4.8 Article

Operando X-ray Diffraction Studies of the Mg-Ion Migration Mechanisms in Spinel Cathodes for Rechargeable Mg-Ion Batteries

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 143, Issue 28, Pages 10649-10658

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.1c04098

Keywords

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Funding

  1. Joint Center for Energy Storage Research (JCESR) of the U.S. Department of Energy (DOE)
  2. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-06CH11357]
  3. National Energy Research Scientific Computing Center (NERSC), a U.S. Department of Energy Office of Science User Facility located at Lawrence Berkeley National Laboratory [DE-AC02-05CH11231]
  4. National Science Foundation [ACI1053575]

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The study successfully synthesized a promising high-voltage spinel oxide cathode material MgCrMnO4 with 18% Mg/Mn inversion, and designed a new custom operando battery device to investigate cation migration mechanisms. The research showed both reversible and partially reversible Mg2+ insertion in the cathode, with inverted Mn believed to be involved in cation migrations causing irreversible structural evolution. The operando techniques developed in this work could play a significant role in optimizing spinel oxide cathodes for multivalent ion batteries.
A promising high-voltage spinel oxide cathode material MgCrMnO4 with 18% Mg/Mn inversion was synthesized successfully. A new custom operando battery device was designed to study the cation migration mechanisms of the MgCrMnO4 cathode using 0.1 M Mg(TPFA)(2) electrolyte dissolved in triglyme and activated carbon as the anode. For the first time in multivalent batteries, high-quality operando diffraction data enabled the accurate quantification of cation contents in the host structure. Besides the exceptional reversibility of 12% Mg2+ insertion in Mg1-xCrMnO4 (x <= 1), a partially reversible insertion of excess Mg2+ during overdischarging was also observed. Moreover, the insertion/extraction reaction was experimentally shown to be accompanied by a series of cation redistributions in the spinel framework, which were further supported by density functional theory calculations. The inverted Mn is believed to be directly involved in the cation migrations, which would cause voltage hysteresis and irreversible structural evolution after overdischarging. Tuning the Mg/Mn inversion rate could provide a direct path to further optimize spinel oxide cathodes for Mg-ion batteries, and more generally, the operando techniques developed in this work should play a key role in understanding the complex mechanisms involved in multivalent ion insertion systems.

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