摘要
Room-temperature sodium–sulfur (Na–S) batteries offer a sustainable energy storage solution to conventional lithium (Li)-based systems 1 , 2 , 3 , owing to the high element abundances and theoretical electrochemical performance 4 , 5 . However, their practical applications have been severely hindered by the low discharge voltages and the need for largely excessive Na metal anode 6 , 7 , 8 . Here we report a 3.6 V class Na–S battery featuring a high-valence sulfur/sulfur tetrachloride (S/SCl 4 ) cathode chemistry and anode-free configuration. We show that sodium dicyanamide (NaDCA) can simultaneously unlock reversible S/SCl 4 conversion and Na plating/stripping in a non-flammable chloroaluminate electrolyte. This design enables the maximum energy and power densities of 1,198 Wh kg −1 and 23,773 W kg −1 , respectively, calculated on the basis of the total electrode mass including both the cathode and the anode. Also, we demonstrate facilitated S/SCl 4 conversion by incorporating a bismuth-coordinated covalent organic framework (Bi-COF) catalyst (8 wt% loading) into the S cathode, which realizes an impressive discharge capacity of 1,206 mAh g (sulfur+catalyst) −1 , contributing to a maximum energy density of 2,021 Wh kg −1 calculated on the basis of the total electrode mass. With an estimated cost of US$5.03 per kWh and excellent scalability, our anode-free Na–S battery shows promise in grid energy storage and wearable electronics.
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