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Understanding improved capacity retention at 4.3 V in modified single crystal Ni-rich NMC//graphite pouch cells at elevated temperature

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Peer-reviewed

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Abstract

Al-surface doped Ni-rich single crystal material translates into better capacity retention in long-term cycling at higher UCV and cycling temperature. The capacity retention of commercially-sourced pouch cells with single crystal Al surface-doped Ni-rich cathodes (LiNi 0.834 Mn 0.095 Co 0.071 O 2 ) is examined. The degradation-induced capacity fade becomes more pronounced as the upper-cut-off voltage (UCV) increases from 4.2 V to 4.3 V ( vs. graphite) at a fixed cycling temperature (either 25 or 40 °C). However, cycles with 4.3 V UCV (slightly below the oxygen loss onset) show better capacity retention upon increasing the cycling temperature from 25 °C to 40 °C. Namely, after 500 cycles at 4.3 V UCV, cycling temperature at 40 °C retains 85.5% of the initial capacity while cycling at 25 °C shows 75.0% capacity retention. By employing a suite of electrochemical, X-ray spectroscopy and secondary ion mass spectrometry techniques, we attribute the temperature-induced improvement of the capacity retention at high UCV to the combined effects of Al surface-dopants, electrochemically resilient single crystal Ni-rich particles, and thermally-improved Li kinetics translating into better electrochemical performance. If cycling remains below the lattice oxygen loss onset, improved capacity retention in industrial cells should be achieved in single crystal Ni-rich cathodes with the appropriate choice of cycling parameter, particle quality, and particle surface dopants.

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Acknowledgements: We thank Ieuan Ellis and Paul Malliband from the Battery Scale Up facility at WMG for their assistance. This work is supported by the Faraday Institution under grant no. FIRG060, no. FIRG024, and no. FIRG061. We acknowledge Diamond Light Source for time on beamline I09 under proposal SI25355-5 and SI27494-2.

Journal Title

RSC Applied Interfaces

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Journal ISSN

2755-3701
2755-3701

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Publisher

Royal Society of Chemistry (RSC)

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Except where otherwised noted, this item's license is described as http://creativecommons.org/licenses/by/3.0/
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Faraday Institution (FIRG060, FIRG024, FIRG061)