Zn-anode stability in additive added perchlorate electrolyte for aqueous Zn-MnO2 battery

被引:3
作者
Sambandam, Balaji [1 ]
Lee, Hyeonseo [1 ]
Kim, Sungjin [1 ]
Zikri, Adi Tiara [1 ]
Lestari, Kiki Rezki [1 ]
Lee, Seunggyeong [1 ]
Kim, Jaekook [1 ]
机构
[1] Chonnam Natl Univ, Dept Mat Sci & Engn, Gwangju 61186, South Korea
基金
新加坡国家研究基金会;
关键词
Zn anode; Zn (ClO (4 )) (2) electrolyte with additive; High DoDs; Zn-MnO (2) aqueous Zn-ion battery; LONG-LIFE; ZINC; STRATEGIES;
D O I
10.1016/j.jpowsour.2024.235413
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Extensive research has been conducted on aqueous Zn-MnO2 batteries in the most common ZnSO4 electrolyte. However, the present study focuses on Zn anode stability and subsequent pairing with the commonly utilized MnO2 cathode in a low-concentration aqueous Zn (ClO4)(2) electrolyte containing an organic additive, triethyl phosphate (TEP). The structural stability of Zn anodes in optimized additive-added and additive-free electrolytes is analyzed by assembling series of Zn parallel to Zn symmetry cells under various electrochemical conditions with varying depth of discharges between 20 and 60 %. As such, additive added electrolyte stabilizes the Zn anode over 250 h under high areal capacity/low areal current density of 38.3 mAh cm(-2)/11.3 mA cm(-2) with 60 % depth of discharge at long half-cycle time of 29.5 h. The Zn-MnO2 paired cells in the Zn (ClO4)(2) electrolyte with and without additives registered reversible capacities of 262 and 247 mAh g(-1), respectively, at 0.05 A g(-1). These electrochemical features are completely different from those of the common ZnSO4 electrolyte, whose electrochemical mechanism is still a subject of debate.
引用
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页数:11
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