Abstract
AbstractThe electrochemical reactions for the storage of Zn2+ while embracing more electron transfer is a foundation of the future high‐energy aqueous zinc batteries. Herein, we report a six‐electron transfer electrochemistry of nano‐sized TeO2/C (n‐TeO2/C) cathode by facilitating the reversible conversion of TeO2↔Te and Te↔ZnTe. Benefitting from the integrated conductive nanostructure and the proton‐rich environment in providing optimized electrochemical kinetics (facilitated Zn2+ uptake and high electronic conductivity) and feasible thermodynamic process (low Gibbs free energy change), the as‐prepared n‐TeO2/C with stable cycling performance exhibits a superior reversible capacity of over 800 mAh g−1 at 0.1 A g−1. A precise understanding of the reaction mechanism via ex situ and in situ characterizations presents that the reversible six‐electron transfer reaction is proton‐dependent, and a proton generating and consuming mechanism of three‐phase conversion n‐TeO2/C in the weakly acidic electrolyte is thoroughly revealed.
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