The raw material selected for this research was Brazil chestnut shells (BCs), which were utilized to gain porous carbon as a positive electrode for lithium–sulfur batteries (LSBs). The effects of N/S co-doped on the electrochemical properties of porous carbon materials were studied using thiourea as nitrogen and sulfur sources. The experimental results indicate that the N/S co-doped carbon materials have a higher mesopore ratio than the undoped porous carbon materials. The porous carbon material NSPC-2 has a lotus-like structure with uniform pore distribution. The N and S doping contents are 2.5% and 5.4%. The prepared N/S co-doped porous carbon materials were combined with S, respectively, and three kinds of sulfur carbon composites were obtained. Among them, the composite NSPC-2/S can achieve the initial specific discharge capacity of 1018.6 mAh g− 1 at 0.2 C rate. At 1 C rate, the initial discharge capacity of the material is 730.6 mAh g− 1, and the coulomb efficiency is 98.6% and the capacity retention rate is 71.5% after 400 charge–discharge cycles.

Electric-propulsion systems for ships, also known as electric propulsion devices, represent the current direction of development for maritime power. Issues concerning the environment and fuel economy have compelled the maritime transport sector to seek solutions that reduce emissions and improve fuel efficiency. In this process, power electronics technology plays a significant role in the propulsion systems of ships. Selecting an efficient battery system is of great importance for enhancing the cruising range of yachts and minimizing environmental impact. The battery model is crucial for revealing the working principles of batteries, and it is extremely critical for the application and development of battery technology. The Battery Management System (BMS) serves a crucial regulatory function, optimizing both the safety and performance of battery cells. Central to its operation is the precise estimation of the battery's State of Charge (SOC), a process dependent on an exacting battery model. This system not only enhances longevity and reliability but also ensures that energy storage solutions meet high standards of efficacy. This study focused on testing the impedance characteristics of lithium-sulfur batteries (LSB) at various SOC points and establishing first- and second-order RC equivalent circuit models. The model parameters were identified through experimental data. Subsequently, a simulation platform was constructed using MATLAB/Simulink to simulate the behavior of LSB under a constant current discharge condition. The simulation results showed that the second-order RC model had significantly lower errors than the first-order model, demonstrating higher accuracy. These achievements can provide technical support for the research of energy storage systems in the green aviation and maritime industries.

We reported the synthesis of dendrite-like carbon nanotube-confined polymeric sulfur composite by modifying the surface of carbon nanotubes (CNTs) with trithiocyanuric acid (TTCA) and then copolymerizing with sulfur. DSC results show the successfully formation of robust chemical bonds between sulfur and TTCA modified CNTs, which effectively avoid the dissolution of polysulfide when used as cathodes for lithium–sulfur batteries. The composite with a high sulfur content of 78 wt% exhibits an initial charge capacity of 698 mAh g− 1 and the residual capacity of 553 mAh g− 1 after 1000 cycles at a rate of 1 C.

We fabricated a Li-S battery with post-treated carbon nanotube (CNT) films which offered better support for sulfur, and investigated the effect of the surface properties and pore structure of the post-treated CNT films on Li-S battery performance. Post-treatments, i.e., acid treatment, unzip process and cetyltrimethylammonium bromide (CTAB) treatment, effectively modified the surface properties and pore structure of the CNT film. The modified pore structure impacted the ability of the CNT films to accommodate the catholyte, resulting in an increase in initial discharge capacity.