Author
Listed:
- Gang Lu
(University of Pennsylvania
City University of Hong Kong)
- Rui Ma
(Norwegian University of Science and Technology)
- Yuanyuan Zhao
(The Hong Kong Polytechnic University)
- Dianyu Wang
(Zhengzhou University)
- Wentao Shang
(City University of Hong Kong
Jinan University)
- Huaguo Chen
(City University of Hong Kong)
- Shahid Ali Khan
(City University of Hong Kong)
- Ming Li
(Imperial College London)
- Eduardo Saiz
(Imperial College London)
Abstract
Developing strong, thermally resistant adhesives for load-bearing applications remains challenging. Here we report a class of solution-sheared supramolecular oligomers that exhibit exceptional adhesive strength and toughness across a broad temperature range. These adhesives achieve a debonding work up to 23.6 kN/m and a lap shear strength exceeding 30.6 MPa, surpassing commercial structural adhesives by up to eightfold on metal and glass surfaces. Impressively, they retain a lap shear strength above 21 MPa even at 120 °C, outperforming current leading commercial alternatives. This performance arises from hierarchical nanostructures formed during solution shearing, which create enlarged, ordered nanocrystals and aligned nanofibrils within the bulk, enhancing mechanical robustness and toughness. Simultaneously, hydrogen-bonded nanocrystals anchored at the surface significantly strengthen interfacial adhesion. This multiscale structural organization enables thermal tolerance, crack resistance, and efficient energy dissipation, setting a new paradigm for high-performance, reusable adhesives capable of multiple rebonding cycles. Our work demonstrates how solution-shearing simultaneously optimizes adhesion chemistry and multiscale nano/microstructural control, achieving synergistic improvements in interfacial adhesion and bulk cohesion.
Suggested Citation
Gang Lu & Rui Ma & Yuanyuan Zhao & Dianyu Wang & Wentao Shang & Huaguo Chen & Shahid Ali Khan & Ming Li & Eduardo Saiz, 2025.
"Solution-sheared supramolecular oligomers with enhanced thermal resistance in interfacial adhesion and bulk cohesion,"
Nature Communications, Nature, vol. 16(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-63123-9
DOI: 10.1038/s41467-025-63123-9
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