TY - JOUR A1 - Gerhard, Reimund A1 - Bauer, Siegfried A1 - Bauer-Gogonea, Simona A1 - Brinker, Walter A1 - Dinger, Claudia A1 - Molzow, Wolf-Dietrich A1 - Wirges, Werner A1 - Yilmaz, Sükrü T1 - Electro-optical investigation of the dipole orientation in poled polymers Y1 - 1995 ER - TY - THES A1 - Nguyen, Quyet Doan T1 - Electro-acoustical probing of space-charge and dipole-polarization profiles in polymer dielectrics for electret and electrical-insulation applications T1 - Elektroakustische Abtastung von elektrischen Ladungs- und Polarisationsprofilen in Polymerfolien für Elektret- und Isolations-Anwendungen N2 - Electrets are dielectrics with quasi-permanent electric charge and/or dipoles, sometimes can be regarded as an electric analogy to a magnet. Since the discovery of the excellent charge retention capacity of poly(tetrafluoro ethylene) and the invention of the electret microphone, electrets have grown out of a scientific curiosity to an important application both in science and technology. The history of electret research goes hand in hand with the quest for new materials with better capacity at charge and/or dipole retention. To be useful, electrets normally have to be charged/poled to render them electro-active. This process involves electric-charge deposition and/or electric dipole orientation within the dielectrics ` surfaces and bulk. Knowledge of the spatial distribution of electric charge and/or dipole polarization after their deposition and subsequent decay is crucial in the task to improve their stability in the dielectrics. Likewise, for dielectrics used in electrical insulation applications, there are also needs for accumulated space-charge and polarization spatial profiling. Traditionally, space-charge accumulation and large dipole polarization within insulating dielectrics is considered undesirable and harmful to the insulating dielectrics as they might cause dielectric loss and could lead to internal electric field distortion and local field enhancement. High local electric field could trigger several aging processes and reduce the insulating dielectrics' lifetime. However, with the advent of high-voltage DC transmission and high-voltage capacitor for energy storage, these are no longer the case. There are some overlapped between the two fields of electrets and electric insulation. While quasi-permanently trapped electric-charge and/or large remanent dipole polarization are the requisites for electret operation, stably trapped electric charge in electric insulation helps reduce electric charge transport and overall reduced electric conductivity. Controlled charge trapping can help in preventing further charge injection and accumulation as well as serving as field grading purpose in insulating dielectrics whereas large dipole polarization can be utilized in energy storage applications. In this thesis, the Piezoelectrically-generated Pressure Steps (PPSs) were employed as a nondestructive method to probe the electric-charge and dipole polarization distribution in a range of thin film (several hundred micron) polymer-based materials, namely polypropylene (PP), low-density polyethylene/magnesium oxide (LDPE/MgO) nanocomposites and poly(vinylidene fluoride-co- trifluoro ethylene) (P(VDF-TrFE)) copolymer. PP film surface-treated with phosphoric acid to introduce surfacial isolated nanostructures serves as example of 2-dimensional nano-composites whereas LDPE/MgO serves as the case of 3-dimensional nano-composites with MgO nano-particles dispersed in LDPE polymer matrix. It is evidenced that the nanoparticles on the surface of acid-treated PP and in the bulk of LDPE/MgO nanocomposites improve charge trapping capacity of the respective material and prevent further charge injection and transport and that the enhanced charge trapping capacity makes PP and LDPE/MgO nanocomposites potential materials for both electret and electrical insulation applications. As for PVDF and VDF-based copolymers, the remanent spatial polarization distribution depends critically on poling method as well as specific parameters used in the respective poling method. In this work, homogeneous polarization poling of P(VDF-TrFE) copolymers with different VDF-contents have been attempted with hysteresis cyclical poling. The behaviour of remanent polarization growth and spatial polarization distribution are reported and discussed. The Piezoelectrically-generated Pressure Steps (PPSs) method has proven as a powerful method for the charge storage and transport characterization of a wide range of polymer material from nonpolar, to polar, to polymer nanocomposites category. N2 - Elektrete sind Dielektrika mit quasi-permanenter elektrischer Ladung und/oder quasi-permanent ausgerichteten elektrischen Dipolen - das elektrische Analogon zu einem Magneten. Seit der Entdeckung der besonders hohen Stabilitaet negativer Raumladungen in Polytetrafluorethylen (PTFE, Handelsname Teflon) und der Erfindung des Elektretmikrofons ist aus der spannenden wissenschaftlichen Fragestellung nach den Ursachen der hervorragenden Ladungsspeicherung in Elektreten auch eine wichtige technische Anwendung geworden. In der Geschichte der Elektretforschung und der Elektretanwendungen geht es neben der Ursachenklaerung auch immer um die Suche nach neuen Materialien mit besserer Ladungsspeicherung und/oder Dipolpolarisation. Elektretmaterialien muessen in der Regel elektrisch aufgeladen oder gepolt werden, um die gewuenschten elektroaktiven Eigenschaften zu erhalten. Dabei werden entweder elektrische Ladungen auf der Oberflaeche oder im Volumen des Elektretmaterials deponiert und/oder elektrische Dipole im Material ausgerichtet. Genaue Informationen ueber die raeumliche Verteilung der elektrischen Ladungen und/oder der Dipolpolarisation sowie deren Entwicklung im Laufe der Zeit sind entscheidend fuer eine gezielte Verbesserung der Elektretstabilitaet. Dielektrika, die zur elektrischen Isolierung von Hochspannungsanlagen eingesetzt werden, koennen ebenfalls elektrische Raumladungen und/oder Dipolpolarisationen enthalten, deren Verteilungen entscheidend fuer die Beherrschung der damit einhergehenden Eigenschaftsaenderungen sind. Traditionell gelten Raumladungen und Dipolpolarisationen in elektrischen Isolierungen als unerwuenscht und schaedlich, da sie zu erheblichen Verlusten und zu Verzerrungen der inneren elektrischen Felder fuehren koennen. Hohe lokale Felder koennen Alterungsprozesse ausloesen und die Lebensdauer der isolierenden Dielektrika erheblich verkuerzen. Mit dem Aufkommen der Hochspannungs-Gleichstromuebertragung und des Hochspannungskondensators zur Energiespeicherung in den letzten Jahren hat sich die Situation jedoch grundlegend geaendert, da Raumladungen prinzipiell nicht mehr vermeidbar sind und bei entsprechender Gestaltung der Isolierung moeglicherweise sogar von Vorteil sein koennen. Hier ergeben sich nun Ueberschneidungen und Synergien zwischen Elektreten und elektrischen Isoliermaterialien, zumal in beiden Faellen hohe elektrische Gleichfelder auftreten. Waehrend quasi-permanent gespeicherte elektrische Ladungen und/oder stark quasi- permanente oder remanente Dipolpolarisationen das wesentliche Merkmal von Elektreten sind, koennen stabil gespeicherte elektrische Ladungen in elektrischen Isolierungen dazu beitragen, den schaedlichen Ladungstransport und damit die effektive elektrische Leitfaehigkeit der Dielektrika zu reduzieren. Ein kontrolliertes Einbringen von Raumladungen kann die Injektion und die Anhaeufung weiterer Ladungen verhindern, waehrend stark Dipolpolarisationen die Kapazitaet von elektrischen Energiespeichern wesentlich erhoehen koennen. In der vorliegenden Arbeit wurden piezoelektrisch erzeugte Druckstufen (Piezoelectrically generated Pressure Steps oder PPSs) eingesetzt, um die Verteilung elektrischer Ladungen und/oder ausgerichteter elektrischer Dipole in relativ duennen polymeren Dielektrika (Mikrometerbereich) zu untersuchen. Wesentliche Probenmaterialien waren Polypropylen (PP), Komposite aus Polyethylen mit Magnesiumoxid-Nanopartikeln in geringen Mengen (LDPE/MgO) sowie Poly(vinyliden fluorid-trifluorethylen)-Copolymere (P(VDF-TrFE)). PP-Folien, die mit Phosphorsaeure oberflaechenbehandelt wurden, um voneinander isolierte Nanostrukturen an der Oberflaeche zu erzeugen, sind ein Beispiel fuer ein zweidimensionales (2-D) Nanokomposit, waehrend LDPE/MgO ein dreidimensionales (3-D) Nanokomposit darstellt. Es konnte nachgewiesen werden, dass die Nanopartikel auf der Oberflaeche von saeurebehandeltem PP und im Volumen von LDPE/MgO-Nanokompositen die Ladungsspeicherfaehigkeit des jeweiligen Materials entscheidend verbessern. Damit werden weitere Ladungsinjektionen und der Ladungstransport verhindert, was die 2-D PP- und die 3-D LDPE/MgO-Nanokomposite zu geeigneten Kandidaten sowohl fuer Elektret- als auch fuer Isolationsanwendungen macht. Bei Polyvinylidenfluorid (PVDF) und Copolymeren auf der Basis von Vinylidenfluorid (VDF) haengt die remanente raeumliche Polarisationsverteilung entscheidend von der jeweiligen Polungsmethode sowie von den Parametern des jeweiligen Polungsvorgangs ab. Hier wurde versucht, eine homogene Polung von P(VDF-TrFE)-Copolymeren mit unterschiedlichen VDF-Gehalten mit dem Verfahren der zyklischen Polung (sogenannte Hysterese-Polung) zu erzeugen. Das Entstehen der remanenten Polarisation und deren raeumliche Verteilung konnten erfasst und interpretiert werden, um Hinweise für eine optimale Polung zu erhalten. An den genannten Beispielen konnte gezeigt werden, dass die Methode der piezoelektrisch erzeugten Druckstufen (PPS) ein leistungsfaehiges Verfahren zur Charakterisierung der Ladungsspeicherung und des Ladungstransports in Dielektrika ist und dass damit ein breites Spektrum von unpolaren Polymeren ueber polare Polymerdielektrika bis hin zu polaren Nanokompositen sinnvoll untersucht werden kann. Es wurden wesentliche Erkenntnisse zur Ladungsspeicherung und zur remanten Polarisation in den untersuchten Polymeren gewonnen. KW - electro-acoustic electric-charge and polarization profiling KW - space charge KW - polypropylene KW - polyethylene nanocomposites KW - magnesium oxide KW - polymer electrets KW - ferroelectrets KW - electrical insulation KW - piezoelectricity KW - ferroelectricity KW - poly(vinylidene fluoride) KW - hysteresis KW - elektroakustische Abtastung elektrischer Ladungen und Dipolpolarisationen KW - elektrische Raumladung KW - Polypropylen KW - Polyethylen-Nanokomposite KW - Magnesiumoxid KW - Polymerelektrete KW - Ferroelektrete KW - elektrische Isolierung KW - Piezoelektrizität KW - Ferroelektrizität KW - Poly(vinylidenfluorid) KW - Hysterese Y1 - 2019 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-445629 ER - TY - JOUR A1 - Feulner, Philine G. D. A1 - Plath, Martin A1 - Engelmann, Jacob A1 - Kirschbaum, Frank A1 - Tiedemann, Ralph T1 - Electrifying love : electric fish use species-specific discharge for mate recognition N2 - Mate choice is mediated by a range of sensory cues, and assortative mating based on these cues can drive reproductive isolation among diverging populations. A specific feature of mormyrid fish, the electric organ discharge (EOD), is used for electrolocation and intraspecific communication. We hypothesized that the EOD also facilitates assortative mating and ultimately promotes prezygotic reproductive isolation in African weakly electric fishes. Our behavioural experiments using live males as well as EOD playback demonstrated that female mate recognition is influenced by EOD signals and that females are attracted to EOD characteristics of conspecific males. The dual function of the EOD for both foraging and social communication (including mate recognition leading to assortative mating) underlines the importance of electric signal differentiation for the divergence of African weakly electric fishes. Thus, the EOD provides an intriguing mechanism promoting trophic divergence and reproductive isolation between two closely related Campylomormyrus species occurring in sympatry in the lower Congo rapids. Y1 - 2009 UR - http://www.journals.royalsoc.ac.uk/link.asp?id=110824 U6 - https://doi.org/10.1098/rsbl.2008.0566 SN - 1744-9561 ER - TY - JOUR A1 - Döring, Sebastian A1 - Kollosche, Matthias A1 - Rabe, Torsten A1 - Stumpe, Joachim A1 - Kofod, Guggi T1 - Electrically tunable polymer DFB laser JF - Advanced materials Y1 - 2011 U6 - https://doi.org/10.1002/adma.201102465 SN - 0935-9648 VL - 23 IS - 37 SP - 4265 EP - 4269 PB - Wiley-VCH CY - Weinheim ER - TY - JOUR A1 - Badalyan, Artavazd A1 - Dierich, Marlen A1 - Stiba, Konstanze A1 - Schwuchow, Viola A1 - Leimkühler, Silke A1 - Wollenberger, Ulla T1 - Electrical wiring of the aldehyde oxidoreductase PaoABC with a polymer containing osmium redox centers BT - biosensors for benzaldehyde and GABA JF - Biosensors N2 - Biosensors for the detection of benzaldehyde and g-aminobutyric acid (GABA) are reported using aldehyde oxidoreductase PaoABC from Escherichia coli immobilized in a polymer containing bound low potential osmium redox complexes. The electrically connected enzyme already electrooxidizes benzaldehyde at potentials below −0.15 V (vs. Ag|AgCl, 1 M KCl). The pH-dependence of benzaldehyde oxidation can be strongly influenced by the ionic strength. The effect is similar with the soluble osmium redox complex and therefore indicates a clear electrostatic effect on the bioelectrocatalytic efficiency of PaoABC in the osmium containing redox polymer. At lower ionic strength, the pH-optimum is high and can be switched to low pH-values at high ionic strength. This offers biosensing at high and low pH-values. A “reagentless” biosensor has been formed with enzyme wired onto a screen-printed electrode in a flow cell device. The response time to addition of benzaldehyde is 30 s, and the measuring range is between 10–150 µM and the detection limit of 5 µM (signal to noise ratio 3:1) of benzaldehyde. The relative standard deviation in a series (n = 13) for 200 µM benzaldehyde is 1.9%. For the biosensor, a response to succinic semialdehyde was also identified. Based on this response and the ability to work at high pH a biosensor for GABA is proposed by coimmobilizing GABA-aminotransferase (GABA-T) and PaoABC in the osmium containing redox polymer. KW - redox polymer KW - aldehyde oxidoreductase KW - ionic strength KW - benzaldehyde KW - GABA KW - biosensor Y1 - 2014 U6 - https://doi.org/10.3390/bios4040403 VL - 4 IS - 4 SP - 403 EP - 421 PB - MDPI CY - Basel ER - TY - GEN A1 - Badalyan, Artavazd A1 - Dierich, Marlen A1 - Stiba, Konstanze A1 - Schwuchow, Viola A1 - Leimkühler, Silke A1 - Wollenberger, Ulla T1 - Electrical wiring of the aldehyde oxidoreductase PaoABC with a polymer containing osmium redox centers BT - biosensors for benzaldehyde and GABA T2 - Postprints der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe N2 - Biosensors for the detection of benzaldehyde and g-aminobutyric acid (GABA) are reported using aldehyde oxidoreductase PaoABC from Escherichia coli immobilized in a polymer containing bound low potential osmium redox complexes. The electrically connected enzyme already electrooxidizes benzaldehyde at potentials below −0.15 V (vs. Ag|AgCl, 1 M KCl). The pH-dependence of benzaldehyde oxidation can be strongly influenced by the ionic strength. The effect is similar with the soluble osmium redox complex and therefore indicates a clear electrostatic effect on the bioelectrocatalytic efficiency of PaoABC in the osmium containing redox polymer. At lower ionic strength, the pH-optimum is high and can be switched to low pH-values at high ionic strength. This offers biosensing at high and low pH-values. A “reagentless” biosensor has been formed with enzyme wired onto a screen-printed electrode in a flow cell device. The response time to addition of benzaldehyde is 30 s, and the measuring range is between 10–150 µM and the detection limit of 5 µM (signal to noise ratio 3:1) of benzaldehyde. The relative standard deviation in a series (n = 13) for 200 µM benzaldehyde is 1.9%. For the biosensor, a response to succinic semialdehyde was also identified. Based on this response and the ability to work at high pH a biosensor for GABA is proposed by coimmobilizing GABA-aminotransferase (GABA-T) and PaoABC in the osmium containing redox polymer. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 1082 KW - redox polymer KW - aldehyde oxidoreductase KW - ionic strength KW - benzaldehyde KW - GABA KW - biosensor Y1 - 2021 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-475070 SN - 1866-8372 IS - 1082 ER - TY - JOUR A1 - Raman Venkatesan, Thulasinath A1 - Gulyakova, Anna A. A1 - Frübing, Peter A1 - Gerhard, Reimund T1 - Electrical polarization phenomena, dielectric relaxations and structural transitions in a relaxor-ferroelectric terpolymer investigated with electrical probing techniques JF - Materials research express N2 - Dielectric Relaxation Spectroscopy (DRS) and Thermally Stimulated Depolarization Current (TSDC) measurements were employed to study dielectric-relaxation processes, structural transitions and electric-polarization phenomena in poly(vinylidenefluoride-trifluoroethylene-chlorofluoroethylene) (P(VDF-TrFE-CFE)) terpolymer films. Results from DRS confirm the existence of two separate dispersion regions related to a para-to-ferroelectric phase transition and to the glass transition. The dipolar TSDC peak correlates with the loss peak of the ? relaxation that represents the glass transition. The electric polarization calculated from the dipolar TSDC peak (glass transition) shows a non-linear electric-field dependence and saturates at high electric poling fields. As the observed behaviour is essentially the same as that of the electric polarization obtained from direct polarization-versus-electric-field hysteresis measurements, TSDC experiments are also suitable for studying the polarization in relaxor-ferroelectric polymers. A saturation polarization of 44 mC m(?2) was found for an electric field of 190 MV m(?1). KW - P(VDF-TrFE-CFE) terpolymer KW - relaxor-ferroelectric polymers KW - dielectric relaxation spectroscopy KW - thermally stimulated depolarization current KW - electrical polarization hysteresis Y1 - 2019 U6 - https://doi.org/10.1088/2053-1591/ab5352 SN - 2053-1591 VL - 6 IS - 12 PB - IOP Publ. Ltd. CY - Bristol ER - TY - JOUR A1 - Poghossian, A. A1 - Weil, M. A1 - Cherstvy, Andrey G. A1 - Schöning, M. J. T1 - Electrical monitoring of polyelectrolyte multilayer formation by means of capacitive field-effect devices JF - Analytical & bioanalytical chemistry N2 - The semiconductor field-effect platform represents a powerful tool for detecting the adsorption and binding of charged macromolecules with direct electrical readout. In this work, a capacitive electrolyte-insulator-semiconductor (EIS) field-effect sensor consisting of an Al-p-Si-SiO2 structure has been applied for real-time in situ electrical monitoring of the layer-by-layer formation of polyelectrolyte (PE) multilayers (PEM). The PEMs were deposited directly onto the SiO2 surface without any precursor layer or drying procedures. Anionic poly(sodium 4-styrene sulfonate) and cationic weak polyelectrolyte poly(allylamine hydrochloride) have been chosen as a model system. The effect of the ionic strength of the solution, polyelectrolyte concentration, number and polarity of the PE layers on the characteristics of the PEM-modified EIS sensors have been studied by means of capacitance-voltage and constant-capacitance methods. In addition, the thickness, surface morphology, roughness and wettabilityof the PE mono- and multilayers have been characterised by ellipsometry, atomic force microscopy and water contact-angle methods, respectively. To explain potential oscillations on the gate surface and signal behaviour of the capacitive field-effect EIS sensor modified with a PEM, a simplified electrostatic model that takes into account the reduced electrostatic screening of PE charges by mobile ions within the PEM has been proposed and discussed. KW - Field-effect KW - Capacitive sensor KW - Polyelectrolyte multilayer KW - Electrical monitoring KW - ConCap Y1 - 2013 U6 - https://doi.org/10.1007/s00216-013-6951-9 SN - 1618-2642 VL - 405 IS - 20 SP - 6425 EP - 6436 PB - Springer CY - Heidelberg ER - TY - JOUR A1 - Bauer-Gogonea, Simona A1 - Wirges, Werner A1 - Bauer, Siegfried A1 - Gerhard, Reimund A1 - Liang, J. A1 - Zyss, Joseph T1 - Electrical determination of the degree of cross-linking in a poled nonlinear optical polymer Y1 - 1996 ER - TY - JOUR A1 - Liperovsky, Viktor A. A1 - Meister, Claudia-Veronika A1 - Haldoupis, Ch. A1 - Schlegel, K. T1 - Electrical currents and Farley-Buneman turbulence in mid-latitude sporadic E-layers Y1 - 1994 ER -