Abstract
Lithium‐sulfur (Li−S) batteries have been highly praised for the key rechargeable batteries due to their numerous advantages. However, the sluggish conversion and shuttling effect of polysulfides restrict their practicality. Here we rationally design the multi‐cavity hollow carbon spheres doped with atomic Fe−N sites (Fe−N/MCHCS) as physically/chemically double‐confined catalytic nanoreactors for the efficient sulfur host materials. The Fe−N/MCHCS with hierarchical porous structure and high pore volume ensures the high loading mass, and the multi‐cavity structures significantly buffer the volume expansion of sulfur and enhance the electronic contact. Meanwhile, atomic Fe offers chemical binding site and efficiently catalyzes the conversion of polysulfides during cycling, thus immobilizing and alleviating the shutting effect of polysulfides. Consequently, the Fe−N/MCHCS nanoreactor based Li−S batteries deliver a long cycling life of 1135 mAh g−1 after 300 cycles at 0.5 C and high‐rate capability of 1055 mAh g−1 at 8 C. Even under practical conditions with a high sulfur mass loading of 5.0 mg cm−2, a steady areal capacity of 4.85 mAh cm−2 is attained. This strategy combing multi‐cavity hollow carbon with single atom catalysis opens a reliable route to design highly stable and high‐performance Li−S batteries.
Sulfur host: A multi‐cavity hollow carbon sphere doped with atomic Fe−N site is designed as a physically/chemically double‐confined catalytic nanoreactor for sulfur host of Li−S batteries. The nanoreactor with hierarchical porous structure and large pore volume ensures the high loading mass and buffers the volume expansion of sulfur, while the atomic Fe offers chemical binding and catalytic conversion for lithium polysulfides, thus offering excellent performance for Li−S batteries.