Fullerene Acceptor (fullerene + acceptor)

Distribution by Scientific Domains


Selected Abstracts


Copolymers of Cyclopentadithiophene and Electron-Deficient Aromatic Units Designed for Photovoltaic Applications

ADVANCED FUNCTIONAL MATERIALS, Issue 20 2009
Johan C. Bijleveld
Abstract Alternating copolymers based on cyclopentadithiophene (CPDT) and five different electron-deficient aromatic units with reduced optical band gaps are synthesized via Suzuki coupling. All polymers show a significant photovoltaic response when mixed with a fullerene acceptor. The frontier orbital levels of the new polymers are designed to minimize energy losses by increasing the open-circuit voltage with respect to the optical band gap, while maintaining a high coverage of the absorption with the solar spectrum. The best cells are obtained for a copolymer of CPDT and benzooxadiazole (BO) with a band gap of 1.47,eV. This cell gives a short-circuit current of 5.4,mA cm,2, an open-circuit voltage of 0.78,V, and a fill factor of 0.6, resulting in a power conversion efficiency of about 2.5%. [source]


Nanoscale Phase Separation and High Photovoltaic Efficiency in Solution-Processed, Small-Molecule Bulk Heterojunction Solar Cells

ADVANCED FUNCTIONAL MATERIALS, Issue 19 2009
Bright Walker
Abstract Research relating to organic solar cells based on solution-processed, bulk heterojunction (BHJ) films has been dominated by polymeric donor materials, as they typically have better film-forming characteristics and film morphology than their small-molecule counterparts. Despite these morphological advantages, semiconducting polymers suffer from synthetic reproducibility and difficult purification procedures, which hinder their commercial viability. Here, a non-polymeric, diketopyrrolopyrrole-based donor material that can be solution processed with a fullerene acceptor to produce good quality films is reported. Thermal annealing leads to suitable phase separation and material distribution so that highly effective BHJ morphologies are obtained. The frontier orbitals of the material are well aligned with those of the fullerene acceptor, allowing efficient electron transfer and suitable open-circuit voltages, leading to power conversion efficiencies of 4.4,±,0.4% under AM1.5G illumination (100,mW cm,2). Small molecules can therefore be solution processed to form high-quality BHJ films, which may be used for low-cost, flexible organic solar cells. [source]


Recent Progress in Polymer Solar Cells: Manipulation of Polymer:Fullerene Morphology and the Formation of Efficient Inverted Polymer Solar Cells

ADVANCED MATERIALS, Issue 14-15 2009
Li-Min Chen
Abstract Polymer morphology has proven to be extremely important in determining the optoelectronic properties in polymer-based devices. The understanding and manipulation of polymer morphology has been the focus of electronic and optoelectronic polymer-device research. In this article, recent advances in the understanding and controlling of polymer morphology are reviewed with respect to the solvent selection and various annealing processes. We also review the mixed-solvent effects on the dynamics of film evolution in selected polymer-blend systems, which facilitate the formation of optimal percolation paths and therefore provide a simple approach to improve photovoltaic performance. Recently, the occurrence of vertical phase separation has been found in some polymer:fullerene bulk heterojunctions.1,3 The origin and applications of this inhomogeneous distribution of the polymer donor and fullerene acceptor are addressed. The current status and device physics of the inverted structure solar cells is also reviewed, including the advantage of utilizing the spontaneous vertical phase separation, which provides a promising alternative to the conventional structure for obtaining higher device performance. [source]


Tuning Conversion Efficiency in Metallo Endohedral Fullerene-Based Organic Photovoltaic Devices

ADVANCED FUNCTIONAL MATERIALS, Issue 14 2009
Russel B. Ross
Abstract Here the influence that 1-(3-hexoxycarbonyl)propyl-1-phenyl-[6,6]-Lu3N@C81, Lu3N@C80,PCBH, a novel acceptor material, has on active layer morphology and the performance of organic photovoltaic (OPV) devices using this material is reported. Polymer/fullerene blend films with poly(3-hexylthiophene), P3HT, donor material and Lu3N@C80,PCBH acceptor material are studied using absorption spectroscopy, grazing incident X-ray diffraction and photocurrent spectra of photovoltaic devices. Due to a smaller molecular orbital offset the OPV devices built with Lu3N@C80,PCBH display increased open circuit voltage over empty cage fullerene acceptors. The photovoltaic performance of these metallo endohedral fullerene blend films is found to be highly impacted by the fullerene loading. The results indicate that the optimized blend ratio in a P3HT matrix differs from a molecular equivalent of an optimized P3HT/[6,6]-phenyl-C61 -butyric methyl ester, C60,PCBM, active layer, and this is related to the physical differences of the C80 fullerene. The influence that active layer annealing has on the OPV performance is further evaluated. Through properly matching the film processing and the donor/acceptor ratio, devices with power conversion efficiency greater than 4% are demonstrated. [source]


Polymer Photovoltaics with Alternating Copolymer/Fullerene Blends and Novel Device Architectures

ADVANCED MATERIALS, Issue 20 2010
Olle Inganäs
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. [source]