Published 2019 | Version v1
Journal article

Cooling Induced Surface Reconstruction during Synthesis of High-Ni Layered Oxides

  • 1. Brookhaven National Laboratory (BNL), Upton, NY (United States). Sustainable Energy Technologies Dept.
  • 2. Peking University, Beijing (China)
  • 3. Brookhaven National Laboratory (BNL), Upton, NY (United States). Condensed Matter Physics and Materials Science Dept.

Description

Transition metal layered oxides have been the dominant cathodes in lithiumion batteries, and among them, high-Ni ones (LiNixMnyCozO2; x ≥ 0.7) with greatly boosted capacity and reduced cost are of particular interest for largescale applications. The high Ni loading, on the other hand, raises the critical issues of surface instability and poor rate performance. The rational design of synthesis leading to layered LiNi0.7Mn0.15Co0.15O2 with greatly enhanced rate capability is demonstrated, by implementing a quenching process alternative to the general slow cooling. In situ synchrotron X-ray diffraction, coupled with surface analysis, is applied to studies of the synthesis process, revealing cooling-induced surface reconstruction involving Li2CO3 accumulation, formation of a Li-deficient layer and Ni reduction at the particle surface. The reconstruction process occurs predominantly at high temperatures (above 350 °C) and is highly cooling-rate dependent, implying that surface reconstruction can be suppressed through synthetic control, i.e., quenching to improve the surface stability and rate performance of the synthesized materials. These findings may provide guidance to rational synthesis of high-Ni cathode materials.

Availability note (English)

Available from https://www.osti.gov/servlets/purl/1574924; https://www.osti.gov/biblio/1574924; DOE Accepted Manuscript full text, or the publishers Best Available Version will be available free of charge after the embargo period

Additional details

Publishing Information

Journal Title
Advanced Energy Materials
Journal Volume
9
Journal Issue
43
Journal Page Range
vp.
ISSN
1614-6832