Urchin-shaped NiCo 2 Se 4 (u-NCSe) nanostructures as efficient sulfur hosts are synthesized to overcome the limitations of lithium-sulfur batteries (LSBs). u-NCSe provides a beneficial hollow structure to relieve volumetric expansion, a superior electrical conductivity to improve electron transfer, a high polarity to promote absorption of lithium polysulfides (LiPS), and outstanding electrocatalytic activity to accelerate LiPS conversion kinetics. Owing to these excellent qualities as cathode for LSBs, S@u-NCSe delivers outstanding initial capacities up to 1403 mAh g −1 at 0.1 C and retains 626 mAh g −1 at 5 C with exceptional rate performance. More significantly, a very low capacity decay rate of only 0.016% per cycle is obtained after 2000 cycles at 3 C. Even at high sulfur loading (3.2 mg cm −2 ), a reversible capacity of 557 mAh g −1 is delivered after 600 cycles at 1 C. Density functional theory calculations further confirm the strong interaction between NCSe and LiPS, and cytotoxicity measurements prove the biocompatibility of NCSe. This work not only demonstrates that transition metal selenides can be promising candidates as sulfur host materials, but also provides a strategy for the rational design and the development of LSBs with long-life and high-rate electrochemical performance.

Original measurement data are available upon reasonable request.

The inhibition of this polysulfide shuttle effect and the promotion of the redox reaction kinetics remains as the key material challenges of lithium-sulfur batteries (LSBs) to be urgently solved.Here we report a new architecture for the cathode material based on nanoreactor of ZnSe/Ndoped hollow carbon (ZnSe/NHC). This material combination and the hollow geometry provide three key benefits to the LSBs cathode: i) The combination of lithiophilic sites of NHC and sulfiphilic sites of ZnSe effectively trap LiPS as demonstrated by experimental results and density functional theory (DFT) calculations; ii) In part related to this promoted adsorption, the ZnSe/NHC material combination is able to facilitate the Li + diffusion, thus promoting the redox reaction kinetics; iii) The hollow nanoreactor design traps LiPS and accommodates volumetric expansion preventing the cathode material decomposition. As a result, LSBs cathodes based on this hybrid material, S@ZnSe/NHC, are characterized by high initial capacities, 1475 mAh g −1 at 0.1 C and 542 mAh g −1 at 3 C, and excellent rate capability. Besides, these cathodes deliver stable operation with only 0.022% capacity decay per cycle after 800 cycles at 3 C. Even at high sulfur loading of 3.2 mg cm −2 , a reversible capacity of 540.5 mAh g −1 is delivered after 600 cycles at 1 C. Overall, this work not only further demonstrates the large potential of transitionmetal selenides as cathode materials in LSBs, but also demonstrates the nanoreactor design to be a highly suitable architecture to enhance cycle stability.

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To meet the application needs of rechargeable Zn−air battery and electrocatalytic overall water splitting (EOWS), developing high-efficiency, cost-effective, and durable trifunctional catalysts for the hydrogen evolution reaction (HER), oxygen evolution, and reduction reaction (OER and ORR) is extremely paramount yet challenging. Herein, the interface engineering concept and nanoscale hollowing design were proposed to fabricate N-doping carbon nanoboxes confined with Co/MoC nanoparticles. Uniform zeolitic imidazolate framework nanocube was employed as the starting material to construct the trifunctional electrocatalyst through the conformal polydopamine−Mo layer coating and the subsequent pyrolysis treatment. The Co@IC/MoC@PC catalyst displayed superior electrochemical ORR performances with a positive half-wave potential of 0.875 V and a high limiting current density of 5.89 mA/cm 2 . When practically employed as an electrocatalyst in regenerative Zn−air battery, a high specific capacity of 728 mAh/g, a large peak power density of 221 mW/cm 2 , a high open-circuit voltage of 1.482 V, and a low charge/discharge voltage gap of 0.41 V were obtained. Moreover, its practicability was further exploited by overall water splitting, affording low overpotentials of 277 and 68 mV at 10 mA/cm 2 for the OER and HER in 1 M KOH solution, respectively, and a decent operating potential of 1.57 V for EOWS. Ultraviolet photoelectron spectroscopy and density functional theory calculation revealed that the Co/MoC interface synergistically facilitated the charge-transfer, thereby contributing to the enhancements of electrocatalytic ORR/OER/HER processes. More importantly, this catalyst design concept can offer some interesting prospects for the construction of outstanding trifunctional catalysts toward various energy conversion and storage devices.