Abstract

AbstractThe electrochemical performance of aqueous zinc metal batteries (AZMBs) is highly dependent on the electric double layer (EDL) properties at Zn electrode/electrolyte interface. Herein, a novel reconfigured EDL is constructed via a double‐charged theanine (TN) additive for super‐stable and deep‐rechargeable AZMBs. Experiments and theoretical computations unravel that the positively charged TN not only serves as preferential anchor to form a water‐poor Helmholtz plane onto the Zn anode, but also its anionic end could coordinate with Zn2+ to tailor the solvation structure in the diffusion layer and further reconstruct the inner H‐bonds networks, thus effectively guiding uniform Zn deposition and suppressing the water‐induced side reactions. Consequently, the Zn//Zn cells acquire outstanding cycling stabilities of nearly 800 h at a high depth of discharge of 80%. Moreover, the Zn//VOX full cells deliver substantial capacity retention (94.12% after 1400 cycles at 2 A g−1) under practical conditions. Importantly, the designed 2.7 Ah Zn//VOX pouch cell harvests a recorded energy density of 42.3 Wh Kgcell−1 and 79.5 Wh Lcell–1, with a remarkable capacity retention of 85.93% after 220 cycles at 50 mA g−1. This innovative design concept to reshape the EDL chemistry would inject fresh vitality into developing advanced AZMBs and beyond.

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