Skip to main content
Article
The s−p Bonded Representatives of the Prominent BaAl4 Structure Type:  A Case Study on Structural Stability of Polar Intermetallic Network Structures
Journal of the American Chemical Society
  • Ulrich Haussermann, Stockholm University
  • Shahrad Amerioun, Stockholm University
  • Lars Ericksson, Stockholm University
  • Chi-Shen Lee, Iowa State University
  • Gordon J. Miller, Iowa State University
Document Type
Article
Publication Version
Published Version
Publication Date
1-1-2002
DOI
10.1021/ja012392v
Abstract
This work presents a detailed, combined experimental and theoretical study on the structural stability of s−p bonded compounds with the BaAl4 structure type (space group I4/mmm, Z = 2) as part of a broad program to investigate the complex questions of structure formation and atomic arrangements in polar intermetallics. From ab initio calculations employing pseudopotentials and a plane wave basis set, we extracted optimized structural parameters, binding energies, and the electronic structure of the systems AeX(III)4, AeX(II)2X(IV)2, AeX(II)2X(III)2 (Ae = Ca, Sr, Ba; X(II) = Mg, Zn; X(III) = Al, Ga; X(IV) = Si, Ge). For all systems we found a pronounced pseudo-gap in the density of states separating network X42- bonding from antibonding electronic states that coincides with the Fermi level for an electron count of 14 electrons per formula unit, the optimum value for stable BaAl4-type polar intermetallics. However, the synthesis and structural characterization (from X-ray single crystal and powder diffraction data) of the new compounds AeZn2-δAl2+δ, AeZn2-δGa2+δ (Ae = Ca, Sr, Ba; δ = 0−0.2) and AeMg0.9Al3.1, AeMg1.7Ga2.3 (Ae = Sr, Ba) manifested that electron deficiency is rather frequent for BaAl4-type polar intermetallics. The site preference for different “X” elements in the ternary systems was quantified by calculating “coloring energies”, which, for some systems, was strongly dependent on the size of the electropositive Ae component. The Ae2+ cations decisively influence the nearest neighbor distances in the encapsulating polyanionic networks X42- and the structures of these networks are surprisingly flexible to the size of the Ae component without changing the overall bonding picture. A monoclinically distorted variant of the BaAl4 structure occurs when the cations become too small for matching the size of encapsulating X42- cages. An even larger size mismatch leads to the formation of the EuIn4 structure type.
Comments

Reprinted (adapted) with permission from J. Am. Chem. Soc., 2002, 124 (16), pp 4371–4383. Copyright 2002 American Chemical Society.

Copyright Owner
American Chemical Society
Language
en
File Format
application/pdf
Citation Information
Ulrich Haussermann, Shahrad Amerioun, Lars Ericksson, Chi-Shen Lee, et al.. "The s−p Bonded Representatives of the Prominent BaAl4 Structure Type:  A Case Study on Structural Stability of Polar Intermetallic Network Structures" Journal of the American Chemical Society Vol. 124 Iss. 16 (2002) p. 4371 - 4383
Available at: http://works.bepress.com/gordon-miller/106/