4.6 Article

Lessons Learned from Long-Term Cycling Experiments with Pouch Cells with Li-Rich and Mn-Rich Positive Electrode Materials

Journal

JOURNAL OF THE ELECTROCHEMICAL SOCIETY
Volume 169, Issue 6, Pages -

Publisher

ELECTROCHEMICAL SOC INC
DOI: 10.1149/1945-7111/ac76e8

Keywords

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Funding

  1. NSERC
  2. Tesla Canada
  3. Ernst Jaakson Memorial Fund
  4. NSERC Vanier CGS
  5. Killam Foundation
  6. Nova Scotia Graduate Scholarship
  7. China Scholarship Council
  8. Walter C. Sumner Foundation
  9. Vidyasirimedhi Institute of Science and Technology (VISTEC)

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In this study, the performance of commercial pouch cells with Li1.11Ni0.34Mn0.53Al0.02O2/graphite (LNMA) and Li1.167Ni0.183Mn0.558Co0.092O2/graphite (LNMC) electrodes was evaluated under different cycling conditions. The best performing electrolyte for high voltage LNMA cells was Control + 2% fluoroethylene carbonate + 1% lithium difluorophosphate + 1% lithium difluoro(oxalato)borate, retaining 87% capacity after 720 cycles. LNMA cells cycled to 4.25 V and LNMC cells cycled to 4.44 V at 40 degrees C could cycle for 1000 cycles with 80% capacity retention.
In this work, the performance of commercial (250-300 mAh) Li1.11Ni0.34Mn0.53Al0.02O2/graphite (LNMA) and Li1.167Ni0.183Mn0.558Co0.092O2/graphite (LNMC) pouch cells was evaluated using different cycling drive profiles, temperatures, formation voltages, cycling upper and lower cut-off voltages. A variety of electrolyte additives and additive combinations were tested in the LNMA cells. The best performing electrolyte in high voltage LNMA cells (4.6 V upper cut-off) was Control + 2% fluoroethylene carbonate (FEC) + 1% lithium difluorophosphate (LFO) + 1% lithium difluoro(oxalato)borate (LiDFOB) with 87% capacity retention after 720 cycles. LNMA cells cycled to 4.25 V and LNMC cells cycled to 4.44 V at 40 degrees C were able to cycle for 1000 cycles before reaching 80% capacity. These materials can have surprisingly good high-voltage performance, but we stress that a fundamental breakthrough that can eliminate the voltage fade that is ubiquitous in Li-rich and Mn-rich materials is necessary to make Li-rich materials competitive with existing cell chemistries. We demonstrate that the high specific capacity of Li-rich materials can be deceptive when making conclusions about the energy density of Li-rich/graphite full cells. Hopefully, these results can set a baseline for other researchers in the Li-rich space.

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