Article ID Journal Published Year Pages File Type
1332170 Journal of Solid State Chemistry 2008 8 Pages PDF
Abstract

Lead-containing members of the hilgardite family of borate halides, M2B5O9X (M=Ca, Sr, Ba, Pb; X=Cl, Br) exhibit an abnormally large nonlinear optical response. In order to establish any underlying crystal-chemical rationale for this we have carried out detailed crystallographic characterisations of the representative members of this series, Sr2B5O9Cl and Pb2B5O9Cl, using powder neutron diffraction. Both adopt the orthorhombic hilgardite structure type, in space group Pnn2. The full solid solution range Pb2−xSrxB5O9Cl has also been prepared, and studied by X-ray Rietveld and second harmonic generation (SHG) measurements. The SHG response shows a linear decrease with increasing x, whereas the unit cell shows an increasing orthorhombic distortion. However, the crystallographic results suggest no significant or systematic changes in the nature of the borate sublattice between Sr2B5O9Cl and Pb2B5O9Cl. We conclude that the enhanced SHG response in Pb-containing hilgardites is due predominantly to the presence of the polarizable nature of Pb2+, in particular the presence of a stereochemically active lone pair.

Graphical abstractSr2B5O9Cl, Pb2B5O9Cl and the solid solution range Pb2−xSrxB5O9Cl has been prepared, and studied by powder neutron and X-ray diffraction and SHG measurements.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Inorganic Chemistry
Authors
, , , , , , , ,