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Structure and X-ray reference diffraction patterns of (Ba6−xSrx)R2Co4O15 (x = 1, 2) (R = lanthanides)

Published online by Cambridge University Press:  25 April 2013

W. Wong-Ng*
Affiliation:
Materials Measurement Science Division, NIST, Gaithersburg, Maryland 20899
G. Liu
Affiliation:
Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100190, People's Republic of China
Y.G. Yan
Affiliation:
State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan, Hubei 430070, People's Republic of China
J.A. Kaduk
Affiliation:
BCPS, Illinois Institute of Technology, Chicago, Illinois 60616
*
a)Author to whom correspondence should be addressed. Electronic mail: winnie.wong-ng@nist.gov

Abstract

The structure and X-ray patterns of two series of barium lanthanide cobaltates, namely, Ba4Sr2R2Co4O15 (R = La, Nd, Sm, Eu, Gd, and Dy), and Ba5SrR2Co4O15 (R = La, Nd, Sm, Eu, and Gd) have been determined. These compounds crystallize in the space group P63mc; the unit-cell parameters of Ba4Sr2R2Co4O15 (R from La to Dy) decrease from a = 11.6128(2) Å to 11. 5266(9) Å, c = 6.869 03(11) to 6. 7630(5) Å, and V = 802.23(3) Å3 to 778.17(15) Å3, respectively. In the Ba5SrR2Co4O15 series (R = La to Gd), the unit-cell parameters decrease from a = 11.735 44(14) Å to 11.619 79(12) Å, c = 6.942 89 (14) Å to 6.836 52(8) Å, and V = 828.08(3) Å3 to 799.40(2) Å3. In the general structure of (Ba6−xSrx)R2Co4O15, there are four Co ions per formula unit occupying one CoO6 octahedral and three CoO4 tetrahedral units. Through corner-sharing of these polyhedra, a larger Co4O15 unit is formed. Sr2+ ions adopt both octahedral and 8-fold coordination environment. R3+ ions adopt 8-fold coordination (mixed site with Sr), while the larger Ba2+ ions assume both 10- and 11-fold coordination environments. The samples were found to be insulators. X-ray diffraction patterns of these samples have been determined and submitted to the Powder Diffraction File (PDF).

Type
Technical Articles
Copyright
Copyright © International Centre for Diffraction Data 2013 

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