Time filter

Source Type

Boudiba S.,Laboratory of Organic Materials and HeterochemistryTebessa UniversityConstantine RoadTebessa12002 Algeria | Ruzicka A.,Czech Institute of Macromolecular Chemical | Ulbricht C.,Linz Institute for Organic Solar Cells LIOS | Enengl S.,Linz Institute for Organic Solar Cells LIOS | And 11 more authors.
Journal of Polymer Science, Part A: Polymer Chemistry | Year: 2016

Four conjugated polymers (P1-P4) consisting of alternating anthracene-9,10-diyl and 1,4-phenylene building blocks connected via ethynylene as well as vinylene (P1 and P2), ethynylene-only (P3), and vinylene-only (P4) moieties, respectively, were synthesized and studied. The phenylene units in all four polymers bear 2-ethylhexyloxy side-chains to promote good solubility. The three polymers with vinylene units (P1, P2, and P4) were prepared using the Horner-Wadsworth-Emmons reaction. For the synthesis of the arylene-ethynylene polymer P3, the palladium-catalyzed Sonogashira cross-coupling reaction was used. The polymers were characterized by NMR, Fourier transform infrared spectroscopy, and Raman spectroscopy. Photophysical, absorption and photoluminescence, and electrochemical properties were studied. Spectroscopic ellipsometry measurements were performed to gain more insight on the optical properties. In addition, the transport properties were investigated using admittance spectroscopy. The bulk hole mobility and its dependence on the electric field were evaluated for P1 and P2. © 2016 Wiley Periodicals, Inc.


Grucela-Zajac M.,University of Silesia | Bijak K.,University of Silesia | Kula S.,University of Silesia | Filapek M.,University of Silesia | And 12 more authors.
Journal of Physical Chemistry C | Year: 2014

New symmetrical arylene bisimide derivatives formed by using electron-donating-electron-accepting systems were synthesized. They consist of a phthalic diimide or naphthalenediimide core and imine linkages and are end-capped with thiophene, bithiophene, and (ethylenedioxy)thiophene units. Moreover, polymers were obtained from a new diamine, N,N′-bis(5- aminonaphthalenyl)naphthalene-1,4,5,8-dicarboximide and 2,5- thiophenedicarboxaldehyde or 2,2′-bithiophene-5,5′-dicarboxaldehyde. The prepared azomethine diimides exhibited glass-forming properties. The obtained compounds emitted blue light with the emission maximum at 470 nm. The value of the absorption coefficient was determined as a function of the photon energy using spectroscopic ellipsometry. All compounds are electrochemically active and undergo reversible electrochemical reduction and irreversible oxidation processes as was found in cyclic voltammetry and differential pulse voltammetry (DPV) studies. They exhibited a low electrochemically (DPV) calculated energy band gap (Eg) from 1.14 to 1.70 eV. The highest occupied molecular orbital and lowest unoccupied molecular orbital levels and Eg were additionally calculated theoretically by density functional theory at the B3LYP/6-31G(d,p) level. The photovoltaic properties of two model compounds as the active layer in organic solar cells in the configuration indium tin oxide/poly(3,4-(ethylenedioxy)thiophene):poly(styrenesulfonate)/active layer/Al under an illumination of 1.3 mW/cm2 were studied. The device comprising poly(3-hexylthiophene) with the compound end-capped with bithiophene rings showed the highest value of Voc (above 1 V). The conversion efficiency of the fabricated solar cell was in the range of 0.69-0.90%. © 2014 American Chemical Society.


Gasiorowski J.,Linz Institute for Organic Solar Cells LIOS | Mardare A.I.,Johannes Kepler University | Sariciftci N.S.,Linz Institute for Organic Solar Cells LIOS | Hassel A.W.,Johannes Kepler University
Electrochimica Acta | Year: 2013

The electrochemical oxidation of a next generation low bandgap high performance photovoltaic material namely poly[4,8-bis-substituted-benzo[1,2-b:4, 5-b0]dithiophene-2,6-diyl-alt-4-substituted-thieno[3,4-b] thiophene-2,6-diyl] (PBDTTT-c) thin film was investigated using a scanning droplet cell microscope. Cyclic voltammetry was used for the basic characterization of the oxidation/doping of PBDTTT-c. Application of the different final potentials during the electrochemical study provides a close look to the oxidation kinetics. The electrical properties of both doped and undoped PBDTTT-c were analyzed in situ by electrochemical impedance spectroscopy giving the possibility to correlate the changes in the doping level with the subsequent changes in the resistance and capacitance. As a result one oxidation peak was found during the cyclic voltammetry and in potentiostatic measurements. From Mott-Schottky analysis a donor concentration of 2.3 × 1020 cm-3 and a flat band potential of 1.00 V vs. SHE were found. The oxidation process resulted in an increase of the conductivity by two orders of magnitude reaching a maximum for the oxidized form of 1.4 S cm-1. © 2013 The Authors. Published by Elsevier Ltd. All rights reserved..


PubMed | Johannes Kepler University and Linz Institute for Organic Solar Cells LIOS
Type: | Journal: Electrochimica acta | Year: 2015

The electrochemical oxidation of a next generation low bandgap high performance photovoltaic material namely poly[4,8-bis-substituted-benzo[1,2-b:4,5-b0]dithiophene-2,6-diyl-alt-4-substituted-thieno[3,4-b] thiophene-2,6-diyl] (PBDTTT-c) thin film was investigated using a scanning droplet cell microscope. Cyclic voltammetry was used for the basic characterization of the oxidation/doping of PBDTTT-c. Application of the different final potentials during the electrochemical study provides a close look to the oxidation kinetics. The electrical properties of both doped and undoped PBDTTT-c were analyzed in situ by electrochemical impedance spectroscopy giving the possibility to correlate the changes in the doping level with the subsequent changes in the resistance and capacitance. As a result one oxidation peak was found during the cyclic voltammetry and in potentiostatic measurements. From Mott-Schottky analysis a donor concentration of 2.310


Apaydin D.H.,Linz Institute for Organic Solar Cells LIOS | Glowacki E.D.,Linz Institute for Organic Solar Cells LIOS | Portenkirchner E.,Linz Institute for Organic Solar Cells LIOS | Sariciftci N.S.,Linz Institute for Organic Solar Cells LIOS
Angewandte Chemie - International Edition | Year: 2014

Limiting anthropogenic carbon dioxide emissions constitutes a major issue faced by scientists today. Herein we report an efficient way of controlled capture and release of carbon dioxide using nature inspired, cheap, abundant and non-toxic, industrial pigment namely, quinacridone. An electrochemically reduced electrode consisting of a quinacridone thin film (ca. 100nm thick)on an ITO support forms a quinacridone carbonate salt. The captured CO2 can be released by electrochemical oxidation. The amount of captured CO2 was quantified by FT-IR. The uptake value for electrochemical release process was 4.61mmolg-1. This value is among the highest reported uptake efficiencies for electrochemical CO2 capture. For comparison, the state-of-the-art aqueous amine industrial capture process has an uptake efficiency of ca. 8mmolg-1. Capture and release: The established industrial colorant quinacridone reacts with CO2 following electrochemical reduction, with an uptake efficiency of 4.6mmol CO2/g quinacridone at room temperature. The CO2 can be released by electrochemical oxidation. © 2014 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

Loading Linz Institute for Organic Solar Cells LIOS collaborators
Loading Linz Institute for Organic Solar Cells LIOS collaborators