Optimizing Li-Excess Cation-Disordered Rocksalt Cathode Design Through Partial Li Deficiency

  • Liliang Huang
  • , Peichen Zhong
  • , Yang Ha
  • , Zijian Cai
  • , Young Woon Byeon
  • , Tzu Yang Huang
  • , Yingzhi Sun
  • , Fengyu Xie
  • , Han Ming Hau
  • , Haegyeom Kim
  • , Mahalingam Balasubramanian
  • , Bryan D. McCloskey
  • , Wanli Yang
  • , Gerbrand Ceder

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

Li-excess disordered rocksalts (DRXs) are emerging as promising cathode materials for Li-ion batteries due to their ability to use earth-abundant transition metals. In this work, a new strategy based on partial Li deficiency engineering is introduced to optimize the overall electrochemical performance of DRX cathodes. Specifically, by using Mn-based DRX as a proof-of-concept, it is demonstrated that the introduction of cation vacancies during synthesis (e.g., Li1.3-xMn2+0.4-xMn3+xNb0.3O1.6F0.4, x = 0, 0.2, and 0.4) improves both the discharge capacity and rate performance due to the more favored short-range order in the presence of Mn3+. Density functional theory calculations and Monte Carlo simulations, in combination with spectroscopic tools, reveal that introducing 10% vacancies (Li1.1Mn2+0.2Mn3+0.2Nb0.3O1.6F0.4) enables both Mn2+/Mn3+ redox and excellent Li percolation. However, a more aggressive vacancy doping (e.g., 20% vacancies in Li0.9Mn3+0.4Nb0.3O1.6F0.4) impairs performance because it induces phase separation between an Mn-rich and a Li-rich phase.

Original languageEnglish
Article number2202345
JournalAdvanced Energy Materials
Volume13
Issue number4
DOIs
StatePublished - Jan 27 2023
Externally publishedYes

Funding

L.H. and P.Z. contributed equally to this work. This work was supported by the Assistant Secretary for Energy Efficiency and Renewable Energy, Vehicle Technologies Office, under the Applied Battery Materials Program, of the US Department of Energy (DOE) under contract no. DE‐AC02‐05CH11231. Research at the Advanced Light Source was supported by the Director, Office of Science, Office of Basic Energy Sciences, of the US DOE under contract no. DE‐AC02‐05CH11231. Research at the Molecular Foundry was supported by the Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy under Contract No. DE‐AC02‐05CH11231. T.‐Y.H. was supported collectively by both the Ministry of Education in Taiwan and the UC Berkeley College of Chemistry through the Taiwan Fellowship Program. The computational work was supported with the computational resources provided by the Extreme Science and Engineering Discovery Environment (XSEDE), which was supported by National Science Foundation grant number ACI1053575; the National Energy Research Scientific Computing Center (NERSC), a U.S. DOE Office of Science User Facility located at Lawrence Berkeley National Laboratory under contract no. DE‐AC02‐05CH11231; and the Lawrencium computational cluster resource provided by the IT Division at the Lawrence Berkeley National Laboratory.

Keywords

  • Li-ion batteries
  • cation vacancies
  • cation-disordered cathodes
  • percolation properties
  • short-range order

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