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Abstract Searching for advanced anode materials with exceptional electrochemical performance is essential for next-generation rechargeable batteries. The selection and structural design of anode materials are pivotal in the development of high-performance batteries. Herein, we demonstrate the preparation of uniform NiCo 2 O 4 nanotubes via a simple and cost-effective electrospinning technique followed by calcination in the air. Impressively, the advantages and importance of NiCo 2 O 4 nanotubes as an anode in lithium-ion batteries (LIBs) is demonstrated, which surpass their respective monometallic oxides in terms of electrochemical performance. Encouragingly, the as-obtained NiCo 2 O 4 nanotubes as an anode for sodium-ion batteries (SIBs) exhibit appealing electrochemical performance, such as high initial discharge capacity (879 mAh g−1 at 100 mA g−1), good rate capability, and excellent cycling stability. Moreover, a reversible capacity of 420 mAh g−1 at a current density of 100 mA g−1 can be maintained even after 100 cycles, corresponding to around 72% of the second cycle discharge capacity (584 mAh g−1). It is worth noting that this facile technique may provide a feasible way for the preparation of other functional materials with tube-like architectures for application in energy-storage device. Graphical abstract An advanced NiCo 2 O 4 nanotubes anode has been successfully prepared through a simple and cost-effective electrospinning technique followed by calcination in air. The as-obtained NiCo 2 O 4 nanotubes exhibits appealing electrochemical performance, such as high initial discharge capacity, good rate capability, and excellent cycling stability. Image 1 Highlights • NiCo 2 O 4 nanotubes are prepared through an electrospinning technique. • The NiCo 2 O 4 nanotubes surpass their respective monometallic oxides in terms of electrochemical performance in LIBs. • The NiCo 2 O 4 nanotubes as anode for SIBs present excellent electrochemical properties. • The electrospinning technique can be extended to prepare other functional materials in energy-storage devices. [ABSTRACT FROM AUTHOR]

The as-prepared binder-free Co 1−x S/MCF anode exhibits the desirable electrochemical performance for LIBs and SIBs, which can be attributed to the unique hierarchical nanostructure which provides enough active sites and internal space for volume expansion. [Display omitted] • The flexible Co 1−x S/MCF electrode is prepared via the electrospinning technique. • The Co 1−x S/MCF presents hierarchically hollow and multichannel structures. • The Co 1−x S/MCF electrode can effectively ease the huge volume expansion. • The Co 1−x S/MCF electrode shows high electrochemical performance for LIBs and SIBs. The exploration of prospective electrode materials represents great challenges for remarkable lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs). Herein, we report a reliable synthetic approach for the in-situ growth of the Co-based zeolitic imidazolate framework (ZIF-67) on electrospun nanofibers, followed by carbonization and sulfurization with the formation of free-standing Co 1−x S hollow polyhedrons anchored on multichannel carbon nanofibers (Co 1−x S/MCF) for LIBs and SIBs. The Co 1−x S/MCF electrode displays a high reversible capacity (813 mAh g−1 over 180 cycles at 0.1 A g−1), and stable cycle performance (559 mAh g−1 for 300 cycles at 1 A g−1) in LIBs. For SIBs, Co 1−x S/MCF electrode exhibits a favorable Na-storage capacity (433 mAh g−1 over 120 cycles at 0.1 A g−1). The as-prepared binder-free Co 1−x S/MCF anode demonstrates the advanced electrochemical properties for LIBs and SIBs. It is attributed to the particular multichannel nanostructure and the Co 1−x S hollow polyhedrons (Co 1−x S HPs), which provide enough active sites, and the internal void space effectively reduces the structural strain and eases the volume expansion to maintain structural integrity. This work gives insights to design a unique structure for promising LIBs and SIBs. [ABSTRACT FROM AUTHOR]

The as-prepared binder-free Co 1−x S/MCF anode exhibits the desirable electrochemical performance for LIBs and SIBs, which can be attributed to the unique hierarchical nanostructure which provides enough active sites and internal space for volume expansion. [Display omitted] • The flexible Co 1−x S/MCF electrode is prepared via the electrospinning technique. • The Co 1−x S/MCF presents hierarchically hollow and multichannel structures. • The Co 1−x S/MCF electrode can effectively ease the huge volume expansion. • The Co 1−x S/MCF electrode shows high electrochemical performance for LIBs and SIBs. The exploration of prospective electrode materials represents great challenges for remarkable lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs). Herein, we report a reliable synthetic approach for the in-situ growth of the Co-based zeolitic imidazolate framework (ZIF-67) on electrospun nanofibers, followed by carbonization and sulfurization with the formation of free-standing Co 1−x S hollow polyhedrons anchored on multichannel carbon nanofibers (Co 1−x S/MCF) for LIBs and SIBs. The Co 1−x S/MCF electrode displays a high reversible capacity (813 mAh g−1 over 180 cycles at 0.1 A g−1), and stable cycle performance (559 mAh g−1 for 300 cycles at 1 A g−1) in LIBs. For SIBs, Co 1−x S/MCF electrode exhibits a favorable Na-storage capacity (433 mAh g−1 over 120 cycles at 0.1 A g−1). The as-prepared binder-free Co 1−x S/MCF anode demonstrates the advanced electrochemical properties for LIBs and SIBs. It is attributed to the particular multichannel nanostructure and the Co 1−x S hollow polyhedrons (Co 1−x S HPs), which provide enough active sites, and the internal void space effectively reduces the structural strain and eases the volume expansion to maintain structural integrity. This work gives insights to design a unique structure for promising LIBs and SIBs. [ABSTRACT FROM AUTHOR]