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Formation of Novel Cluster Compounds from Ternary Molybdenum Oxides by In- Situ Deintercalation

Published online by Cambridge University Press:  02 July 2020

R. Ramlau
Affiliation:
; Max-Planck-Institut für Festkörperforschung, D-70569Stuttgart, Germany
A. Simon
Affiliation:
; Max-Planck-Institut für Festkörperforschung, D-70569Stuttgart, Germany
R. E. McCarley
Affiliation:
Ames Laboratory, U.S.D.O.E., and, Iowa State University, Ames, Iowa50011
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Extract

Comprehensive studies by HREM, SAED, and EDXS have been recently devoted to the real structure of the ternary reduced molybdenum oxides in the series Mn±δMo4n+2O6n+4 with M = Sn,In. These compounds contain condensed clusters Mo4n+2O8n+10 with a core of n transedge-sharing molybdenum octahedra. The individual clusters are interconnected via common oxygen atoms. of course, the appropriate choice of counter-cations M is essential for the stability of the clusters, whose core of condensed molybdenum octahedra is a more or less extended metal-metal bonded structure. In tin oxomolybdates condensed clusters with n = 2,3 have been observed, in indium oxomolybdates with n = 3,4,5,6. In Sn2Mo10O16 and Sn2.8Mo14O22 each Sn atom provides 2 electrons to the cluster, in In5Mo18O28, e.g., with n = 4 an In57+ polycation, a metal-metal bonded unit itself, provides 7 electrons.

It became obvitalicous that both tin and indium oxomolybdates undergo a structure transformatitalicon when irradiated a 300kV electron mitaliccroscope (Philips CM30/ST, Cs = 1.15mm).

Type
In Situ Studies in Microscopy
Copyright
Copyright © Microscopy Society of America 1997

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References

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