith
  • Paul Barnes
  • Paul F. McMillan
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<mark>Journal publication date</mark>13/12/2011
<mark>Journal</mark>Chemistry of Materials
Issue number23
Volume23
Number of pages8
Pages (from-to)5160-5167
Publication StatusPublished
<mark>Original language</mark>English

Abstract

Silicon clathrates are unusual open-framework solids formed by tetrahedrally bonded silicon that show remarkable electronic and thermal properties. The type I structure has a primitive cubic unit cell containing cages occupied by metal atoms to give compositions such as Na8Si46 and Na2Ba6Si46. Although their structure and properties are well described, there is little understanding of the formation mechanism. Na8Si46 is typically produced by metastable thermal decomposition under vacuum conditions from NaSi, itself an unusual structure containing Si44– polyanions. In this study, we used in situ synchrotron X-ray diffraction combined with rapid X-ray detection on samples taken through a controlled temperature ramp (25–500 °C at 8 °C/min) under vacuum conditions (10–4 bar) to study the clathrate formation reaction. We also carried out complementary in situ high-temperature solid-state 23Na NMR experiments using a sealed tube loaded under inert-gas-atmosphere conditions. We find no evidence for an intermediate amorphous phase during clathrate formation. Instead, we observe an unexpectedly high degree of structural coherency between the Na8Si46 clathrate and its NaSi precursor, evidenced by a smooth passage of several X-ray reflections from one structure into the other. The results indicate the possibility of an unusual, epitaxial-like, growth of the clathrate phase as Na atoms are removed from the NaSi precursor into the vacuum.