Abstract

The structure of bulk and nondefective compounds is generally described with crystal models built from well mastered techniques such the analysis of an X-ray diffractogram. The presence of defects, such as cationic vacancies, locally disrupt the long-range order, with the appearance of local structures with order extending only a few nanometers. To probe and describe the electrochemical properties of cation-deficient anatase, we investigated a series of materials having different concentrations of vacancies, i.e., Ti1–x–y□x+yO2–4(x+y)F4x(OH)4y, and compared their properties with respect to defect-free stoichiometric anatase TiO2. At first, we characterized the series of materials Ti1–x–y□x+yO2–4(x+y)F4x(OH)4y by means of pair distribution function (PDF), 19F nuclear magnetic resonance (NMR), Raman and X-ray photoelectron spectroscopies, to probe the compositional and structural features. Second, we characterized the insertion electrochemical properties vs metallic lithium where we emphasized the beneficia...

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