Zeng Chaozhi, Huang Chun
The Interdisciplinary Research Center, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai 201210, China.
Key Laboratory of Low-Carbon Conversion Science and Engineering, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai 201210, China.
ACS Omega. 2021 Dec 22;7(1):688-695. doi: 10.1021/acsomega.1c05341. eCollection 2022 Jan 11.
A new lithium-ion battery cathode material of LiF@C-coated FeF·0.33HO of 20 nm primary particles and 200-500 nm secondary particles is synthesized. The redox reaction mechanisms of the new cathode material and the influence of different electrolytes on the electrochemical performance of LiF@C-coated FeF·0.33HO are investigated. We show that LiF@C-coated FeF·0.33HO using a LiFSI/Pyr FSI ionic liquid electrolyte exhibits high reversible capacities of 330.2 and 147.6 mAh g at 200 and 3600 mA g, respectively, as well as maintains high capacity over cycling. Electrochemical characterization shows that the high performance is attributed to higher electronic conductivity of the coating, continuous compensation of the loss of LiF product through the coating, higher ionic conductivity of both the coating and the electrolyte, and higher stability of the electrolyte.
合成了一种新型锂离子电池正极材料,其为LiF@C包覆的FeF·0.33HO,初级颗粒为20nm,次级颗粒为200 - 500nm。研究了这种新型正极材料的氧化还原反应机理以及不同电解质对LiF@C包覆的FeF·0.33HO电化学性能的影响。我们发现,使用LiFSI/Pyr FSI离子液体电解质的LiF@C包覆的FeF·0.33HO在200和3600 mA g下分别表现出330.2和147.6 mAh g的高可逆容量,并且在循环过程中保持高容量。电化学表征表明,高性能归因于涂层较高的电子电导率、通过涂层对LiF产物损失的持续补偿、涂层和电解质两者较高的离子电导率以及电解质较高的稳定性。