4.8 Article

Dynamic imaging of crystalline defects in lithium-manganese oxide electrodes during electrochemical activation to high voltage

Journal

NATURE COMMUNICATIONS
Volume 10, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-019-09408-2

Keywords

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Funding

  1. US Department of Energy (DOE), Office of Science, Basic Energy Sciences [DE-AC02-06CH11357]
  2. Samsung Advanced Institute of Technology (SAIT)'s Global Research Outreach (GRO) Program
  3. Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF) [ECCS-1542205]
  4. MRSEC program (NSF) at the Materials Research Center [DMR-1720139]
  5. International Institute for Nanotechnology (IIN)
  6. Keck Foundation
  7. state of Illinois, through the IIN
  8. Office of Science of the DOE [DE-AC02-05CH11231]
  9. National Natural Science Foundation of China [51702207]
  10. Fundamental Research Funds for the Central Universities [WUT: 2019III012GX]

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Crystalline defects are commonly generated in lithium-metal-oxide electrodes during cycling of lithium-ion batteries. Their role in electrochemical reactions is not yet fully understood because, until recently, there has not been an effective operando technique to image dynamic processes at the atomic level. In this study, two types of defects were monitored dynamically during delithiation and concomitant oxidation of oxygen ions by using in situ high-resolution transmission electron microscopy supported by density functional theory calculations. One stacking fault with a fault vector b/6[110] and low mobility contributes minimally to oxygen release from the structure. In contrast, dissociated dislocations with Burgers vector of c/2[001] have high gliding and transverse mobility; they lead to the formation, transport and release subsequently of oxygen related species at the surface of the electrode particles. This work advances the scientific understanding of how oxygen participates and the structural response during the activation process at high potentials.

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