4.8 Article

Origin of structural degradation in Li-rich layered oxide cathode

Journal

NATURE
Volume 606, Issue 7913, Pages 305-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41586-022-04689-y

Keywords

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Funding

  1. US Department of Energy (DOE), Office of Energy Efficiency and Renewable Energy, Vehicle Technologies Office
  2. Clean Vehicles, US-China Clean Energy Research Centre (CERC-CVC2) under US DOE EERE Vehicle Technologies Office
  3. DOE Office of Science by UChicago Argonne, LLC [DE-AC02-06CH11357]
  4. National Key R&D Program of China [2016YFB0700600]
  5. Soft Science Research Project of Guangdong Province [2017B030301013]
  6. Shenzhen Science and Technology Research Grants [ZDSYS201707281026184]
  7. DOE Office of Science by Argonne National Laboratory [DE-AC02-06CH11357]
  8. DOE, Office of Science, Office of Basic Energy Sciences [DE-SC0012704]
  9. US Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-06CH11357]

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Utilizing Li- and Mn-rich (LMR) cathode materials can increase battery energy density. However, voltage decay issues impede commercialization. In this study, it is revealed that nanostrain and lattice displacement accumulate continuously during operation, leading to structure degradation and oxygen loss, which cause rapid voltage decay. The heterogeneous nature of LMR cathodes results in pernicious phase displacement/strain. Mesostructural design is proposed as a strategy to mitigate lattice displacement and achieve stable voltage and capacity profiles.
Li- and Mn-rich (LMR) cathode materials that utilize both cation and anion redox can yield substantial increases in battery energy density(1-3). However, although voltage decay issues cause continuous energy loss and impede commercialization, the prerequisite driving force for this phenomenon remains a mystery(3-6) Here, with in situ nanoscale sensitive coherent X-ray diffraction imaging techniques, we reveal that nanostrain and lattice displacement accumulate continuously during operation of the cell. Evidence shows that this effect is the driving force for both structure degradation and oxygen loss, which trigger the well-known rapid voltage decay in LMR cathodes. By carrying out micro- to macro-length characterizations that span atomic structure, the primary particle, multiparticle and electrode levels, we demonstrate that the heterogeneous nature of LMR cathodes inevitably causes pernicious phase displacement/strain, which cannot be eliminated by conventional doping or coating methods. We therefore propose mesostructural design as a strategy to mitigate lattice displacement and inhomogeneous electrochemical/structural evolutions, thereby achieving stable voltage and capacity profiles. These findings highlight the significance of lattice strain/displacement in causing voltage decay and will inspire a wave of efforts to unlock the potential of the broad-scale commercialization of LMR cathode materials.

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