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 Fe7S8 nanoparticles anchored on a
porous N-doped carbon nanosheet (CN) skeleton (denoted as Fe7S8/NC) with high conductivity and numerous active sites via 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 Fe7S8 can not only ensure enhanced Na+ adsorption
ability but also promote the charge transfer kinetics of the Fe7S8/NC electrode. Accordingly, the designed Fe7S8/NC electrode exhibits remarkable electrochemical
performance with superior high-rate capability (451.4 mAh g–1 at 6 A g–1) and excellent long-term cycling stability
(508.5 mAh g–1 over 1000 cycles at 4 A g–1) 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.