Exploring Lithium-Cobalt-Nickel Oxide Spinel Electrodes for ≥3.5 V Li-Ion Cells
Abstract
Some recent reports have indicated that a manganese oxide spinel component, when embedded in a relatively small concentration in layered xLi2MnO3center dot(1-x)LiMO2 (M = Ni, Mn, or Co) electrode systems, can act as a stabilizer that increases their capacity, rate capability, cycle life, and first-cycle efficiency. Our findings prompted us to explore the possibility of exploiting lithiated cobalt oxide spinel stabilizers by taking advantage of (1) the low mobility of cobalt ions relative to that of manganese and nickel ions in close-packed oxides and (2) their higher potential (similar to 3.6 V vs Li0) relative to manganese oxide spinels (similar to 2.9 V vs Li0) for the spinel-to-lithiated spinel electrochemical reaction. In particular, we revisited the structural and electrochemical properties of lithiated spinels in the LiCo1-xNixO2 (0 <= x <= 0.2) system, first reported almost 25 years ago, by means of high-resolution (synchrotron) X-ray diffraction, transmission electron microscopy, nuclear magnetic resonance spectroscopy, electrochemical cell tests, and theoretical calculations. These results provide a deeper understanding of the complexity of intergrown layered/lithiated spinel LiCo1-xNixO2 structures when prepared in air between 400 and 800 degrees C and the impact of structural variations on their electrochemical behavior. These structures, when used in low concentrations,more »
- Authors:
-
- Argonne National Lab. (ANL), Argonne, IL (United States). Chemical Sciences and Engineering Division
- Northwestern Univ., Evanston, IL (United States). Dept. of Materials Science and Engineering, NUANCE Center
- Pacific Northwest National Lab. (PNNL), Richland, WA (United States). Environmental Molecular Sciences Lab.
- Northwestern Univ., Evanston, IL (United States). Dept. of Materials Science and Engineering
- Publication Date:
- Research Org.:
- Argonne National Lab. (ANL), Argonne, IL (United States); Energy Frontier Research Centers (EFRC) (United States). Center for Electrical Energy Storage (CEES)
- Sponsoring Org.:
- USDOE Office of Science (SC), Basic Energy Sciences (BES); USDOE Office of Energy Efficiency and Renewable Energy (EERE), Vehicle Technologies Office (EE-3V)
- OSTI Identifier:
- 1392304
- Grant/Contract Number:
- AC02-06CH11357; AC02-05CH11231
- Resource Type:
- Accepted Manuscript
- Journal Name:
- ACS Applied Materials and Interfaces
- Additional Journal Information:
- Journal Volume: 8; Journal Issue: 41; Journal ID: ISSN 1944-8244
- Publisher:
- American Chemical Society (ACS)
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 25 ENERGY STORAGE; 36 MATERIALS SCIENCE; lithium-cobalt-nickel oxide; lithium-ion battery; spinel; stabilizer; structure
Citation Formats
Lee, Eungje, Blauwkamp, Joel, Castro, Fernando C., Wu, Jinsong, Dravid, Vinayak P., Yan, Pengfei, Wang, Chongmin, Kim, Soo, Wolverton, Christopher, Benedek, Roy, Dogan, Fulya, Park, Joong Sun, Croy, Jason R., and Thackeray, Michael M. Exploring Lithium-Cobalt-Nickel Oxide Spinel Electrodes for ≥3.5 V Li-Ion Cells. United States: N. p., 2016.
Web. doi:10.1021/acsami.6b09073.
Lee, Eungje, Blauwkamp, Joel, Castro, Fernando C., Wu, Jinsong, Dravid, Vinayak P., Yan, Pengfei, Wang, Chongmin, Kim, Soo, Wolverton, Christopher, Benedek, Roy, Dogan, Fulya, Park, Joong Sun, Croy, Jason R., & Thackeray, Michael M. Exploring Lithium-Cobalt-Nickel Oxide Spinel Electrodes for ≥3.5 V Li-Ion Cells. United States. https://doi.org/10.1021/acsami.6b09073
Lee, Eungje, Blauwkamp, Joel, Castro, Fernando C., Wu, Jinsong, Dravid, Vinayak P., Yan, Pengfei, Wang, Chongmin, Kim, Soo, Wolverton, Christopher, Benedek, Roy, Dogan, Fulya, Park, Joong Sun, Croy, Jason R., and Thackeray, Michael M. Tue .
"Exploring Lithium-Cobalt-Nickel Oxide Spinel Electrodes for ≥3.5 V Li-Ion Cells". United States. https://doi.org/10.1021/acsami.6b09073. https://www.osti.gov/servlets/purl/1392304.
@article{osti_1392304,
title = {Exploring Lithium-Cobalt-Nickel Oxide Spinel Electrodes for ≥3.5 V Li-Ion Cells},
author = {Lee, Eungje and Blauwkamp, Joel and Castro, Fernando C. and Wu, Jinsong and Dravid, Vinayak P. and Yan, Pengfei and Wang, Chongmin and Kim, Soo and Wolverton, Christopher and Benedek, Roy and Dogan, Fulya and Park, Joong Sun and Croy, Jason R. and Thackeray, Michael M.},
abstractNote = {Some recent reports have indicated that a manganese oxide spinel component, when embedded in a relatively small concentration in layered xLi2MnO3center dot(1-x)LiMO2 (M = Ni, Mn, or Co) electrode systems, can act as a stabilizer that increases their capacity, rate capability, cycle life, and first-cycle efficiency. Our findings prompted us to explore the possibility of exploiting lithiated cobalt oxide spinel stabilizers by taking advantage of (1) the low mobility of cobalt ions relative to that of manganese and nickel ions in close-packed oxides and (2) their higher potential (similar to 3.6 V vs Li0) relative to manganese oxide spinels (similar to 2.9 V vs Li0) for the spinel-to-lithiated spinel electrochemical reaction. In particular, we revisited the structural and electrochemical properties of lithiated spinels in the LiCo1-xNixO2 (0 <= x <= 0.2) system, first reported almost 25 years ago, by means of high-resolution (synchrotron) X-ray diffraction, transmission electron microscopy, nuclear magnetic resonance spectroscopy, electrochemical cell tests, and theoretical calculations. These results provide a deeper understanding of the complexity of intergrown layered/lithiated spinel LiCo1-xNixO2 structures when prepared in air between 400 and 800 degrees C and the impact of structural variations on their electrochemical behavior. These structures, when used in low concentrations, offer the possibility of improving the cycling stability, energy, and power of high energy (>= 3.5 V) lithium-ion cells.},
doi = {10.1021/acsami.6b09073},
journal = {ACS Applied Materials and Interfaces},
number = 41,
volume = 8,
place = {United States},
year = {Tue Oct 04 00:00:00 EDT 2016},
month = {Tue Oct 04 00:00:00 EDT 2016}
}
Web of Science
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