| 1. |
- Abdollahi Sani, Negar, et al.
(författare)
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A ferroelectric polymer introduces addressability in electrophoretic display cells
- 2019
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Ingår i: FLEXIBLE AND PRINTED ELECTRONICS. - : IOP PUBLISHING LTD. - 2058-8585. ; 4:3
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Tidskriftsartikel (refereegranskat)abstract
- During the last decades, tremendous efforts have been carried out to develop flexible electronics for a vast array of applications. Among all different applications investigated in this area, flexible displays have gained significant attention, being a vital part of large-area devices, portable systems and electronic labels etc electrophoretic (EP) ink displays have outstanding properties such as a superior optical switch contrast and low power consumption, besides being compatible with flexible electronics. However, the EP ink technology requires an active matrix-addressing scheme to enable exclusive addressing of individual pixels. EP ink pixels cannot be incorporated in low cost and easily manufactured passive matrix circuits due to the lack of threshold voltage and nonlinearity, necessities to provide addressability. Here, we suggest a simple method to introduce nonlinearity and threshold voltage in EP ink display cells in order to make them passively addressable. Our method exploits the nonlinearity of an organic ferroelectric capacitor that introduces passive addressability in display cells. The organic ferroelectric material poly(vinylidene fluoride-co-trifluoroethylene) (P(VDF-TrFE)) is here chosen because of its simple manufacturing protocol and good polarizability. We demonstrate that a nonlinear EP cell with bistable states can be produced by depositing a P(VDF-TrFE) film on the bottom electrode of the display cell. The P(VDF-TrFE) capacitor and the EP ink cell are separately characterized in order to match the surface charge at their respective interfaces and to achieve and optimize bistable operation of display pixels.
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| 2. |
- Abdollahi Sani, Negar, et al.
(författare)
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Flexible lamination-fabricated ultra-high frequency diodes based on self-supporting semiconducting composite film of silicon micro-particles and nano-fibrillated cellulose
- 2016
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Ingår i: Scientific Reports. - : Springer Science and Business Media LLC. - 2045-2322. ; 6
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Tidskriftsartikel (refereegranskat)abstract
- Low cost and flexible devices such as wearable electronics, e-labels and distributed sensors will make the future "internet of things" viable. To power and communicate with such systems, high frequency rectifiers are crucial components. We present a simple method to manufacture flexible diodes, operating at GHz frequencies, based on self-adhesive composite films of silicon micro-particles (Si-ΌPs) and glycerol dispersed in nanofibrillated cellulose (NFC). NFC, Si-ΌPs and glycerol are mixed in a water suspension, forming a self-supporting nanocellulose-silicon composite film after drying. This film is cut and laminated between a flexible pre-patterned Al bottom electrode and a conductive Ni-coated carbon tape top contact. A Schottky junction is established between the Al electrode and the Si-ΌPs. The resulting flexible diodes show current levels on the order of mA for an area of 2 mm2, a current rectification ratio up to 4 × 103 between 1 and 2 V bias and a cut-off frequency of 1.8 GHz. Energy harvesting experiments have been demonstrated using resistors as the load at 900 MHz and 1.8 GHz. The diode stack can be delaminated away from the Al electrode and then later on be transferred and reconfigured to another substrate. This provides us with reconfigurable GHz-operating diode circuits.
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| 3. |
- Belaineh, Dagmawi, et al.
(författare)
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Controlling the Organization of PEDOT:PSS on Cellulose Structures
- 2019
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Ingår i: ACS APPLIED POLYMER MATERIALS. - : AMER CHEMICAL SOC. - 2637-6105. ; 1:9, s. 2342-2351
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Tidskriftsartikel (refereegranskat)abstract
- Composites of biopolymers and conducting polymers are emerging as promising candidates for a green technological future and are actively being explored in various applications, such as in energy storage, bioelectronics, and thermoelectrics. While the device characteristics of these composites have been actively investigated, there is limited knowledge concerning the fundamental intracomponent interactions and the modes of molecular structuring. Here, by use of cellulose and poly(3,4-ethylene-dioxythiophene):poly(styrenesulfonate) (PEDOT:PSS), it is shown that the chemical and structural makeup of the surfaces of the composite components are critical factors that determine the materials organization at relevant dimensions. AFM, TEM, and GIVVAXS measurements show that when mixed with cellulose nanofibrils, PEDOT:PSS organizes into continuous nanosized beadlike structures with an average diameter of 13 nm on the nanofibrils. In contrast, when PEDOT:PSS is blended with molecular cellulose, a phase-segregated conducting network morphology is reached, with a distinctly relatively lower electric conductivity. These results provide insight into the mechanisms of PEDOT:PSS crystallization and may have significant implications for the design of conducting biopolymer composites for a vast array of applications.
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| 4. |
- Brooke, Robert, et al.
(författare)
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Controlling the electrochromic properties of conductive polymers using UV-light
- 2018
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Ingår i: Journal of Materials Chemistry C. - : ROYAL SOC CHEMISTRY. - 2050-7526 .- 2050-7534. ; 6:17, s. 4663-4670
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Tidskriftsartikel (refereegranskat)abstract
- The phenomenon of electrochromism in conductive polymers is well known and has been exploited in many scientific reports. Using a newly developed patterning technique for conductive polymers, we manufactured high-resolution electrochromic devices from the complementary polymers PEDOT and polypyrrole. The technique, which combines UV-light exposure with vapor phase polymerization, has previously only been demonstrated with the conductive polymer PEDOT. We further demonstrated how the same technique can be used to control the optical properties and the electrochromic contrast in these polymers. Oxidant exposure to UV-light prior to vapor phase polymerization showed a reduction in polymer electrochromic contrast allowing high-resolution (100 mu m) patterns to completely disappear while applying a voltage bias due to their optical similarity in one redox state and dissimilarity in the other. This unique electrochromic property enabled us to construct devices displaying images that appear and disappear with the change in applied voltage. Finally, a modification of the electrochromic device architecture permitted a dual image electrochromic device incorporating patterned PEDOT and patterned polypyrrole on the same electrode, allowing the switching between two different images.
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| 5. |
- 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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| 6. |
- Brooke, Robert, 1989-, et al.
(författare)
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Supercapacitors on demand : All-printed energy storage devices with adaptable design
- 2019
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Ingår i: Flexible and Printed Electronics. - : Institute of Physics Publishing. - 2058-8585. ; 4:1
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Tidskriftsartikel (refereegranskat)abstract
- Demands on the storage of energy have increased for many reasons, in part driven by household photovoltaics, electric grid balancing, along with portable and wearable electronics. These are fast-growing and differentiated applications that need large volume and/or highly distributed electrical energy storage, which then requires environmentally friendly, scalable and flexible materials and manufacturing techniques. However, the limitations on current inorganic technologies have driven research efforts to explore organic and carbon-based alternatives. Here, we report a conducting polymer:cellulose composite that serves as the active material in supercapacitors which has been incorporated into all-printed energy storage devices. These devices exhibit a specific capacitance of ≈90 F g -1 and an excellent cyclability (>10 000 cycles). Further, a design concept coined 'supercapacitors on demand' is presented, which is based on a printing-cutting-folding procedure, that provides us with a flexible production protocol to manufacture supercapacitors with adaptable configuration and electrical characteristics.
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| 7. |
- Edberg, Jesper, et al.
(författare)
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Boosting the capacity of all-organic paper supercapacitors using wood derivatives
- 2018
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Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry (RSC). - 2050-7488 .- 2050-7496. ; 6:1, s. 145-152
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Tidskriftsartikel (refereegranskat)abstract
- Printed and flexible organic electronics is a steadily expanding field of research and applications. One of the most attractive features of this technology is the possibility of large area and high throughput production to form low-cost electronics on different flexible substrates. With an increasing demand for sustainable energy production, low-cost and large volume technologies to store high-quality energy become equally important. These devices should be environmentally friendly with respect to their entire life cycle. Supercapacitors and batteries based on paper hold great promise for such applications due to the low cost and abundance of cellulose and other forest-derived components. We report a thick-film paper-supercapacitor system based on cellulose nanofibrils, the mixed ion-electron conducting polymer PEDOT: PSS and sulfonated lignin. We demonstrate that the introduction of sulfonated lignin into the cellulose-conducting polymer system increases the specific capacitance from 110 to 230 F g(-1) and the areal capacitance from 160 mF cm(-2) to 1 F cm(-2). By introducing lignosulfonate also into the electrolyte solution, equilibrium, with respect to the concentration of the redox molecule, was established between the electrode and the electrolyte, thus allowing us to perform beyond 700 charge/discharge cycles with no observed decrease in performance.
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| 8. |
- Edberg, Jesper, et al.
(författare)
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Electrochemical circuits from 'cut and stick' PEDOT : PSS-nanocellulose composite
- 2017
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Ingår i: Flexible and Printed Electronics. - : Institute of Physics Publishing (IOPP). - 2058-8585. ; 2:4
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Tidskriftsartikel (refereegranskat)abstract
- We report a flexible self-standing adhesive composite made from PEDOT:PSS and nanofibrillated cellulose. The material exhibits good combined mechanical and electrical characteristics (an elastic modulus of 4.4 MPa, and an electrical conductivity of 30 S cm(-1)). The inherent self-adhesiveness of the material enables it to be laminated and delaminated repeatedly to form and reconfigure devices and circuits. This modular property opens the door for a plethora of applications where reconfigurability and ease-of-manufacturing are of prime importance. We also demonstrate a paper composite with ionic conductivity and combine the two materials to construct electrochemical devices, namely transistors, capacitors and diodes with high values of transconductance, charge storage capacity and current rectification. We have further used these devices to construct digital circuits such as NOT, NAND and NORlogic.
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| 9. |
- Edberg, Jesper, 1988-
(författare)
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Flexible and Cellulose-based Organic Electronics
- 2017
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Organic electronics is the study of organic materials with electronic functionality and the applications of such materials. In the 1970s, the discovery that polymers can be made electrically conductive led to an explosion within this field which has continued to grow year by year. One of the attractive features of organic electronic materials is their inherent mechanical flexibility, which has led to the development of numerous flexible electronics technologies such as organic light emitting diodes and solar cells on flexible substrates. The possibility to produce electronics on flexible substrates like plastic or paper has also had a large impact on the field of printed, electronics where inks with electronic functionality are used for large area fabrication of electronic devices using classical printing methods, such as screen printing, inkjet printing and flexography.Recently, there has been a growing interest in the use of cellulose in organic and printed electronics, not only as a paper substrate but also as a component in composite materials where the cellulose provides mechanical strength and favorable 3D-microstructures. Nanofibrillated cellulose is composed of cellulose fibers with high aspect-ratio and diameters in the nanometer range. Due to its remarkable mechanical strength, large area-to-volume ratio, optical transparency and solution processability it has been widely used as a scaffold or binder for electronically active materials in applications such as batteries, supercapacitors and optoelectronics.The focus of this thesis is on flexible devices based on conductive polymers and can be divided into two parts: (1) Composite materials of nanofibrillated cellulose and the conductive polymer PEDOT:PSS and (2) patterning of vapor phase polymerized conductive polymers. In the first part, it is demonstrated how the combination of cellulose and conductive polymers can be used to make electronic materials of various form factors and functionality. Thick, freestanding and flexible “papers” are used to realize electrochemical devices such as transistors and supercapacitors while lightweight, porous and elastic aerogels are used for sensor applications. The second focus of the thesis is on a novel method of patterning conductive polymers produced by vapor phase polymerization using UV-light. This method is used to realize flexible electrochromic smart windows with high-resolution images and tunable optical contrast.
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| 10. |
- Edberg, Jesper, et al.
(författare)
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Improving the Performance of Paper Supercapacitors Using Redox Molecules from Plants
- 2019
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Ingår i: ADVANCED SUSTAINABLE SYSTEMS. - : WILEY-V C H VERLAG GMBH. - 2366-7486. ; 3:8
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Tidskriftsartikel (refereegranskat)abstract
- A supercapacitor made from organic and nature-based materials, such as conductive polymers (PEDOT:PSS), nanocellulose, and an the organic dye molecule (alizarin), is demonstrated. The dye molecule, which historically was extracted from the roots of the plant rubia tinctorum, is here responsible for the improvement in energy storage capacity, while the conductive polymer provides bulk charge transport within the composite electrode. The forest-based nanocellulose component provides a mechanically strong and nonporous network onto which the conductive polymer self-organizes. The electrical and electrochemical properties of the material composition are investigated and prototype redox-enhanced supercapacitor devices with excellent specific capacitance exceeding 400 F g(-1) and an operational stability over >1000 cycles are demonstrated. This new class of supercapacitors, which in part are based on organic materials from plants, represents an important step toward a green and sustainable energy technology.
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