Ammonium-ion hybrid supercapacitors (AIHSCs) have gained extensive attention due to their high safety and environmental friendliness. Manganese oxides are among the most promising cathode materials; however, the side electrochemical reactions occurring in aqueous electrolytes limit their reversible capacities and energy densities. This work prepares the β-/γ-MnO2 electrode and reveals the side electrochemical reactions occurring in the (NH4)2SO4 electrolyte. Besides the widely recognized dissolution of MnO2, the re-deposition of MnO2 and irreversible insertion of NH4 + exist simultaneously during cycling, resulting in irreversible structural changes of MnO2. A portion of β-/γ-MnO2 converts to δ-MnO2, and a layer of 7Mn(OH)2·2MnSO4·H2O forms on the electrode surface, modifying the ionic accessibility and structural stability of the electrode. The structural changes, along with the competition among the three types of side reactions, cause capacity decay and uprise during cycling. Accordingly, the self-adjusting mechanism is proposed, and trace Mn2+ is added to the electrolyte to facilitate this mechanism, thereby improving performance. Finally, the AIHSC, featuring the MnO2 cathode and activated carbon anode in the Mn2+-added (NH4)2SO4 electrolyte, shows 60.2 mAh g-1 at 0.5 A g-1 under 0-2 V. The maximum energy and power densities of 60.2 Wh kg-1 and 5000 W kg-1 are achieved.
Keywords: Mn2+ electrolyte additive; aqueous ammonium‐ion hybrid supercapacitors; manganese dioxide cathode; self‐adjusting mechanism; side electrochemical reactions.
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