Inverse design of cellular structures with the targeted nonlinear mechanical response

Advanced additive manufacturing capabilities have enabled a transformational ability to create sophisticated cellular structures using diverse materials. By altering the topology of the unit cell, the mechanical behavior, such as the stress-strain response during compression, can be modulated. Nevertheless, identifying a printable topology within an enormous design space that would precisely deliver the targeted nonlinear material response is challenging. We propose a data-driven generative framework based on a conditional variational autoencoder (cVAE) architecture that can inverse design the cellular structure based on the intended nonlinear stress-strain response. Trained on a dataset of structure-property pairs, the cVAE learns a compact and expressive latent space that enables efficient mapping from targets to feasible geometries. Two inference modes are explored: (1) decoder-only generation, which enables the exploration of diverse designs conditioned solely on the desired mechanical response, and (2) encoder-decoder generation, which further allows for the incorporation of desired topologies, ensuring the generated structure conforms to both mechanical properties and to desired-topology constraints. The results demonstrate that the model can generate structurally plausible and mechanically accurate designs, with the predicted stress-strain curves closely matching the targets. Even under joint conditioning, the model effectively balances geometric fidelity and functional performance.

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Publication Details

Journal
Scientific Reports
Published
2025-12-25
DOI
https://doi.org/10.1038/s41598-025-33184-3
Primary Topic
Topology Optimization in Engineering
Type
article
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article

Inverse design of cellular structures with the targeted nonlinear mechanical response

Darby J. Luscher, Nitin Daphalapurkar, Dana M. Dattelbaum, Jeffery A. Leiding et al.
Scientific Reports
Topology Optimization in Engineering
article

Inverse design of cellular structures with the targeted nonlinear mechanical response

Darby J. Luscher, Nitin Daphalapurkar, Dana M. Dattelbaum, Jeffery A. Leiding, Sushan Nakarmi, Kwan‐Soo Lee, Jihyeon Kim
article en

Abstract

Advanced additive manufacturing capabilities have enabled a transformational ability to create sophisticated cellular structures using diverse materials. By altering the topology of the unit cell, the mechanical behavior, such as the stress-strain response during compression, can be modulated. Nevertheless, identifying a printable topology within an enormous design space that would precisely deliver the targeted nonlinear material response is challenging. We propose a data-driven generative framework based on a conditional variational autoencoder (cVAE) architecture that can inverse design the cellular structure based on the intended nonlinear stress-strain response. Trained on a dataset of structure-property pairs, the cVAE learns a compact and expressive latent space that enables efficient mapping from targets to feasible geometries. Two inference modes are explored: (1) decoder-only generation, which enables the exploration of diverse designs conditioned solely on the desired mechanical response, and (2) encoder-decoder generation, which further allows for the incorporation of desired topologies, ensuring the generated structure conforms to both mechanical properties and to desired-topology constraints. The results demonstrate that the model can generate structurally plausible and mechanically accurate designs, with the predicted stress-strain curves closely matching the targets. Even under joint conditioning, the model effectively balances geometric fidelity and functional performance.

Scientific ReportsVol. 16(1)
Los Alamos National Laboratory (US), Computational Physics (United States) (US)
Openalex Percentile: Top 37%
Topology Optimization in Engineering
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Inverse design of cellular structures with the targeted nonlinear mechanical response — Darby J. Luscher, Nitin Daphalapurkar, et al. · Scientific Reports (2025) | TGRS Research Map | TGRS