| 1. |
- Aasmundtveit, K.E., et al.
(författare)
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Structural anisotropy of poly(alkylthiophene) films
- 2000
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Ingår i: Macromolecules. - : American Chemical Society (ACS). - 0024-9297 .- 1520-5835. ; 33:8, s. 3120-3127
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Tidskriftsartikel (refereegranskat)abstract
- The structural anisotropy of various poly(alkylthiophene) films have been studied by X-ray diffraction, using both conventional methods and synchrotron radiation at grazing incidence. Solution-cast films orient with the side chains preferably normal to the film surface, whereas spin-cast films of nonstereoregular material orient with both the main and the side chains in the film plane. For thick (10-50 µm) solution-cast films, the degree of orientation depends strongly on the solvent used for casting, and on the stereoregularity of the polymer, films of stereoregular materials being more oriented than those of nonregular materials. The most oriented nonregular films are those cast from mixtures of chloroform and tetrahydrofuran. Thin (50-500 nm) solution-cast films are more oriented than the thicker ones, and the effects of different stereoregularity or different casting solvents are small. For spin-cast films, the degree of orientation is independent of substrate and solvent. Spin-cast films of stereoregular material have two different phases: One with the side chains normal to the substrate, and another where they are parallel to the substrate. The diffraction peaks of spin-cast poly(octylthiophene) narrow considerably upon heating.
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| 2. |
- Aasmundtveit, K.E., et al.
(författare)
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Structural aspects of electrochemical doping and dedoping of poly(3,4-ethylenedioxythiophene)
- 2000
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Ingår i: Synthetic metals. - 0379-6779 .- 1879-3290. ; 113:1, s. 93-97
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Tidskriftsartikel (refereegranskat)abstract
- Electrochemical dedoping and redoping of p-toluene sulfonate doped poly(3,4-ethylenedioxythiophene) (PEDOT) has been studied with in situ grazing incidence diffraction with water used as an electrolyte. The diffraction peak positions and integrated intensities do not change significantly during doping and dedoping, while the peak widths increase upon dedoping and decrease upon doping. This implies that the lattice parameters and the relative positions of the polymer chains and the p-toluene sulfonate ions remain unchanged, the redox processes being carried out by the motion of smaller ions between the polymer and the electrolyte, and that the structural order decreases upon dedoping and increases upon doping in a reversible manner.
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| 3. |
- Aasmundtveit, K.E., et al.
(författare)
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Structural ordering in phenyl-substituted polythiophenes
- 2000
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Ingår i: Macromolecules. - : American Chemical Society (ACS). - 0024-9297 .- 1520-5835. ; 33:15, s. 5481-5489
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Tidskriftsartikel (refereegranskat)abstract
- Various substituted poly(phenylthiophene)s have been studied by X-ray diffraction. They are semicrystalline, with very different degrees of crystallinity. Those with para-substituted phenyl groups have a low degree of crystallinity, whereas those with ortho-substituted phenyl groups are more crystalline. The most crystalline materials in this study have two equally long substituents on the phenyl ring, one at the ortho position and the other at the ortho or meta position on the opposite side of the phenyl ring. Poly(3-(2,5-dioctylphenyl)thiophene) (PDOPT) was most thoroughly studied, and a structural model is proposed. The structure of PDOPT is quite different from previously studied substituted polythiophenes in that the octyl side chains are directed normal to the thiophene planes. In this way, the conjugated polymer chains are kept separated from each other. Solution-cast and spin-cast PDOPT films are anisotropic, with the octyl side chains oriented normal to the film surface in both cases. This is contrary to the situation for poly(3-alkylthiophene)s, where solution-cast and spin-cast films orient in different ways.
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| 4. |
- Abramavicius, V., et al.
(författare)
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Role of coherence and delocalization in photo-induced electron transfer at organic interfaces
- 2016
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Ingår i: Scientific Reports. - : NATURE PUBLISHING GROUP. - 2045-2322. ; 6:32914
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Tidskriftsartikel (refereegranskat)abstract
- Photo-induced charge transfer at molecular heterojunctions has gained particular interest due to the development of organic solar cells (OSC) based on blends of electron donating and accepting materials. While charge transfer between donor and acceptor molecules can be described by Marcus theory, additional carrier delocalization and coherent propagation might play the dominant role. Here, we describe ultrafast charge separation at the interface of a conjugated polymer and an aggregate of the fullerene derivative PCBM using the stochastic Schrodinger equation (SSE) and reveal the complex time evolution of electron transfer, mediated by electronic coherence and delocalization. By fitting the model to ultrafast charge separation experiments, we estimate the extent of electron delocalization and establish the transition from coherent electron propagation to incoherent hopping. Our results indicate that even a relatively weak coupling between PCBM molecules is sufficient to facilitate electron delocalization and efficient charge separation at organic interfaces.
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| 5. |
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| 6. |
- Admassie, Shimelis, et al.
(författare)
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A renewable biopolymer cathode with multivalent metal ions for enhanced charge storage
- 2014
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Ingår i: JOURNAL OF MATERIALS CHEMISTRY A. - : Royal Society of Chemistry. - 2050-7488. ; 2:6, s. 1974-1979
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Tidskriftsartikel (refereegranskat)abstract
- A ternary composite supercapacitor electrode consisting of phosphomolybdic acid (HMA), a renewable biopolymer, lignin, and polypyrrole was synthesized by a simple one-step simultaneous electrochemical deposition and characterized by electrochemical methods. It was found that the addition of HMA increased the specific capacitance of the polypyrrole-lignin composite from 477 to 682 F g(-1) ( at a discharge current of 1 A g(-1)) and also significantly improved the charge storage capacity from 6(to 128 mA h g(-1).
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| 7. |
- Admassie, Shimelis, et al.
(författare)
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Biopolymer hybrid electrodes for scalable electricity storage
- 2016
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Ingår i: Materials Horizons. - : ROYAL SOC CHEMISTRY. - 2051-6347 .- 2051-6355. ; 3:3, s. 174-185
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Forskningsöversikt (refereegranskat)abstract
- Powering the future, while maintaining a cleaner environment and a strong socioeconomic growth, is going to be one of the biggest challenges faced by mankind in the 21st century. The first step in overcoming the challenge for a sustainable future is to use energy more efficiently so that the demand for fossil fuels can be reduced drastically. The second step is a transition from the use of fossil fuels to renewable energy sources. In this sense, organic electrode materials are becoming increasingly attractive compared to inorganic electrode materials which have reached a plateau regarding performance and have severe drawbacks in terms of cost, safety and environmental friendliness. Using organic composites based on conducting polymers, such as polypyrrole, and abundant, cheap and naturally occurring biopolymers rich in quinones, such as lignin, has recently emerged as an interesting alternative. These materials, which exhibit electronic and ionic conductivity, provide challenging opportunities in the development of new charge storage materials. This review presents an overview of recent developments in organic biopolymer composite electrodes as renewable electroactive materials towards sustainable, cheap and scalable energy storage devices.
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| 8. |
- Admassie, Shimelis, et al.
(författare)
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Electrochemical and optical studies of the band gaps of alternating polyfluorene copolymers
- 2006
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Ingår i: Synthetic metals. - : Elsevier BV. - 0379-6779 .- 1879-3290. ; 156:7-8, s. 614-623
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Tidskriftsartikel (refereegranskat)abstract
- The electrochemical and optical properties of a series of alternating polyfluorene copolymers with low band gaps were determined. These polymers incorporated fluorene units alternating with groups including electron-withdrawing (A) and electron-donating (D) groups in donor-acceptor-donor (DAD) sequence to achieve the lowering of band gaps. The polymers were solvent-casted on platinum disk electrode and the band gaps were estimated from cyclic voltammetry (CV). These values were compared with values obtained from optical absorption measurements. Although the electrochemically determined band gaps were found to be slightly higher than the optical band gap in most cases, values are well correlated. The values of the band gaps determined range from 2.1 to 1.3 eV. © 2006 Elsevier B.V. All rights reserved.
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| 9. |
- Admassie, S., et al.
(författare)
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Electrochromism in diffractive conducting polymer gratings
- 2004
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Ingår i: Journal of the Electrochemical Society. - : The Electrochemical Society. - 0013-4651 .- 1945-7111. ; 151:6
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Tidskriftsartikel (refereegranskat)abstract
- The electrochromic polymer poly(3,4-ethylenedioxythiophene)-poly(styrene sulfonate) (PEDOT-PSS) spin-coated on ITO/glass was patterned with a soft lithographic method in order to diffract the incident light and thereby modify absorption of light by the film to improve the electrochromic efficiency of the polymer. The absorbance peak at around 610 nm was found to be much higher in the patterned PEDOT-PSS film than the one observed in the unpatterned film. Values of coloration efficiencies varying from 107 to 174 cm2/C were obtained for three different unpatterned PEDOT-PSS films, whereas for three different patterned PEDOT-PSS films higher values ranging from 211 to 371 cm2/C were found. These increased values of the electrochromic efficiencies are attributed to diffraction. © 2004 The Electrochemical Society. All rights reserved.
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| 10. |
- Ail, Ujwala, et al.
(författare)
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Effect of Sulfonation Level on Lignin/Carbon Composite Electrodes for Large-Scale Organic Batteries
- 2020
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Ingår i: ACS Sustainable Chemistry and Engineering. - : AMER CHEMICAL SOC. - 2168-0485. ; 8:49, s. 17933-17944
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Tidskriftsartikel (refereegranskat)abstract
- The key figure-of-merit for materials in stationary energy storage applications, such as large-scale energy storage for buildings and grids, is the cost per kilo per electrochemical cycle, rather than the energy density. In this regard, forest-based biopolymers such as lignin, are attractive, as they are abundant on Earth. Here, we explored lignin as an electroactive battery material, able to store two electrons per hydroquinone aromatic ring, with the targeted operation in aqueous electrolytes. The impact of the sulfonation level of lignin on the performance of its composite electrode with carbon was investigated by considering three lignin derivatives: lignosulfonate (LS), partially desulfonated lignosulfonate (DSLS), and fully desulfonated lignin (KL, lignin produced by the kraft process). Partial desulfonation helped in better stability of the composite in aqueous media, simultaneously favoring its water processability. In this way, a route to promote ionic conductivity within the lignin/carbon composite electrodes was developed, facilitating the access to the entire bulk of the volumetric electrodes. Electrochemical performance of DSLS/C showed highly dominant Faradaic contribution (66%) towards the total capacity, indicating an efficient mixed ionic-electronic transport within the lignin-carbon phase, displaying a capacity of 38 mAh/g at 0.25 A/g and 69% of capacity retention after 2200 cycles at a rate of 1 A/g.
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| 11. |
- Ajjan, Fátima, 1986-, et al.
(författare)
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Doped Conjugated Polymer Enclosing a Redox Polymer : Wiring Polyquinones with Poly(3,4‐Ethylenedioxythiophene)
- 2020
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Ingår i: Advanced Energy & Sustainability Research. - : John Wiley & Sons. - 2699-9412. ; 1:2
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Tidskriftsartikel (refereegranskat)abstract
- The mass implementation of renewable energies is limited by the absence of efficient and affordable technology to store electrical energy. Thus, the development of new materials is needed to improve the performance of actual devices such as batteries or supercapacitors. Herein, the facile consecutive chemically oxidative polymerization of poly(1-amino-5-chloroanthraquinone) (PACA) and poly(3,4-ethylenedioxythiophene (PEDOT) resulting in a water dispersible material PACA-PEDOT is shown. The water-based slurry made of PACA-PEDOT nanoparticles can be processed as film coated in ambient atmosphere, a critical feature for scaling up the electrode manufacturing. The novel redox polymer electrode is a nanocomposite that withstands rapid charging (16 A g−1) and delivers high power (5000 W kg−1). At lower current density its storage capacity is high (198 mAh g−1) and displays improved cycling stability (60% after 5000 cycles). Its great electrochemical performance results from the combination of the redox reversibility of the quinone groups in PACA that allows a high amount of charge storage via Faradaic reactions and the high electronic conductivity of PEDOT to access to the redox-active sites. These promising results demonstrate the potential of PACA-PEDOT to make easily organic electrodes from a water-coating process, without toxic metals, and operating in non-flammable aqueous electrolyte for large scale pseudocapacitors.
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| 12. |
- Ajjan, Fátima, et al.
(författare)
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Enhancing Energy Storage Devices with Biomacromolecules in Hybrid Electrodes
- 2019
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Ingår i: Biotechnology Journal. - : WILEY-V C H VERLAG GMBH. - 1860-6768 .- 1860-7314. ; 14:12
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Forskningsöversikt (refereegranskat)abstract
- The development of energy storage devices with higher energy and power outputs, and long cycling stability is urgently required in the pursuit of the expanding challenges of electrical energy storage. The utilization of biologically renewable redox compounds holds a great potential in designing sustainable energy storage systems and contributes in reducing the dependence on fossil fuels for energy materials. Quinones are the principal redox centers in natural organic materials and play a key role as charge storage electrode materials because of their abundance, multiple forms and integration into the materials flow through the biosphere. Electrical energy storage devices and systems can be significantly improved by the combination of scalable quinone-based biomaterials with good electronic conductors. This review uses recent examples to show how biopolymers are providing new directions in the development of renewable biohybrid electrodes for energy storage devices.
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| 13. |
- Ajjan, Fátima, et al.
(författare)
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High performance PEDOT/lignin biopolymer composites for electrochemical supercapacitors
- 2016
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Ingår i: Journal of Materials Chemistry A. - : ROYAL SOC CHEMISTRY. - 2050-7488 .- 2050-7496. ; 4:5, s. 1838-1847
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Tidskriftsartikel (refereegranskat)abstract
- Developing sustainable organic electrode materials for energy storage applications is an urgent task. We present a promising candidate based on the use of lignin, the second most abundant biopolymer in nature. This polymer is combined with a conducting polymer, where lignin as a polyanion can behave both as a dopant and surfactant. The synthesis of PEDOT/Lig biocomposites by both oxidative chemical and electrochemical polymerization of EDOT in the presence of lignin sulfonate is presented. The characterization of PEDOT/Lig was performed by UV-Vis-NIR spectroscopy, FTIR infrared spectroscopy, thermogravimetric analysis, scanning electron microscopy, cyclic voltammetry and galvanostatic charge-discharge. PEDOT doped with lignin doubles the specific capacitance (170.4 F g(-1)) compared to reference PEDOT electrodes (80.4 F g(-1)). The enhanced energy storage performance is a consequence of the additional pseudocapacitance generated by the quinone moieties in lignin, which give rise to faradaic reactions. Furthermore PEDOT/Lig is a highly stable biocomposite, retaining about 83% of its electroactivity after 1000 charge/discharge cycles. These results illustrate that the redox doping strategy is a facile and straightforward approach to improve the electroactive performance of PEDOT.
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| 14. |
- Ajjan, Fátima, et al.
(författare)
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Innovative polyelectrolytes/poly(ionic liquid)s for energy and the environment
- 2017
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Ingår i: Polymer international. - : WILEY. - 0959-8103 .- 1097-0126. ; 66:8, s. 1119-1128
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Forskningsöversikt (refereegranskat)abstract
- This paper presents the work carried out within the European project RENAISSANCE-ITN, which was dedicated to the development of innovative polyelectrolytes for energy and environmental applications. Within the project different types of innovative polyelectrolytes were synthesized such as poly(ionic liquid)s coming from renewable or natural ions, thiazolium cations, catechol functionalities or from a new generation of cheap deep eutectic monomers. Further, macromolecular architectures such as new poly(ionic liquid) block copolymers and new (semi)conducting polymer/polyelectrolyte complexes were also developed. As the final goal, the application of these innovative polymers in energy and the environment was investigated. Important advances in energy storage technologies included the development of new carbonaceous materials, new lignin/conducting polymer biopolymer electrodes, new iongels and single-ion conducting polymer electrolytes for supercapacitors and batteries and new poly(ionic liquid) binders for batteries. On the other hand, the use of innovative polyelectrolytes in sustainable environmental technologies led to the development of new liquid and dry water, new materials for water cleaning technologies such as flocculants, oil absorbers, new recyclable organocatalyst platforms and new multifunctional polymer coatings with antifouling and antimicrobial properties. All in all this paper demonstrates the potential of poly(ionic liquid)s for high-value applications in energy and enviromental areas. (c) 2017 Society of Chemical Industry
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| 15. |
- Ajjan, Fátima, et al.
(författare)
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Scalable Asymmetric Supercapacitors Based on Hybrid Organic/Biopolymer Electrodes
- 2017
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Ingår i: ADVANCED SUSTAINABLE SYSTEMS. - : WILEY-V C H VERLAG GMBH. - 2366-7486. ; 1:8
-
Tidskriftsartikel (refereegranskat)abstract
- A trihybrid bioelectrode composed of lignin, poly(3,4-ethylenedioxythiophene) (PEDOT), and poly(aminoanthraquinone) (PAAQ) is prepared by a two-step galvanostatic electropolymerization, and characterized for supercapacitor applications. Using PEDOT/Lignin as a base layer, followed by the consecutive deposition of PAAQ, the hybrid electrode PEDOT/Lignin/PAAQ shows a high specific capacitance of 418 F g(-1) with small self-discharge. This trihybrid electrode material can be assembled into symmetric and asymmetric super-capacitors. The asymmetric supercapacitor uses PEDOT + Lignin/PAAQ as positive electrode and PEDOT/PAAQ as negative electrode, and exhibits superior electrochemical performance due to the synergistic effect of the two electrodes, which leads to a specific capacitance of 74 F g(-1). It can be reversibly cycled in the voltage range of 0-0.7 V. More than 80% capacitance is retained after 10 000 cycles. These remarkable features reveal the exciting potential of a full organic energy storage device with long cycle life.
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| 16. |
- Ajjan, Fátima, et al.
(författare)
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Spectroelectrochemical investigation of redox states in a polypyrrole/lignin composite electrode material
- 2015
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Ingår i: Journal of Materials Chemistry A. - : ROYAL SOC CHEMISTRY. - 2050-7488 .- 2050-7496. ; 3:24, s. 12927-12937
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Tidskriftsartikel (refereegranskat)abstract
- We report spectroelectrochemical studies to investigate the charge storage mechanism of composite polypyrrole/lignin electrodes. Renewable bioorganic electrode materials were produced by electropolymerization of pyrrole in the presence of a water-soluble lignin derivative acting as a dopant. The resulting composite exhibited enhanced charge storage abilities due to a lignin-based faradaic process, which was expressed after repeated electrochemical redox of the material. The in situ FTIR spectroelectrochemistry results show the formation of quinone groups, and reversible oxidation-reduction of these groups during charge-discharge experiments in the electrode materials. The most significant IR bands include carbonyl absorption near 1705 cm(-1), which is attributed to the creation of quinone moieties during oxidation, and absorption at 1045 cm(-1) which is due to hydroquinone moieties.
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| 17. |
- Ajjan Godoy, Fátima Nadia
(författare)
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Biohybrid Polymer Electrodes for Renewable Energy Storage
- 2017
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Daily and seasonally fluctuating energy supply and demand requires adequate energy storage solutions. In recent years electrochemical supercapacitors have attracted considerable attention due to their ability to both store and deliver electrical energy efficiently. Our efforts are focused on developing and optimizing sustainable organic electrode materials for supercapacitors based on renewable bioorganic materials, offering a cheap, environmentally friendly and scalable alternative to store energy. In particular, we are using the second most abundant biopolymer in nature, lignin (Lig), which is an insulating material. However, when used in combination with electroactive and conducting polymers such as polypyrrole (PPy) and poly(3,4-ethylenedioxythiophene) (PEDOT), the biohybrid electrodes PPy/Lig and PEDOT/Lig display significantly enhanced energy storage performance as compared to the pristine conducting polymers without the lignin. Redox cyclic voltammetry and galvanostatic charge/discharge measurements indicate that the enhanced performance is due to the additional pseudocapacitance generated by the quinone moieties in lignin. Moreover, a conjugated redoxpolymer poly(aminoanthraquinone) PAAQ, with intrinsic quinone functions and excellentstability, has been combined with lignin and PEDOT resulting in a trihybrid bioelectrode. PEDOT compensates the low conductivity of PAAQ and provides electrical pathways to the quinone groups. The electrochemically generated quinones undergo a two electron, two protonredox process within the biohybrid electrodes as revealed by FTIR spectroelectrochemistry.These remarkable features reveal the exciting potential of a full organic energy storage device with long cycle life. Therefore, supercapacitor devices were designed in symmetric or asymmetric two electrode configuration. The best electrochemical performance was achieved by the asymmetric supercapacitor based on PEDOT+Lignin/PAAQ as the positive electrode and PEDOT/PAAQ as the negative electrode. This device exhibits superior electrochemical performance and outstanding stability after 10000 charge/discharge cycles due to the synergistic effect of the two electrodes. Finally, we have characterized the response of this supercapacitor device when charged with the intermittent power supply from an organic photovoltaic module. We have designed charging/discharging conditions such that reserve power was available in the storage device at all times. This work has resulted in an inexpensive fully organic system witht he dual function of energy conversion and storage.
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| 18. |
- Anctil, Annick, et al.
(författare)
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Status report on emerging photovoltaics
- 2023
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Ingår i: JOURNAL OF PHOTONICS FOR ENERGY. - : SPIE-SOC PHOTO-OPTICAL INSTRUMENTATION ENGINEERS. - 1947-7988. ; 13:4
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Tidskriftsartikel (refereegranskat)abstract
- This report provides a snapshot of emerging photovoltaic (PV) technologies. It consists of concise contributions from experts in a wide range of fields including silicon, thin film, III-V, perovskite, organic, and dye-sensitized PVs. Strategies for exceeding the detailed balance limit and for light managing are presented, followed by a section detailing key applications and commercialization pathways. A section on sustainability then discusses the need for minimization of the environmental footprint in PV manufacturing and recycling. The report concludes with a perspective based on broad survey questions presented to the contributing authors regarding the needs and future evolution of PV.(c) 2023 Society of Photo-Optical Instrumentation Engineers (SPIE)
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| 19. |
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| 20. |
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| 21. |
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| 22. |
- Andersson, Lars Mattias, et al.
(författare)
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Acceptor influence on hole mobility in fullerene blends with alternating copolymers of fluorene
- 2006
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Ingår i: Applied Physics Letters. - : AIP Publishing. - 0003-6951 .- 1077-3118. ; 88, s. 082103-
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Tidskriftsartikel (refereegranskat)abstract
- Hole mobility in polyfluorene/fullerene blends has been studied with field effect transistors. Two different C60 derivatives and one C70 derivative have been investigated together with two different polyfluorenes. Mobility is presented as a function of acceptor loading at ratios suitable for photovoltaics and varies between 10–3 and 10–5 cm2 V–1 s–1 depending on the polymer/acceptor combination. The hole mobility is increased in blends with the commonly used acceptor [6-6]-phenyl-C61-butyric acid methylester (PCBM). With related C60 and C70 derivatives the hole mobility is decreased under the same circumstances.
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| 23. |
- Andersson, Lars Mattias, et al.
(författare)
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Bipolar transport observed through extraction currents on organic photovoltaic blend materials
- 2006
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Ingår i: Applied Physics Letters. - : AIP Publishing. - 0003-6951 .- 1077-3118. ; 89, s. 142111-
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Tidskriftsartikel (refereegranskat)abstract
- Both electron and hole mobilities have been simultaneously measured through charge extraction by linearly increasing voltage on polymer heterojunction solar cells with varying stoichiometry of polymer and acceptor. The polymer is a low band gap copolymer of fluorene, thiophene, and electron accepting groups named APFO-Green 5, and the acceptor is [6,6]-phenyl-C61-butyric acid methylester. Results are correlated to field effect transistor measurements on the same material system. A monotonous increase in mobility for both carrier types is observed with increased acceptor loading.
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| 24. |
- Andersson, Lars Mattias, 1976-
(författare)
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Electronic Transport in Polymeric Solar Cells and Transistors
- 2007
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- The main topic of this dissertation is electronic charge transport in polymeric and molecular organic materials and material blends intended for solar cell applications. Charge transport in polymers is a strange beast and carrier mobility is rarely a well-defined number. Measurements on different sample geometries and under different conditions tend to give different results and when everything is to be related to solar cell performance it is imperative that there is a way to correlate the results from different measurements. Polymer solar cells utilize composite materials for their function. This puts an additional twist on charge transport studies, as there will also be interaction between the different phases to take into account.Several measurement techniques have been used and their interrelationships as well as information on their relevance for solar cells have been investigated. Field effect transistors (FET) with an organic active layer have proved to be one of the more versatile measurement geometries and are also an interesting topic in itself. FETs are discussed both as a route for material characterization and as components. A main result correlates bias stress in organic field effect transistors with the electronic structure of the material.Power conversion efficiency in solar cells is discussed with respect to electrical properties. The interaction of different blend materials and the impact of stoichiometry on transport properties in the active layer have been investigated. Results indicate that charge transport properties frequently are a key determining factor for which material combinations and ratios that works best.Some work on the conductive properties of nano-fibers coated with semiconducting polymers has also been done and is briefly discussed. The conductive properties of nano-fibers have been studied through potential imaging.
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| 25. |
- Andersson, Lars Mattias, et al.
(författare)
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Non-equilibrium effects on electronic transport in organic field effect transistors
- 2007
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Ingår i: Organic electronics. - : Elsevier BV. - 1566-1199 .- 1878-5530. ; 8:4, s. 423-430
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Tidskriftsartikel (refereegranskat)abstract
- Non-ideal behavior in organic field effect transistors, in particular threshold voltage drift and light sensitivity, is argued to be due to intrinsic carrier dynamics. The discussion is based on the theory for hopping transport within a Gaussian density of states. Carrier concentration is shown to be of fundamental importance, and the time required to reach equilibrium at different bias is responsible for device behavior, with implications for mobility evaluation. Experimental results from various conjugated polymers in a field effect transistor illustrate the theory.
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