| 1. |
- 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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| 2. |
- Negash, Asfaw, et al.
(författare)
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Diketopyrrolopyrrole-based terpolymers with tunable broad band absorption for fullerene and fullerene-free polymer solar cells
- 2019
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Ingår i: Journal of Materials Chemistry C. - : Royal Society of Chemistry (RSC). - 2050-7534 .- 2050-7526. ; 7:11, s. 3375-3384
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Tidskriftsartikel (refereegranskat)abstract
- A series of random terpolymers with donor-acceptor-donor-acceptor molecular configuration, comprising fluorinated benzotriazole (FTAZ) and thienothiophene-capped diketopyrrolopyrrole (TTDPP) as the first and second electron-accepting moieties and thienyl-substituted benzodithiophene (BDTT) as the electron-donating unit, are designed for polymer solar cells. By tuning the ratio of TTDPP and FTAZ, the optoelectronic properties of the terpolymers are systematically varied. All materials exhibit a broad absorption window spanning from 300 to 900 nm, illustrating the success of the terpolymer approach. Fullerene-based polymer solar cells fabricated from the terpolymer with the highest content of TTDPP afford a power conversion efficiency of 5.7%, with a short-circuit current density of 15.2 mA cm -2 . On the other hand, solar cell devices composed of the terpolymer with the lowest content of TTDPP and the narrow gap non-fullerene acceptor IEICO-4F exhibit a higher efficiency of 6.3%, with an enhanced short-circuit current density of 17.5 mA cm -2 , as a result of a better complementarity in the absorption of the donor and acceptor materials and well-balanced charge carrier mobilities. This efficiency represents the best value for fullerene-free polymer solar cells based on DPP-containing polymers to date.
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| 3. |
- Negash, Asfaw, et al.
(författare)
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Ladder-type high gap conjugated polymers based on indacenodithieno[3,2-b]thiophene and bithiazole for organic photovoltaics
- 2019
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Ingår i: Organic Electronics: physics, materials, applications. - : Elsevier BV. - 1566-1199. ; 74, s. 211-217
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Tidskriftsartikel (refereegranskat)abstract
- © 2019 Elsevier B.V. Two push-pull type conjugated polymers - PIDTT−BTz and PIDTT−DTBTz, based on the ladder-type donor unit indacenodithieno[3,2-b]thiophene (IDTT) and bithiazole (BTz) as acceptor component - are designed and synthesized for photovoltaic applications. The polymers exhibit relatively high optical gaps of ~2.0 eV with strong absorption in the range of 400–600 nm, rendering them of particular interest for the harvesting of indoor light and/or multijunction devices. Electrochemical investigations indicate a lower highest occupied molecular orbital energy level (−5.44 eV) for PIDTT−BTz as compared to PIDTT−DTBTz (−5.36 eV), enabling to achieve a higher open-circuit voltage. Under solar illumination, the best power conversion efficiency (5.1%) is achieved for the combination PIDTT−DTBTz:PC71BM (compared to 4.6% for PIDTT−BTz:PC71BM).
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| 4. |
- Patil, Nagaraj, et al.
(författare)
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Bioinspired Redox-Active Catechol-Bearing Polymers as Ultrarobust Organic Cathodes for Lithium Storage
- 2017
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Ingår i: Advanced Materials. - : WILEY-V C H VERLAG GMBH. - 0935-9648 .- 1521-4095. ; 29:40
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Tidskriftsartikel (refereegranskat)abstract
- Redox-active catechols are bioinspired precursors for ortho-quinones that are characterized by higher discharge potentials than para-quinones, the latter being extensively used as organic cathode materials for lithium ion batteries (LIBs). Here, this study demonstrates that the rational molecular design of copolymers bearing catechol-and Li+ ion-conducting anionic pendants endow redox-active polymers (RAPs) with ultrarobust electrochemical energy storage features when combined to carbon nanotubes as a flexible, binder-, and metal current collector-free buckypaper electrode. The importance of the structure and functionality of the RAPs on the battery performances in LIBs is discussed. The structure-optimized RAPs can store high-capacities of 360 mA h g(-1) at 5C and 320 mA h g(-1) at 30C in LIBs. The high ion and electron mobilities within the buckypaper also enable to register 96 mA h g(-1) (24% capacity retention) at an extreme C-rate of 600C (6 s for total discharge). Moreover, excellent cyclability is noted with a capacity retention of 98% over 3400 cycles at 30C. The high capacity, superior active-material utilization, ultralong cyclability, and excellent rate performances of RAPs-based electrode clearly rival most of the state-of-the-art Li+ ion organic cathodes, and opens up new horizons for large-scalable fabrication of electrode materials for ultrarobust Li storage.
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