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Electronic Polymers and DNA Self-assembled in Nanowire Transistors
Linköpings universitet, Institutionen för fysik, kemi och biologi, Biomolekylär och Organisk Elektronik. Linköpings universitet, Tekniska högskolan.
Linköpings universitet, Institutionen för fysik, kemi och biologi, Biomolekylär och Organisk Elektronik. Linköpings universitet, Tekniska högskolan.
Linköpings universitet, Institutionen för fysik, kemi och biologi, Organisk Kemi. Linköpings universitet, Tekniska högskolan.
Linköpings universitet, Institutionen för fysik, kemi och biologi, Biomolekylär och Organisk Elektronik. Linköpings universitet, Tekniska högskolan.
2013 (Engelska)Ingår i: Small, ISSN 1613-6810, E-ISSN 1613-6829, Vol. 9, nr 3, s. 363-368Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

In this study the fully acidic form of PEDOT-S was used for the purpose of self-assembly onto DNA. We have previously shown that PEDOT-S is a short polymer that is self-doped with !1/3 of the sulfonate side groups acting as the self-doping sites (see supporting info.). The remaining sulfonate groups contribute to a net anionic charge, and a water-soluble polymer, with an intrinsic bulk conductivity of around 30 S/cm. It has been shown that PEDOT-S can bind to oppositely charged cationic amyloid protein structures in water and form conducting nano fibrillar networks, and it has also been shown to form hybrid structures with synthetic peptides, and gold nanoparticles.

Ort, förlag, år, upplaga, sidor
Wiley-VCH Verlag Berlin , 2013. Vol. 9, nr 3, s. 363-368
Nyckelord [en]
Organic electronics, conducting polymers, DNA nanotechnology, molecular selfassembly, organic electrochemical transistors
Nationell ämneskategori
Naturvetenskap Teknik och teknologier
Identifikatorer
URN: urn:nbn:se:liu:diva-81344DOI: 10.1002/smll.201201771ISI: 000314547200005OAI: oai:DiVA.org:liu-81344DiVA, id: diva2:551796
Anmärkning

Funding Agencies|Strategic Research Foundation SSF through the program OPEN||

Tillgänglig från: 2012-09-12 Skapad: 2012-09-12 Senast uppdaterad: 2017-12-07Bibliografiskt granskad
Ingår i avhandling
1. Electroactive Conjugated Polyelectrolytes Based on EDOT From Synthesis to Organic Electronics
Öppna denna publikation i ny flik eller fönster >>Electroactive Conjugated Polyelectrolytes Based on EDOT From Synthesis to Organic Electronics
2012 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

Conjugated polyelectrolytes (CP) show interesting electrical and optical properties for organic electronics as well as for life science applications. Their possibilities of supramolecular assembly with nanowire like misfolded proteins, amyloids, as well as synthetic polypeptides or DNA forming conducting nano composites is highly interesting as being a truly bottom up approach for fabrication of OLEDs, photovoltaic’s as well as logic devices.

A special class of CPs is that of electroactive cojugated polymers (ECPs), which, due to their structure, will exhibits a unique combination of properties, including the following; electrically conducting, ability to store an electric charge and ability to exchange ions. The positive or negative excess charge can be introduced into the conjugated polymer by means of chemical or electrochemical oxidation/reduction (a process called doping) following the polymerization reaction. In order to preserve overall electroneutrality of the polymer during introduction of excess charge, ionexhange processes occurs between the polymer phase and the surrounding electrolyte solution. This charge/discharge process can be utilized for application such as; pseudo super capacitors (energy storage through oxidation/reduction processes), electro mechanical actuators (convert electrical energy to mechanical energy) and sensors (converts a chemical signal to electrical conductivity).

In this thesis we describes the synthetic challenges with ECPs for applications vide supra. These mostly relates to solubility, ionic functionalization, conductivity and macromolecular properties such as size and shape of the ECPs. The key requirement in the synthesis of ECPs is that the conjugated nature of the monomer is conserved in the synthesis process and that insertion of excess charge (doping) can be obtained. This limits both the choice of monomer and the choice of polymerization process. Monomers of great complexity have been synthesized with this careful goal in mind. Furthermore, the development of novel monomers must also target the appropriate functionality for polymerization. As such, most ECP monomers are electron-rich molecules with pendant groups containing pyrroles, thiophenes, or 3,4-ethylenedioxythiophenes. These three well known ECP monomers are excellent additions to conjugated systems as they typically enable electrochemical polymerization and direct the polymerizations toward linear polymers with good stability towards doping.

The first topic of this thesis we demonstrate how we can obtain water soluble ECPs with good electrical conductivity by controlling the polymerization techniques and proper ionic functionalization of the monomer. We also show how these polymers can be incorporated by self-assembly with biomolecular templates, such as, DNA and amyloid fibrils, thus generating novel electrically conductive nanowires.

The second topics of this thesis demonstrate how hydrogels of ECPs can be used as bioand charge storage materials, were we demonstrate electronically controlled cell release for biology applications. Both applications are based on ECPs ability to ionexhange processes during electrochemical redox reactions. As well as ions, solvent and other neutral molecules may enter the film during charge/discharge processes. This cause a swelling or shrinking of the ECP films and the expansion and contraction of the polymer network in conjugation with the sorption/desorption of solvent molecules and ions can be described in terms of mechanical work.

In the first case we were able to synthesize a water soluble ECP with high amphiphilic character. The polymer was immobilized onto a flexible electrode, suitable for cell growth and subjected to a cell growth media. When the desired cell layer was formed we applied a potential to the flexible electrode. This resulted in that the mechanical work of the immobilized ECP during the applied potential overcame the week adhesive forces to the flexible electrode, which resulted in super swelling and disintegration of the ICP and the cell layer could be harvested.

In the second case the possibilities of using synthetically modified ECPs as a dopant during electropolymerization of another ECP monomer to obtain a polymer integrated network with high charge density and good charge transport properties. We demonstrate how this polymer network can be used as porous electrodes suitable for supercapacitors.

Ort, förlag, år, upplaga, sidor
Linköping: Linköping University Electronic Press, 2012. s. 75
Serie
Linköping Studies in Science and Technology. Dissertations, ISSN 0345-7524 ; 1470
Nyckelord
Conjugated polyelectrolytes, Electroactive conjugated polyelectrolytes, Intrinsically conducting polyelectrolytes
Nationell ämneskategori
Naturvetenskap
Identifikatorer
urn:nbn:se:liu:diva-81347 (URN)978-91-7519-812-5 (ISBN)
Disputation
2012-09-28, Planck, Fysikhuset, Campus Valla, Linköpings universitet, Linköping, 10:15 (Engelska)
Opponent
Handledare
Tillgänglig från: 2012-09-12 Skapad: 2012-09-12 Senast uppdaterad: 2013-07-01Bibliografiskt granskad
2. On decoration of biomolecular scaffolds with a conjugated polyelectrolyte
Öppna denna publikation i ny flik eller fönster >>On decoration of biomolecular scaffolds with a conjugated polyelectrolyte
2017 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

Biotemplating is the art of using a biological structure as a scaffold which is decorated with a functional material. In this fashion the structures will gain new functionalities and biotemplating offers a simple route of mass-producing mesoscopic material with new interesting properties. Biological structures are abundant and come in a great variety of elaborate and due to their natural origin they could be more suitable for interaction with biological systems than wholly synthetic materials. Conducting polymers are a novel class of material which was developed just 40 years ago and are well suited for interaction with biological material due to their organic composition. Furthermore the electronic properties of the conducting polymers can be tuned giving rise to dynamic control of the behavior of the material. Self-assembly processes are interesting since they do not require complicated or energy demanding processing conditions. This is particularly important as most biological materials are unstable at elevated temperatures or harsh environments. The main aim of this thesis is to show the possibility of using self-assembly to decorate a conducting polymer onto various biotemplates. Due to the intrinsic variety in charge, size and structure between the available natural scaffolds it is difficult, if not impossible, to find a universal method.

In this thesis we show how biotemplating can be used to create new hybrid materials by self-assembling a conducting polymer with biological structures based on DNA, protein, lipids and cellulose, and in this fashion create material with novel optical and electronic properties.

Ort, förlag, år, upplaga, sidor
Linköping: Linköping University Electronic Press, 2017. s. 51
Serie
Linköping Studies in Science and Technology. Dissertations, ISSN 0345-7524 ; 1885
Nationell ämneskategori
Polymerkemi
Identifikatorer
urn:nbn:se:liu:diva-141675 (URN)10.3384/diss.diva-141675 (DOI)9789176854372 (ISBN)
Disputation
2017-10-19, Planck, Fysikhuset, Campus Valla, Linköping, 10:15 (Engelska)
Opponent
Handledare
Forskningsfinansiär
Stiftelsen för strategisk forskning (SSF)Knut och Alice Wallenbergs Stiftelse
Tillgänglig från: 2017-10-04 Skapad: 2017-10-04 Senast uppdaterad: 2019-10-11Bibliografiskt granskad

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