As
one of the most promising candidates for next-generation energy
storage technology, lithium–sulfur (Li–S) battery has
been attracting increasing attention due to its high theoretical specific
capacity (1675 mA h g–1), natural abundance, and
environmental friendliness. However, the notorious shuttle effect
caused by the soluble polysulfides as well as the sluggish redox kinetics
significantly hinders the practical application. Herein, sulfiphilic
iron disulfide (FeS2) nanoparticles caged in the hollow
carbon shell have been facilely fabricated as the sulfur host (FeS2@C-S) for Li–S batteries. The deposited amorphous carbon
cage with hollow space can provide efficient pathways for electrons,
facilitate electrolyte penetration, and effectively accommodate the
volume change during the repeated charge/discharge process. In addition,
polar FeS2 nanoparticles have strong chemical interaction
on the polysulfides and can promote the redox conversion of polysulfides
as an electrocatalyst. Visible adsorption and electrochemical analysis
have been conducted to confirm the static polysulfide trapping capability
and dynamic polysulfide conversion reversibility. Synergistically,
the FeS2@C-S cathode with a sulfur loading of ∼1.5
mg cm–2 exhibits high cycle stability with a reversible
capacity of ca. 800 mA h g–1 after 200 cycles at
a current density of 0.2 C and excellent rate performance. Even at
the current density of 5 C, a capacity of ca. 400 mA h g–1 can still be achieved after 400 cycles. This work provides a feasible
approach to provide both physical and chemical protection against
polysulfides resulting from the synergistic effects of multifunctional
units during the sulfur cathode development.