Overpotential-Dependent Phase Transformation Pathways in Lithium Iron Phosphate Battery Electrodes
- Massachusetts Institute of Technology (MIT)
- Lawrence Livermore National Laboratory (LLNL)
- Khon Kaen University
- University of Tennessee, Knoxville (UTK)
An objective in battery development for higher storage energy density is the design of compounds that can accommodate maximum ion concentration change over useful electrochemical windows. Not surprisingly, many storage compounds undergo phase transitions in-situ, including production of metastable phases. Unique to this environment is the frequent application of electrical over- and underpotentials, which are the electrical analogs to undercooling and superheating. Surprisingly, overpotential effects on phase stability and transformation mechanisms have not been studied in detail. Here we use synchrotron X-ray diffraction performed in-situ during potentiostatic and galvanostatic cycling, combined with phase-field modeling, to reveal a remarkable dependence of phase transition pathway on overpotential in the model olivine Li1-xFePO4. At both low (e.g., <20 mV) and high (>75 mV) overpotentials a crystal-to-crystal olivine transformation is preferred, whereas at intermediate overpotentials a crystalline-to-amorphous phase transition dominates. At nanoscale particle size, amorphization is further emphasized. Implications for battery use and design are considered.
- Research Organization:
- Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). High Temperature Materials Lab. (HTML)
- Sponsoring Organization:
- USDOE Office of Energy Efficiency and Renewable Energy (EERE)
- DOE Contract Number:
- DE-AC05-00OR22725
- OSTI ID:
- 992090
- Journal Information:
- Chemistry of Materials, Vol. 22, Issue 21; ISSN 0897-4756
- Country of Publication:
- United States
- Language:
- English
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