SwePub
Sök i SwePub databas

  Utökad sökning

Träfflista för sökning "WFRF:(Zhang Fengling) srt2:(2011)"

Sökning: WFRF:(Zhang Fengling) > (2011)

  • Resultat 1-10 av 11
Sortera/gruppera träfflistan
   
NumreringReferensOmslagsbildHitta
1.
  • Wang, Ergang, et al. (författare)
  • An Easily Accessible Isoindigo-Based Polymer for High-Performance Polymer Solar Cells
  • 2011
  • Ingår i: Journal of the American Chemical Society. - 0002-7863. ; 133:36, s. 14244-14247
  • Tidskriftsartikel (refereegranskat)abstract
    • A new, low-band-gap alternating copolymer consisting of terthiophene and isoindigo has been designed and synthesized. Solar cells based on this polymer and PC(71)BM show a power conversion efficiency of 6.3%, which is a record for polymer solar cells based on a polymer with an optical band gap below 1.5 eV. This work demonstrates the great potential of isoindigo moieties as electron-deficient units for building donor-acceptor-type polymers for high-performance polymer solar cells.
  •  
2.
  • Wang, Ergang, et al. (författare)
  • An isoindigo-based low band gap polymer for efficient polymer solar cells with high photo-voltage
  • 2011
  • Ingår i: Chemical Communications. - 1359-7345. ; 47:17, s. 4908-4910
  • Tidskriftsartikel (refereegranskat)abstract
    • A new low band gap polymer (E-g = 1.6 eV) with alternating thiophene and isoindigo units was synthesized and characterized. A PCE of 3.0% and high open-circuit voltage of 0.89 V were realized in polymer solar cells, which demonstrated the promise of isoindigo as an electron deficient unit in the design of donor-acceptor conjugated polymers for polymer solar cells.
  •  
3.
  • Andersson, Mattias, et al. (författare)
  • Mobility and fill factor correlation in geminate recombination limited solar cells
  • 2011
  • Ingår i: Journal of Applied Physics. - American Institute of Physics (AIP). - 0021-8979. ; 110:2, s. 024509
  • Tidskriftsartikel (refereegranskat)abstract
    • Empirical data for the fill factor as a function of charge carrier mobility for two different polymer: fullerene systems is presented and analyzed. The results indicate that charge extraction depth limitations and space charge effects are inconsistent with the observed behavior, and the decrease in the fill factor is, instead, attributed to the field-dependent charge separation and geminate recombination. A solar cell photocurrent limited by the Onsager-Braun charge transfer exciton dissociation is shown to be able to accommodate the experimental observations. Charge dissociation limited solar cells always benefit from increased mobilities, and the negative contribution from the reduced charge separation is shown to be much more important for the fill factor in these material systems than any adverse effects from charge carrier extraction depth limitations or space charge effects due to unbalanced mobilities. The logarithmic dependence of the fill factor on the mobility for such a process is also shown to imply that simply increasing the mobilities is an impractical way to reach very high fill factors under these conditions since unrealistically high mobilities are required. A more controlled morphology is, instead, argued to be necessary for high performance.
4.
  • Du, Chun, et al. (författare)
  • 9-Alkylidene-9H-Fluorene-Containing Polymer for High-Efficiency Polymer Solar Cells
  • 2011
  • Ingår i: Macromolecules. - American Chemical Society. - 0024-9297. ; 44:19, s. 7617-7624
  • Tidskriftsartikel (refereegranskat)abstract
    • A novel donor-acceptor copolymer containing 9-alkylidene-9H-fluorene unit in the main chain, poly[9-(1-hexylheptylidene)-2,7-fluorene-alt-5, 5-(4,7-di-2-thienyl-5,6-dialkoxy-2,1,3-benzothiadiazole)] (PAFDTBT), has been synthesized and evaluated in bulk heterojunction polymer solar cells (BHJ PSCs). The polymer possesses a low band gap of 1.84 eV, a low-lying HOMO energy level (5.32 eV), and excellent solubility in common organic solvents. PSCs based on PAFDTBT and (6,6)-phenyl-C(71)-butyric add methyl ester (PC(71)BM) demonstrate a power conversion efficiency (PCE) of 6.2% with a high fill factor (FF) of 0.70, which indicates that 9-alkylidene-9H-fluorene can be a very useful building block for constructing narrow band gap conjugated polymers for high-efficiency BHJ PSCs.
  •  
5.
  • Hou, Lintao, et al. (författare)
  • Lateral Phase Separation Gradients in Spin-Coated Thin Films of High-Performance Polymer: : Fullerene Photovoltaic Blends
  • 2011
  • Ingår i: Advanced Functional Materials. - Wiley-VCH Verlag Berlin. - 1616-301X. ; 21:16, s. 3169-3175
  • Tidskriftsartikel (refereegranskat)abstract
    • In this study, it is demonstrated that a finer nanostructure produced under a rapid rate of solvent removal significantly improves charge separation in a high-performance polymer: fullerene bulk-heterojunction blend. During spin-coating, variations in solvent evaporation rate give rise to lateral phase separation gradients with the degree of coarseness decreasing away from the center of rotation. As a result, across spin-coated thin films the photocurrent at the first interference maximum varies as much as 25%, which is much larger than any optical effect. This is investigated by combining information on the surface morphology of the active layer imaged by atomic force microscopy, the 3D nanostructure imaged by electron tomography, film formation during the spin coating process imaged by optical interference and photocurrent generation distribution in devices imaged by a scanning light pulse technique. The observation that the nanostructure of organic photovoltaic blends can strongly vary across spin-coated thin films will aid the design of solvent mixtures suitable for high molecular-weight polymers and of coating techniques amenable to large area processing.
  •  
6.
  • Li, Weiwei, et al. (författare)
  • The Effect of additive on performance and shelf-stability of HSX-1/PCBM photovoltaic devices
  • 2011
  • Ingår i: Organic electronics. - Elsevier Science B.V., Amsterdam.. - 1566-1199. ; 12:9, s. 1544-1551
  • Tidskriftsartikel (refereegranskat)abstract
    • How 1,8-diiodooctane (DIO) enhances performance of polymer solar cells based on polymer HXS-1 and fullerene [6,6]-phenyl C(71)-butyric acid methyl ester (PC(71)BM) from 3.6% to 5.4% is scrutinized with several techniques by comparing devices or blend films spin-coated from dichlorobenzene (DCB) to those from DCB/DIO (97.5:2.5 v/v). Morphology of blend films is examined with atomic force microscopy (AFM), transmission electron microscopy (TEM) and electron tomography (3-D TEM), respectively. Charge generation and recombination is studied with photoluminescence, and charge transport with field effect transistors. The morphology with domain size in 10-20 nm and vertical elongated clusters formed in DIO system is supposed to facilitate charge transport and minimize charge carrier recombination, which are the main reasons for enhancing power conversion efficiency (PCE) from 3.6% (without DIO) to 5.4% (with DIO). Furthermore, a two year inspection shows no significant impact of DIO on the shelf-stability of the solar cells. No visible degradation in the second year indicates that the morphology of the active layers in the devices is relatively stable after initial relaxation in the first year.
7.
  • Ma, Zaifei, et al. (författare)
  • Enhance performance of organic solar cells based on an isoindigo-based copolymer by balancing absorption and miscibility of electron acceptor
  • 2011
  • Ingår i: Applied Physics Letters. - American Institute of Physics (AIP). - 0003-6951. ; 99:14, s. 143302
  • Tidskriftsartikel (refereegranskat)abstract
    • Superior absorption of PC(71)BM in visible region to that of PC(61)BM makes PC(71)BM a predominant acceptor for most high efficient polymer solar cells (PSCs). However, we will demonstrate that power conversion efficiencies (PCEs) of PSCs based on poly[N,N-bis(2-hexyldecyl)isoindigo-6, 6-diyl-alt-thiophene-2,5-diyl] (PTI-1) with PC(61)BM as acceptor are 50% higher than their PC71BM counterparts under illumination of AM1.5G. AFM images reveal different topographies of the blends between PTI-1:PC(61)BM and PTI-1:PC(71)BM, which suggests that acceptors miscibility plays a more important role than absorption. The photocurrent of 9.1 mA/cm(2) is among the highest value in PSCs with a driving force for exciton dissociation less than 0.2 eV.
8.
  • O Reese, Matthew, et al. (författare)
  • Consensus stability testing protocols for organic photovoltaic materials and devices
  • 2011
  • Ingår i: SOLAR ENERGY MATERIALS AND SOLAR CELLS. - Elsevier Science B.V., Amsterdam.. - 0927-0248. ; 95:5, s. 1253-1267
  • Tidskriftsartikel (refereegranskat)abstract
    • Procedures for testing organic solar cell devices and modules with respect to stability and operational lifetime are described. The descriptions represent a consensus of the discussion and conclusions reached during the first 3 years of the international summit on OPV stability (ISOS). The procedures include directions for shelf life testing, outdoor testing, laboratory weathering testing and thermal cycling testing, as well as guidelines for reporting data. These procedures are not meant to be qualification tests, but rather generally agreed test conditions and practices to allow ready comparison between laboratories and to help improving the reliability of reported values. Failure mechanisms and detailed degradation mechanisms are not covered in this report.
  •  
9.
  • Wang, Ergang, et al. (författare)
  • Side-Chain Architectures of 2,7-Carbazole and Quinoxaline-Based Polymers for Efficient Polymer Solar Cells
  • 2011
  • Ingår i: Macromolecules. - 0024-9297. ; 44:7, s. 2067-2073
  • Tidskriftsartikel (refereegranskat)abstract
    • Three polymers bearing a common carbazole thiophene quinoxaline thiophene backbone, but different side chains, were designed and synthesized in order to investigate the effect of side chains on their photovoltaic performance. Their photophysical, electrochemical, and photovoltaic properties were investigated and compared. The polymer EWC3, with the largest amount of side chains, showed the highest power conversion efficiency of 3.7% with an open-circuit voltage (V-oc) of 0.92 V. The atomic force microscopy images of the active layers of the devices showed that the morphology was highly influenced by the choice of the solvent and processing additive. It is worth noting that polymer solar cells (PSCs) fabricated from EWC3, with branched side chains on the carbazole units, gave a much higher V-oc than the devices made from EWC1, which bears the same electron-deficient segment as EWC3 but straight side chains on carbazole units. This study offered a useful and important guideline for designing 2,7-carbazole-based polymers for high-performance PSCs.
  •  
10.
  • Wang, Yaling, et al. (författare)
  • Enhanced performance and stability in polymer photovoltaic cells using lithium benzoate as cathode interfacial layer
  • 2011
  • Ingår i: SOLAR ENERGY MATERIALS AND SOLAR CELLS. - Elsevier Science B.V., Amsterdam.. - 0927-0248. ; 95:4, s. 1243-1247
  • Tidskriftsartikel (refereegranskat)abstract
    • We report the enhanced performance and stability of polymer solar cells based on regioregular poly(3-hexylthiophene)(P3HT) and methanofullerene [6,6]-phenyl C-61-butyric acid methyl ester (PCBM) blend using lithium benzoate (C6H5COOLi) as cathode buffer layer between the active layer and the Al cathode. The effects of the C6H5COOLi thickness on the performance of polymer solar cell are also investigated. Under 100 mW/cm(2) white light illumination, the device with 1 nm thick C6H5COOLi as cathode buffer layer exhibits power conversion efficiency (PCE) as high as 3.41 +/- 0.07% and the device stability is greatly extended. Compared to the solar cell with LiF/AI cathode, the PCE is increased ca. 9.4%. Introduction of C6H5COOLi buffer layer effectively increases the shunt resistance and improves the photo-generated charge collection. The improved performance may attribute to the dissociation of semi-conducting C6H5COOLi upon deposition to liberate Li with a low work function, which reduces the interface resistance of the active layer and the cathode and enhances the interior electric field that may result in efficient charge transportion. In addition, the C6H5COOLi layer may serve as an effective oxygen and moisture diffusion barrier for the organic solar cells. Therefore. C6H5COOLi is a promising candidate as an interlayer to improve the efficiency of electron collection and to reduce the ambience influence on the stability of polymer solar cells.
  •  
Skapa referenser, mejla, bekava och länka
  • Resultat 1-10 av 11
 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy