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Programmable metal ion-induced patterned multicolour carboxymethylcellulose-based fluorescent hydrogels for
Qiuyan Luo1, Jia Jiang1, Juguo Dai1
1College of Materials, Fujian Provincial Key Laboratory of Fire Retardant Materials, Xiamen Key Laboratory of Fire Retardant Materials, Xiamen University, Xiamen 361005, China.
International Journal of Biological Macromolecules
|July 14, 2025
Summary
This study presents a novel fluorescent hydrogel for secure information encryption. The material changes color with metal ions, enabling programmable data storage and smartphone-readable encryption.
Area of Science:
- Materials Science
- Polymer Chemistry
- Nanotechnology
Background:
- Developing advanced materials for information encryption is crucial for data security.
- Existing encryption methods face challenges in usability, security, and data capacity.
Purpose of the Study:
- To create a novel interpenetrating polymer network hydrogel for enhanced information encryption.
- To develop a multi-color fluorescent material responsive to specific stimuli for data encoding.
Main Methods:
- Copolymerization of carboxymethyl cellulose and acrylamide to form an interpenetrating polymer network.
- Incorporation of gold nanoclusters and coumarin derivatives for tunable fluorescence (red, blue, green).
- Utilizing metal ion (Hg 2+ , Fe 3+ ) induced fluorescence changes for patterning and immobilization on various surfaces.
Main Results:
- Successfully synthesized three types of fluorescent hydrogels with distinct emission colors.
- Demonstrated responsive fluorescence changes to Hg 2+ and Fe 3+ ions, enabling precise patterning.
- Achieved information encoding and encryption via physical/chemical stimuli, UV light, and smartphone scanning.
Conclusions:
- The developed carboxymethyl cellulose-based fluorescent hydrogel offers a novel platform for advanced information storage.
- The metal ion-induced, multi-color patterning strategy integrated with smartphone scanning meets demands for digital encryption.
- The fluorescence quenching mechanism was elucidated, linked to specific functional groups within the hydrogel matrix.
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