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Deep-learning-based inverse design of three-dimensional architected cellular materials with the target porosity and stiffness using voxelized Voronoi lattices

Architected cellular materials are a class of artificial materials with cellular architecture-dependent properties. Typically, designing cellular architectures paves the way to generate architected cellular materials with specific properties. However, most previous studies have primarily focused on...

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Autores principales: Zheng, Xiaoyang, Chen, Ta-Te, Jiang, Xiaoyu, Naito, Masanobu, Watanabe, Ikumu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9815236/
https://www.ncbi.nlm.nih.gov/pubmed/36620090
http://dx.doi.org/10.1080/14686996.2022.2157682
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author Zheng, Xiaoyang
Chen, Ta-Te
Jiang, Xiaoyu
Naito, Masanobu
Watanabe, Ikumu
author_facet Zheng, Xiaoyang
Chen, Ta-Te
Jiang, Xiaoyu
Naito, Masanobu
Watanabe, Ikumu
author_sort Zheng, Xiaoyang
collection PubMed
description Architected cellular materials are a class of artificial materials with cellular architecture-dependent properties. Typically, designing cellular architectures paves the way to generate architected cellular materials with specific properties. However, most previous studies have primarily focused on a forward design strategy, wherein a geometry is generated using computer-aided design modeling, and its properties are investigated experimentally or via simulations. In this study, we developed an inverse design framework for a disordered architected cellular material (Voronoi lattices) using deep learning. This inverse design framework is a three-dimensional conditional generative adversarial network (3D-CGAN) trained based on supervised learning using a dataset consisting of voxelized Voronoi lattices and their corresponding relative densities and Young’s moduli. A well-trained 3D-CGAN adopts variational sampling to generate multiple distinct Voronoi lattices with the target relative density and Young’s modulus. Consequently, the mechanical properties of the 3D-CGAN generated Voronoi lattices are validated through uniaxial compression tests and finite element simulations. The inverse design framework demonstrates potential for use in bone implants, where scaffold implants can be automatically generated with the target relative density and Young’s modulus.
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spelling pubmed-98152362023-01-06 Deep-learning-based inverse design of three-dimensional architected cellular materials with the target porosity and stiffness using voxelized Voronoi lattices Zheng, Xiaoyang Chen, Ta-Te Jiang, Xiaoyu Naito, Masanobu Watanabe, Ikumu Sci Technol Adv Mater Materials Informatics Architected cellular materials are a class of artificial materials with cellular architecture-dependent properties. Typically, designing cellular architectures paves the way to generate architected cellular materials with specific properties. However, most previous studies have primarily focused on a forward design strategy, wherein a geometry is generated using computer-aided design modeling, and its properties are investigated experimentally or via simulations. In this study, we developed an inverse design framework for a disordered architected cellular material (Voronoi lattices) using deep learning. This inverse design framework is a three-dimensional conditional generative adversarial network (3D-CGAN) trained based on supervised learning using a dataset consisting of voxelized Voronoi lattices and their corresponding relative densities and Young’s moduli. A well-trained 3D-CGAN adopts variational sampling to generate multiple distinct Voronoi lattices with the target relative density and Young’s modulus. Consequently, the mechanical properties of the 3D-CGAN generated Voronoi lattices are validated through uniaxial compression tests and finite element simulations. The inverse design framework demonstrates potential for use in bone implants, where scaffold implants can be automatically generated with the target relative density and Young’s modulus. Taylor & Francis 2023-01-04 /pmc/articles/PMC9815236/ /pubmed/36620090 http://dx.doi.org/10.1080/14686996.2022.2157682 Text en © 2023 The Author(s). Published by National Institute for Materials Science in partnership with Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Materials Informatics
Zheng, Xiaoyang
Chen, Ta-Te
Jiang, Xiaoyu
Naito, Masanobu
Watanabe, Ikumu
Deep-learning-based inverse design of three-dimensional architected cellular materials with the target porosity and stiffness using voxelized Voronoi lattices
title Deep-learning-based inverse design of three-dimensional architected cellular materials with the target porosity and stiffness using voxelized Voronoi lattices
title_full Deep-learning-based inverse design of three-dimensional architected cellular materials with the target porosity and stiffness using voxelized Voronoi lattices
title_fullStr Deep-learning-based inverse design of three-dimensional architected cellular materials with the target porosity and stiffness using voxelized Voronoi lattices
title_full_unstemmed Deep-learning-based inverse design of three-dimensional architected cellular materials with the target porosity and stiffness using voxelized Voronoi lattices
title_short Deep-learning-based inverse design of three-dimensional architected cellular materials with the target porosity and stiffness using voxelized Voronoi lattices
title_sort deep-learning-based inverse design of three-dimensional architected cellular materials with the target porosity and stiffness using voxelized voronoi lattices
topic Materials Informatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9815236/
https://www.ncbi.nlm.nih.gov/pubmed/36620090
http://dx.doi.org/10.1080/14686996.2022.2157682
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