Rapid photocontrollable dopamine polymerization for instant adaptive wet adhesion

Dopamine-based adhesives offer strong, versatile adhesion through diverse interactions but are limited by slow, poorly controlled oxidative polymerization and dopamine's inhibition of radical polymerization. We present an efficient photochemical strategy for in-situ fabrication of high-performance polydopamine-containing hydrogels with instant wet adhesion. By integrating a scalable synthesis of a protected dopamine derivative with rational photochemical design, we enable simultaneous, light-controlled oxidative and radical polymerizations, forming interpenetrated hydrogel networks within seconds. The resulting tough adhesives exhibit high polydopamine content and strong adhesion across diverse wet and dry substrates, outperforming conventional polydopamine-coated systems. This rapid, light-driven process is compatible with extrusion-based 3D printing, allowing spatially programmable adhesion and the creation of complex biomimetic architectures. Furthermore, the instant, robust adhesion enables integration of flexible electroluminescent devices that remain stable under large deformations. This work establishes a versatile platform for rapid, programmable adhesion in soft electronics and biointerfacing systems.

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Publication Details

Journal
Nature Communications
Published
2026-01-07
DOI
https://doi.org/10.1038/s41467-025-66530-0
Primary Topic
Polymer Surface Interaction Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Rapid photocontrollable dopamine polymerization for instant adaptive wet adhesion

P. Zhang, You Yu, Hao Lü, Jie Yu et al.
Nature Communications
Polymer Surface Interaction Studies
article

Rapid photocontrollable dopamine polymerization for instant adaptive wet adhesion

P. Zhang, You Yu, Hao Lü, Jie Yu, Zhenhao Zhu, Zhe Lu, Shi Bai, Qian Lu, Zijian Zheng, Qian Wang
article en

Abstract

Dopamine-based adhesives offer strong, versatile adhesion through diverse interactions but are limited by slow, poorly controlled oxidative polymerization and dopamine's inhibition of radical polymerization. We present an efficient photochemical strategy for in-situ fabrication of high-performance polydopamine-containing hydrogels with instant wet adhesion. By integrating a scalable synthesis of a protected dopamine derivative with rational photochemical design, we enable simultaneous, light-controlled oxidative and radical polymerizations, forming interpenetrated hydrogel networks within seconds. The resulting tough adhesives exhibit high polydopamine content and strong adhesion across diverse wet and dry substrates, outperforming conventional polydopamine-coated systems. This rapid, light-driven process is compatible with extrusion-based 3D printing, allowing spatially programmable adhesion and the creation of complex biomimetic architectures. Furthermore, the instant, robust adhesion enables integration of flexible electroluminescent devices that remain stable under large deformations. This work establishes a versatile platform for rapid, programmable adhesion in soft electronics and biointerfacing systems.

Nature CommunicationsVol. 16(1)
Guangzhou University of Chinese Medicine (CN), Ministry of Education of the People's Republic of China (CN), Hong Kong Polytechnic University (HK)
National Natural Science Foundation of China
Affordable and clean energy
Openalex Percentile: Top 95%
Polymer Surface Interaction Studies
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