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Ion Exchange and Structural Aging in the Layered Perovskite Phases H(1-x)Li(x)LaTiO4

Ion Exchange and Structural Aging in the Layered Perovskite Phases H(1-x)Li(x)LaTiO4

T W S Yip, E J Cussen

Inorg Chem. 2013 Jun 17;52(12):6985-93.

PMID: 23713950

Abstract:

Grinding together the solid acid HLaTiO4 with stoichiometric quantities of lithium hydroxide monohydrate gives the solid solution H(1-x)Li(x)LaTiO4. The structures of these crystalline phases have been refined against neutron powder diffraction data to show that all of these compounds crystallize in the centrosymmetric space group P4/nmm. The protons and lithium cations occupy sites between the perovskite layers; the former in hydroxide groups that hydrogen-bond to adjacent layers while Li(+) is in four-coordinate sites that bridge the perovskite slabs with a geometry intermediate between square-planar and tetrahedral. The reaction proceeds rapidly, but the unit cell size continues to evolve over the course of days with a gradual compression along the interlayer direction that can be modeled using a power law dependence reminiscent of an Ostwald ripening process. On heating, these materials undergo a mass loss because of dehydration but retain the layered Ruddlesden-Popper structure up to 480 °C before a substantial loss of crystallinity on further heating to 600 °C. Impedance spectroscopy studies of the dehydrated materials shows that Li(+) mobility in these materials is lower than the LiLaTiO4 end member, possibly because of microstructural effects causing large intergrain resistance through the defective phases.

Chemicals Related in the Paper:

Catalog Number	Product Name	Structure	CAS Number	Price
AP1310663	Lithium hydroxide monohydrate		1310-66-3	Price

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