TY - JOUR
T1 - High Energy Density Rechargeable Batteries Based on Li Metal Anodes. The Role of Unique Surface Chemistry Developed in Solutions Containing Fluorinated Organic Co-solvents
AU - Aurbach, Doron
AU - Markevich, Elena
AU - Salitra, Gregory
N1 - Publisher Copyright: © 2021 American Chemical Society
PY - 2021/12/22
Y1 - 2021/12/22
N2 - To date, lithium ion batteries are considered as a leading energy storage and conversion technology, ensuring a combination of high energy and power densities and prolonged cycle life. A critical point for elaboration of high energy density secondary Li batteries is the use of high specific capacity positive and negative electrodes. Among anode materials, Li metal anodes are considerably superior due to having the highest theoretical specific capacity (3860 mAh g–1) and lowest negative redox potential (−3.040 V vs a standard hydrogen electrode). Combination of Li metal anodes with Li[NiCoM]O2-layered cathodes with a high stable specific capacity of about 200 up to 250 mAh g–1 is particularly attractive. The development of advanced electrolyte solutions which ensure effective passivation of the electrodes’ surfaces is of critical importance. Considerable efforts have been focused on fluorinated organic co-solvents and specifically fluoroethylene carbonate (FEC) due to the formation of thin, flexible Li-ions-conducting surface films with excellent protective properties. However, in the FEC-based solutions, detrimental “cross talk” between the Li anodes and the Li[NiCoM]O2 cathodes leads to worsening of the passivation of Li metal anodes, consumption of the electrolyte solutions, and limited cycle life of full Li|Li[NiCoM]O2 cells cycled with a low amount of the electrolyte solution and practical cycling parameters. The addition of difluoroethylene carbonate (DFEC) co-solvent with lower LUMO energy leads to a significant improvement in the cycling behavior of full cells. Using fluorinated co-solvents possessing synergistic effects is very promising and paves the way for developing rechargeable batteries with the highest energy density.
AB - To date, lithium ion batteries are considered as a leading energy storage and conversion technology, ensuring a combination of high energy and power densities and prolonged cycle life. A critical point for elaboration of high energy density secondary Li batteries is the use of high specific capacity positive and negative electrodes. Among anode materials, Li metal anodes are considerably superior due to having the highest theoretical specific capacity (3860 mAh g–1) and lowest negative redox potential (−3.040 V vs a standard hydrogen electrode). Combination of Li metal anodes with Li[NiCoM]O2-layered cathodes with a high stable specific capacity of about 200 up to 250 mAh g–1 is particularly attractive. The development of advanced electrolyte solutions which ensure effective passivation of the electrodes’ surfaces is of critical importance. Considerable efforts have been focused on fluorinated organic co-solvents and specifically fluoroethylene carbonate (FEC) due to the formation of thin, flexible Li-ions-conducting surface films with excellent protective properties. However, in the FEC-based solutions, detrimental “cross talk” between the Li anodes and the Li[NiCoM]O2 cathodes leads to worsening of the passivation of Li metal anodes, consumption of the electrolyte solutions, and limited cycle life of full Li|Li[NiCoM]O2 cells cycled with a low amount of the electrolyte solution and practical cycling parameters. The addition of difluoroethylene carbonate (DFEC) co-solvent with lower LUMO energy leads to a significant improvement in the cycling behavior of full cells. Using fluorinated co-solvents possessing synergistic effects is very promising and paves the way for developing rechargeable batteries with the highest energy density.
UR - http://www.scopus.com/inward/record.url?scp=85120305038&partnerID=8YFLogxK
U2 - 10.1021/jacs.1c11315
DO - 10.1021/jacs.1c11315
M3 - مقالة مرجعية
C2 - 34807588
SN - 0002-7863
VL - 143
SP - 21161
EP - 21176
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 50
ER -