High ionic conductivity electrolyte and intimate interfacial contact are crucial factors to realize high-performance all-solid-state sodium batteries. NaPSSe electrolyte with reduced particle size of 500 nm is first synthesized by a simple liquid-phase method and exhibits a high ionic conductivity of 1.21 × 10 S cm, which is comparable with that synthesized with a solid-state reaction. Meanwhile, a general interfacial architecture, that is, NaPSSe electrolyte uniformly anchored on FeS nanorods, is designed and successfully prepared by an in situ liquid-phase coating approach, forming core-shell structured FeS@NaPSSe nanorods and thus realizing an intimate contact interface. The FeS@NaPSSe/NaPSSe/Na all-solid-state sodium battery demonstrates high specific capacity and excellent rate capability at room temperature, showing reversible discharge capacities of 899.2, 795.5, 655.1, 437.9, and 300.4 mAh g at current densities of 20, 50, 100, 150, and 200 mA g, respectively. The obtained all-solid-state sodium batteries show very high energy and power densities up to 910.6 Wh kg and 201.6 W kg based on the mass of FeS at current densities of 20 and 200 mA g, respectively. Moreover, the reaction mechanism of FeS is confirmed by means of ex situ X-ray diffraction techniques, showing that partially reversible reaction occurs in the FeS electrode after the second cycle, which gives the obtained all-solid-state sodium battery an exceptional cycling stability, exhibiting a high capacity of 494.3 mAh g after cycling at 100 mA g for 100 cycles. This contribution provides a strategy for designing high-performance room temperature all-solid-state sodium battery.

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http://dx.doi.org/10.1021/acsnano.8b00073DOI Listing

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