共 39 条
Dilute dual-salt electrolyte for successful passivation of in-situ deposited Li anode and permit effective cycling of high voltage anode free batteries
被引:14
作者:

Beyene, Tamene Tadesse
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Jimma Univ, Coll Nat Sci, Dept Chem, POB 378, Jimma, Ethiopia Jimma Univ, Coll Nat Sci, Dept Chem, POB 378, Jimma, Ethiopia

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[1] Jimma Univ, Coll Nat Sci, Dept Chem, POB 378, Jimma, Ethiopia
[2] Natl Taiwan Univ Sci & Technol, Grad Inst Appl Sci Technol, Nano Electrochem Lab, Taipei 106, Taiwan
[3] Natl Taiwan Univ Sci & Technol, Appl Res Ctr Thin Film Met Glass, Dept Chem Engn, Nano Electrochem Lab, Taipei 106, Taiwan
[4] Natl Synchrotron Radiat Res Ctr, Hsinchu 300 76, Taiwan
关键词:
Imide-orthoborate;
Dual-salt;
Anode free;
Interfacial chemistry;
High voltage battery;
RENEWABLE ENERGY;
METAL;
PERFORMANCE;
DISSOLUTION;
CATHODES;
STORAGE;
LITFSI;
LIODFB;
ETHER;
D O I:
10.1016/j.jpowsour.2022.231752
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:
An investigation of the cycling stability of anode-free batteries (AFBs) using dilute dual-salt electrolytes is conducted in a mixture of ether and carbonate solvents. Using the AFB configuration, various compositions of the dual-salt electrolyte were optimized and it was found that 0.9M-LiTFSI+0.3M-LiDFOB in FEC/TTE (2:3, v/v) is the best. An in-depth investigation of the electrochemical performance of AFB was conducted in this optimized dual-salt composition in comparison to 1.2 M LiTFSI in the same solvent ratio. Accordingly, the performance of Cu||NMC cell in the dual-salt electrolyte surpassed that of the single-salt. The relative better performance of the AFB in the dual-salt electrolyte is attributed to the co-existence of dual-ion (TFSI-&DFOB-) in the electrolyte, which enhanced conductivity and introduces entirely new interphases via preferential decomposition mechanisms. The newly formed interface is stable, ionically conductive, and able to intercept parasitic side reactions between the electrolyte solvent and the deposited Li by blocking electron and solvent flow towards the deposit. As a result of the unique interfacial chemistry brought by this dual-salt system, this electrolyte supports a unique CE (98.6%) and capacity retention (63%) in 4.5V Cu||NMC cell and exhibited >27% improvement over the single salt electrolyte after 50 cycles.
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Natl Taiwan Univ Sci & Technol, Nanoelectrochem Lab, Dept Chem Engn, Taipei 106, Taiwan Stanford Univ, Dept Chem, Stanford, CA 94305 USA

Bezabh, Hailemariam Kassa
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Natl Taiwan Univ Sci & Technol, Nanoelectrochem Lab, Dept Chem Engn, Taipei 106, Taiwan Stanford Univ, Dept Chem, Stanford, CA 94305 USA

Berhe, Gebregziabher Brhane
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Natl Taiwan Univ Sci & Technol, Nanoelectrochem Lab, Dept Chem Engn, Taipei 106, Taiwan Stanford Univ, Dept Chem, Stanford, CA 94305 USA

Abrha, Ljalem Hadush
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Natl Taiwan Univ Sci & Technol, Nanoelectrochem Lab, Dept Chem Engn, Taipei 106, Taiwan Stanford Univ, Dept Chem, Stanford, CA 94305 USA

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Huang, Chen-Jui
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Natl Taiwan Univ Sci & Technol, Nanoelectrochem Lab, Dept Chem Engn, Taipei 106, Taiwan Stanford Univ, Dept Chem, Stanford, CA 94305 USA

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Dai, Hongjie
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Stanford Univ, Dept Chem, Stanford, CA 94305 USA Stanford Univ, Dept Chem, Stanford, CA 94305 USA

Hwang, Bing Joe
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Natl Synchrotron Radiat Res Ctr NSRRC, Hsinchu 30076, Taiwan Stanford Univ, Dept Chem, Stanford, CA 94305 USA