The practical deployment of lithium sulfur batteries demands stable cycling of high loading and dense sulfur cathodes under lean electrolyte conditions, which is very difficult to realize. We describe here a strategy of fabricating extremely dense sulfur cathodes, designed by integrating MoS nanoparticles as a multifunctional mediator with a Li-ion conducting binder and a high-performance FeO@N-carbon sulfur host. The MoS nanoparticles have substantially faster Li-ion insertion kinetics compared with sulfur, and the produced LiMoS particles have spontaneous redox reactivity with relevant polysulfide species (such as LiMoS + LiS ↔ LiMoS + LiS, Δ = -84 kJ mol), which deliver a true redox catalytic sulfur conversion mechanism. In addition, LiMoS particles strongly absorb polysulfide during battery cycling, which provides a quasi-solid sulfur conversion pathway and almost eliminated polysulfide dissolution. Such a pathway not only promotes growth of uniform LiS that can be readily charged back with nearly no overpotential, but also mitigates the polysulfide-induced Li metal corrosion issue. The combination of these benefits enables stable and high capacity cycling of dense sulfur cathodes under a low electrolyte to sulfur ratio (4.2 μL mg), as demonstrated with cathodes with volumetric capacities of at least 1.3 Ah cm and capacity retentions of ∼80% for 300 cycles. Furthermore, stable cycling of batteries under a practically relevant N/P ratio of 2.4 is also demonstrated.
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http://dx.doi.org/10.1021/acsnano.9b08516 | DOI Listing |
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