Abstract
The proficient realization of Na-ion batteries (NIBs) having exceptional electrochemical behavior is considered to bridge the hurdles triggered by inadequate resources and costly manufacturing of Li-ion batteries. Herein, we report a facile synthesis of Ni0.06Co2.94O4/CNTs hybrid using the solvothermal route and Ni0.06Co2.94O4 using the hydrothermal approach. The formation of a nest-like conductive framework of Ni0.06Co2.94O4/CNT composites, aligning favorably to form an assembly of a layered structure, supports an efficient Na-ion insertion/extraction process. A high initial charge capacity of 621 and 582 mAh g-1 is delivered by Ni0.06Co2.94O4/CNTs and Ni0.06Co2.94O4 electrodes, respectively which retained up to 328 and 239 mAh g-1 after 100 cycles. The electrodes also delivered excellent rate performance with 119 and 93 mAh g-1 at 5.0C and retained 77 and 64% of initial capacity, respectively when recovered from 0.05C. Additionally, Ni0.06Co2.94O4/CNTs exhibited low impedance over a wide range of frequencies resulting in more Na ions storage and a faster Na insertion/extraction process. The exceptional performance shown by the hybrid electrode is due to the synergistic influence flanked by binary metal oxides and CNTs. Hence, the hybrid of Ni-doped metal oxide and carbonaceous species emerge as an excellent choice for use as an electrode for electrochemical energy storage devices.
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