Conductive, self-healable and reusable poly(3,4-ethylenedioxythiophene)-based hydrogels for highly sensitive pressure arrays

Although challenging, the preparation of pure conducting polymer (CP) hydrogels as conductive flexible networks for developing high-performance functional platforms is an outstanding alternative to conventional approaches, as for example those based on the cross-linking of insulating polymers with C...

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Detalhes bibliográficos
Autores: Babeli Aguilera, Ismael, Ruano Torres, Guillem, Casanovas Salas, Jordi|||0000-0002-4914-9194, Ginebra Molins, Maria Pau|||0000-0002-4700-5621, García Torres, José Manuel|||0000-0002-3996-0274, Alemán Llansó, Carlos|||0000-0003-4462-6075
Formato: artículo
Fecha de publicación:2020
País:España
Recursos:Universitat Politècnica de Catalunya (UPC)
Repositorio:UPCommons. Portal del coneixement obert de la UPC
Idioma:inglés
OAI Identifier:oai:upcommons.upc.edu:2117/340563
Acesso em linha:https://hdl.handle.net/2117/340563
https://dx.doi.org/10.1039/d0tc01947j
Access Level:acceso abierto
Palavra-chave:Polymers -- Testing
Conducting polymers
Conducting polymer
hydrogel
Polímers -- Proves
Polímers conductors
Àrees temàtiques de la UPC::Enginyeria dels materials
Descrição
Resumo:Although challenging, the preparation of pure conducting polymer (CP) hydrogels as conductive flexible networks for developing high-performance functional platforms is an outstanding alternative to conventional approaches, as for example those based on the cross-linking of insulating polymers with CP segments and the simple utilization of CPs as fillers of insulating hydrogel networks. In this work, we propose the employment of poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) to prepare conductive hydrogels by partially replacing the PSS dopant by alginate (Alg) chains, which is energetically favoured. The capacity of Alg chains to be electrostatically cross-linked by Ca2+ ions has allowed us to obtain hydrogels with good electrical percolation response and mechanical properties. Hydrogels were prepared in a very simple one-step process by adding CaCl2 to different mixtures of PEDOT : PSS and alginic acid (1 : 3, 1 : 1 and 3 : 1). After structural, chemical and physical characterization, the 1 : 3 PEDOT/Alg hydrogel was moulded to fabricate stretchable touch-pressure sensor arrays, which exhibited fast response and good spatial resolution of the pressure distribution. In addition, the PEDOT/Alg hydrogel is self-healable which allowed us to prepare reusable pressure sensors (i.e. devices that can be reprocessed to be used in their original application) thanks to the reversibility of the noncovalent Ca2+ crosslinks. Reusable devices are different to reclaimed and recycled devices as these are no longer used for the same application because the materials lose their properties. With our hydrogels we are a step closer to a circular economy by allowing the reuse of electronic devices and reducing electronic waste worldwide. Moreover, the superior performance of the PEDOT/Alg hydrogel opens up its utilization as an efficient and flexible pressure sensor for wearable human-electronic interfaces, in which reusability would be an added value.