Abstract
Aqueous Zn‒I2 batteries based on four-electron conversion chemistry have been extensive explored due to their high voltage and large specific capacity. However, the intrinsic instability of I+ generated during the high-voltage conversion process and the severe electrochemical corrosion of Zn anode in aqueous electrolyte primarily hinder the construction of high-performance Zn‒I2 batteries. Herein, trimethylammonium bromide (TMBr) with functional cation and anion has been selected as a dual-side shielding electrolyte additive to concurrently resolve these problems. On the one hand, Br− in TMBr could incorporate into the electrolyte solvation structure and reconstitute the hydrogen-bond (H-bond) network, suppressing the activity of free H2O molecules and consequently enhancing the Zn anode stability. On the other hand, the Br− could electrochemically activate I+, followed by the stabilization of I+ via complexation interactions with trimethylamine cations (TM+) and Br−, synergistically achieving facile high-voltage conversion chemistry of I2 cathode. As a result, the TMBr additive enables the four-electron conversion-type Zn‒I2 batteries to demonstrate a remarkable capacity of 250 mAh g−1 coupled with stable cycling exceeding 15000 cycles at 3 A g−1. Additionally, the 160 mAh pouch cell delivers an energy density of 367.4 Wh kg−1 (based on I2 mass) with a lifetime of over 300 cycles.

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