Spatially Confined FeS Nanoparticles Anchored on a Porous Nitrogen-Doped Carbon Nanosheet Skeleton for High-Rate and Durable Sodium Storage.

Iron sulfides are widely explored as anodes of sodium-ion batteries (SIBs) owing to high theoretical capacities and low cost, but their practical application is still impeded by poor rate capability and fast capacity decay. Herein, for the first time, we construct highly dispersed FeS nanoparticles anchored on a porous N-doped carbon nanosheet (CN) skeleton (denoted as FeS/NC) with high conductivity and numerous active sites facile ion adsorption and thermal evaporation combined procedures coupled with a gas sulfurization treatment. Nanoscale design coupled with a conductive carbon skeleton can simultaneously mitigate the above obstacles to obtain enhanced structural stability and faster electrode reaction kinetics. With the aid of density functional theory (DFT) calculations, the synergistic interaction between CNs and FeS can not only ensure enhanced Na adsorption ability but also promote the charge transfer kinetics of the FeS/NC electrode. Accordingly, the designed FeS/NC electrode exhibits remarkable electrochemical performance with superior high-rate capability (451.4 mAh g at 6 A g) and excellent long-term cycling stability (508.5 mAh g over 1000 cycles at 4 A g) due to effectively alleviated volumetric variation, accelerated charge transfer kinetics, and strengthened structural integrity. Our work provides a feasible and effective design strategy toward the low-cost and scalable production of high-performance metal sulfide anode materials for SIBs.