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Multi-modal characterization methods of solid-electrolyte interphase in silicon-graphite composite electrodes
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Ha, Yeyoung
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Natl Renewable Energy Lab, 15013 Denver West Pkwy, Golden, CO 80401 USA Natl Renewable Energy Lab, 15013 Denver West Pkwy, Golden, CO 80401 USA

Frisco, Sarah
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Natl Renewable Energy Lab, 15013 Denver West Pkwy, Golden, CO 80401 USA Natl Renewable Energy Lab, 15013 Denver West Pkwy, Golden, CO 80401 USA

Norman, Andrew
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Natl Renewable Energy Lab, 15013 Denver West Pkwy, Golden, CO 80401 USA Natl Renewable Energy Lab, 15013 Denver West Pkwy, Golden, CO 80401 USA

Teeter, Glenn
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Natl Renewable Energy Lab, 15013 Denver West Pkwy, Golden, CO 80401 USA Natl Renewable Energy Lab, 15013 Denver West Pkwy, Golden, CO 80401 USA

Jiang, Chun-Sheng
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Natl Renewable Energy Lab, 15013 Denver West Pkwy, Golden, CO 80401 USA Natl Renewable Energy Lab, 15013 Denver West Pkwy, Golden, CO 80401 USA

DeCaluwe, Steven C.
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Colorado Sch Mines, 1500 Illinois St, Golden, CO 80401 USA Natl Renewable Energy Lab, 15013 Denver West Pkwy, Golden, CO 80401 USA
机构:
[1] Natl Renewable Energy Lab, 15013 Denver West Pkwy, Golden, CO 80401 USA
[2] Colorado Sch Mines, 1500 Illinois St, Golden, CO 80401 USA
关键词:
Solid electrolyte interphase;
Surface characterization;
Silicon electrodes;
Lithium ion batteries;
LITHIUM-ION-BATTERY;
FLUOROETHYLENE CARBONATE;
NEGATIVE ELECTRODES;
ANODE;
SEI;
EVOLUTION;
XPS;
REDUCTION;
CHEMISTRY;
FILM;
D O I:
10.1016/j.jpowsour.2023.232804
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Composite silicon-graphite (Si-Gr) anodes can improve battery energy density, due to Si's high gravimetric capacity, while mitigating mechanical degradation of the anode and solid-electrolyte interphase (SEI) caused by Si volumetric expansion. Optimizing these anodes is challenging, in part due to difficulty characterizing the SEI structure and composition. In this work, we present multi-modal characterization of the SEI on composite Si-Gr anodes to relate SEI chemical composition and structure to functional properties. Discrepancies in elemental concentrations from X-ray photoelectron spectroscopy, Auger electron spectroscopy, and energy-dispersive X-ray spectroscopy (EDS) are attributed to varying information depth and lateral resolution of the individual probes. However, by combining quantitative composition information with spatially resolved element mapping from scanning transmission electron microscopy, EDS, and electron energy loss spectroscopy, a holistic picture of the SEI emerges. We observe the bilayer SEI structure and a direct correlation between elemental Li and F, suggesting that most Li in the SEI exists as lithium fluoride (LiF). Further, LiF concentration is directly proportional to the maximum SEI resistivity, as determined by scanning spreading resistance microscopy. Lastly, there is an inverse relationship between lithium carbonate and LiF concentration in the SEI, providing insight into the detailed chemistry of SEI formation and evolution.
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