Abstract
Layered cathode materials (LCMs), because of their high energy density and relatively stable performance, represent an important class of cathode materials for alkali metal ion (e.g., Li+ and Na+) batteries. Chemomechanical behaviors of LCMs, which affect battery performance dramatically, have drawn extensive attention in recent years. Most chemomechanical processes have some common chemical and structural origins that are at the center of materials chemistry, for example, defects and local bonding environments in the solid state. In this review, we first discuss the chemomechanical breakdown of LCMs by introducing their categories and negative effects on the battery performance. We then systematically analyze factors that govern the initiation and propagation of chemomechanical breakdown and summarize their formation mechanisms. Strategies that can enhance the chemomechanical properties of LCMs or reduce the destructive effects of chemomechanical breakdown are then discussed. Finally, light is shed on the new state-of-the-art techniques that have been applied to study chemomechanical breakdown. This review virtually includes most aspects of the chemomechanical behaviors of LCMs and provides some insights into the important chemical motifs that determine the chemomechanical properties. Therefore, we believe that advanced design protocols of LCMs can be developed to effectively address the chemomechanical breakdown issue of LCMs.
Original language | English |
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Pages (from-to) | 21859-21884 |
Number of pages | 26 |
Journal | Journal of Materials Chemistry A |
Volume | 6 |
Issue number | 44 |
DOIs | |
State | Published - 2018 |
Externally published | Yes |
Funding
The authors acknowledge support from the National Science Foundation under Grant no. DMR-1832613. The work was also supported by the Department of Chemistry Startup at Virginia Tech. Use of the SSRL, SLAC National Accelerator Laboratory, is supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences under Contract No. DE-AC02-76SF00515. The authors acknowledge Yao Wang (Rice University, TX, USA) for her help in making figures. The authors acknowledge support from the National Science Foundation under Grant no. DMR-1832613. The work was also supported by the Department of Chemistry Startup at Virginia Tech. Use of the SSRL, SLAC National Accelerator Laboratory, is supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences under Contract No. DE-AC02-76SF00515. The authors acknowledge Yao Wang (Rice University, TX, USA) for her help in making gures.
Funders | Funder number |
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Office of Basic Energy Sciences | |
SSRL | |
National Science Foundation | 1832613 |
U.S. Department of Energy | |
Office of Science | |
SLAC National Accelerator Laboratory | |
National Science Foundation | DMR-1832613 |