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Simultaneously constructing solid cathode/anode-electrolyte interphase by anions decomposition in aqueous Zn battery
被引:0
|作者:
Zhu, Chaoqiong
[1
]
Ruan, Hao
[1
,2
]
Zheng, Limin
[1
]
Dong, Xiaodong
[3
]
Pu, Zewei
[3
]
Wan, Fang
[1
]
Guo, Xiaodong
[1
]
机构:
[1] Sichuan Univ, Sch Chem Engn, Chengdu 610065, Peoples R China
[2] Chengdu Univ, Sch Mech Engn, Chengdu 610106, Peoples R China
[3] Xizang Autonomous Reg Energy Res Demonstrat Ctr, Lasa 850000, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Aqueous Zn batteries;
Solid electrode-electrolyte interphase;
Solvation structure;
Low current density;
IN-SALT ELECTROLYTE;
CHALLENGES;
D O I:
10.1016/j.cej.2024.158241
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
Aqueous Zn batteries exhibit enormous potential in large-scale energy storage. However, complex interfacial side reactions between electrode and electrolyte fast deteriorate the electrochemical performance. Directly constructing solid electrode-electrolyte interphase is an effective strategy to enhance the interface stability, while it is difficult to form solid electrode-electrolyte interphase in conventional electrolytes. Herein, propylene carbonate was introduced into water-in-salts electrolytes to regulate Zn2+ solvation structure, which reduces the HOMO and LUMO energy gap of Zn2+ solvation complexes. As a result, anion-derived cathode-electrolyte interphase (CEI) and anode-electrolyte interphase (SEI) are formed simultaneously. Assembled Zn||Zn symmetrical cell achieves high cycling stability over 9000 h at 8 mA cm- 2 with 8 mAh cm- 2 . Moreover, Zn||Alx- V2O5 & sdot;nH2O battery displays excellent cycling performance at low current density (capacity retention rate of 92 %/94 % after 400/1300 cycles of 0.2/0.5 A g- 1 ). This work provides a simple and effective strategy to simultaneously construct CEI layer and SEI layer, achieving long life aqueous Zn batteries.
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