4D Printing of Self-Healing, Thermally, and Near-Infrared Light-Responsive Granular Hydrogels with Segmental Directed Movement for Soft Robotic

Soft robots with intelligent shape-changing capabilities and spatially controlled actuation are essential for enhancing their performance. Here, three-dimensional printing of self-healing, near-infrared light-responsive shape memory granular hydrogels (SLSH) was introduced. The hydrogels were formulated using four distinct microgels: β-cyclodextrin-functionalized microgels (CDMGs) and 1-adamantylamine-functionalized microgels (AMGs) to promote host–guest physical interactions for self-healing and shear-thinning properties; polydopamine-functionalized microgels (PMGs) for photothermal conversion and antibacterial activity; and microgels with epoxy groups (MG) to enable chemical cross-linking with Jeffamine, forming a shape memory framework. The shear-thinning, shape memory, and self-healing characteristics were influenced by physical interactions within the ink as well as the chemical bonds formed after postprinting treatment. The viscosity and yield strength of the inks showed an increasing trend with a higher fraction of CDMG and AMG, indicating stronger reversible attractions within the jammed assembly of particles. Upon irradiation with an intensity of 1000 mW·cm–2 for 2 min, the internal temperature of the hydrogels increased to 38.2–43.0 °C, depending on the hydrogel type. For SLSH70, a distinct melting peak was recorded at 35–41 °C, associated with the melting of crystalline domains of Jeffamine, which was essential for the thermal shape recovery of the construct. After 1 h of fixation, the hydrogels SLSH30, SLSH50, and SLSH70 demonstrated a shape-fixing efficiency of 98.22 ± 0.45, 99.38 ± 0.68, and 98.54 ± 0.26%, respectively, with shape recovery efficiency approaching approximately 100%. During the self-healing process, complete reattachment occurred after 24 h at 25 °C for SLSH30, while the other samples exhibited a weaker healing ability. Finally, the results of antibacterial investigations highlighted the synergistic effects of PMG’s inherent antibacterial properties and its photothermal activity within the bacterial environment.

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Publication Details

Journal
ACS Applied Polymer Materials
Published
2025-01-29
DOI
https://doi.org/10.1021/acsapm.4c03518
Citations
14
Primary Topic
Advanced Materials and Mechanics
Type
article
Field-Weighted Citation Impact
9.99

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article

4D Printing of Self-Healing, Thermally, and Near-Infrared Light-Responsive Granular Hydrogels with Segmental Directed Movement for Soft Robotic

Mehdi Sheikhi, Fatemeh Rafiemanzelat, Ali Ramazani, Shaghayegh Vakili et al.
14 citations
ACS Applied Polymer Materials
Advanced Materials and Mechanics
9.99
article

4D Printing of Self-Healing, Thermally, and Near-Infrared Light-Responsive Granular Hydrogels with Segmental Directed Movement for Soft Robotic

Mehdi Sheikhi, Fatemeh Rafiemanzelat, Ali Ramazani, Shaghayegh Vakili, Zahra Mohamadnia, Ashkan Taheri, Aziz Maleki, Niyosha Karimi
article en
14 citations

Abstract

Soft robots with intelligent shape-changing capabilities and spatially controlled actuation are essential for enhancing their performance. Here, three-dimensional printing of self-healing, near-infrared light-responsive shape memory granular hydrogels (SLSH) was introduced. The hydrogels were formulated using four distinct microgels: β-cyclodextrin-functionalized microgels (CDMGs) and 1-adamantylamine-functionalized microgels (AMGs) to promote host–guest physical interactions for self-healing and shear-thinning properties; polydopamine-functionalized microgels (PMGs) for photothermal conversion and antibacterial activity; and microgels with epoxy groups (MG) to enable chemical cross-linking with Jeffamine, forming a shape memory framework. The shear-thinning, shape memory, and self-healing characteristics were influenced by physical interactions within the ink as well as the chemical bonds formed after postprinting treatment. The viscosity and yield strength of the inks showed an increasing trend with a higher fraction of CDMG and AMG, indicating stronger reversible attractions within the jammed assembly of particles. Upon irradiation with an intensity of 1000 mW·cm–2 for 2 min, the internal temperature of the hydrogels increased to 38.2–43.0 °C, depending on the hydrogel type. For SLSH70, a distinct melting peak was recorded at 35–41 °C, associated with the melting of crystalline domains of Jeffamine, which was essential for the thermal shape recovery of the construct. After 1 h of fixation, the hydrogels SLSH30, SLSH50, and SLSH70 demonstrated a shape-fixing efficiency of 98.22 ± 0.45, 99.38 ± 0.68, and 98.54 ± 0.26%, respectively, with shape recovery efficiency approaching approximately 100%. During the self-healing process, complete reattachment occurred after 24 h at 25 °C for SLSH30, while the other samples exhibited a weaker healing ability. Finally, the results of antibacterial investigations highlighted the synergistic effects of PMG’s inherent antibacterial properties and its photothermal activity within the bacterial environment.

ACS Applied Polymer MaterialsVol. 7(3)
Zanjan University of Medical Sciences (IR), Institute for Advanced Studies in Basic Sciences (IR), University of Isfahan (IR), Applied Nanotech (United States) (US), Ingenierie des Materiaux polymeres (FR), BioMarin (United States) (US), University of Zanjan (IR)
Iran National Science Foundation, Zanjan University of Medical Sciences, Office of Vice Chancellor for Research and Technology, University of Isfahan
Openalex Percentile: Top 1%
Advanced Materials and Mechanics
9.99
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