Structure Stabilization by Mixed Anions in Oxyfluoride Cathodes for High-Energy Lithium Batteries
Abstract
Mixed-anion oxyfluorides (i.e., FeOxF2-x) are an appealing alternative to pure fluorides as high-capacity cathodes in lithium batteries, with enhanced cyclability via oxygen substitution. Yet, it is still unclear how the mixed anions impact the local phase transformation and structural stability of oxyfluorides during cycling due to the complexity of electrochemical reactions, involving both lithium intercalation and conversion. Herein, we investigated the local chemical and structural ordering in FeO0.7F1.3 at length scales spanning from single particles to the bulk electrode, via a combination of electron spectrum-imaging, magnetization, electrochemistry, and synchrotron X-ray measurements. The FeO0.7F1.3 nanoparticles retain a FeF2-like rutile structure but chemically heterogeneous, with an F-rich core covered by thin O-rich shell. Upon lithiation the O-rich rutile phase is transformed into Li—Fe—O(—F) rocksalt that has high lattice coherency with converted metallic Fe, a feature that may facilitate the local electron and ion transport. The O-rich rocksalt is highly stable over lithiation/delithiation and thus advantageous to maintain the integrity of the particle, and due to its predominant distribution on the surface, it is expected to prevent the catalytic interaction of Fe with electrolyte. Our findings of the structural origin of cycling stability in oxyfluorides may provide insights into developing viable high-energymore »
- Authors:
-
- Brookhaven National Lab. (BNL), Upton, NY (United States); Korea Atomic Energy Research Institute, Daejeon (Korea)
- Rutgers Univ., New Brunswick, NJ (United States)
- State Univ. of New York at Binghampton, Binghampton, NY (United States)
- Brookhaven National Lab. (BNL), Upton, NY (United States)
- Publication Date:
- Research Org.:
- Brookhaven National Laboratory (BNL), Upton, NY (United States); Energy Frontier Research Centers (EFRC) (United States). Northeastern Center for Chemical Energy Storage (NECCES)
- Sponsoring Org.:
- USDOE Office of Science (SC), Basic Energy Sciences (BES)
- OSTI Identifier:
- 1239785
- Report Number(s):
- BNL-111677-2015-JA
Journal ID: ISSN 1936-0851; YN0100000
- Grant/Contract Number:
- SC0012704; SC0001294
- Resource Type:
- Accepted Manuscript
- Journal Name:
- ACS Nano
- Additional Journal Information:
- Journal Volume: 9; Journal Issue: 10; Journal ID: ISSN 1936-0851
- Publisher:
- American Chemical Society (ACS)
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 25 ENERGY STORAGE; lithium batteries; mixed-anion cathodes; iron oxyfluoride; scanning transmission electron microscopy (STEM); electron energy loss spectroscopy (EELS)
Citation Formats
Kim, Sung-Wook, Pereira, Nathalie, Chernova, Natasha A., Omenya, Fredrick, Gao, Peng, Whittingham, M. Stanley, Amatucci, Glenn G., Su, Dong, and Wang, Feng. Structure Stabilization by Mixed Anions in Oxyfluoride Cathodes for High-Energy Lithium Batteries. United States: N. p., 2015.
Web. doi:10.1021/acsnano.5b03643.
Kim, Sung-Wook, Pereira, Nathalie, Chernova, Natasha A., Omenya, Fredrick, Gao, Peng, Whittingham, M. Stanley, Amatucci, Glenn G., Su, Dong, & Wang, Feng. Structure Stabilization by Mixed Anions in Oxyfluoride Cathodes for High-Energy Lithium Batteries. United States. https://doi.org/10.1021/acsnano.5b03643
Kim, Sung-Wook, Pereira, Nathalie, Chernova, Natasha A., Omenya, Fredrick, Gao, Peng, Whittingham, M. Stanley, Amatucci, Glenn G., Su, Dong, and Wang, Feng. Mon .
"Structure Stabilization by Mixed Anions in Oxyfluoride Cathodes for High-Energy Lithium Batteries". United States. https://doi.org/10.1021/acsnano.5b03643. https://www.osti.gov/servlets/purl/1239785.
@article{osti_1239785,
title = {Structure Stabilization by Mixed Anions in Oxyfluoride Cathodes for High-Energy Lithium Batteries},
author = {Kim, Sung-Wook and Pereira, Nathalie and Chernova, Natasha A. and Omenya, Fredrick and Gao, Peng and Whittingham, M. Stanley and Amatucci, Glenn G. and Su, Dong and Wang, Feng},
abstractNote = {Mixed-anion oxyfluorides (i.e., FeOxF2-x) are an appealing alternative to pure fluorides as high-capacity cathodes in lithium batteries, with enhanced cyclability via oxygen substitution. Yet, it is still unclear how the mixed anions impact the local phase transformation and structural stability of oxyfluorides during cycling due to the complexity of electrochemical reactions, involving both lithium intercalation and conversion. Herein, we investigated the local chemical and structural ordering in FeO0.7F1.3 at length scales spanning from single particles to the bulk electrode, via a combination of electron spectrum-imaging, magnetization, electrochemistry, and synchrotron X-ray measurements. The FeO0.7F1.3 nanoparticles retain a FeF2-like rutile structure but chemically heterogeneous, with an F-rich core covered by thin O-rich shell. Upon lithiation the O-rich rutile phase is transformed into Li—Fe—O(—F) rocksalt that has high lattice coherency with converted metallic Fe, a feature that may facilitate the local electron and ion transport. The O-rich rocksalt is highly stable over lithiation/delithiation and thus advantageous to maintain the integrity of the particle, and due to its predominant distribution on the surface, it is expected to prevent the catalytic interaction of Fe with electrolyte. Our findings of the structural origin of cycling stability in oxyfluorides may provide insights into developing viable high-energy electrodes for lithium batteries.},
doi = {10.1021/acsnano.5b03643},
journal = {ACS Nano},
number = 10,
volume = 9,
place = {United States},
year = {Mon Aug 24 00:00:00 EDT 2015},
month = {Mon Aug 24 00:00:00 EDT 2015}
}
Web of Science
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