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Electrochemically Controlled Hydrogels with Electrotunable Permeability and Uniaxial Actuation
Department of Fibre and Polymer Technology School of Engineering Sciences in Chemistry Biotechnology and Health KTH Royal Institute of Technology Stockholm 100 44 Sweden.ORCID-id: 0000-0003-4388-8970
Department of Fibre and Polymer Technology School of Engineering Sciences in Chemistry Biotechnology and Health KTH Royal Institute of Technology Stockholm 100 44 Sweden.ORCID-id: 0000-0001-6403-2755
Robotic Materials Department Max Planck Institute for Intelligent Systems 70569 Stuttgart Germany.ORCID-id: 0000-0002-0588-6993
Department of Management and Engineering Division of Solid Mechanics Linköping University Linköping 58183 Sweden.ORCID-id: 0000-0002-1503-8293
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2023 (Engelska)Ingår i: Advanced Materials, ISSN 0935-9648, E-ISSN 1521-4095, Vol. 35, nr 45, artikel-id 2303255Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

The unique properties of hydrogels enable the design of life-like soft intelligent systems. However, stimuli-responsive hydrogels still suffer from limited actuation control. Direct electronic control of electronically conductive hydrogels can solve this challenge and allow direct integration with modern electronic systems. An electrochemically controlled nanowire composite hydrogel with high in-plane conductivity that stimulates a uniaxial electrochemical osmotic expansion is demonstrated. This materials system allows precisely controlled shape-morphing at only −1 V, where capacitive charging of the hydrogel bulk leads to a large uniaxial expansion of up to 300%, caused by the ingress of ≈700 water molecules per electron–ion pair. The material retains its state when turned off, which is ideal for electrotunable membranes as the inherent coupling between the expansion and mesoporosity enables electronic control of permeability for adaptive separation, fractionation, and distribution. Used as electrochemical osmotic hydrogel actuators, they achieve an electroactive pressure of up to 0.7 MPa (1.4 MPa vs dry) and a work density of ≈150 kJ m−3 (2 MJ m−3 vs dry). This new materials system paves the way to integrate actuation, sensing, and controlled permeation into advanced soft intelligent systems.

Ort, förlag, år, upplaga, sidor
Wiley , 2023. Vol. 35, nr 45, artikel-id 2303255
Nationell ämneskategori
Polymerkemi
Identifikatorer
URN: urn:nbn:se:miun:diva-49879DOI: 10.1002/adma.202303255Scopus ID: 2-s2.0-85167722724OAI: oai:DiVA.org:miun-49879DiVA, id: diva2:1813038
Forskningsfinansiär
Knut och Alice Wallenbergs Stiftelse, 2019.0564Olle Engkvists stiftelseTillgänglig från: 2023-11-18 Skapad: 2023-11-18 Senast uppdaterad: 2025-09-25Bibliografiskt granskad

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Lindström, Stefan B

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Benselfelt, TobiasShakya, JyotiRothemund, PhilippLindström, Stefan BPiper, AndrewWinkler, Thomas E.Hajian, AlirezaWågberg, LarsKeplinger, ChristophHamedi, Mahiar Max
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Advanced Materials
Polymerkemi

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