X-Ray Absorption Spectroscopic Studies on Layered FeWO 4Cl and Its Lithium Intercalate

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Copyright (c) 1997 The Japan Society of Applied Physics
, , Citation Jin-Ho Choy et al 1997 Jpn. J. Appl. Phys. 36 5605 DOI 10.1143/JJAP.36.5605

1347-4065/36/9R/5605

Abstract

Lithium intercalation into FeWO4Cl leads to the structural phase transformation from tetragonal to monoclinic. According to Fe K-edge X-ray absorption near edge structure (XANES) spectroscopic analysis, only the Fe3+ ion in the FeWO4Cl lattice is reduced to Fe2+ with an increment of site symmetry from C4v to Oh upon lithium intercalation. On the other hand, the white line intensity at the W L-edge XANES becomes slightly enhanced after intercalation, indicating an increase of the (W6+–O) bond covalency due to a decrease of the competing (Fe2+–O) bond strength. W L3-edge extended X-ray absorption fine structure (EXAFS) analyses for FeWO4Cl and LiFeWO4Cl show that the regular tetrahedron of the WO42- group in FeWO4Cl becomes distorted upon lithium intercalation.

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10.1143/JJAP.36.5605