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Decoupled Attraction and Repulsion for Fast, Large, and Reversible Thermal Actuation in Hydrogels.

Created on 09 Nov 2026

Authors

Jaewon Choi, Taehun Chung, Byungho Lee, Youngkwang Kim, Jihyeok Kwak, Jaeyoung Kim, Jihoon Han, Im Kyung Han, Junwoo Son, Anna Lee, Youn Soo Kim

Published in

ACS applied materials & interfaces. Nov 09, 2026. Epub Nov 09, 2026.

Abstract

In thermoresponsive poly(N-isopropylacrylamide) (PNIPAAm) hydrogels, strategies that accelerate heating-induced shrinking often slow down subsequent re-swelling upon cooling, because the driving forces favorable for shrinking and those favorable for re-swelling are fundamentally opposed within a single homogeneous network. This kinetic asymmetry limits the reversibility and cyclability of thermoresponsive actuators. To resolve this trade-off, we propose decoupled attraction and repulsion for thermal actuation (DART), in which the shrinking and re-swelling driving forces are assigned to separate structural components of a hydrogel rather than sharing a single network. Water-swollen, negatively charged poly(2-acrylamido-2-methyl-1-propanesulfonic acid) (PAMPS) nanogels, produced by planetary milling of bulk PAMPS hydrogels, were dispersed throughout a phase-separated PNIPAAm matrix to construct a composite hydrogel (PSG-Pn). The porous, phase-separated matrix enables rapid heating-induced water expulsion, while thermally modulated electrostatic repulsion among the PAMPS nanogels, governed by the temperature-dependent dielectric constant and Debye screening length, drives fast re-swelling upon cooling without impeding the shrinking process. PSG-Pn exhibited shrinking and re-swelling relaxation times of 2.24 and 219 s, respectively, approximately 1250-fold and 14-fold faster than those of a conventional non-phase-separated PNIPAAm hydrogel. PSG-Pn sustained ∼90% volume recovery over 20 heating-cooling cycles in water, and it also maintained repeated shrinking and re-swelling under open-air conditions without drying or structural failure. Building on this response, a near-infrared-responsive bilayer combining PSG-Pn with graphene oxide was steered to crawl in either direction across an unpatterned flat surface simply by switching the irradiation site, without any built-in ratchet or friction asymmetry, a behavior further supported by finite-element analysis of the localized contraction-recovery cycle. Together, these results indicate that partitioning attractive and repulsive driving forces into distinct structural elements offers a broadly applicable strategy for engineering thermoresponsive soft actuators with fast, large-amplitude, and reversible motion.

PMID:
43002134
Bibliographic data and abstract were imported from PubMed on 09 Nov 2026.

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