3D Printing–In Situ Curing of Soft Organogels Using Frontal Polymerizable Inks

Q Qing Li Y Ya‐Lan Zhao (State Key Laboratory of Materials‐Oriented Chemical Engineering, College of Chemical Engineering and Jiangsu Key Laboratory of Fine Chemicals and Functional Polymer Materials Nanjing Tech University Nanjing 210009 P. R. China) H Hai‐Xia Shen (State Key Laboratory of Materials‐Oriented Chemical Engineering, College of Chemical Engineering and Jiangsu Key Laboratory of Fine Chemicals and Functional Polymer Materials Nanjing Tech University Nanjing 210009 P. R. China) Y Yong‐Chun Hou (State Key Laboratory of Materials‐Oriented Chemical Engineering, College of Chemical Engineering and Jiangsu Key Laboratory of Fine Chemicals and Functional Polymer Materials Nanjing Tech University Nanjing 210009 P. R. China) J Jia‐Le Lu (State Key Laboratory of Materials‐Oriented Chemical Engineering, College of Chemical Engineering and Jiangsu Key Laboratory of Fine Chemicals and Functional Polymer Materials Nanjing Tech University Nanjing 210009 P. R. China) L Liangliang Zhu (State Key Laboratory of Molecular Engineering of Polymers, Department of Macromolecular Science) S Su Chen (State Key Laboratory of High Pressure and Superhard Materials, College of Physics)

Abstract

Abstract 3D printing has gained immense recognition owing to its fascinating ability for rapid prototyping and customization. However, the current methods usually require post‐processing (direct ink writing) or continuous energy input (stereolithography) for polymer gel curing. The former lowers the fidelity and integrity of the printed layers, whereas the latter suffers from high energy consumption. To address these issues, a frontal polymerization (FP)–3D printing–in situ‐curing method is developed to construct printable and polymerizable inks for acrylate‐based monomers and soft organogel materials. Once initiated, no external energy supply is required, which allows for real‐time conversion of monomers into polymers within seconds. Thus, the energy requirements are reduced by several orders of magnitude. More importantly, the printed structure is closely bonded, effectively avoiding the collapse and deformation of soft materials. The as‐printed organogel is used as an evaporator and achieves a high water‐evaporation rate of 3.77 kg m −2  h −1 . This FP–3D printing–in situ‐curing strategy is an alternative, energy‐saving method for fabricating soft materials, enabling high fidelity and integrity of printed patterns with wide applicability.

Article Details

Volume / Issue Vol. 37, Issue 35
Published September 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (7)

Q

Qing Li

Y

Ya‐Lan Zhao

State Key Laboratory of Materials‐Oriented Chemical Engineering, College of Chemical Engineering and Jiangsu Key Laboratory of Fine Chemicals and Functional Polymer Materials Nanjing Tech University Nanjing 210009 P. R. China

H

Hai‐Xia Shen

State Key Laboratory of Materials‐Oriented Chemical Engineering, College of Chemical Engineering and Jiangsu Key Laboratory of Fine Chemicals and Functional Polymer Materials Nanjing Tech University Nanjing 210009 P. R. China

Y

Yong‐Chun Hou

State Key Laboratory of Materials‐Oriented Chemical Engineering, College of Chemical Engineering and Jiangsu Key Laboratory of Fine Chemicals and Functional Polymer Materials Nanjing Tech University Nanjing 210009 P. R. China

J

Jia‐Le Lu

State Key Laboratory of Materials‐Oriented Chemical Engineering, College of Chemical Engineering and Jiangsu Key Laboratory of Fine Chemicals and Functional Polymer Materials Nanjing Tech University Nanjing 210009 P. R. China

L

Liangliang Zhu

State Key Laboratory of Molecular Engineering of Polymers, Department of Macromolecular Science

S

Su Chen

State Key Laboratory of High Pressure and Superhard Materials, College of Physics