Quasi-Solid Sulfur Conversion for Energetic All-Solid-State Na-S Battery

The high theoretical energy density (1274 Wh kg-1) and high safety enable the all-solid-state Na-S batteries with great promise for stationary energy storage system. However, the uncontrollable solid-liquid-solid multiphase conversion and its associated sluggish polysulfides redox kinetics pose a great challenge in tunning the sulfur speciation pathway for practical Na-S electrochemistry. Herein, we propose a new design methodology for matrix featuring separated bi-catalytic sites that control the multi-step polysulfide transformation in tandem and direct quasi-solid reversible sulfur conversion during battery cycling. It is revealed that the N, P heteroatom hotspots are more favorable for catalyzing the long-chain polysulfides reduction, while PtNi nanocrystals manipulate the direct and full Na2S4 to Na2S low-kinetic conversion during discharging. The electrodeposited Na2S on strongly coupled PtNi and N, P-codoped carbon host is extremely electroreactive and can be readily recovered back to S8 without passivation of active species during battery recharging, which delivers a true tandem electrocatalytic quasi-solid sulfur conversion mechanism. Accordingly, stable cycling of the all-solid-state soft-package Na-S pouch cells with an attractive specific capacity of 876 mAh gS-1 and a high energy of 608 Wh kgcathode-1 (172 Wh kg-1, based on the total mass of cathode and anode) at 60 degrees C are demonstrated. A new design methodology for matrix featuring separated bi-catalytic sites that direct one-step reversible sulfur conversion during battery cycling was proposed. And the tandem electrocatalysis manipulated tunable quasi-solid sulfur redox chemistry smoothen the efficient entrapping-catalysis-conversion polysulfide speciation for practical all-solid-state Na-S batteries.+ image