4.8 Article

Li-Rich Mn-Mg Layered Oxide as a Novel Ni-/Co-Free Cathode

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume 32, Issue 36, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202204354

Keywords

cathodes; high energy; Li-ion batteries; Li-rich layered oxides; low costs

Funding

  1. National Research Foundation of Korea (NRF) - Korea government (MSIT) [2019M2A2A6A05102365, 2020M2D8A2070870, 2021R1A2C1014280, 2021R1C1C1006721, 2022M3H4A1A01010832]
  2. Korea Institute of Science and Technology (KIST) [2E31851]
  3. National Research Foundation of Korea [2021R1A2C1014280, 2020M2D8A2070870, 2021R1C1C1006721, 2022M3H4A1A01010832] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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A novel cathode material, Li1.8Mg0.3Mn0.9O3, has been proposed to enhance the capacity and energy density of Li2MnO3 by partially substituting Li+ and Mn4+ with inactive Mg2+. The Mg substitution effectively suppresses Mn migration and mitigates oxygen release, resulting in improved power-capability and cycle performance.
Although Li2MnO3 exhibits high capacity via anionic oxygen redox, it suffers from rapid capacity decay owing to structural disordering accompanying irreversible Mn migration and O-2 release. To promote the reversibility of the anionic redox reaction, Li1.8Mg0.3Mn0.9O3 as a novel cathode material, prepared by partially substituting Li+ and Mn4+ of Li2MnO3 with the redox-inactive Mg2+ as a structural stabilizer is proposed. Li1.8Mg0.3Mn0.9O3 delivers a high specific capacity and energy density of approximate to 310 mAh g(-1) and approximate to 915 Wh kg(-1), respectively. In particular, the power-capability and cycle performance of Li1.8Mg0.3Mn0.9O3 greatly surpass those of Li2MnO3. Through first-principles calculations and various experiments, it is revealed that Mg substitution effectively suppresses the Mn migration by stabilizing Mn cations in the original sites at the charged state. The energetically stabilized layered structure disfavors the distortion of the MnO6 octahedra, which induces the oxygen dimer (O-O) formation through the metal-oxygen decoordination, thus mitigating oxygen release.

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