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Lithium–sulfur batteries (LSBs) are regarded as one of the most promising energy-recycling storage systems due to their high energy density (up to 2600 Wh kg−1), high theoretical specific capacity (as much as 1672 mAh g−1), environmental friendliness, and low cost. Originating from the complicated redox of lithium polysulfide intermediates, Li–S batteries suffer from several problems, restricting their application and commercialization. Such problems include the shuttle effect of polysulfides (Li2Sx (2 < x ≤ 8)), low electronic conductivity of S/Li2S/Li2S2, and large volumetric expansion of S upon lithiation. In this study, a lotus root-like nitrogen-doped carbon nanofiber (NCNF) structure, assembled with vanadium nitride (VN) catalysts, was fabricated as a 3D freestanding current collector for high performance LSBs. The lotus root-like NCNF structure, which had a multichannel porous nanostructure, was able to provide excellent (ionically/electronically) conductive networks, which promoted ion transport and physical confinement of lithium polysulfides. Further, the structure provided good electrolyte penetration, thereby enhancing the interface contact with active S. VN, with its narrow resolved band gap, showed high electrical conductivity, high catalytic effect and polar chemical adsorption of lithium polysulfides, which is ideal for accelerating the reversible redox kinetics of intermediate polysulfides to improve the utilization of S. Tests showed that the VN-decorated multichannel porous carbon nanofiber structure retained a high specific capacity of 1325 mAh g−1 after 100 cycles at 0.1 C, with a low capacity decay of 0.05% per cycle, and demonstrated excellent rate capability. [ABSTRACT FROM AUTHOR]

In this work, black phosphorus quantum dots (BPQDs) were decorated on hexagonal ZnIn2S4 flower-like microspheres to form zero-dimensional/two-dimensional (0D/2D) structures. Interface interactions between the BPQDs and ZnIn2S4 resulted in optimum effective charge transfer, thereby improving the photocatalytic performance of the material. Thus, the 0.2% BPQD–ZnIn2S4 sample showed 30% higher H2 evolution rates compared to pure ZnIn2S4. This study provides a simple route for the synthesis of photocatalysts. The results obtained herein can pave the way for designing effective catalysts for solar-to-chemical energy conversion and feasible approaches to obtain cheap, clean, and efficient photocatalysts. [ABSTRACT FROM AUTHOR]