4.8 Article

Enabling Ether-Based Electrolytes for Long Cycle Life of Lithium-Ion Batteries at High Charge Voltage

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 12, 期 49, 页码 54893-54903

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c18177

关键词

lithium-ion battery; ether electrolyte; graphite compatibility; high voltage stability; long cycle life; electrode/electrolyte interphase

资金

  1. U.S. Department of Energy (DOE)'s Office of Energy Efficiency and Renewable Energy (EERE) through the Applied Battery Research Program [DE-EE0008444, DE-AC0576RL01830]
  2. Office of Vehicle Technologies of the U.S. DOE under the Advanced Cathode Materials Program [DE-LC-000L053]
  3. DOE's Office of Biological and Environmental Research
  4. DOE [DE-AC05-76RL01830]

向作者/读者索取更多资源

Lithium-ion batteries (LIBs) with high-nickel (Ni) content LiNixMnyCozO2 (x + y + z = 1) (NMC with Ni >= 0.6) cathodes operated at high charge voltages have been considered as one of the most promising candidates for addressing the challenge of increasing energy density demand. Conventional LiPF6-organocarbonate electrolytes exhibit incompatibility with such cell chemistries under certain testing conditions because of the instability of electrode/electrolyte interphases. In response to this challenge, ether-based electrolytes with finely tuned structure and composition of solvation sheaths were developed and evaluated in graphite (Gr)parallel to NMC811 cell chemistry in 2.5-4.4 V, despite ethers being conventionally considered to be unfavorable electrolyte solvents for LIBs because of their anodic instability above 4.0 V and cointercalation into Gr electrodes. The functional ether-based electrolytes in this work enable both excellent cycle life and high rate capability of Gr parallel to NMC811 cells. Mechanistic studies reveal that the unique structure and composition of the solvation sheath of the functional ether electrolytes are the main reasons behind their excellent anodic stability and effective protection of the Gr electrode and, consequently, the extraordinary cell performances when operated at high charge cutoff voltages. This work also provides a feasible approach in developing highly stable functional electrolytes for high-energy density LIBs.

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