Ultrathin
TiO<sub>2</sub>(B) Nanorods with Superior Lithium-Ion Storage Performance
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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)