Light-Responsive Shape Memory Polymer Network Containing Azobenzene: Shape Manipulation, Mechanical Regulation, and Intelligent Lubrication

Light-responsive materials have garnered significant attention in fields such as robotics and actuators due to their flexibility in remote and localized control, presenting immense application potential. In this work, we demonstrate intelligent responsive applications through the introduction of a liquid crystal network formed by azobenzene, showcasing photoinduced shape memory performance, light-reversible tribological behavior, and thermally driven force modulation. By copolymerizing the liquid crystal monomer 1,4-bis-[4-(6-acryloyloxyhexyloxy)benzoyloxy]-2-methylbenzene with a functional azobenzene monomer, we can adjust the cross-linking density and mechanical properties of the yield liquid crystal elastomer networks (LCNs) by varying the azobenzene content, resulting in a high-strength elastomer with a tensile strength of 23.6 MPa. The unique microstructure of this material, which readily crystallizes at low temperatures, allows LCN-20 to generate a high actuating stress of ∼5.6 MPa when cooled from 15 °C to −45 °C, significantly expanding its potential as an actuator. The presence of azobenzene enables photoisomerization, imparting reversible changes in the surface contact angle and modulus. Additionally, the photothermal effect of azobenzene facilitates light-controlled shape memory performance. By integrating the tunable surface and mechanical properties, the LCNs demonstrate reversible tribological switching upon UV–visible light irradiation, significantly expanding their potential as smart adaptive materials. This work provides a heuristic perspective for designing multiresponsive and performance-adjustable materials.

Authors

Institutions

Publication Details

Journal
ACS Applied Polymer Materials
Published
2025-06-07
DOI
https://doi.org/10.1021/acsapm.5c00822
Citations
3
Primary Topic
Polymer composites and self-healing
Type
article
Field-Weighted Citation Impact
1.82

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Light-Responsive Shape Memory Polymer Network Containing Azobenzene: Shape Manipulation, Mechanical Regulation, and Intelligent Lubrication

Zhangzhang Tang, Junhui Gong, Yaoming Zhang, Tingmei Wang et al.
3 citations
ACS Applied Polymer Materials
Polymer composites and self-healing
1.82
article

Light-Responsive Shape Memory Polymer Network Containing Azobenzene: Shape Manipulation, Mechanical Regulation, and Intelligent Lubrication

Zhangzhang Tang, Junhui Gong, Yaoming Zhang, Tingmei Wang, Qihua Wang, Xinrui Zhang, Xianqiang Pei, Hangyu Shen
article en
3 citations

Abstract

Light-responsive materials have garnered significant attention in fields such as robotics and actuators due to their flexibility in remote and localized control, presenting immense application potential. In this work, we demonstrate intelligent responsive applications through the introduction of a liquid crystal network formed by azobenzene, showcasing photoinduced shape memory performance, light-reversible tribological behavior, and thermally driven force modulation. By copolymerizing the liquid crystal monomer 1,4-bis-[4-(6-acryloyloxyhexyloxy)benzoyloxy]-2-methylbenzene with a functional azobenzene monomer, we can adjust the cross-linking density and mechanical properties of the yield liquid crystal elastomer networks (LCNs) by varying the azobenzene content, resulting in a high-strength elastomer with a tensile strength of 23.6 MPa. The unique microstructure of this material, which readily crystallizes at low temperatures, allows LCN-20 to generate a high actuating stress of ∼5.6 MPa when cooled from 15 °C to −45 °C, significantly expanding its potential as an actuator. The presence of azobenzene enables photoisomerization, imparting reversible changes in the surface contact angle and modulus. Additionally, the photothermal effect of azobenzene facilitates light-controlled shape memory performance. By integrating the tunable surface and mechanical properties, the LCNs demonstrate reversible tribological switching upon UV–visible light irradiation, significantly expanding their potential as smart adaptive materials. This work provides a heuristic perspective for designing multiresponsive and performance-adjustable materials.

ACS Applied Polymer MaterialsVol. 7(12)
Chinese Academy of Sciences (CN), Lanzhou Institute of Chemical Physics (CN), University of Chinese Academy of Sciences (CN), State Key Laboratory of Solid Lubrication
National Natural Science Foundation of China, Chinese Academy of Sciences
Affordable and clean energy
Openalex Percentile: Top 16%
Polymer composites and self-healing
1.82
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.