Abstract
Natural graphite powders were subjected to a series of thermal treatments to improve the anode irreversible capacity loss and capacity retention during long-term cycling of lithium-ion batteries. A baseline thermal treatment in inert Ar or N2 atmosphere was compared to cases with a proprietary additive to the furnace gas. This additive substantially altered the surface chemistry of the uncoated natural graphite powders and resulted in significantly improved long-term cycling performance of the lithium ion batteries over the commercial, carbon-coated natural graphite baseline. Different heat-treatment temperatures were investigated ranging from 950 to 2900 C to achieve the desired long-term cycling performance with a significantly reduced thermal budget. A detailed summary of the characterization data is also presented, which includes X-ray diffraction, X-ray photoelectron spectroscopy, Raman spectroscopy, and temperature-programmed desorption-mass spectroscopy. Characterization data was correlated to the observed capacity fade improvements over the course of long-term cycling at high charge-discharge rates in full lithium-ion cells. It is believed that the long-term performance improvements are a result of forming a more stable solid electrolyte interface (SEI) layer on the anode graphite surfaces, which is directly related to the surface chemistry modifications imparted by the proprietary gas environment during thermal treatment.
Original language | English |
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Pages (from-to) | 393-401 |
Number of pages | 9 |
Journal | Carbon |
Volume | 72 |
DOIs | |
State | Published - Jun 2014 |
Funding
This research at Oak Ridge National Laboratory, managed by UT Battelle, LLC, for the U.S. Department of Energy (DOE) under contract DE-AC05-00OR22725, was sponsored by the Office of Energy Efficiency and Renewable Energy (EERE) Advanced Manufacturing Office (Program Manager: Steve Sikirica) and Vehicle Technologies Office (VTO) (Program Manager: David Howell). The work was also sponsored by A123 Systems, Inc. under Cooperative Research and Development Agreement (CRADA) NFE-10-02757. SEM analysis was carried out at ORNL’s Center for Nanophase Materials Science (CNMS) User Facility, sponsored by the Office of Basic Energy Sciences, U.S. DOE. The authors would also like to thank Mike Wixom and Claus Daniel for helpful discussions throughout the course of this research project.
Funders | Funder number |
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A123 Systems, Inc. | |
CRADA | NFE-10-02757 |
U.S. Department of Energy | DE-AC05-00OR22725 |
Office of Energy Efficiency and Renewable Energy | |
Basic Energy Sciences | |
Oak Ridge National Laboratory | |
UT-Battelle |