@article{AltafimAltafimQiuetal.2012, author = {Altafim, Ruy Alberto Pisani and Altafim, Ruy Alberto Pisani and Qiu, Xunlin and Raabe, Sebastian and Wirges, Werner and Basso, Heitor Cury and Gerhard, Reimund}, title = {Fluoropolymer piezoelectrets with tubular channels resonance behavior controlled by channel geometry}, series = {Applied physics : A, Materials science \& processing}, volume = {107}, journal = {Applied physics : A, Materials science \& processing}, number = {4}, publisher = {Springer}, address = {New York}, issn = {0947-8396}, doi = {10.1007/s00339-012-6848-z}, pages = {965 -- 970}, year = {2012}, abstract = {Ferro- or piezoelectrets are dielectric materials with two elastically very different macroscopic phases and electrically charged interfaces between them. One of the newer piezoelectret variants is a system of two fluoroethylenepropylene (FEP) films that are first laminated around a polytetrafluoroethylene (PTFE) template. Then, by removing the PTFE template, a two-layer FEP structure with open tubular channels is obtained. After electrical charging, the channels form easily deformable macroscopic electric dipoles whose changes under mechanical or electrical stress lead to significant direct or inverse piezoelectricity, respectively. Here, different PTFE templates are employed to generate channel geometries that vary in height or width. It is shown that the control of the channel geometry allows a direct adjustment of the resonance frequencies in the tubular-channel piezoelectrets. By combining several different channel widths in a single ferroelectret, it is possible to obtain multiple resonance peaks that may lead to a rather flat frequency-response region of the transducer material. A phenomenological relation between the resonance frequency and the geometrical parameters of a tubular channel is also presented. This relation may help to design piezoelectrets with a specific frequency response.}, language = {en} } @article{AltafimRychkovWirgesetal.2012, author = {Altafim, Ruy Alberto Pisani and Rychkov, Dmitry and Wirges, Werner and Gerhard, Reimund and Basso, Heitor Cury and Altafim, Ruy Alberto Pisani and Melzer, Martin}, title = {Laminated tubular-channel ferroelectret systems from low-density Polyethylene Films and from Fluoroethylene-propylene Copolymer Films - A comparison}, series = {IEEE transactions on dielectrics and electrical insulation}, volume = {19}, journal = {IEEE transactions on dielectrics and electrical insulation}, number = {4}, publisher = {Inst. of Electr. and Electronics Engineers}, address = {Piscataway}, issn = {1070-9878}, pages = {1116 -- 1123}, year = {2012}, abstract = {A template-based lamination technique for the manufacture of ferroelectrets from uniform electret films was recently reported. In the present work, this technique is used to prepare similar ferroelectret structures from low-density polyethylene (LDPE) films and from fluoro-ethylene-propylene (FEP) copolymer films. A comparative analysis of the pressure-, temperature-, and frequency-dependent piezoelectric properties has been performed on the two ferroelectret systems. It is observed that the FEP ferroelectrets exhibit better piezoelectric responses and are thermally more stable. The difference between the piezoelectric d(33) coefficients of the two ferroelectret systems is partially explained here by their different elastic moduli. The anti-resonance peaks of both structures have been investigated by means of dielectric resonance spectroscopy and electroacoustic sound-pressure measurements. A difference of more than 10 kHz is observed between the anti-resonance frequencies of the two ferroelectret systems.}, language = {en} } @article{FangHollaenderWirgesetal.2012, author = {Fang, Peng and Hollaender, Lars and Wirges, Werner and Gerhard, Reimund}, title = {Piezoelectric d(33) coefficients in foamed and layered polymer piezoelectrets from dynamic mechano-electrical experiments, electro-mechanical resonance spectroscopy and acoustic-transducer measurements}, series = {Measurement science and technology}, volume = {23}, journal = {Measurement science and technology}, number = {3}, publisher = {IOP Publ. Ltd.}, address = {Bristol}, issn = {0957-0233}, doi = {10.1088/0957-0233/23/3/035604}, pages = {9}, year = {2012}, abstract = {Piezoelectrets are novel transducer materials which can be widely applied in sensors and actuators. Here, three techniques for determining piezoelectric d(33) coefficients of piezoelectrets are reviewed and compared. Two types of piezoelectrets, polyethylene-naphthalate (PEN) polymer-foam piezoelectrets and fluorinated ethylene-propylene (FEP) copolymer-layer piezoelectrets, have been prepared and measured by means of dynamic, resonance, and acoustical methods. The dynamic measurements show that the d(33) coefficient of PEN-foam samples clearly decreases with increasing stress, but 80\% of the initial d(33) can be retained after 1800 cycles of a continuous dynamic measurement in a mechanical fatigue test. The resonance measurements demonstrate that both PEN-foam and FEP-layer samples exhibit clear electro-mechanical resonances. PEN-foam samples show elastic moduli in the range from 1 to 12 MPa and d(33) values up to 500 pC N-1, while FEP-layer samples show homogeneous elastic moduli of about 0.3 MPa and d(33) values of about 280 pC N-1. The acoustical measurements reveal that both PEN-foam and FEP-layer samples exhibit stable frequency responses in the range from 5.7 to 20 kHz. In addition, d(33) coefficients obtained with different experimental methods are in good agreement with each other, which confirms the reliability of all three techniques.}, language = {en} } @article{KalbitzGerhardTaylor2012, author = {Kalbitz, Rene and Gerhard, Reimund and Taylor, D. M.}, title = {Fixed negative interface charges compromise organic ferroelectric field-effect transistors}, series = {Organic electronics : physics, materials and applications}, volume = {13}, journal = {Organic electronics : physics, materials and applications}, number = {5}, publisher = {Elsevier}, address = {Amsterdam}, issn = {1566-1199}, doi = {10.1016/j.orgel.2012.01.034}, pages = {875 -- 884}, year = {2012}, abstract = {Capacitance-voltage (C-V) and current-voltage measurements have been undertaken on metal-ferroelectric-semiconductor capacitors and ferroelectric field-effect transistors (FeFETs) using the ferroelectric polymer poly(vinylidenefluoride-trifluoroethylene) as the gate insulator and poly(3-hexylthiophene) as the active semiconductor. C-V measurements, voltage-dependence of gate currents and FeFET transfer characteristics all confirm that ferroelectric polarization is stable and only reverses when positive/negative coercive fields are exceeded for the first time. The apparent instability observed following the application of depletion voltages arises from the development of a negative interfacial charge which more than compensates the ferroelectric-induced shift, resulting in a permanent shift in threshold voltage to positive values. Application of successive bipolar voltage sweeps to a diode-connected FeFET show that significant remanent polarization is only induced in an unpoled device when the coercive field is exceeded during the first application of accumulation voltages. This initial polarization and its growth during subsequent bipolar voltage sweeps is accompanied by the accumulation of the fixed interfacial negative charges which cause the positive turn on voltages seen in C-V and transfer characteristics. The origin of the negative charge is ascribed either to layers of irreversible ferroelectric domains at the insulator surface or to the drift to the insulator-semiconductor interface of F-ions produced electrolytically during the application of accumulation voltages.}, language = {en} } @article{KollscheKalbitzKappeletal.2012, author = {Kollsche, Matthias and Kalbitz, Rene and Kappel, Marcel and Fr{\"u}bing, Peter and Gerhard, Reimund}, title = {Vermittlung von Schl{\"u}sselkompetenzen f{\"u}r Biologen in der Studieneingangsphase}, isbn = {978-3- 937026-77-0}, year = {2012}, language = {de} } @article{RychkovAltafimQiuetal.2012, author = {Rychkov, Dmitry and Altafim, Ruy Alberto Pisani and Qiu, Xunlin and Gerhard, Reimund}, title = {Treatment with orthophosphoric acid enhances the thermal stability of the piezoelectricity in low-density polyethylene ferroelectrets}, series = {Journal of applied physics}, volume = {111}, journal = {Journal of applied physics}, number = {12}, publisher = {American Institute of Physics}, address = {Melville}, issn = {0021-8979}, doi = {10.1063/1.4729866}, pages = {5}, year = {2012}, abstract = {Ferroelectrets have been fabricated from low-density polyethylene (LDPE) films by means of a template-based lamination. The temperature dependence of the piezoelectric d(33) coefficient has been investigated. It was found that low-density polyethylene ferroelectrets have rather low thermal stability with the piezoelectric coefficient decaying almost to zero already at 100 degrees C. This behavior is attributed to the poor electret properties of the polyethylene films used for the fabrication of the ferroelectrets. In order to improve the charge trapping and the thermal stability of electret charge and piezoelectricity, LDPE ferroelectrets were treated with orthophosphoric acid. The treatment resulted in considerable improvements of the charge stability in LDPE films and in ferroelectret systems made from them. For example, the charge and piezoelectric-coefficient decay curves shifted to higher temperatures by 60 K and 40 K, respectively. It is shown that the decay of the piezoelectric coefficient in LDPE ferroelectrets is governed by the relaxation of less stable positive charges. The treatment also leads to noticeable changes in the chemical composition of the LDPE surface. Infrared spectroscopy reveals absorption bands attributed to phosphorus-containing structures, while scanning electron microscopy shows new island-like structures, 50-200 nm in diameter, on the modified surface.}, language = {en} } @article{RychkovGerhardIvanovetal.2012, author = {Rychkov, Dmitry and Gerhard, Reimund and Ivanov, Vadim and Rychkov, Andrey}, title = {Enhanced electret charge stability on Polyethylene Films treated with Titanium-Tetrachloride vapor}, series = {IEEE transactions on dielectrics and electrical insulation}, volume = {19}, journal = {IEEE transactions on dielectrics and electrical insulation}, number = {4}, publisher = {Inst. of Electr. and Electronics Engineers}, address = {Piscataway}, issn = {1070-9878}, pages = {1305 -- 1311}, year = {2012}, abstract = {Low-density polyethylene (LDPE) films have been treated with titanium-tetrachloride vapor by means of the molecular-layer-deposition method. It is shown that such a treatment leads to a considerable improvement of the electret properties for both positively and negatively charged films. The temperature stability of the electret homo-charge has been increased by approximately 60 degrees C. At the same time, the temporal stability of charge is also considerably improved. Modified low-density polyethylene films show no "cross-over phenomenon" when charged to higher voltages. Thus, it is now possible to produce electrets from polyethylene films with high initial charge densities, but without a strongly reduced charge stability. The influence of a chemical treatment with titanium-tetrachloride vapor on charge injection from aluminum electrodes into polyethylene films was also investigated. It is found that the interface between an aluminum electrode and a modified LDPE surface layer has different injection properties for positive and negative charges. Electrons can be injected across the modified interface, whereas injection of holes is either very limited or non-existent.}, language = {en} } @article{WangLackXieetal.2012, author = {Wang, Feipeng and Lack, Alexander and Xie, Zailai and Fr{\"u}bing, Peter and Taubert, Andreas and Gerhard, Reimund}, title = {Ionic-liquid-induced ferroelectric polarization in poly(vinylidene fluoride) thin films}, series = {Applied physics letters}, volume = {100}, journal = {Applied physics letters}, number = {6}, publisher = {American Institute of Physics}, address = {Melville}, issn = {0003-6951}, doi = {10.1063/1.3683526}, pages = {4}, year = {2012}, abstract = {Thin films of ferroelectric beta-phase poly(vinylidene fluoride) (PVDF) were spin-coated from a solution that contained small amounts of the ionic liquid (IL) 1-ethyl-3-methylimidazolium nitrate. A remanent polarization of 60 mC/m(2) and a quasi-static pyroelectric coefficient of 19 mu C/m(2)K at 30 degrees C were observed in the films. It is suggested that the IL promotes the formation of the beta phase through dipolar interactions between PVDF chain-molecules and the IL. The dipolar interactions are identified as Coulomb attraction between hydrogen atoms in PVDF chains and anions in IL. The strong crystallinity increase is probably caused by the same dipolar interaction as well.}, language = {en} } @article{WertheimerStGeorgesRobillardLerougeetal.2012, author = {Wertheimer, Michael R. and St-Georges-Robillard, Amelie and Lerouge, Sophie and Mwale, Fackson and Elkin, Bentsian and Oehr, Christian and Wirges, Werner and Gerhard, Reimund}, title = {Amine-rich organic thin films for cell culture - possible electrostatic effects in cell-surface interactions}, series = {Japanese journal of applied physics}, volume = {51}, journal = {Japanese journal of applied physics}, number = {11}, publisher = {Japan Soc. of Applied Physics}, address = {Tokyo}, issn = {0021-4922}, doi = {10.1143/JJAP.51.11PJ04}, pages = {5}, year = {2012}, abstract = {In recent communications from these laboratories, we observed that amine-rich thin organic layers are very efficient surfaces for the adhesion of mammalian cells. We prepare such deposits by plasma polymerization at low pressure, atmospheric pressure, or by vacuum-ultraviolet photo-polymerization. More recently, we have also investigated a commercially available material, Parylene diX AM. In this article we first briefly introduce literature relating to electrostatic interactions between cells, proteins, and charged surfaces. We then present certain selected cell-response results that pertain to applications in orthopedic and cardiovascular medicine: we discuss the influence of surface properties on the observed behaviors of two particular cell lines, human U937 monocytes, and Chinese hamster ovary cells. Particular emphasis is placed on possible electrostatic attractive forces due to positively charged R-NH3+ groups and negatively charged proteins and cells, respectively. Experiments carried out with electrets, polymers with high positive or negative surface potentials are added for comparison.}, language = {en} }