Developing high-performance cathode host materials is fundamental to solve the low utilization of sulfur, the sluggish redox kinetics, and the lithium polysulfide (LiPS) shuttle effect in lithium–sulfur batteries (LSBs). Here, a multifunctional Ag/VN@Co/NCNT nanocomposite with multiple adsorption and catalytic sites within hierarchical nanoreactors is reported as a robust sulfur host for LSB cathodes. In this hierarchical nanoreactor, heterostructured Ag/VN nanorods serve as a highly conductive backbone structure and provide internal catalytic and adsorption sites for LiPS conversion. Interconnected nitrogen-doped carbon nanotubes (NCNTs), in situ grown from the Ag/VN surface, greatly improve the overall specific surface area for sulfur dispersion and accommodate volume changes in the reaction process. Owing to their high LiPS adsorption ability, outer Co nanoparticles at the top of the NCNTs catch escaped LiPS, thus effectively suppressing the shuttle effect and enhancing kinetics. Benefiting from the multiple adsorption and catalytic sites of the developed hierarchical nanoreactors, Ag/VN@Co/NCNTs@S cathodes display outstanding electrochemical performances, including a superior rate performance of 609.7 mAh g–1 at 4 C and a good stability with a capacity decay of 0.018% per cycle after 2000 cycles at 2 C. These properties demonstrate the exceptional potential of Ag/VN@Co/NCNTs@S nanocomposites and approach LSBs closer to their real-world application.

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Searching for high-performance Ni-based cathodes plays an important role in developing better aqueous nickel–zinc (Ni–Zn) batteries. For this purpose, herein, we demonstrate the design and synthesis of ultrathin α-Ni­(OH)2 nanosheets branched onto metal–organic frameworks (MOFs)-derived 3D cross-linked N-doped carbon nanotubes encapsulated with tiny Co nanoparticles (denoted as Co@NCNTs/α-Ni­(OH)2), which are directly supported on a flexible carbon cloth (CC). An aqueous Ni–Zn battery employing the hierarchical CC/Co@NCNTs/α-Ni­(OH)2 as the binder-free cathode and a commercial Zn plate as the anode is fabricated, which displays an ultrahigh capacity (316 mAh g–1) and energy density (540.4 Wh kg–1) at 1 A g–1 as well as excellent rate capability (238 mAh g–1 at 10 A g–1) and superior cycling performance (about 84% capacity retention after 2000 cycles at 10 A g–1). The impressive electrochemical performance might benefit from the rich active sites, rapid electron transfer, cushy electrolyte access, rapid ion transport, and robust structural stability. In addition, the quasi-solid-state CC/Co@NCNTs/α-Ni­(OH)2//Zn batteries are also successfully assembled with polymer electrolyte, indicating the great potential for portable and wearable electronics. This work might provide important guidance for constructing carbon-based hybrid materials directly supported on conductive substrates as high-performance electrodes for energy-related devices.

Vanadium (V)-based cathode materials hold great potential for rechargeable aqueous zinc-ion batteries (AZIBs). However, the shortcomings of poor electrical conductivity, large volume change, serious V dissolution and complicated electrochemical reaction...

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