Abstract
Despite the impressive merits of low-cost and high-safety electrochemical energy storage for aqueous zinc ion batteries, researchers have long struggled against the unresolved issues of dendrite growth and the side reactions of zinc metal anodes. Herein, a new strategy of zinc-electrolyte interface charge engineering induced by amino acid additives is demonstrated for highly reversible zinc plating/stripping. Through electrostatic preferential absorption of positively charged arginine molecules on the surface of the zinc metal anode, a self-adaptive zinc-electrolyte interface is established for the inhibition of water adsorption/hydrogen evolution and the guidance of uniform zinc deposition. Consequently, an ultra-long stable cycling up to 2200 h at a high current density of 5 mA cm−2 is achieved under an areal capacity of 4 mAh cm−2. Even cycled at an ultra-high current density of 10 mA cm−2, 900 h-long stable cycling is still demonstrated, demonstrating the reliable self-adaptive feature of the zinc-electrolyte interface. This work provides a new perspective of interface charge engineering in realizing highly reversible bulk zinc anode that can prompt its practical application in aqueous rechargeable zinc batteries.
Original language | English |
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Article number | 2103514 |
Number of pages | 9 |
Journal | Advanced Functional Materials |
Volume | 31 |
Issue number | 45 |
Early online date | 6 Aug 2021 |
DOIs | |
Publication status | Published - 3 Nov 2021 |
Keywords
- amino acid additives
- aqueous rechargeable zinc batteries
- cycling stability
- interface charge engineering
- zinc anodes