The charge-storage kinetics of amorphous TiO x nanotube electrodes formed by anodizing three-dimensional porous Ti scaffolds are reported. The resultant electrodes demonstrated not only superior storage capacities and rate capability to anatase TiO x nanotube electrodes but also improved areal capacities (324 μAh cm-2 at 50 μA cm-2 and 182 μAh cm-2 at 5 mA cm-2) and cycling stability (over 2000 cycles) over previously reported TiO x nanotube electrodes using planar current collectors. Amorphous TiO x exhibits very different electrochemical storage behavior from its anatase counterpart as the majority of its storage capacity can be attributed to capacitive-like processes with more than 74 and 95% relative contributions being attained at 0.05 and 1 mV s-1, respectively. The kinetic analysis revealed that the insertion/extraction process of Li+ in amorphous TiO x is significantly faster than in anatase structure and controlled by both solid-state diffusion and interfacial charge-transfer kinetics. It is concluded that the large capacitive contribution in amorphous TiO x originates from its highly defective and loosely packed structure and lack of long-range ordering, which facilitate not only a significantly faster Li+ diffusion process (diffusion coefficients of 2 × 10-14 to 3 × 10-13 cm2 s-1) but also more facile interfacial charge-transfer kinetics than anatase TiO x.
Keywords: amorphous TiO2 nanotubes; anode material; high-rate energy storage; insertion kinetics; lithium-ion battery; lithium-ion diffusion; potentiostatic intermittent titration technique.