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Abstract Lithium–sulfur batteries (LSBs) are a class of new‐generation rechargeable high‐energy‐density batteries. However, the persisting issue of lithium polysulfides (LiPs) dissolution and the shuttling effect that impedes the efficiency of LSBs are challenging to resolve. Herein a general synthesis of highly dispersed pyrrhotite Fe 1− x S nanoparticles embedded in hierarchically porous nitrogen‐doped carbon spheres (Fe 1− x S‐NC) is proposed. Fe 1− x S‐NC has a high specific surface area (627 m 2 g −1 ), large pore volume (0.41 cm 3 g −1 ), and enhanced adsorption and electrocatalytic transition toward LiPs. Furthermore, in situ generated large mesoporous pores within carbon spheres can accommodate high sulfur loading of up to 75%, and sustain volume variations during charge/discharge cycles as well as improve ionic/mass transfer. The exceptional adsorption properties of Fe 1− x S‐NC for LiPs are predicted theoretically and confirmed experimentally. Subsequently, the electrocatalytic activity of Fe 1− x S‐NC is thoroughly verified. The results confirm Fe 1− x S‐NC is a highly efficient nanoreactor for sulfur loading. Consequently, the Fe 1− x S‐NC nanoreactor performs extremely well as a cathodic material for LSBs, exhibiting a high initial capacity of 1070 mAh g −1 with nearly no capacity loss after 200 cycles at 0.5 C. Furthermore, the resulting LSBs display remarkably enhanced rate capability and cyclability even at a high sulfur loading of 8.14 mg cm −2 .
Boyjoo et al. (Thu,) studied this question.