Abstract

The peculiar architecture of a novel class of anisotropic TiO<sub>2</sub>(B) nanocrystals, which were synthesized by an surfactant-assisted nonaqueous sol–gel route, was profitably exploited to fabricate highly efficient mesoporous electrodes for Li storage. These electrodes are composed of a continuous spongy network of interconnected nanoscale units with a rod-shaped profile that terminates into one or two bulgelike or branch-shaped apexes spanning areas of about 5 × 10 nm<sup>2</sup>. This architecture transcribes into a superior cycling performance (a charge capacitance of 222 mAh g<sup>–1</sup> was achieved by a carbon-free TiO<sub>2</sub>(B)-nanorods-based electrode vs 110 mAh g<sup>–1</sup> exhibited by a comparable TiO<sub>2</sub>-anatase electrode) and good chemical stability (more than 90% of the initial capacity remains after 100 charging/discharging cycles). Their outstanding lithiation/delithiation capabilities were also exploited to fabricate electrochromic devices that revealed an excellent coloration efficiency (130 cm<sup>2</sup> C<sup>–1</sup> at 800 nm) upon the application of 1.5 V as well as an extremely fast electrochromic switching (coloration time ∼5 s)

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