Over‐Stoichiometric Metastabilization of Cation‐Disordered Rock Salts

Author:

Wang You1,Outka Alexandra1,Takele Wassie Mersha1,Avdeev Maxim23,Sainio Sami4,Liu Rui5,Kee Vanessa6,Choe Wonu7,Raji‐Adefila Basirat1,Nordlund Dennis4,Zhou Shan6,Kan Wang Hay89,Habteyes Terefe G.1,Chen Dongchang1ORCID

Affiliation:

1. Department of Chemistry and Chemical Biology University of New Mexico Albuquerque NM 87131 USA

2. Australian Nuclear Science and Technology Organization (ANSTO) Lucas Heights NSW 2234 Australia

3. School of Chemistry The University of Sydney Sydney NSW 2006 Australia

4. SLAC National Accelerator Laboratory Menlo Park CA 94025 USA

5. College of Pharmacy, University of New Mexico Albuquerque NM 87131 USA

6. Nanoscience & Biomedical Engineering South Dakota School of Mines & Technology Rapid City SD 57701 USA

7. Albuquerque Institute for Math & Science Albuquerque NM 87106 USA

8. Spallation Neutron Source Science Center Dongguan 523803 China

9. Institute of High Energy Physics Chinese Academy of Sciences Beijing 100049 China

Abstract

AbstractCation‐disordered rock salts (DRXs) are well known for their potential to realize the goal of achieving scalable Ni‐ and Co‐free high‐energy‐density Li‐ion batteries. Unlike in most cathode materials, the disordered cation distribution may lead to more factors that control the electrochemistry of DRXs. An important variable that is not emphasized by research community is regarding whether a DRX exists in a more thermodynamically stable form or a more metastable form. Moreover, within the scope of metastable DRXs, over‐stoichiometric DRXs, which allow relaxation of the site balance constraint of a rock salt structure, are particularly underexplored. In this work, these findings are reported in locating a generally applicable approach to “metastabilize” thermodynamically stable Mn‐based DRXs to metastable ones by introducing Li over‐stoichiometry. The over‐stoichiometric metastabilization greatly stimulates more redox activities, enables better reversibility of Li deintercalation/intercalation, and changes the energy storage mechanism. The metastabilized DRXs can be transformed back to the thermodynamically stable form, which also reverts the electrochemical properties, further contrasting the two categories of DRXs. This work enriches the structural and compositional space of DRX families and adds new pathways for rationally tuning the properties of DRX cathodes.

Funder

University of New Mexico

Oak Ridge Associated Universities

Publisher

Wiley

Subject

Mechanical Engineering,Mechanics of Materials,General Materials Science

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