We report the electrochemical performance of Si nanotube vertical arrays possessing thin porous sidewalls for Li-ion batteries. Porous Si nanotubes were fabricated on stainless steel substrates using a sacrificial ZnO nanowire template method. These porous Si nanotubes are stable at multiple C-rates. A second discharge capacity of 3095 mAh g(-1) with a Coulombic efficiency of 63% is attained at a rate of C/20 and a stable gravimetric capacity of 1670 mAh g(-1) obtained after 30 cycles. The high capacity values are attributed to the large surface area offered by the porosity of the 3D nanostructures, thereby promoting lithium-ion storage according to a pseudocapacitive mechanism.
Self‐supported titanium dioxide nanotube is explored as a potential negative electrode for 3D Li‐ion (micro) batteries. Apart from the direct contact of the nanotubes with the substrate, the 1D porous structure effectively facilitates the flow of electrolyte into the bulk, alleviates any volume expansion during cycling, and provides a short lithium‐ion diffusion length. The fabrication of self‐supported Nb rich titanium dioxide nanotubes by electrochemical anodization of Ti–Nb alloys is reported. The structure, morphology, and the composition of the Nb alloyed TiO2 nanotubes are studied using scanning electron microscopy, X‐ray diffraction, and X‐ray photoelectron spectroscopy. The electrochemical behavior of the alloyed and the pristine TiO2 nanotubes is investigated by cyclic voltammetry, chronopotentiometry, and electrochemical impedance spectroscopy. The electrochemical performance of the pristine and the alloyed titania nanotubes reveals that as the niobium concentration increases the capacity increases. The titania nanotubes containing 10 wt% of Nb deliver a higher capacity, with good capacity retention and coulombic efficiency. Electrochemical impedance spectroscopy analysis shows that Nb alloying can decrease the overall cell impedance by reducing the charge transfer resistance.
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