Electrochemical Properties of Laser-Printed Multilayer Anodes for Lithium-Ion Batteries

New electrode architectures promise huge potential for improving batteries’ electrochemical properties, such as power density, energy density, and lifetime. In this work, the use of laser-induced forward transfer (LIFT) was employed and evaluated as a tool for the development of advanced electrode a...

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Bibliographic Details
Published in:Nanomaterials (Basel, Switzerland) Switzerland), 2023-08, Vol.13 (17), p.2411
Main Authors: Rist, Ulrich, Falkowski, Viktoria, Pfleging, Wilhelm
Format: Article
Language:English
Subjects:
anode
Anodes
Carbon black
Electrochemical analysis
Electrochemistry
Electrodes
Energy storage
Graphite
Investigations
laser-induced forward transfer
Lasers
Lithium
Lithium-ion batteries
lithium-ion battery
multilayer
Multilayers
N-Methyl-2-pyrrolidone
Optimization
Particle size
Polyvinylidene fluorides
Printing
Rechargeable batteries
Silicon
Specific capacity
Viscosity
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Summary:New electrode architectures promise huge potential for improving batteries’ electrochemical properties, such as power density, energy density, and lifetime. In this work, the use of laser-induced forward transfer (LIFT) was employed and evaluated as a tool for the development of advanced electrode architectures. For this purpose, it was first confirmed that the printing process has no effect on the transferred battery material by comparing the electrochemical performance of the printed anodes with state-of-the-art coated ones. For this, polyvinylidene fluoride (PVDF) was used as a binder and n-methyl-2-pyrrolidone (NMP) as a solvent, which is reported to be printable. Subsequently, multilayer electrodes with flake-like and spherical graphite particles were printed to test if a combination of their electrochemical related properties can be realized with measured specific capacities ranging from 321 mAh·g−1 to 351 mAh·g−1. Further, a multilayer anode design with a silicon-rich intermediate layer was printed and electrochemically characterized. The initial specific capacity was found to be 745 mAh·g−1. The presented results show that the LIFT technology offers the possibility to generate alternative electrode designs, promoting research in the optimization of 3D battery systems.
ISSN:2079-4991
2079-4991
DOI:10.3390/nano13172411