EventsThe 1st International Online Conference on Gels
Published
This submission belongs to the session S2. Hydrogels, Organogels, Xerogels, and Aerogels of the event The 1st International Online Conference on Gels
Published date
28 Nov, 2025
Academic Editor
author-avatarSIDI A. BENCHERIF
Citation
Pietro Tordi, Soft, Stretchable, and Smart: Alginate/Gelatin Organohydrogels for Wearable Electronics, in Proceedings of The 1st International Online Conference on Gels, 3 December–5 December 2025, MDPI: Basel, Switzerland
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Soft, Stretchable, and Smart: Alginate/Gelatin Organohydrogels for Wearable Electronics

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1. Institut de Science et d’Ingénierie Supramoléculaires (ISIS), Université de Strasbourg & CNRS, Strasbourg, 67000, France, Italy
Abstract

Alginate, a naturally abundant polysaccharide, offers exceptional versatility in functional material design due to its charged backbone and its ability to form ionically crosslinked networks with multivalent cations[1,2]. When combined with gelatin in a glycerol-rich medium, it gives rise to a class of organohydrogels that are not only soft and stretchable, but also responsive, robust, and fully biocompatible.

We harness this platform to engineer multifunctional hydrogels tailored for both sensing and energy-related applications. By tuning the crosslinking chemistry with Cu2+, Mn2+, Fe3+, and Zr4+ ions, we access highly adaptable materials that respond sensitively to mechanical strain (gauge factor > 1.6), temperature (0.19 K-1), humidity (0.022 RH(%)-1), and light (up to 9.2 μA/W)—while retaining performance over 2500 mechanical cycles. These multiresponsive materials are ideal candidates for next-generation wearable sensors and electronic skins[3].

Building on this concept, we developed a complementary formulation serving as a gel polymer electrolyte for flexible supercapacitors. Through the synergistic interplay of Cu2+/Mn2+ crosslinking and Li+ doping, we modulate the nanoscale polymer structure (via SAXS) to enable high capacitance (up to 591.8 mF/cm2), excellent rate performance, and long-term stability (> 88% over 5000 cycles). This work demonstrates how ionic coordination directly governs electrochemical function and mechanical resilience[4].

Together, these studies showcase a green, modular strategy for designing biopolymer-based systems that seamlessly integrate soft sensing and energy delivery—offering a scalable path toward self-powered, sustainable devices.

[1] Jeong, Y.; Tordi, P.; Tamayo, A.; Han, B.; Bonini, M.; Samorì, P. Adv. Funct. Mater. 2025, e09607. DOI: 10.1002/adfm.202509607

[2] Tordi, P.; Ridi, F.; Samorì, P.; Bonini, M. Adv. Funct. Mater. 2025, 35 (9), 2416390. DOI: 10.1002/adfm.202416390

[3] Tordi, P.; Tamayo, A.; Jeong, Y.; Bonini, M.; Samorì, P. Adv. Funct. Mater. 2024, 34 (52), 2410663. DOI: 10.1002/adfm.202410663

[4] Tordi, P.; Montes-García, V.; Tamayo, A.; Bonini, M.; Samorì, P.; Ciesielski, A. Small. 2025, 2503937. DOI: 10.1002/smll.202503937

Keywords
alginate
organohydrogels
gel polymer electrolytes
organic electronics
wearable sensors
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