Abstract

Titanium dioxide in the TiO2–B phase, which can be stabilized in nanoparticle form, is a promising anode material for lithium ion batteries. Here the structural and electronic changes between nanoribbons in TiO2–B and the thermodynamic stable anatase phase are studied using nanoscale X-ray absorption spectroscopy and first-principles calculations. The oxygen K-edge spectra of the two phases display marked differences which are very well reproduced in the calculations. Strong linear dichroism is observed in single nanoribbons, reflecting preferential O-2p to Ti-3d bond orientation in the low symmetry crystal structures. A simple bond counting model is developed which semiquantitatively accounts for the major dichroic effect. It is shown that the crystal orientation of the nanoparticles can be inferred from the dichroic spectra.

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