Insights into the structural evolution and Li/O loss in high-Ni layered oxide cathodes
Creators
- 1. School of Advanced Materials, Peking University, Shenzhen Graduate School, Shenzhen 518055 (China)
- 2. Sustainable Energy Technologies Department, Brookhaven National Laboratory, Upton, NY 11973 (United States)
Description
Highlights: • The thermal-induced structural evolution and Li/O loss are investigated in a high-Ni layered oxide LiNi0.9Co0.1O2. • Heterogenous Li/O loss kinetics in the bulk and at the surface are quantitatively tracked by XRD and XPS. • In-situ TEM during calcination uncovers the local structural evolution and Li/O loss within single primary particles. -- Abstract: High-Ni layered oxides are one class of the most promising cathodes for Lithium ion batteries (LIBs) due to the high capacity and low cost. Accompanying with the high Ni content, Li/O loss from the layered structure, as well as the relevant structural evolution, have been extensively considered as a general origin for various detrimental phenomena, such as cationic disordering during high-temperature solid-state synthesis, chemical weathering at the surface during storage, and the capacity fading at high upper voltages (> 4.3 V) during electrochemical tests. Herein, multiple macroscopic/microscopic characterization techniques, including in-situ transmission electron microscopy (TEM), ex-situ X-ray diffraction (XRD), and X-ray photoelectron spectra (XPS), are combined to comprehensively investigate the thermal-induced local structural evolution vs Li/O loss in a representative binary high-Ni layered oxide LiNi0.9Co0.1O2. The heterogenous Li/O loss kinetics in the bulk and at the surface are simultaneously tracked based on a rational structural model, revealing a quantitative relationship between Li/O loss and the phase transformation. The local structural evolution within single primary particles monitored by in-situ TEM further uncovers that, Li/O loss at the particle surface is accelerated via the large Li+ diffusivity at high temperatures, finally leads to a phase transformation process from the bulk to the surface, in which a peculiar "anti-core-shell" structure within single primary particles is observed. The quantitative analysis combined with the direct observation not only demonstrate a feasible route to investigate the Li/O loss kinetics, but also provide valuable insights into the performance improvement of high-Ni layered oxides from the aspect of Li/O loss.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.nanoen.2019.02.059Additional details
Identifiers
- DOI
- 10.1016/j.nanoen.2019.02.059;
- PII
- S2211285519301727;
Publishing Information
- Journal Title
- Nano Energy (Print)
- Journal Volume
- 59
- Journal Page Range
- p. 327-335
- ISSN
- 2211-2855
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54115212
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
- Descriptors DEI
- CALCINATION; CATHODES; ELECTRIC POTENTIAL; ELECTROCHEMISTRY; KINETICS; LITHIUM ION BATTERIES; LITHIUM IONS; OXIDES; PERFORMANCE; PHASE TRANSFORMATIONS; STRUCTURAL MODELS; SURFACES; TRANSMISSION ELECTRON MICROSCOPY; X-RAY DIFFRACTION; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- CHALCOGENIDES; CHARGED PARTICLES; CHEMICAL REACTIONS; CHEMISTRY; COHERENT SCATTERING; DECOMPOSITION; DIFFRACTION; ELECTRIC BATTERIES; ELECTROCHEMICAL CELLS; ELECTRODES; ELECTRON MICROSCOPY; ELECTRON SPECTROSCOPY; ENERGY STORAGE SYSTEMS; ENERGY SYSTEMS; IONS; MICROSCOPY; OXYGEN COMPOUNDS; PHOTOELECTRON SPECTROSCOPY; PYROLYSIS; SCATTERING; SPECTROSCOPY; THERMOCHEMICAL PROCESSES
Optional Information
- Copyright
- Copyright (c) 2019 Elsevier Ltd. All rights reserved.