Hydrogel-Based Iontronic Sensing

Hydrogel-based iontronic sensing (HBIS) is emerging as a compelling frontier at the interface of soft matter, electrochemistry, and bioelectronics, driven by the unique ability of hydrogels to communicate with living systems through hydrated ionic networks rather than electronic conduction in rigid solids. This ionic mode of signal transduction enables intrinsically compliant interactions with biological tissues, electrolytes, and dynamic fluidic microenvironments, making HBIS highly attractive for flexible bioelectronics. As the field evolves from material optimization toward integrated and intelligent systems, a unifying understanding of material design, ion transport, and device function remains lacking. Here, a multiscale quantitative framework is established to bridge structure, transport, and sensing performance in HBIS. Representative material platforms, including polyelectrolytes, ionogels, and nanocomposite hydrogels, are examined alongside key transport mechanisms, such as diffusion, electromigration, convection, electroosmotic flow, adsorption-site hopping, and Grotthuss-type conduction. Quantitative modeling approaches based on electrochemical impedance spectroscopy and Poisson-Nernst-Planck theory are further highlighted, together with emerging applications in iontronic skins, soft robotics, human-machine interfaces, and energy conversion. This review provides a design blueprint for next-generation hydrogel iontronic sensors with improved predictability, adaptability, and operational stability across biological interfaces.

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Publication Details

Journal
Sustainable Engineering Novit
Published
2026-04-28
DOI
https://doi.org/10.53941/sen.2026.100006
Primary Topic
Advanced Sensor and Energy Harvesting Materials
Type
article
Field-Weighted Citation Impact
0.00

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article

Hydrogel-Based Iontronic Sensing

Yigang Shen, Weijun Li, Junhua Zhang, Shihao Wang et al.
Sustainable Engineering Novit
Advanced Sensor and Energy Harvesting Materials
article

Hydrogel-Based Iontronic Sensing

Yigang Shen, Weijun Li, Junhua Zhang, Shihao Wang, J Liu
article en

Abstract

Hydrogel-based iontronic sensing (HBIS) is emerging as a compelling frontier at the interface of soft matter, electrochemistry, and bioelectronics, driven by the unique ability of hydrogels to communicate with living systems through hydrated ionic networks rather than electronic conduction in rigid solids. This ionic mode of signal transduction enables intrinsically compliant interactions with biological tissues, electrolytes, and dynamic fluidic microenvironments, making HBIS highly attractive for flexible bioelectronics. As the field evolves from material optimization toward integrated and intelligent systems, a unifying understanding of material design, ion transport, and device function remains lacking. Here, a multiscale quantitative framework is established to bridge structure, transport, and sensing performance in HBIS. Representative material platforms, including polyelectrolytes, ionogels, and nanocomposite hydrogels, are examined alongside key transport mechanisms, such as diffusion, electromigration, convection, electroosmotic flow, adsorption-site hopping, and Grotthuss-type conduction. Quantitative modeling approaches based on electrochemical impedance spectroscopy and Poisson-Nernst-Planck theory are further highlighted, together with emerging applications in iontronic skins, soft robotics, human-machine interfaces, and energy conversion. This review provides a design blueprint for next-generation hydrogel iontronic sensors with improved predictability, adaptability, and operational stability across biological interfaces.

Sustainable Engineering NovitVol. 2(2)
University of Science and Technology of China (CN), Zhejiang Normal University (CN), Jinan University (CN), Suzhou University of Science and Technology (CN), Xiamen University of Technology (CN), Cardiff University (GB)
China Postdoctoral Science Foundation
Affordable and clean energy
Openalex Percentile: Top 8%
Advanced Sensor and Energy Harvesting Materials
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