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Reversible Fluorescence/Photochromic Switching of Repeated-Response Cellulose-Based Hydrogels for Information Encryption

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The rapid development of anti-counterfeiting technology has put forward new challenges on the repeated-response and stability of reversible fluorescence/photochromic switching hydrogels. To address this issue, a series of chemical cross-linked cellulose-based intelligent responsive hydrogels were synthesized by free-radical graft copolymerization in a hydrothermal process. This strategy allows for the creation of a chemical cross-linked three-dimensional structure that anchors photochromic ammonium molybdate/fluorescent carbon dots bifocals, resulting in enhanced stability and mechanical properties. Especially, the tensile and compressive strength of hydrogel reached a maximum value of 280 kPa and 560 kPa, respectively, which far exceeds that of some reported hydrogels. The resultant hydrogels exhibited desired reversible fluorescence/photochromic switching, reversible printing and erasing of patterns, and information encryption/decryption. Notably, the change of photochromism from yellow to green can be realized, and the self-fading process can be shortened to 25 minutes at 60 ℃ instead of 6 h at room temperature. More importantly, the fluorescence quenching phenomenon of the hydrogel occurs gradually after 2 min of continuous irradiation, and it can be recovered by selective treatment with ethanol. Overall, this study provides a simple strategy for the preparation of environmentally friendly reversible fluorescence/photochromic switching cellulose-based hydrogels for information encryption.
Title: Reversible Fluorescence/Photochromic Switching of Repeated-Response Cellulose-Based Hydrogels for Information Encryption
Description:
The rapid development of anti-counterfeiting technology has put forward new challenges on the repeated-response and stability of reversible fluorescence/photochromic switching hydrogels.
To address this issue, a series of chemical cross-linked cellulose-based intelligent responsive hydrogels were synthesized by free-radical graft copolymerization in a hydrothermal process.
This strategy allows for the creation of a chemical cross-linked three-dimensional structure that anchors photochromic ammonium molybdate/fluorescent carbon dots bifocals, resulting in enhanced stability and mechanical properties.
Especially, the tensile and compressive strength of hydrogel reached a maximum value of 280 kPa and 560 kPa, respectively, which far exceeds that of some reported hydrogels.
The resultant hydrogels exhibited desired reversible fluorescence/photochromic switching, reversible printing and erasing of patterns, and information encryption/decryption.
Notably, the change of photochromism from yellow to green can be realized, and the self-fading process can be shortened to 25 minutes at 60 ℃ instead of 6 h at room temperature.
More importantly, the fluorescence quenching phenomenon of the hydrogel occurs gradually after 2 min of continuous irradiation, and it can be recovered by selective treatment with ethanol.
Overall, this study provides a simple strategy for the preparation of environmentally friendly reversible fluorescence/photochromic switching cellulose-based hydrogels for information encryption.

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