Hysteresis-free and high sensitivity strain sensing of ionically conductive hydrogels.
Hysteresis-free and high sensitivity strain sensing of ionically conductive hydrogels.
复制标题
离子导电水凝胶的无滞后和高灵敏度应变传感。
DOI:
10.1002/anbr.202200132
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发表时间:
2022-12
影响因子:
3.4
通讯作者:
Jiwoo Song;Chenchen Mou;G. Balakrishnan;Yingqiao Wang;Mahathy Rajagopalan;Audrey Schreiner;Durva Naik;Tzahi Cohen-Karni;M. S. Halbreiner;C. Bettinger
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文献类型:
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作者:
Jiwoo Song;Chenchen Mou;G. Balakrishnan;Yingqiao Wang;Mahathy Rajagopalan;Audrey Schreiner;Durva Naik;Tzahi Cohen-Karni;M. S. Halbreiner;C. Bettinger
Hydrogels are promising materials for soft and implantable strain sensors owing to their large compliance (E500%) compared to other polymer networks. Further, hydrogels can be functionalized to seamlessly integrate with many types of tissues. However, most current methods attempt to imbue additional electronic functionality to structural hydrogel materials by incorporating fillers with orthogonal properties such as electronic or mixed ionic conduction. Although composite strategies may improve performance or facilitate heterogeneous integration with downstream hardware, composites complicate the path for regulatory approval and may compromise the otherwise compelling properties of the underlying structural material. Here we report hydrogel strain sensors composed of genipin-crosslinked gelatin and dopamine-functionalized poly(ethylene glycol) for in vivo monitoring of cardiac function. By measuring their impedance only in their resistive regime (>10 kHz), hysteresis is reduced and the resulting gauge factor is increased by ~50x to 1.02±0.05 and 1.46±0.05 from approximately 0.03-0.05 for PEG-Dopa and genipin-crosslinked gelatin respectively. Adhesion and in vivo biocompatibility are studied to support implementation of strain sensors for monitoring cardiac output in porcine models. Impedance-based strain sensing in the kilohertz regime simplifies the piezoresistive behavior of these materials and expands the range of hydrogel-based strain sensors.