TY - JOUR
T1 - The Evolution of LiNi0.5Mn0.3Co0.2O2Particle Damage from Fast Charging in Optimized, Full Li-Ion Cells
AU - Preefer, Molleigh B.
AU - Tanim, Tanvir R.
AU - Welborn, Samuel S.
AU - Agyeman-Budu, David N.
AU - Dunlop, Alison R.
AU - Trask, Stephen E.
AU - Dufek, Eric J.
AU - Jansen, Andrew N.
AU - Nelson Weker, Johanna
N1 - Funding Information:
This work was supported by the Vehicle Technologies Office of the U.S. Department of Energy’s Office of Energy Efficiency and Renewable Energy under the Advanced Battery Cell Research Program (eXtreme fast charge Cell Evaluation of Lithium-ion batteries, XCEL). Stanford Synchrotron Radiation Lightsource, SLAC National Accelerator Laboratory, is supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, under contract no. DE-AC02-76SF00515. Idaho National Laboratory is managed by Battelle Energy Alliance, LLC, under contract no. DE-AC07-05ID14517 with the U.S. Department of Energy. Argonne National Laboratory is operated for DOE Office of Science by UChicago Argonne, LLC, under contract number DE-AC02-06CH11357. S.S.W. is supported by the Office of Science Graduate Student Research (SCGSR) program through the U.S. Department of Energy, Office of Science, Office of Workforce Development for Teachers and Scientists. The SCGSR program is administered by the Oak Ridge Institute for Science and Education for the DOE under contract number DE-SC0014664. We thank Mike Marsh at Dragonfly ORS for helpful discussions about image segmentation.
Publisher Copyright:
© 2022 American Chemical Society.
PY - 2022/12/22
Y1 - 2022/12/22
N2 - Fast charging batteries are critical to the widespread adoption of electric vehicles to compete with refueling times of combustion-based vehicles. In the near term, adapting current commercial battery technologies to perform better under fast charging conditions through engineering optimizations will greatly expedite the process while exploratory fast-charging electrode materials are being pursued. To do so, the degradation modes in optimized Li-ion batteries need to be completely explored to understand fast charging limits while maintaining a high energy density and a long cycle life. While lithium plating on graphite still remains a challenge, cathode degradation also plays a key role in battery performance. We used nano- and micro-X-ray computed tomography to characterize the mechanical degradation of LiNi0.5Mn0.3Co0.2O2 (NMC532) in optimized Li-ion batteries cycled at three rates, 1C, 6C, and 9C, and at different stages of cycle life, 225 and 600 cycles. Despite using a conservative upper voltage cutoff limit aimed to minimize extensive cathode degradation, higher charging rates and increased cycling caused the polycrystalline NMC532 particles to fracture and pulverize, which likely drives cathode capacity fade and contributes to the decrease in overall cell performance.
AB - Fast charging batteries are critical to the widespread adoption of electric vehicles to compete with refueling times of combustion-based vehicles. In the near term, adapting current commercial battery technologies to perform better under fast charging conditions through engineering optimizations will greatly expedite the process while exploratory fast-charging electrode materials are being pursued. To do so, the degradation modes in optimized Li-ion batteries need to be completely explored to understand fast charging limits while maintaining a high energy density and a long cycle life. While lithium plating on graphite still remains a challenge, cathode degradation also plays a key role in battery performance. We used nano- and micro-X-ray computed tomography to characterize the mechanical degradation of LiNi0.5Mn0.3Co0.2O2 (NMC532) in optimized Li-ion batteries cycled at three rates, 1C, 6C, and 9C, and at different stages of cycle life, 225 and 600 cycles. Despite using a conservative upper voltage cutoff limit aimed to minimize extensive cathode degradation, higher charging rates and increased cycling caused the polycrystalline NMC532 particles to fracture and pulverize, which likely drives cathode capacity fade and contributes to the decrease in overall cell performance.
UR - https://www.scopus.com/pages/publications/85144126953
UR - https://www.mendeley.com/catalogue/3a352561-43a2-3939-8619-9565df43aae8/
U2 - 10.1021/acs.jpcc.2c06977
DO - 10.1021/acs.jpcc.2c06977
M3 - Article
AN - SCOPUS:85144126953
SN - 1932-7447
VL - 126
SP - 21196
EP - 21204
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 50
ER -