Design of Tough 3D Printable Elastomers with Human‐in‐the‐Loop Reinforcement Learning

J Johann L. Rapp (Department of Chemistry, University of North Carolina at Chapel Hill) D Dylan M. Anstine (Department of Chemical Engineering and Materials Science Michigan State University East Lansing MI 48824 United States) F Filipp Gusev (Department of Chemistry Mellon College of Science Carnegie Mellon University Pittsburgh Pennsylvania 15213 USA) F Filipp Nikitin (Department of Chemistry Mellon College of Science Carnegie Mellon University Pittsburgh Pennsylvania 15213 USA) K Kelly H. Yun (Department of Chemistry University of North Carolina at Chapel Hill Chapel Hill North Carolina 27599 USA) M Meredith A. Borden (Department of Chemistry University of North Carolina At Chapel Hill Chapel Hill North Carolina USA) V Vittal Bhat (Department of Chemistry, Stanford University, Stanford, California 94305, United States) O Olexandr Isayev F Frank A. Leibfarth (Department of Chemistry)

Abstract

Abstract The development of high‐performance elastomers for additive manufacturing requires overcoming complex property trade‐offs that challenge conventional material discovery pipelines. Here, a human‐in‐the‐loop reinforcement learning (RL) approach is used to discover polyurethane elastomers that overcome pervasive stress–strain property tradeoffs. Starting with a diverse training set of 92 formulations, a coupled multi‐component reward system was identified that guides RL agents toward materials with both high strength and extensibility. Through three rounds of iterative optimization combining RL predictions with human chemical intuition, we identified elastomers with more than double the average toughness compared to the initial training set. The final exploitation round, aided by solubility prescreening, predicted twelve materials exhibiting both high strength (>10 MPa) and high strain at break (>200%). Analysis of the high‐performing materials revealed structure‐property insights, including the benefits of high molar mass urethane oligomers, a high density of urethane functional groups, and incorporation of rigid low molecular weight diols and unsymmetric diisocyanates. These findings demonstrate that machine‐guided, human‐augmented design is a powerful strategy for accelerating polymer discovery in applications where data is scarce and expensive to acquire, with broad applicability to multi‐objective materials optimization.

Article Details

Volume / Issue Vol. 64, Issue 36
Published September 01, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (9)

J

Johann L. Rapp

Department of Chemistry, University of North Carolina at Chapel Hill

D

Dylan M. Anstine

Department of Chemical Engineering and Materials Science Michigan State University East Lansing MI 48824 United States

F

Filipp Gusev

Department of Chemistry Mellon College of Science Carnegie Mellon University Pittsburgh Pennsylvania 15213 USA

F

Filipp Nikitin

Department of Chemistry Mellon College of Science Carnegie Mellon University Pittsburgh Pennsylvania 15213 USA

K

Kelly H. Yun

Department of Chemistry University of North Carolina at Chapel Hill Chapel Hill North Carolina 27599 USA

M

Meredith A. Borden

Department of Chemistry University of North Carolina At Chapel Hill Chapel Hill North Carolina USA

V

Vittal Bhat

Department of Chemistry, Stanford University, Stanford, California 94305, United States

O

Olexandr Isayev

F

Frank A. Leibfarth

Department of Chemistry