4.6 Article

Lithium-Rich O2-Type Li0.66[Li0.22Ru0.78]O2 Positive Electrode Material

Journal

JOURNAL OF THE ELECTROCHEMICAL SOCIETY
Volume 169, Issue 4, Pages -

Publisher

ELECTROCHEMICAL SOC INC
DOI: 10.1149/1945-7111/ac6459

Keywords

-

Funding

  1. Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan [20H05673]
  2. JSPS [20J14291]
  3. [21H04697]
  4. [19H05816]
  5. Grants-in-Aid for Scientific Research [20J14291, 20H05673] Funding Source: KAKEN

Ask authors/readers for more resources

This research reports on a high-capacity O2-type lithium-rich layered oxide Li1.22-x Ru0.78O2, which can achieve stable redox reactions and deliver a high capacity of 200 mAh g(-1).
Increasing the energy density of lithium-ion batteries is an important step towards flexible electricity supply, which can be achieved by developing large-capacity positive electrodes. Lithium-rich oxides have been a longstanding research target because of their large capacity involving extra oxygen-redox reactions. In this work, we report the synthesis, electrochemical properties, electronic structure, and structural evolution of O2-type lithium-rich layered oxide Li1.22-x Ru0.78O2. A robust Ru-O layered framework without Ru migration allows for unveiling the solid-state electrochemistry of O2-type lithium-rich layered oxides with possibility of a large yet stable extra capacity for oxygen-redox reaction. Using a combination of X-ray photoelectron spectroscopy, X-ray absorption/emission spectroscopy, and in situ/ex situ X-ray diffraction, we clarified that O2-Li1.22-x Ru0.78O2 delivers a large capacity of 200 mAh g(-1) in association with Ru5+/Ru4+ and Ru4+/Ru3+ two-electron redox reactions under a solid-solution process, but with no contribution from the extra oxygen-redox reaction.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available