Abstract

We have prepared the first known lithium manganese oxynitride, , and characterized both its structure and electrochemistry. Powder diffraction experiments show that it adopts a cubic antifluorite lattice, while electron microscopy studies reveal the existence of an incommensurate modulated superstructure due to partial and/or ordering. This is consistent with the magic angle spinning–nuclear magnetic resonance spectra, which show only a limited number of Li local environments. is electrochemically active when tested as an electrode in a lithium battery and can be reversibly oxidized up to . Additional reversible capacity is obtained on reduction down to due to the insertion of Li onto the existing lithium-ion vacancies. In situ X-ray diffraction experiments indicate that the redox mechanism is single-phase and involves the formation of a solid solution . This compound exhibits an overall specific capacity of , with only a 4% loss after the 40th cycle. The higher capacity retention of when compared to that of is due to both the easier diffusion of the lithium within the structure caused by the additional cationic vacancies, and the fact that its lithium exchange mechanism goes through the formation of a solid solution, with no biphasic regions.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.