Dual robust electrode-electrolyte interfaces enabled by fluorinated electrolyte for high-performance zinc metal batteries

被引:0
|
作者
Guo, Xun [1 ]
Hong, Hu [1 ]
Li, Qing [1 ]
Zhu, Jiaxiong [1 ]
Wu, Zhuoxi [1 ]
Wang, Yanbo [1 ]
Yang, Shuo [1 ]
Huang, Zhaodong [1 ]
Huang, Yan [2 ]
Li, Nan [1 ]
Zhi, Chunyi [3 ,4 ]
机构
[1] City Univ Hong Kong, Dept Mat Sci & Engn, 83 Tat Chee Ave, Hong Kong 999077, Peoples R China
[2] Harbin Inst Technol, Sch Mat Sci & Engn, Sauvage Lab Smart Mat, Shenzhen 518055, Guangdong, Peoples R China
[3] Hong Kong Ctr Cerebro Cardiovasc Hlth Engn COCHE, Shatin, Hong Kong 999077, Peoples R China
[4] City Univ Hong Kong, Ctr Adv Nucl Safety & Sustainable Dev, Kowloon, Hong Kong 999077, Peoples R China
关键词
ION BATTERIES; INTERPHASES; WATER; LAYER;
D O I
10.1016/j.matt.2024.08.002
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Rechargeable zinc metal batteries (ZMBs) are promising for fabricating low-cost, safe, and high-energy-density storage systems. However, ZMBs typically undergo interfacial side reactions and cathode dissolution during cycling, resulting in the depletion of active materials and performance decay of batteries. Here, we develop a localized high-concentration fluorinated electrolyte featuring a high fluorine/oxygen atomic ratio (388.72%) with beneficial solvation chemistry, fostering the simultaneous formation of a cathode-electrolyte interphase (CEI) enriched with C-F bonds and a ZnF2-dominant solid-electrolyte interphase (SEI). The constructed robust electrode-electrolyte interfaces (EEIs) contribute to dendrite-free zinc deposition and a highly stable cathode, demonstrating soft-packed Zn||Mn-doped V2O5 batteries with an exceptional energy density (91.25 Wh kg- 1cathode+anode ) and capacity retention (90.5%) over 500 cycles employing a limited zinc supply. The anode-free ZMBs deliver a record power density of 153.9 Wh kg- 1 cathode+ anode with a high capacity retention of 80.2% over 1,500 cycles. This research provides significant insights for interface construction in multivalent ion batteries.
引用
收藏
页码:4014 / 4030
页数:18
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