| 1. |
- Brooke, Robert, 1989-, et al.
(författare)
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Greyscale and paper electrochromic polymer displays by UV patterning
- 2019
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Ingår i: Polymers. - : MDPI AG. - 2073-4360. ; 11:2
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Tidskriftsartikel (refereegranskat)abstract
- Electrochromic devices have important implications as smart windows for energy efficient buildings, internet of things devices, and in low-cost advertising applications. While inorganics have so far dominated the market, organic conductive polymers possess certain advantages such as high throughput and low temperature processing, faster switching, and superior optical memory. Here, we present organic electrochromic devices that can switch between two high-resolution images, based on UV-patterning and vapor phase polymerization of poly(3,4- ethylenedioxythiophene) films. We demonstrate that this technique can provide switchable greyscale images through the spatial control of a UV-light dose. The color space was able to be further altered via optimization of the oxidant concentration. Finally, we utilized a UV-patterning technique to produce functional paper with electrochromic patterns deposited on porous paper, allowing for environmentally friendly electrochromic displays.
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| 2. |
- Che, Canyan, 1988-, et al.
(författare)
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Twinning Lignosulfonate with a Conducting Polymer via Counter-Ion Exchange for Large-Scale Electrical Storage
- 2019
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Ingår i: Advanced Sustainable Systems. - : Wiley-VCH Verlag. - 2366-7486. ; 3:9
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Tidskriftsartikel (refereegranskat)abstract
- Lignosulfonate (LS) is a large-scale surplus product of the forest and paper industries, and has primarily been utilized as a low-cost plasticizer in making concrete for the construction industry. LS is an anionic redox-active polyelectrolyte and is a promising candidate to boost the charge capacity of the positive electrode (positrode) in redox-supercapacitors. Here, the physical-chemical investigation of how this biopolymer incorporates into the conducting polymer PEDOT matrix, of the positrode, by means of counter-ion exchange is reported. Upon successful incorporation, an optimal access to redox moieties is achieved, which provides a 63% increase of the resulting stored electrical charge by reversible redox interconversion. The effects of pH, ionic strength, and concentrations, of included components, on the polymer–polymer interactions are optimized to exploit the biopolymer-associated redox currents. Further, the explored LS-conducting polymer incorporation strategy, via aqueous synthesis, is evaluated in an up-scaling effort toward large-scale electrical energy storage technology. By using an up-scaled production protocol, integration of the biopolymer within the conducting polymer matrix by counter-ion exchange is confirmed and the PEDOT-LS synthesized through optimized strategy reaches an improved charge capacity of 44.6 mAh g−1.
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| 3. |
- Chen, Shangzhi, et al.
(författare)
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Redox-tunable structural colour images by UV-patterned conducting polymer nanofilms on metal surfaces
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Annan publikation (övrigt vetenskapligt/konstnärligt)abstract
- Precise manipulation of light-matter interaction has enabled a wide variety of approaches to create bright and vivid structural colours. Techniques utilizing photonic crystals, Fabry-Pérot cavities, plasmonics, or high-refractive index dielectric metasurfaces have been studied for applications ranging from optical coatings to reflective displays. However, complicated fabrication procedures for sub-wavelength nanostructures, limited active areas, and inherent absence of tunability of these approaches significantly impede their further development towards flexible, large-scale, and switchable devices compatible with facile and cost-effective production. Herein, we present a simple and efficient method to generate structural colours based on nanoscale conducting polymer films prepared on metallic surfaces via vapour phase polymerization and ultraviolet (UV) light patterning. Varying the UV dose enables synergistic control of both nanoscale film thickness and polymer permittivity, which generates controllable colours from violet to red. Together with greyscale photomasks this enables fabrication of high-resolution colour images using single exposure steps. We further demonstrate spatiotemporal tuning of the structurally coloured surfaces and images via electrochemical modulation of the polymer redox state. The simple structure, facile fabrication, wide colour gamut, and dynamic colour tuning make this concept competitive for future multi-functional and smart displays.
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| 4. |
- Kim, Nara, 1985-, et al.
(författare)
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Electric transport properties in PEDOT thin films
- 2019. - 4
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Ingår i: Conjugated polymers. - Boca Raton : CRC Press. - 9780429190520 ; , s. 45-128
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Bokkapitel (refereegranskat)abstract
- In this chapter, the authors summarize their understanding of Poly(3,4-ethylenedioxythiophene) (PEDOT), with respect to its chemical and physical fundamentals. They focus upon the structure of several PEDOT systems, from the angstrom level and up, and the impact on both electronic and ionic transport. The authors discuss the structural properties of PEDOT:X and PEDOT:poly(styrenesulfonate) based on experimental data probed at the scale ranging from angstrom to submicrometer. The morphology of PEDOT is influenced by the nature of counter-ions, especially at high oxidation levels. The doping anions intercalate between PEDOT chains to form a “sandwich” structure to screen the positive charges in PEDOT chains. The authors provide the main transport coefficients such as electrical conductivity s, Seebeck coefficient S, and Peltier coefficient σ, starting from a general thermodynamic consideration. The optical conductivity of PEDOT has also been examined based on the effective medium approximation, which is normally used to describe microscopic permittivity properties of composites made from several different constituents.
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| 5. |
- Mitraka, Evangelia, 1986-
(författare)
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Conducting Polymer Electrodes for Oxygen Reduction Reaction
- 2018
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Both the pollution level of the environment and the increasing energy demands have stimulated intense research on the development of low-cost environmentally-friendly energy conversion and storage systems with high efficiency, such as metal-air batteries and fuel cells.One of the most essential parts of both fuel cells and metal–air batteries is the air-electrode which is responsible for the reduction of O2. The air-electrode can use O2 from air facilitating the layout of the device; however, the process taking place on it is significantly complex. Currently, platinum (Pt) is the benchmark for air-electrodes in such technologies, although it is expensive and exhibits other important disadvantages which diminish the fuel cell performance. Therefore, extensive research has been devoted to reduce the amount of Pt used in air-electrodes and to develop a noble metal-free version of these electrodes.The area of printed electronics could facilitate the development of low-cost electrodes produced in high volume for such applications. Conducting polymers are attractive materials for this technology because they may combine several desired properties, like electronic conduction, ionic conduction and catalysis of electrochemical reactions.Among other conducting polymers, poly(3,4-ethylenedioxythiophene) (PEDOT) emerged as an alternative cathode catalyst material to Pt, due to its ability to effectively catalyze the oxygen reduction reaction (ORR), while it also exhibits high electrical and ionic conductivity.The focus of this thesis is to study the electrocatalytic activity and mechanism of the conducting polymer poly(3,4-ethylenedioxythiophene) (PEDOT) when employed as an airelectrode in energy storage devices, such as fuel cells and metal-air batteries. Although PEDOT is extensively studied during the last decade as an air-electrode for fuel cell and metal-air batteries, vital pieces of the catalytic mechanism that PEDOT follows remain unknown, namely: (i) the sites of PEDOT on which O2 interacts and (ii) the intermediate species which are formed during the ORR. The content of this thesis tackles these topics, both from experimental and theoretical point of view. Moreover, it investigates the use of PEDOT as an active electrocatalyst in a polymer exchange membrane (PEM) fuel cell, by embedding the polymer in a cellulose matrix, aiming to fabricate a gas diffusion electrode for the ORR side of the device. Finally, the goal of the thesis surpasses the limit of the p-doped PEDOT and undertakes the evaluation of a n-type conjugated polymer of high electron affinity as a cathode in reduction processes.
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| 6. |
- Shiran Chaharsoughi, Mina, 1986-, et al.
(författare)
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Hybrid Plasmonic and Pyroelectric Harvesting of Light Fluctuations
- 2018
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Ingår i: Advanced Optical Materials. - : Wiley-Blackwell. - 2162-7568 .- 2195-1071.
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Tidskriftsartikel (refereegranskat)abstract
- State-of-the-art solar energy harvesting systems based on photovoltaic technology require constant illumination for optimal operation. However, weather conditions and solar illumination tend to fluctuate. Here, a device is presented that extracts electrical energy from such light fluctuations. The concept combines light-induced heating of gold nanodisks (acting as plasmonic optical nanoantennas), and an organic pyroelectric copolymer film (poly(vinylidenefluoride-co-trifluoroethylene)), that converts temperature changes into electrical signals. This hybrid device can repeatedly generate current pulses, not only upon the onset of illumination, but also when illumination is blocked. Detailed characterization highlights the key role of the polarization state of the copolymer, while the copolymer thickness has minor influence on performance. The results are fully consistent with plasmon-assisted pyroelectric effects, as corroborated by combined optical and thermal simulations that match the experimental results. Owing to the tunability of plasmonic resonances, the presented concept is compatible with harvesting near infrared light while concurrently maintaining visible transparency.
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| 7. |
- Wu, Zhixing, 1990-, et al.
(författare)
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Conducting Polymer‐Based e‐Refinery for Sustainable Hydrogen Peroxide Production
- 2023
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Ingår i: Energy & Environmental Materials. - : Wiley-Blackwell. - 2575-0356.
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Tidskriftsartikel (refereegranskat)abstract
- Electrocatalysis enables the industrial transition to sustainable production of chemicals using abundant precursors and electricity from renewable sources. De-centralized production of hydrogen peroxide (H2O2) from water and oxygen of air is highly desirable for daily life and industry. We report an effective electrochemical refinery (e-refinery) for H2O2 by means of electrocatalysis-controlled comproportionation reaction (2(H)O + O -> 2(HO)), feeding pure water and oxygen only. Mesoporous nickel (II) oxide (NiO) was used as electrocatalyst for oxygen evolution reaction (OER), producing oxygen at the anode. Conducting polymer poly(3,4-ethylenedioxythiophene): poly(styrene sulfonate) (PEDOT:PSS) drove the oxygen reduction reaction (ORR), forming H2O2 on the cathode. The reactions were evaluated in both half-cell and device configurations. The performance of the H2O2 e-refinery, assembled on anion-exchange solid electrolyte and fed with pure water, was limited by the unbalanced ionic transport. Optimization of the operation conditions allowed a conversion efficiency of 80%.
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| 8. |
- Abrahamsson, Tobias, 1991-
(författare)
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Synthetic Functionalities for Ion and Electron Conductive Polymers : Applications in Organic Electronics and Biological Interfaces
- 2021
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- In the search for understanding and communicating with all biological systems, in humans, animals, plants, and even microorganisms, we find a common language of all communicating via electrons, ions and molecules. Since the discovery of organic electronics, the ability to bridge the gap and communicate be-tween modern technology and biology has emerged. Organic chemistry pro-vides us with tools for understanding and a material platform of polymer electronics for communication. Such insights give us not only the ability to observe fundamental phenomenon but to actively design and construct materials with chemical functionalities towards better interfaces and applications. Organic electronic materials and devices have found their way to be implemented in the field of medicine for diagnostic and therapeutic purposes, but also in water purification and to help tackle the monumental task in creating the next generation of sustainable energy production and storage. Ultimately it’s safe to say that organic electronics are not going to replace our traditional technology based on inorganic materials but rather the two fields can find a way to complement each other for various purposes and applications. Compared to conventional silicon based technology, production of carbon-based organic electronic polymer materials are extremely cheap and devices can even be made flexible and soft with great compatibility towards biology. The main focus of this thesis has been developing and synthesizing new types of organic electronic and ionic conductive polymeric materials. Rational chemical design and modifications of the materials have been utilized to introduce specific functionalities to the materials. The functionalities serving the purpose to facilitate ion and electron conductive charge transport for organic electronics and with biological interface implementation of the polymer materials. Multi-functional ionic conductive hyperbranched polyglycerol polyelectrolytes (dendrolytes) were developed comprising both ionically charged groups and cross-linkable groups. The hyperbranched polyglycerol core structure of the material possesses a hydrophilic solvating platform for both ions and maintenance of solvent molecules, while being a biocompatible structure. Coupled with the peripheral charged ionic functionalities of the polymer, the dendrolyte materials are highly ionic conductive and selective towards cationic and anionic charged atoms and large molecules when implemented as ion-exchange membranes. Homogenous ion-exchange membrane casting has been achieved by the implementation of cross-linkable functionalities in the dendrolytes, utilizing robust click-chemistry for efficient micro and macro fabrication processing of the ion-ex-change membranes for organic electronic devices. The ion-exchange membrane material was implemented in electrophoretic drug delivery devices (organic electronic ion pumps), which are used for delivery of ions and neurotransmitters with spatiotemporal resolution and are able to communicate and be used for therapeutic drug delivery purposes in biological interfaces. The dendrolyte materials were also able to form free-standing membranes, making it possible for implementation in fuel cell and desalination purposes. Trimeric conjugated thiophene pre-polymer structures were also developed in the thesis and synthesized for the purpose of implementation of the material in vivo to form electrically conductive polymer structures, and in such manner to be able to create electrodes and ultimately to connect with the central nervous system. The conjugated pre-polymers being both water soluble and enzymatically polymerizable serve as a platform to realize such a concept. Also, modifying the trimeric structure with cross-linkable functionality created the capability to form better interfaces and stability towards biological environments.
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| 9. |
- Ahmed, Fareed, et al.
(författare)
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Manufacturing Poly(3,4-Ethylenedioxythiophene) Electrocatalytic Sheets for Large-Scale H2O2 Production
- 2022
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Ingår i: Advanced Sustainable Systems. - : John Wiley and Sons Inc. - 2366-7486. ; 6:1
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Tidskriftsartikel (refereegranskat)abstract
- Producing thick films of conducting polymers by a low-cost manufacturing technique would enable new applications. However, removing huge solvent volume from diluted suspension or dispersion (1–3 wt%) in which conducting polymers are typically obtained is a true manufacturing challenge. In this work, a procedure is proposed to quickly remove water from the conducting polymer poly(3,4-ethylenedioxythiophene:poly(4-styrene sulfonate) (PEDOT:PSS) suspension. The PEDOT:PSS suspension is first flocculated with 1 m H2SO4 transforming PEDOT nanoparticles (≈50–500 nm) into soft microparticles. A filtration process inspired by pulp dewatering in a paper machine on a wire mesh with apertures dimension between 60 µm and 0.5 mm leads to thick free-standing films (≈0.5 mm). Wire mesh clogging that hinders dewatering (known as dead-end filtration) is overcome by adding to the flocculated PEDOT:PSS dispersion carbon fibers that aggregate and form efficient water channels. Moreover, this enables fast formation of thick layers under simple atmospheric pressure filtration, thus making the process truly scalable. Thick freestanding PEDOT films thus obtained are used as electrocatalysts for efficient reduction of oxygen to hydrogen peroxide, a promising green chemical and fuel. The inhomogeneity of the films does not affect their electrochemical function. © 2021 The Authors.
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| 10. |
- Ail, Ujwala, 1980-, et al.
(författare)
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Optimization of Non-Pyrolyzed Lignin Electrodes for Sustainable Batteries
- 2023
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Ingår i: ADVANCED SUSTAINABLE SYSTEMS. - : WILEY-V C H VERLAG GMBH. - 2366-7486. ; 7:2
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Tidskriftsartikel (refereegranskat)abstract
- Lignin, a byproduct from the pulp industry, is one of the redox active biopolymers being investigated as a component in the electrodes for sustainable energy storage applications. Due to its insulating nature, it needs to be combined with a conductor such as carbon or conducting polymer for efficient charge storage. Here, the lignin/carbon composite electrodes manufactured via mechanical milling (ball milling) are reported. The composite formation, correlation between performance and morphology is studied by comparison with manual mixing and jet milling. Superior charge storage capacity with approximate to 70% of the total contribution from the Faradaic process involving the redox functionality of lignin is observed in a mechanically milled composite. In comparison, manual mix shows only approximate to 30% from the lignin storage participation while the rest is due to the electric double layer at the carbon-electrolyte interface. The significant participation of lignin in the ball milled composite is attributed to the homogeneous, intimate mixing of the carbon and the lignin leading the electronic carrier transported in the carbon phase to reach most of the redox group of lignin. A maximum capacity of 49 mAh g(-1) is obtained at charge/discharge rate of 0.25 A g(-1) for the sample milled for 60 min.
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