Nanoconfinement Enabled High‐Efficiency and Long‐Lifetime Multicolor Afterglow Hydrogels for Advanced Spatiotemporal Encryption and Pathogen Eradication

S Shuman Zhang X Xiaoye Li X Xiaolong Liu J Jiaxin Chen (Department of Chemistry, The Hong Kong University of Science and Technology, Clearwater Bay, Kowloon, Hong Kong 999077, China) Y Yixin Ouyang (State Key Laboratory of Flexible Electronics & Institute of Advanced Materials) Z Zhisheng Gao H Huanhuan Li H Hui Li G Gaozhan Xie Y Ye Tao (State Key Laboratory of Radiation Medicine and Protection, School of Radiation Medicine and Protection, Collaborative Innovation Center of Radiological Medicine of Jiangsu Higher Education Institutions, Biomedical Basic Research Center (BBRC) of Jiangsu) H Heng Dong R Runfeng Chen (Key Laboratory for Organic Electronics & Information Displays (KOLED), Jiangsu-Singapore Joint Research Center on Organic/Bio- Electronics and Information Displays & Institute of Advanced Materials (IAM)) W Wei Huang G Guangliang Hong (The Department of Emergency Medicine Quzhou People's Hospital, The Quzhou Affiliated Hospital of Wenzhou Medical University Quzhou Zhejiang China)

Abstract

ABSTRACT Multicolor organic afterglow hydrogels that simultaneously possess efficient exciton harvesting, ultralong lifetimes and large deformations are still rare. Here, a nano‐restriction engineered strategy that embeds a rigid and chromatically diverse hydrogen bond supramolecular framework into hydrogel networks is presented. The confined microenvironment of the supramolecular framework suppresses non‐radiative quenching to prolong triplet lifetimes and acts as stress‐dissipating nodes to reinforce the polymer matrix. The synthesized hydrogels exhibit tunable afterglow emissions from deep blue to orange–red, lifetimes up to 2535 ms, and quantum yields above 29.4%, while retaining a compressive strength of 7.7 MPa and fracture strain near 1400%, with excellent stability under repeated cycling. Programmable color and decay dynamics of afterglow hydrogels enable spatiotemporally resolved encryption. Moreover, the long‐lived triplet excitons efficiently sensitize singlet oxygen, delivering >99.9% antibacterial efficacy to accelerate infected wound healing. This approach provides a general route to develop multifunctional afterglow soft materials that couple high exciton utilization and ultralong lifetime with mechanical robustness.

Article Details

Volume / Issue Vol. 65, Issue 23
Published June 01, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (14)

S

Shuman Zhang

X

Xiaoye Li

X

Xiaolong Liu

J

Jiaxin Chen

Department of Chemistry, The Hong Kong University of Science and Technology, Clearwater Bay, Kowloon, Hong Kong 999077, China

Y

Yixin Ouyang

State Key Laboratory of Flexible Electronics & Institute of Advanced Materials

Z

Zhisheng Gao

H

Huanhuan Li

H

Hui Li

G

Gaozhan Xie

Y

Ye Tao

State Key Laboratory of Radiation Medicine and Protection, School of Radiation Medicine and Protection, Collaborative Innovation Center of Radiological Medicine of Jiangsu Higher Education Institutions, Biomedical Basic Research Center (BBRC) of Jiangsu

H

Heng Dong

R

Runfeng Chen

Key Laboratory for Organic Electronics & Information Displays (KOLED), Jiangsu-Singapore Joint Research Center on Organic/Bio- Electronics and Information Displays & Institute of Advanced Materials (IAM)

W

Wei Huang

G

Guangliang Hong

The Department of Emergency Medicine Quzhou People's Hospital, The Quzhou Affiliated Hospital of Wenzhou Medical University Quzhou Zhejiang China