TY - JOUR A1 - Altafim, Ruy Alberto Pisani A1 - Altafim, Ruy Alberto Pisani A1 - Qiu, Xunlin A1 - Raabe, Sebastian A1 - Wirges, Werner A1 - Basso, Heitor Cury A1 - Gerhard, Reimund T1 - Fluoropolymer piezoelectrets with tubular channels resonance behavior controlled by channel geometry JF - Applied physics : A, Materials science & processing N2 - 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. Y1 - 2012 U6 - https://doi.org/10.1007/s00339-012-6848-z SN - 0947-8396 VL - 107 IS - 4 SP - 965 EP - 970 PB - Springer CY - New York ER - TY - JOUR A1 - Altafim, Ruy Alberto Pisani A1 - Qiu, Xunlin A1 - Wirges, Werner A1 - Gerhard, Reimund A1 - Altafim, Ruy Alberto Pisani A1 - Basso, Heitor Cury A1 - Jenninger, Werner A1 - Wagner, Joachim T1 - Template-based fluoroethylenepropylene piezoelectrets with tubular channels for transducer applications N2 - We describe the concept, the fabrication, and the most relevant properties of a piezoelectric-polymer system: Two fluoroethylenepropylene (FEP) films with good electret properties are laminated around a specifically designed and prepared polytetrafluoroethylene (PTFE) template at 300 degrees C. After removing the PTFE template, a two-layer FEP film with open tubular channels is obtained. For electric charging, the two-layer FEP system is subjected to a high electric field. The resulting dielectric barrier discharges inside the tubular channels yield a ferroelectret with high piezoelectricity. d(33) coefficients of up to 160 pC/N have already been achieved on the ferroelectret films. After charging at suitable elevated temperatures, the piezoelectricity is stable at temperatures of at least 130 degrees C. Advantages of the transducer films include ease of fabrication at laboratory or industrial scales, a wide range of possible geometrical and processing parameters, straightforward control of the uniformity of the polymer system, flexibility, and versatility of the soft ferroelectrets, and a large potential for device applications e.g., in the areas of biomedicine, communications, production engineering, sensor systems, environmental monitoring, etc. Y1 - 2009 UR - http://jap.aip.org/ U6 - https://doi.org/10.1063/1.3159039 SN - 0021-8979 ER - TY - JOUR A1 - Basso, Heitor Cury A1 - Qiu, Xunlin A1 - Wirges, Werner A1 - Gerhard, Reimund T1 - Temporal evolution of the re-breakdown voltage in small gaps from nanoseconds to milliseconds JF - Applied physics letters N2 - A detailed understanding of electric breakdown in dielectrics is of scientific and technological interest. In gaseous dielectrics, a so-called re-breakdown is sometimes observed after extinction of the previous discharge. Although time-dependent re-breakdown voltage is essentially known, its behavior immediately after the previous discharge is not precisely understood. We present an electronic circuit for accurate measurements of the time-dependent re-breakdown voltage in small gaps from tens of nanoseconds to several milliseconds after the previous spark. Results from such experiments are compared with earlier findings, and relevant physical mechanisms such as heating of the gas, decay of the plasma, and ionization of excited atoms and molecules are discussed. It is confirmed that the thermal model is not valid at times below several microseconds. Y1 - 2013 U6 - https://doi.org/10.1063/1.4773518 SN - 0003-6951 VL - 102 IS - 1 PB - American Institute of Physics CY - Melville ER - TY - JOUR A1 - Fang, Peng A1 - Ma, Xingchen A1 - Li, Xiangxin A1 - Qiu, Xunlin A1 - Gerhard, Reimund A1 - Zhang, Xiaoqing A1 - Li, Guanglin T1 - Fabrication, Structure Characterization, and Performance Testing of Piezoelectret-Film Sensors for Recording Body Motion JF - IEEE Sensors Journal N2 - During muscle contractions, radial-force distributions are generated on muscle surfaces due to muscle-volume changes, from which the corresponding body motions can be recorded by means of so-called force myography (FMG). Piezo- or ferroelectrets are flexible piezoelectric materials with attractive materials and sensing properties. In addition to several other applications, they are suitable for detecting force variations by means of wearable devices. In this paper, we prepared piezoelectrets from cellular polypropylene films by optimizing the fabrication procedures, and developed an FMG-recording system based on piezoelectret sensors. Different hand and wrist movements were successfully detected on able-bodied subjects with the FMG system. The FMG patterns were evaluated and identified by means of linear discriminant analysis and artificial neural network algorithms, and average motion-classification accuracies of 96.1% and 94.8%, respectively, were obtained. This paper demonstrates the feasibility of using piezoelectret-film sensors for FMG and may thus lead to alternative methods for detecting body motion and to related applications, e.g., in biomedical engineering or structural-health monitoring. KW - Forcemyography KW - motion registration KW - piezoelectret KW - film sensor KW - wearable Y1 - 2017 U6 - https://doi.org/10.1109/JSEN.2017.2766663 SN - 1530-437X SN - 1558-1748 VL - 18 IS - 1 SP - 401 EP - 412 PB - Inst. of Electr. and Electronics Engineers CY - Piscataway ER - TY - JOUR A1 - Fang, Peng A1 - Qiu, Xunlin A1 - Wirges, Werner A1 - Gerhard, Reimund A1 - Zirkel, Larissa T1 - Polyethylene-naphthalate (PEN) ferroelectrets : cellular structure, piezoelectricity and thermal stability N2 - Cellular polyethylene-naphthalate (PEN) ferroelectrets are useful as soft and flexible electromechanical transducer materials. Improved cellular PEN foams are prepared by means of a "voiding + inflation + stretching" process and investigated with respect to their structure and their applications-relevant properties. It is found that most of the cellular voids have heights below 8 mu m. The polymer walls do not allow sufficient gas exchange between the voids and the ambient atmosphere, when the cellular films are exposed to atmospheric pressures between a millibar and a few bars. As expected for ferroelectrets, a threshold voltage for charging is observed: A reasonable piezoelectric coefficient d(33) is only found when the charging voltage is higher than 4 kV. Furthermore, d(33) increases with charging voltage and reaches saturation at approximately 8 kV. Annealing after charging or charging at elevated temperatures may enhance the thermal stability of the PEN ferroelectrets. The d(33) of properly annealed samples is stable up to the respective annealing temperatures, but the annealing process reduces the piezoelectric activity of charged ferroelectret films to some extent. Samples charged at suitable elevated temperatures show much better thermal stability than those charged at room temperature, but the charging temperature should be limited to values below the material's glass-transition temperature T-g. Furthermore, the relevant elastic modulus c(33) of PEN ferroelectrets may decrease upon thermal treatment. Y1 - 2010 UR - http://ieeexplore.ieee.org/servlet/opac?punumber=94 U6 - https://doi.org/10.1109/TDEI.2010.5539678 SN - 1070-9878 ER - TY - JOUR A1 - Li, Changsheng A1 - Chen, Gangjin A1 - Qiu, Xunlin A1 - Gao, Meng A1 - Gerhard, Reimund T1 - Modified polytetrafluoroethylene BT - towards easy-to-process space-charge electret materials JF - Applied physics express : APEX N2 - Three poly(tetrafluoroethylene-hexafluoropropylene-vinylidenefluoride) (TFE-HFP-VDF or THV) terpolymers (Dyneon (R)) with different monomer ratios are investigated to demonstrate the concept of "modified" PTFE for space-charge electrets. HFP and VDF monomers distort the highly ordered PTFE molecules, which effectively enhances processability and adversely affects space-charge storage. Particularly, VDF component renders the material polar and probably also more conductive, partially undermining the space-charge-storage capabilities of PTFE. Nevertheless, the terpolymer THV815 with a TFE/HFP/VDF wt% ratio of 76.1/10.9/13 combines easy processability and relatively good space-charge stability. Our results shed light on novel concepts for space-charge electret materials with enhanced processing properties and reasonable charge-storage capabilities. Y1 - 2019 U6 - https://doi.org/10.7567/1882-0786/ab5b23 SN - 1882-0778 SN - 1882-0786 VL - 13 IS - 1 PB - IOP Publ. Ltd. CY - Bristol ER - TY - JOUR A1 - Men, Yongiun A1 - Siebenbürger, Miriam A1 - Qiu, Xunlin A1 - Antonietti, Markus A1 - Yuan, Jiayin T1 - Low fractions of ionic liquid or poly(ionic liquid) can activate polysaccaride biomass into shaped, flexible and fire-retardant porous carbons N2 - Sugar-based molecules and polysaccharide biomass can be turned into porous functional carbonaceous products at comparably low temperatures of 400 °C under a nitrogen atmosphere in the presence of an ionic liquid (IL) or a poly(ionic liquid) (PIL). The IL and PIL act as "activation agents" with own structural contribution, and effectively promote the conversion and pore generation in the biomaterials even at a rather low doping ratio (7 wt%). In addition, this "induced carbonization" and pore forming phenomenon enables the preservation of the biotemplate shape to the highest extent and was employed to fabricate shaped porous carbonaceous materials from carbohydrate-based biotemplates, exemplified here with cellulose filter membranes, coffee filter paper and natural cotton. These carbonized hybrids exhibit comparably good mechanical properties, such as bendability of membranes or shape recovery of foams. Moreover, the nitrogen atoms incorporated in the final products from the IL/PIL precursors further improve the oxidation stability in the fire-retardant tests. Y1 - 2013 UR - http://pubs.rsc.org/en/content/articlepdf/2013/ta/c3ta12302b U6 - https://doi.org/10.1039/c3ta12302b ER - TY - GEN A1 - Men, Yongjun A1 - Siebenbürger, Miriam A1 - Qiu, Xunlin A1 - Antonietti, Markus A1 - Yuan, Jiayin T1 - Low fractions of ionic liquid or poly(ionic liquid) can activate polysaccharide biomass into shaped, flexible and fire-retardant porous carbons N2 - Sugar-based molecules and polysaccharide biomass can be turned into porous functional carbonaceous products at comparably low temperatures of 400 °C under a nitrogen atmosphere in the presence of an ionic liquid (IL) or a poly(ionic liquid) (PIL). The IL and PIL act as “activation agents” with own structural contribution, and effectively promote the conversion and pore generation in the biomaterials even at a rather low doping ratio (7 wt%). In addition, this “induced carbonization” and pore forming phenomenon enables the preservation of the biotemplate shape to the highest extent and was employed to fabricate shaped porous carbonaceous materials from carbohydrate-based biotemplates, exemplified here with cellulose filter membranes, coffee filter paper and natural cotton. These carbonized hybrids exhibit comparably good mechanical properties, such as bendability of membranes or shape recovery of foams. Moreover, the nitrogen atoms incorporated in the final products from the IL/PIL precursors further improve the oxidation stability in the fire-retardant tests. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 248 Y1 - 2013 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-95250 SP - 11887 EP - 11887 ER - TY - JOUR A1 - Men, Yongjun A1 - Siebenbürger, Miriam A1 - Qiu, Xunlin A1 - Antonietti, Markus A1 - Yuan, Jiayin T1 - Low fractions of ionic liquid or poly(ionic liquid) can activate polysaccharide biomass into shaped, flexible and fire-retardant porous carbons JF - Journal of materials chemistry : A, Materials for energy and sustainability N2 - Sugar-based molecules and polysaccharide biomass can be turned into porous functional carbonaceous products at comparably low temperatures of 400 degrees C under a nitrogen atmosphere in the presence of an ionic liquid (IL) or a poly(ionic liquid) (PIL). The IL and PIL act as "activation agents" with own structural contribution, and effectively promote the conversion and pore generation in the biomaterials even at a rather low doping ratio (7 wt%). In addition, this "induced carbonization" and pore forming phenomenon enables the preservation of the biotemplate shape to the highest extent and was employed to fabricate shaped porous carbonaceous materials from carbohydrate-based biotemplates, exemplified here with cellulose filter membranes, coffee filter paper and natural cotton. These carbonized hybrids exhibit comparably good mechanical properties, such as bendability of membranes or shape recovery of foams. Moreover, the nitrogen atoms incorporated in the final products from the IL/PIL precursors further improve the oxidation stability in the fire-retardant tests. Y1 - 2013 U6 - https://doi.org/10.1039/c3ta12302b SN - 2050-7488 VL - 1 IS - 38 SP - 11887 EP - 11893 PB - Royal Society of Chemistry CY - Cambridge ER - TY - GEN A1 - Qiu, Xunlin T1 - Patterned piezo-, pyro-, and ferroelectricity of poled polymer electrets T2 - Journal of applied physics Y1 - 2011 U6 - https://doi.org/10.1063/1.3638069 SN - 0021-8979 VL - 110 IS - 5 PB - American Institute of Physics CY - Melville ER -