Lithium insertion into Sn-doped TiO 2 anatase was studied in order to clarify the mechanism responsible for the first plateau observed at 1.75 V vs Li. One of the other aims of this study was to get deeper insight into the process responsible for the appearance of a first domain observed at a small amount of lithium (before the plateau) and a third domain between 1.7 and 1.2 V (after the plateau). Pure and Sn-substituted anatase were synthesized by several synthetic methods with different precursors and solvents. These materials are expected to have different electrochemical properties because crystallite size modifies the Li-insertion process. Their electrochemical behavior is discussed in order to establish a relationship between the materials properties and the electrochemical performances. Three processes have been identified from both X-ray diffraction and 119 Sn Mössbauer spectroscopy: (i) topotactic insertion into the Li-poor compound Li x TiO 2, with the x value depending on the particle size; (ii) a two-phase system mechanism leading to the phase transition Li x TiO 2 (Anatase, I 4 1 / a md ) → Li y TiO 2 (orthorhombic distortion, Imma ); and (iii) another topotactic insertion into the Li-rich compound Li y TiO 2 . Crystallite size governs the topotactic mechanism but does not improve the overall electrochemical capacity of the material.
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Aldon et al. (2006) studied this question.
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