Closed‐Loop and Sustainable 4D Printing of Multi‐Stimuli‐Responsive Sulfur‐Rich Polymer Composites for Autonomous Task Execution

J Jae Hyuk Hwang (Advanced Materials Division Korea Research Institute of Chemical Technology 141 Gajeong‐ro Yuseong‐gu Daejeon 34114 Republic of Korea) S Sukyoung Won (Department of Organic and Nano Engineering Hanyang University 222 Wangsimni‐ro, Seondong‐gu Seoul 04763 Republic of Korea) J Ji Mok Lee (Dow Chemical Silicones Korea Ltd. 24 Gwanghyewonsandan‐gil, Gwanghyewon‐myeon, Chungcheongbuk‐do Jincheon‐gun 27841 Republic of Korea) W Woongbi Cho (Department of Organic and Nano Engineering Hanyang University 222 Wangsimni‐ro, Seondong‐gu Seoul 04763 Republic of Korea) S Sungmin Park (IT Materials & Components Research Center) H Hyun Kim C Chang‐Geun Chae (Advanced Materials Division Korea Research Institute of Chemical Technology 141 Gajeong‐ro Yuseong‐gu Daejeon 34114 Republic of Korea) W Woohwa Lee (Advanced Materials Division Korea Research Institute of Chemical Technology 141 Gajeong‐ro Yuseong‐gu Daejeon 34114 Republic of Korea) D Dong‐Gyun Kim (Advanced Materials Division Korea Research Institute of Chemical Technology 141 Gajeong‐ro Yuseong‐gu Daejeon 34114 Republic of Korea) J Jeong Jae Wie (Department of Organic and Nano Engineering Hanyang University Seoul Republic of Korea) Y Yong Seok Kim

Abstract

Abstract Shape‐programmable polymer networks derived from waste elemental sulfur hold great potential for diverse applications such as 4D printing and soft robotics. However, their crosslinked nature makes it challenging to 3D print complex geometry for soft robots. Herein, a closed‐loop 4D printing strategy is reported of poly(phenylene polysulfide) networks (PSNs) and their magnetic particle composites (MPSNs) to fabricate multi‐functional soft robots with programmable shape‐morphing capabilities. The dynamic S─S bonds within the loosely crosslinked PSNs impart shear‐thinning behavior, enabling hot‐melt extrusion of both PSNs and MPSNs into complex architectures. After shape‐programming, 3D‐printed PSN and MPSN structures exhibit heat‐ or light‐triggered shape recovery and allow modular assembly for spatially selective shape‐morphing governed by the distinct glass transition temperatures of the PSN series. These architectures can be readily reprinted into new form factors, demonstrating a closed‐loop and sustainable 4D printing. With multi‐stimuli responsiveness and solvent resistance provided by the PSN composites, the MPSN capsule serves as an on‐demand catalyst‐releasing magnetic stirring bar in a reagent‐containing solution, autonomously releasing catalysts at a preset temperature to facilitate carbamate synthesis. The 4D printable MPSNs offer a sustainable platform not only for adaptable shape‐morphing and dynamic actuation but also for autonomous task execution in next‐generation soft robotic applications.

Article Details

Volume / Issue Vol. 37, Issue 44
Published November 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (11)

J

Jae Hyuk Hwang

Advanced Materials Division Korea Research Institute of Chemical Technology 141 Gajeong‐ro Yuseong‐gu Daejeon 34114 Republic of Korea

S

Sukyoung Won

Department of Organic and Nano Engineering Hanyang University 222 Wangsimni‐ro, Seondong‐gu Seoul 04763 Republic of Korea

J

Ji Mok Lee

Dow Chemical Silicones Korea Ltd. 24 Gwanghyewonsandan‐gil, Gwanghyewon‐myeon, Chungcheongbuk‐do Jincheon‐gun 27841 Republic of Korea

W

Woongbi Cho

Department of Organic and Nano Engineering Hanyang University 222 Wangsimni‐ro, Seondong‐gu Seoul 04763 Republic of Korea

S

Sungmin Park

IT Materials & Components Research Center

H

Hyun Kim

C

Chang‐Geun Chae

Advanced Materials Division Korea Research Institute of Chemical Technology 141 Gajeong‐ro Yuseong‐gu Daejeon 34114 Republic of Korea

W

Woohwa Lee

Advanced Materials Division Korea Research Institute of Chemical Technology 141 Gajeong‐ro Yuseong‐gu Daejeon 34114 Republic of Korea

D

Dong‐Gyun Kim

Advanced Materials Division Korea Research Institute of Chemical Technology 141 Gajeong‐ro Yuseong‐gu Daejeon 34114 Republic of Korea

J

Jeong Jae Wie

Department of Organic and Nano Engineering Hanyang University Seoul Republic of Korea

Y

Yong Seok Kim