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.