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Institution

Johannes Kepler University of Linz

EducationLinz, Oberösterreich, Austria
About: Johannes Kepler University of Linz is a education organization based out in Linz, Oberösterreich, Austria. It is known for research contribution in the topics: Computer science & Thin film. The organization has 6605 authors who have published 19243 publications receiving 385667 citations.


Papers
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Journal ArticleDOI
TL;DR: In this paper, a systematic investigation was carried out on the influence of carrier electrolyte composition on separation selectivity in capillary zone electrophoresis of inorganic anions.

107 citations

Journal ArticleDOI
TL;DR: In this article, the authors address the steps that need to be taken to create a new European industrial policy and discuss the structural challenges and instruments of the EU's industrial policy, and should the EU be engaged in picking winners or is the market better at making such judgements.
Abstract: One lesson of the Great Recession has been that countries with higher shares of industry in their GDP seemed to be less affected by the crisis. Consequently, the call for an industrial renaissance has become stronger. Industrial policy has now become a top priority in countries where it was not explicitly considered in the past. A strong EU-wide industrial policy is expected to foster growth and job creation. However, cultivating industrial development is a complex challenge. This Forum addresses the steps that need to be taken to create a new European industrial policy. What are the structural challenges that need to be addressed? What are the instruments of the EU’s industrial policy? And should the EU be engaged in picking winners, or is the market better at making such judgements?

107 citations

Journal ArticleDOI
TL;DR: The results indicate the formation of polarons at low doping levels and the existence of bipolarons at high doping levels, both of which are indicated by the presented spectroscopic data.
Abstract: In this work, we focus on the formation of different kinds of charge carriers such as polarons and bipolarons upon p-type doping (oxidation) of the organic semiconductor poly(3- hexylthiophene-2,5-diyl) (P3HT). We elucidate the cyclic voltammogram during oxidation of this polymer and present spectroscopic changes upon doping in the UV/Vis/near-IR range as well as in the mid-IR range. In the low-oxidation regime, two absorption bands related to sub-gap transitions appear, one in the UV/Vis range and another one in the mid-IR range. The UV/Vis absorption gradually decreases upon further doping while the mid-IR absorption shifts to lower energy. Additionally, electron paramagnetic resonance (EPR) measurements are performed, showing an increase of the EPR signal up to a certain doping level, which significantly decreases upon further doping. Furthermore, the absorption spectra in the UV/Vis range are analyzed in relation to the morphology (crystalline vs. amorphous) by using theoretical models. Finally, the calculated charge carriers from cyclic voltammogram are linked together with optical transitions as well as with the EPR signals upon p-type doping. We stress that our results indicate the formation of polarons at low doping levels and the existence of bipolarons at high doping levels. The presented spectroscopic data are an experimental evidence of the formation of bipolarons in P3HT.

107 citations

Journal ArticleDOI
TL;DR: In this paper, a multilayers of self-assembled Ge-rich dot embedded in silicon grown by molecular-beam epitaxy using high resolution x-ray reciprocal space mapping and reflectivity was studied.
Abstract: We have studied multilayers of self-assembled Ge-rich dots embedded in silicon grown by molecular-beam epitaxy using high resolution x-ray reciprocal space mapping and reflectivity. The Si spacer thicknesses between the dot arrays were in the range of 10‐40 nm, the typical dot size was about 150 nm for the diameter and 7 nm for the height. The measured reciprocal space maps were simulated using statistical kinematical x-ray-diffraction theory, and a good agreement between experimental and simulated data has been achieved. From the measurements, the in-plane strain in the dot lattice was determined. We derived the degree of the vertical correlation of the dot positions ~‘‘stacking’’ ! and a lateral ordering of the dots in a square array with main axes parallel to the ^100& directions, with an array lattice constant of about 500 nm. @S0163-1829~97!05623-3#

107 citations

Journal ArticleDOI
TL;DR: This review focuses in particular on the preparation of (macro)porous polymer monoliths by simple free-radical processes and the key events in their formation, and the effect of resistance to mass transfer arising from the nanoscale gel porosity.
Abstract: Porous polymer monoliths are considered to be one of the major breakthroughs in separation science. These materials are well known to be best suited for the separation of large molecules, specifically proteins, an observation most often explained by convective mass transfer and the absence of small pores in the polymer scaffold. However, this conception is not sufficient to explain the performance of small molecules. This review focuses in particular on the preparation of (macro)porous polymer monoliths by simple free-radical processes and the key events in their formation. There is special focus on the fluid transport properties in the heterogeneous macropore space (flow dispersion) and on the transport of small molecules in the swollen, and sometimes permanently porous, globule-scale polymer matrix. For small molecule applications in liquid chromatography, it is consistently found in the literature that the major limit for the application of macroporous polymer monoliths lies not in the optimization of surface area and/or modification of the material and microscopic morphological properties only, but in the improvement of mass transfer properties. In this review we discuss the effect of resistance to mass transfer arising from the nanoscale gel porosity. Gel porosity induces stagnant mass transfer zones in chromatographic processes, which hamper mass transfer efficiency and have a detrimental effect on macroscopic chromatographic dispersion under equilibrium (isocratic) elution conditions. The inherent inhomogeneity of polymer networks derived from free-radical cross-linking polymerization, and hence the absence of a rigid (meso)porous pore space, represents a major challenge for the preparation of efficient polymeric materials for the separation of small molecules.

107 citations


Authors

Showing all 6718 results

NameH-indexPapersCitations
Wolfgang Wagner1562342123391
A. Paul Alivisatos146470101741
Klaus-Robert Müller12976479391
Christoph J. Brabec12089668188
Andreas Heinz108107845002
Niyazi Serdar Sariciftci9959154055
Lars Samuelson9685036931
Peter J. Oefner9034830729
Dmitri V. Talapin9030339572
Tomás Torres8862528223
Ramesh Raskar8667030675
Siegfried Bauer8442226759
Alexander Eychmüller8244423688
Friedrich Schneider8255427383
Maksym V. Kovalenko8136034805
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20242
202354
2022187
20211,404
20201,412
20191,365