Evaluating 3D printed mesh geometries in ceramic LiB electrodes

Additive manufacturing techniques have the potential to promote a paradigmatic change in the electrode fabrication processes for lithium-ion batteries (LiBs) as they may offer alternative component designs to boost their performance or to customise the application. The present research work explores...

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Main Authors: J R Marín-Rueda, J F Valera-Jiménez, J M Ramos-Fajardo, I M Peláez-Tirado, S Tair, M Castro-García, J Canales-Vázquez, J C Pérez-Flores
Format: Article
Language:English
Published: IOP Publishing 2024-01-01
Series:JPhys Energy
Subjects:
Online Access:https://doi.org/10.1088/2515-7655/ad2497
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author J R Marín-Rueda
J F Valera-Jiménez
J M Ramos-Fajardo
I M Peláez-Tirado
S Tair
M Castro-García
J Canales-Vázquez
J C Pérez-Flores
author_facet J R Marín-Rueda
J F Valera-Jiménez
J M Ramos-Fajardo
I M Peláez-Tirado
S Tair
M Castro-García
J Canales-Vázquez
J C Pérez-Flores
author_sort J R Marín-Rueda
collection DOAJ
description Additive manufacturing techniques have the potential to promote a paradigmatic change in the electrode fabrication processes for lithium-ion batteries (LiBs) as they may offer alternative component designs to boost their performance or to customise the application. The present research work explores the use of low-cost fused filament fabrication (FFF) 3D printing to fabricate Li _4 Ti _5 O _12 (LTO) mesh electrodes in the search for enlarged electrochemically active areas. Using different nozzle diameters (ND), we have 3D printed several mesh electrodes that after sintering allow an increase in the surface to volume ratio by up to ≈290% compared to conventional flat cylindrical geometries. As the conventional route to produce 3D printed meshes, i.e. stacking of consecutive layers with a 90° rotation, leads to problems of vertical misalignment that may affect the electrical contact, we have developed a new compact design that maximises the contact between layers. All the 3D printed mesh electrodes with thicknesses of 400 and 800 μ m, exhibit electrochemical performance very close to those of thin (70 μ m) electrodes, e.g. 175 mAh g ^−1 at C/2 in the case of ND = 100 μ m, which is the theoretical capacity value for LTO. At higher C-rates, 800 μ m-thick mesh electrodes with larger ND exhibit a marked drop in the reversible capacity (28 mAh g ^−1 at 8 C), although the values obtained improve notably those of the equivalent thick solid electrode (almost null at 8 C). The compact design demonstrated superior performance at high C-rates, improving by ≈70% the results of the best conventional mesh electrode at 8 C for 800 μ m electrodes. These results highlight the potential of FFF-3D printing to generate novel high aspect ratio geometries and the impact of design and printing parameters on the performance of LiB electrode materials. Exploring alternative efficient geometries may facilitate the integration of thick electrodes in high energy density LiBs.
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spelling doaj.art-a46ae3111bc340e391d97aa639e3e3632024-02-14T11:50:17ZengIOP PublishingJPhys Energy2515-76552024-01-016202500810.1088/2515-7655/ad2497Evaluating 3D printed mesh geometries in ceramic LiB electrodesJ R Marín-Rueda0https://orcid.org/0000-0002-6075-829XJ F Valera-Jiménez1https://orcid.org/0000-0001-9126-7154J M Ramos-Fajardo2https://orcid.org/0009-0000-6840-7905I M Peláez-Tirado3https://orcid.org/0000-0001-8289-4367S Tair4https://orcid.org/0009-0001-3373-7450M Castro-García5https://orcid.org/0000-0003-4157-6164J Canales-Vázquez6https://orcid.org/0000-0003-4089-2034J C Pérez-Flores7https://orcid.org/0000-0002-7641-6374Energy Materials & 3D Printing Laboratory (3D-ENERMAT), Renewable Energy Research Institute, University of Castilla-La Mancha (UCLM) , C/ de la Investigación 1, Building 3, Albacete 02071, SpainEnergy Materials & 3D Printing Laboratory (3D-ENERMAT), Renewable Energy Research Institute, University of Castilla-La Mancha (UCLM) , C/ de la Investigación 1, Building 3, Albacete 02071, SpainEnergy Materials & 3D Printing Laboratory (3D-ENERMAT), Renewable Energy Research Institute, University of Castilla-La Mancha (UCLM) , C/ de la Investigación 1, Building 3, Albacete 02071, SpainEnergy Materials & 3D Printing Laboratory (3D-ENERMAT), Renewable Energy Research Institute, University of Castilla-La Mancha (UCLM) , C/ de la Investigación 1, Building 3, Albacete 02071, SpainEnergy Materials & 3D Printing Laboratory (3D-ENERMAT), Renewable Energy Research Institute, University of Castilla-La Mancha (UCLM) , C/ de la Investigación 1, Building 3, Albacete 02071, SpainEnergy Materials & 3D Printing Laboratory (3D-ENERMAT), Renewable Energy Research Institute, University of Castilla-La Mancha (UCLM) , C/ de la Investigación 1, Building 3, Albacete 02071, SpainEnergy Materials & 3D Printing Laboratory (3D-ENERMAT), Renewable Energy Research Institute, University of Castilla-La Mancha (UCLM) , C/ de la Investigación 1, Building 3, Albacete 02071, SpainEnergy Materials & 3D Printing Laboratory (3D-ENERMAT), Renewable Energy Research Institute, University of Castilla-La Mancha (UCLM) , C/ de la Investigación 1, Building 3, Albacete 02071, SpainAdditive manufacturing techniques have the potential to promote a paradigmatic change in the electrode fabrication processes for lithium-ion batteries (LiBs) as they may offer alternative component designs to boost their performance or to customise the application. The present research work explores the use of low-cost fused filament fabrication (FFF) 3D printing to fabricate Li _4 Ti _5 O _12 (LTO) mesh electrodes in the search for enlarged electrochemically active areas. Using different nozzle diameters (ND), we have 3D printed several mesh electrodes that after sintering allow an increase in the surface to volume ratio by up to ≈290% compared to conventional flat cylindrical geometries. As the conventional route to produce 3D printed meshes, i.e. stacking of consecutive layers with a 90° rotation, leads to problems of vertical misalignment that may affect the electrical contact, we have developed a new compact design that maximises the contact between layers. All the 3D printed mesh electrodes with thicknesses of 400 and 800 μ m, exhibit electrochemical performance very close to those of thin (70 μ m) electrodes, e.g. 175 mAh g ^−1 at C/2 in the case of ND = 100 μ m, which is the theoretical capacity value for LTO. At higher C-rates, 800 μ m-thick mesh electrodes with larger ND exhibit a marked drop in the reversible capacity (28 mAh g ^−1 at 8 C), although the values obtained improve notably those of the equivalent thick solid electrode (almost null at 8 C). The compact design demonstrated superior performance at high C-rates, improving by ≈70% the results of the best conventional mesh electrode at 8 C for 800 μ m electrodes. These results highlight the potential of FFF-3D printing to generate novel high aspect ratio geometries and the impact of design and printing parameters on the performance of LiB electrode materials. Exploring alternative efficient geometries may facilitate the integration of thick electrodes in high energy density LiBs.https://doi.org/10.1088/2515-7655/ad2497mesh electrodesFFF-3D printing of ceramicsLiB LTO electrodes3D designperformance enhancement
spellingShingle J R Marín-Rueda
J F Valera-Jiménez
J M Ramos-Fajardo
I M Peláez-Tirado
S Tair
M Castro-García
J Canales-Vázquez
J C Pérez-Flores
Evaluating 3D printed mesh geometries in ceramic LiB electrodes
JPhys Energy
mesh electrodes
FFF-3D printing of ceramics
LiB LTO electrodes
3D design
performance enhancement
title Evaluating 3D printed mesh geometries in ceramic LiB electrodes
title_full Evaluating 3D printed mesh geometries in ceramic LiB electrodes
title_fullStr Evaluating 3D printed mesh geometries in ceramic LiB electrodes
title_full_unstemmed Evaluating 3D printed mesh geometries in ceramic LiB electrodes
title_short Evaluating 3D printed mesh geometries in ceramic LiB electrodes
title_sort evaluating 3d printed mesh geometries in ceramic lib electrodes
topic mesh electrodes
FFF-3D printing of ceramics
LiB LTO electrodes
3D design
performance enhancement
url https://doi.org/10.1088/2515-7655/ad2497
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