Achieving high loading of active sulfur yet rational regulating the shuttle effect of lithium polysulfide (LiPS) is of great significance in pursuit of high-performance lithium-sulfur (Li-S) battery. Herein, we develop a free-standing graphene-nitrogen (N), phosphorus (P) and fluorine (F) co-doped mesoporous carbon-sulfur (G-NPFMC-S) film, which was used as a binder-free cathode in Li-S battery. The developed mesoporous carbon (MC) achieved a high specific surface area of 921 m²·g^–1 with a uniform pore size distribution of 15 nm. The inserted graphene network inside G-NPFMC-S cathode can effectively improve its electrical conductivity and simultaneously restrict the shuttle of LiPS. A high sulfur loading of 86% was achieved due to the excellent porous structures of graphene-NPFMC (G-NPFMC) composite. When implemented as a freestanding cathode in Li-S battery, this G-NPFMC-S achieved a high specific capacity (1,356 mAh·g^–1), favorable rate capability, and long-term cycling stability up to 500 cycles with a minimum capacity fading rate of 0.025% per cycle, outperforming the corresponding performances of NPFMC-sulfur (NPFMC-S) and MC-sulfur (MC-S). These promising results can be ascribed to the featured structures that formed inside G-NPFMC-S film, as that highly porous NPFMC can provide sufficient storage space for the loading of sulfur, while, the N, P, F-doped carbonic interface and the inserted graphene network help hinder the shuttle of LiPS via chemical adsorption and physical barrier effect. This proposed unique structure can provide a bright prospect in that high mass loading of active sulfur and restriction the shuttle of LiPS can be simultaneously achieved for Li-S battery.

Metal-organic framework (MOF)-derived functional carbon matrices have recently attracted considerable attention as energy-storage materials. However, the development of MOF-derived carbon materials with hierarchical structures, capable of thoroughly preventing the "shuttling" of polysulfides, is still a major challenge. Herein, we synthesized cobalt nanoparticle-containing porous carbon polyhedra with in situ grown N-doped carbon nanotube (CNT) backbone (NCCNT-Co), using zeolitic imidazolate framework-67 (ZIF-67) as starting material. The obtained NCCNT-Co, with interconnected N-doped CNTs on both inner and outer surfaces, possesses an integrated conductive network, which can further accelerate the transport of electrons/ions inside the whole sulfur cathode. The mesoporous structure derived from the ZIF-67 matrix and the densely immobilized CNTs, coupled with the homogeneously doped N atoms and Co nanoparticles, can efficiently trap lithium polysulfides (LiPSs) by physical confinement and chemical interactions. Furthermore, the hierarchical structure of the porous carbon polyhedra enables a high sulfur loading of up to 76 wt.% and can also buffer the volume changes of active sulfur during the lithiation process. As a result, the NCCNT-Co-S cathode delivers a high initial specific capacity of 1, 300 mAh·g^-1 at 0.1 C, along with a high capacity of 860 mAh·g^-1 after 500 cycles at 1 C, with an extremely low capacity decay of 0.024% per cycle.