A free-standing sulfur/nitrogen-doped carbon nanotube (S/N-CNT) composite prepared via a simple solution method was first studied as a cathode material for lithium/sulfur batteries. By taking advantage of the self-weaving behavior of N-CNT, binders and current collectors are rendered unnecessary in the cathode, thereby simplifying its manufacturing and increasing the sulfur weight ratio in the electrode. Transmission electronic microscopy showed the formation of a highly developed core-shell tubular structure consisting of S/N-CNT composite with uniform sulfur coating on the surface of N-CNT. As a core in the composite, the N-CNT with N functionalization provides a highly conductive and mechanically flexible framework, enhancing the electronic conductivity and consequently the rate capability of the material.

Carbon-coated silica nanoparticles anchored on multi-walled carbon nanotubes (SiO2@C/MWNT composite) were synthesized via a simple and facile sol-gel method followed by heat treatment. Scanning and transmission electron microscopy (SEM and TEM) studies confirmed densely anchoring the carbon-coated SiO2 nanoparticles onto a flexible MWNT conductive network, which facilitated fast electron and lithium-ion transport and improved structural stability of the composite. As prepared, ternary composite anode showed superior cyclability and rate capability compared to a carbon-coated silica counterpart without MWNT (SiO2@C). The SiO2@C/MWNT composite exhibited a high reversible discharge capacity of 744 mAh g−1 at the second discharge cycle conducted at a current density of 100 mA g−1 as well as an excellent rate capability, delivering a capacity of 475 mAh g−1 even at 1000 mA g−1. This enhanced electrochemical performance of SiO2@C/MWNT ternary composite anode was associated with its unique core-shell and networking structure and a strong mutual synergistic effect among the individual components.

In this work, a facile strategy to synthesize oxygen and nitrogen co-doped porous carbon (ONPC) is reported by one-step pyrolysis of waste coffee grounds. As-prepared ONPC possesses highly rich micro/mesopores as well as abundant oxygen and nitrogen co-doping, which is applied to sulfur hosts as lithium/sulfur batteries’ appropriate cathodes. In battery testing, the sulfur/oxygen and nitrogen co-doped porous carbon (S/ONPC) composite materials reveal a high initial capacity of 1150 mAh·g⁻¹ as well as a reversible capacity of 613 mAh·g⁻¹ after the 100th cycle at 0.2 C. Furthermore, when current density increases to 1 C, a discharge capacity of 331 mAh·g⁻¹ is still attainable. Due to the hierarchical porous framework and oxygen/nitrogen co-doping, the S/ONPC composite exhibits a high utilization of sulfur and good electrochemical performance via the immobilization of the polysulfides through strong chemical binding.

A novel sulfur/graphene nanosheet (S/GNS) composite was prepared via a simple ball milling of sulfur with commercial multi-layer graphene nanosheet, followed by a heat treatment. High-resolution transmission and scanning electronic microscopy observations showed the formation of irregularly interlaced nanosheet-like structure consisting of graphene with uniform sulfur coating on its surface. The electrochemical properties of the resulting composite cathode were investigated in a lithium cell with a gel polymer electrolyte (GPE) prepared by trapping 1 mol dm⁻³ solution of lithium bistrifluoromethanesulfonamide in tetraethylene glycol dimethyl ether in a polymer matrix composed of poly(vinylidene fluoride-co-hexafluoropropylene)/poly(methylmethacrylate)/silicon dioxide (PVDF-HFP/PMMA/SiO₂). The GPE battery delivered reversible discharge capacities of 809 and 413 mAh g⁻¹ at the 1st and 50th cycles at 0.2C, respectively, along with a high coulombic efficiency over 50 cycles. This performance enhancement of the cell was attributed to the suppression of the polysulfide shuttle effect by a collective effect of S/GNS composite cathode and GPE, providing a higher sulfur utilization.

A novel nitrogen doped mesoporous carbon (NMPC) with a hierarchical porous structure is prepared by simple carbonizing the green algae, which is applied as a host material to encapsulate sulfur for lithium/sulfur (Li/S) battery. The NMPC exhibits high pore volume as well as large specific surface area, and thus sulfur content in the S/NMPC composite reaches up to 63 wt %. When tested in a Li/S battery, the S/NMPC composite yields a high initial capacity of 1327 mAh·g⁻¹ as well as 757 mAh·g⁻¹ after 100 cycles at a current rate of 0.1 C, a reversible capacity of 642 was achieved even at 1 C. This good electrochemical performance of the S/NMPC composite could be attributed to a unique combination of mesopority and surface chemistry, allowing for the retention of the intermediate polysuflides within the carbon framework.

Mesoporous ZnO nanosheets are synthesized through a room temperature solvothermal method. Transmission and scanning electronic microscopy observations indicate that as-prepared ZnO hierarchical aggregates are composed and assembled by nanosheets with a length of 1–2 μm and a thickness of 10–20 nm, and interlaced ZnO nanosheets irregularly stack together, forming a three-dimensional network. Furthermore, large mesopores are embedded in the walls of ZnO nanosheets, confirmed by Brunauer-Emmett-Teller (BET) measurement. Accordingly, the resulting ZnO anode exhibits a high and stable specific discharge capacity of 421 mAh g−1 after 100 cycles at 200 mA g−1 and a good rate capability. Such electrochemical performance could be attributed to the multiple synergistic effects of its mesoporous nanosheet structure, which can not only provide a large specific surface area for lithium storage, but also favor the ion transport and electrolyte diffusion.