| 1. |
- Dyer, Aubrey L., et al.
(författare)
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A Vertically Integrated Solar-Powered Electrochromic Window for Energy Efficient Buildings
- 2014
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Ingår i: Advanced Materials. - : Wiley-VCH Verlag. - 0935-9648 .- 1521-4095. ; 26:28, s. 4895-4900
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Tidskriftsartikel (refereegranskat)abstract
- A solution-processed self-powered polymer electrochromic/photovoltaic (EC/PV) device is realized by vertically integrating two transparent PV cells with an ECD. The EC/PV cell is a net energy positive dual functional device, which can be reversibly switched between transparent and colored states by PV cells for regulating incoming sunlight through windows. The two PV cells can individually, or in pairs, generate electricity.
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| 2. |
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| 3. |
- Inganäs, Olle, et al.
(författare)
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Polymer Photovoltaics with Alternating Copolymer/Fullerene Blends and Novel Device Architectures
- 2010
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Ingår i: Advanced Materials. - : Wiley. - 0935-9648 .- 1521-4095. ; 22:20, s. E100-E116
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Tidskriftsartikel (refereegranskat)abstract
- The synthesis of novel conjugated polymers, designed for the purpose of photovoltaic energy conversion, and their properties in polymer/fullerene materials and photovoltaic devices are reviewed. Two families of main chain polymer donors, based on fluorene or phenylene and donor-acceptor-donor comonomers in alternating copolymers, are used to absorb the high-energy parts of the solar spectrum and to give high photovoltages in combinations with fullerene acceptors in devices. These materials are used in alternative photovoltaic device geometries with enhanced light incoupling to collect larger photocurrents or to enable tandem devices and enhance photovoltage.
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| 4. |
- Jiang, Qinglin, et al.
(författare)
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High Thermoelectric Performance in n-Type Perylene Bisimide Induced by the Soret Effect
- 2020
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Ingår i: Advanced Materials. - : WILEY-V C H VERLAG GMBH. - 0935-9648 .- 1521-4095. ; 32:45
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Tidskriftsartikel (refereegranskat)abstract
- Low-cost, non-toxic, abundant organic thermoelectric materials are currently under investigation for use as potential alternatives for the production of electricity from waste heat. While organic conductors reach electrical conductivities as high as their inorganic counterparts, they suffer from an overall low thermoelectric figure of merit (ZT) due to their small Seebeck coefficient. Moreover, the lack of efficient n-type organic materials still represents a major challenge when trying to fabricate efficient organic thermoelectric modules. Here, a novel strategy is proposed both to increase the Seebeck coefficient and achieve the highest thermoelectric efficiency for n-type organic thermoelectrics to date. An organic mixed ion-electron n-type conductor based on highly crystalline and reduced perylene bisimide is developed. Quasi-frozen ionic carriers yield a large ionic Seebeck coefficient of -3021 mu V K-1, while the electronic carriers dominate the electrical conductivity which is as high as 0.18 S cm(-1)at 60% relative humidity. The overall power factor is remarkably high (165 mu W m(-1)K(-2)), with aZT= 0.23 at room temperature. The resulting single leg thermoelectric generators display a high quasi-constant power output. This work paves the way for the design and development of efficient organic thermoelectrics by the rational control of the mobility of the electronic and ionic carriers.
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| 5. |
- Jin, Yingzhi, et al.
(författare)
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Limitations and Perspectives on Triplet-Material-Based Organic Photovoltaic Devices
- 2019
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Ingår i: Advanced Materials. - : WILEY-V C H VERLAG GMBH. - 0935-9648 .- 1521-4095. ; 31:22
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Tidskriftsartikel (refereegranskat)abstract
- Organic photovoltaic cells (OPVs) have attracted broad attention and become a very energetic field after the emergence of nonfullerene acceptors. Long-lifetime triplet excitons are expected to be good candidates for efficiently harvesting a photocurrent. Parallel with the development of OPVs based on singlet materials (S-OPVs), the potential of triplet materials as photoactive layers has been explored. However, so far, OPVs employing triplet materials in a bulk heterojunction have not exhibited better performance than S-OPVs. Here, the recent progress of representative OPVs based on triplet materials (T-OPVs) is briefly summarized. Based on that, the performance limitations of T-OPVs are analyzed. The shortage of desired triplet materials with favorable optoelectronic properties for OPVs, the tradeoff between long lifetime and high binding energy of triplet excitons, as well as the low charge mobility in most triplet materials are crucial issues restraining the efficiencies of T-OPVs. To overcome these limitations, first, novel materials with desired optoelectronic properties are urgently demanded; second, systematic investigation on the contribution and dynamics of triplet excitons in T-OPVs is necessary; third, close multidisciplinary collaboration is required, as proved by the development of S-OPVs.
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| 6. |
- Li, Shuixing, et al.
(författare)
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Asymmetric Electron Acceptors for High-Efficiency and Low-Energy-Loss Organic Photovoltaics
- 2020
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Ingår i: Advanced Materials. - : WILEY-V C H VERLAG GMBH. - 0935-9648 .- 1521-4095. ; 32
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Tidskriftsartikel (refereegranskat)abstract
- Low energy loss and efficient charge separation under small driving forces are the prerequisites for realizing high power conversion efficiency (PCE) in organic photovoltaics (OPVs). Here, a new molecular design of nonfullerene acceptors (NFAs) is proposed to address above two issues simultaneously by introducing asymmetric terminals. Two NFAs, BTP-S1 and BTP-S2, are constructed by introducing halogenated indandione (A(1)) and 3-dicyanomethylene-1-indanone (A(2)) as two different conjugated terminals on the central fused core (D), wherein they share the same backbone as well-known NFA Y6, but at different terminals. Such asymmetric NFAs with A(1)-D-A(2) structure exhibit superior photovoltaic properties when blended with polymer donor PM6. Energy loss analysis reveals that asymmetric molecule BTP-S2 with six chlorine atoms attached at the terminals enables the corresponding devices to give an outstanding electroluminescence quantum efficiency of 2.3 x 10(-2)%, one order of magnitude higher than devices based on symmetric Y6 (4.4 x 10(-3)%), thus significantly lowering the nonradiative loss and energy loss of the corresponding devices. Besides, asymmetric BTP-S1 and BTP-S2 with multiple halogen atoms at the terminals exhibit fast hole transfer to the donor PM6. As a result, OPVs based on the PM6:BTP-S2 blend realize a PCE of 16.37%, higher than that (15.79%) of PM6:Y6-based OPVs. A further optimization of the ternary blend (PM6:Y6:BTP-S2) results in a best PCE of 17.43%, which is among the highest efficiencies for single-junction OPVs. This work provides an effective approach to simultaneously lower the energy loss and promote the charge separation of OPVs by molecular design strategy.
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| 7. |
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| 8. |
- Svanstrom, C. M. B., et al.
(författare)
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Device Performance of APFO-3/PCBM Solar Cells with Controlled Morphology
- 2009
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Ingår i: Advanced Materials. - Weinheim : Wiley. - 0935-9648 .- 1521-4095. ; 21:43, s. 4398-
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Tidskriftsartikel (refereegranskat)abstract
- Polymer/fullerene solar cells with three different device structures: A) diffuse bilayer, B) spontaneously formed multilayer and C) vertically homogeneous thin films, are fabricated. The photocurrent/voltage performance is compared and it is found that the self-stratified structure (B) yields the highest energy conversion efficiency.
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| 9. |
- Svensson, M., et al.
(författare)
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High-performance polymer solar cells of an alternating polyfluorene copolymer and a fullerene derivative
- 2003
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Ingår i: Advanced Materials. - : Wiley. - 0935-9648 .- 1521-4095. ; 15:12, s. 988-991
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Tidskriftsartikel (refereegranskat)abstract
- High-performance polymer solar cells of an alternating polyfluorene copolymer, PFDTBT, and a fullerene derivative were studied. It was shown that PFDTBT is a promising candidate for obtaining high energy conversion efficiency when combined with a suitable electron acceptor. Results showed that high-performance solar cells with extended spectral coverage and increased open-circuit voltage could be prepared from composites prepared from electron acceptor.
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| 10. |
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