AI Article Synopsis

  • Nickel-rich layered materials are promising for increasing the energy density of lithium batteries, but they face stability challenges due to lattice oxygen release during high-voltage cycling.
  • Surface coatings can help mitigate oxygen release but are often complex and not durable during cycling.
  • A new approach involving a multifunctional cathode/electrolyte interphase (CEI) shows promise by continuously capturing active oxygen, improving stability and performance in tough conditions, with experimental results showing 600 cycles of effective operation.

Article Abstract

The use of nickel-rich layered materials as cathodes can boost the energy density of lithium batteries. However, developing a safe and long-term stable nickel-rich layered cathode is challenging primarily due to the release of lattice oxygen from the cathode during cycling, especially at high voltages, which will cause a series of adverse effects, leading to battery failure and thermal runaway. Surface coating is often considered effective in capturing active oxygen species; however, its process is rather complicated, and it is difficult to maintain intact on the cathode with large volume changes during cycling. Here, we propose an in situ construction of a multifunctional cathode/electrolyte interphase (CEI), which is easy to prepare, repairable, and, most importantly, capable of continuously capturing active oxygen species during the entire life span. This unique protective mechanism notably improves the cycling stability of Li||LiNiCoMnO (NCM811) cells at rigorous working conditions, including ultrahigh voltage (4.8 V), high temperature (60 °C), and fast charging (10 C). An industrial 1 A h graphite||NCM811 pouch cell achieved stable operation of 600 cycles with a capacity retention of 79.6% at 4.4 V, exhibiting great potential for practical use. This work provides insightful guidance for constructing a multifunctional CEI to bypass limitations associated with high-voltage operations of nickel-rich layered cathodes.

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Source
http://dx.doi.org/10.1021/jacs.4c02345DOI Listing

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