Dieter Schmeißer
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Dieter Schmeißer has a total of 32 co-authors. Here are the top co-authors by number of shared publications:
- Karsten Henkel
Applied Physics and Semiconductor Spectroscopy Brandenburg University of Technology Cottbus-Senftenberg Konrad-Zuse-Strasse 1 03046 Cottbus Germany
3 shared publications - F. J. Himpsel
Department of Physics University of Wisconsin Madison 1150 University Ave. 53706 Madison WI USA
2 shared publications F. Zheng
University of Wisconsin-Madison, Department of Physics, B408 Sterling Hall, 1150 University Avenue, Madison, WI 53706-1390, USA
2 shared publications- Hans-Juergen Engelmann
AMD Saxony LLC & Co. KG, Wilschdorfer Landstrasse 101, Dresden, Saxony, D-01109, Germany
2 shared publications - Massimo Tallarida
ALBA Synchrotron Light Source
2 shared publications - Carola Schwiertz
BTU Cottbus, Angewandte Physik-Sensorik, K.-Wachsmann-Allee 17, Cottbus, 03046, Germany
1 shared publication
Latest Publications
- 27 February 2014
- Published by Royal Society of Chemistry (RSC) in Physical Chemistry Chemical Physics
- Vol. 16 (22) , 10403-10407
Improved performance of a polymer nanogenerator based on silver nanoparticles doped electrospun P(VDF–HFP) nanofibers
We report on the electrospinning of poly(vinylidene fluoride–hexafluoropropylene) [P(VDF–HFP)] nanofibers doped with silver nanoparticles for the preparation of a polymer based nanogenerator (PNG). It has been found that the yield of the piezoelectric phase is increased by the addition of silver nanoparticles. Furthermore, defects in the P(VDF–HFP) electrospun fibers are removed resulting in a significant enhancement in the output power of the PNG. A maximum generated PNG output voltage of 3 V with a current density of 0.9 μA cm−2 is achieved.
- 27 February 2014
- Published by Royal Society of Chemistry (RSC) in Physical Chemistry Chemical Physics
- Vol. 16 (22) , 10403-10407
Improved performance of a polymer nanogenerator based on silver nanoparticles doped electrospun P(VDF–HFP) nanofibers
We report on the electrospinning of poly(vinylidene fluoride–hexafluoropropylene) [P(VDF–HFP)] nanofibers doped with silver nanoparticles for the preparation of a polymer based nanogenerator (PNG). It has been found that the yield of the piezoelectric phase is increased by the addition of silver nanoparticles. Furthermore, defects in the P(VDF–HFP) electrospun fibers are removed resulting in a significant enhancement in the output power of the PNG. A maximum generated PNG output voltage of 3 V with a current density of 0.9 μA cm−2 is achieved.
- 23 October 2013
- Published by Springer Nature in Environmental Earth Sciences
- Vol. 70 (8) , 3785-3795
Linear dichroism in ALD layers of TiO2
- 23 October 2013
- Published by Springer Nature in Environmental Earth Sciences
- Vol. 70 (8) , 3785-3795
Linear dichroism in ALD layers of TiO2
- 8 April 2009
- Published by Wiley in Advanced Engineering Materials
- Vol. 11 (4) , 269-274
Interface Reactions in Ultrathin Functional Dielectric Films
- 8 April 2009
- Published by Wiley in Advanced Engineering Materials
- Vol. 11 (4) , 269-274
Interface Reactions in Ultrathin Functional Dielectric Films
- 1 January 2007
- Published by Springer Nature in MRS Proceedings
- Vol. 997
No Interfacial Layer for PEDOT Electrodes on PVDF: Characterization of Reactions at the Interface P(VDF/TrFE)/Al and P(VDF/TrFE)/PEDOT:PSS
With photoelectron spectroscopy, we study the interface chemistry of the copolymer poly(vinylidene fluoride trifluoroethylene) (P(VDF-TrFE)) and different electrode materials. We compare the interfaces aluminum/P(VDF-TrFE) and PEDOT:PSS/P(VDF-TrFE). PEDOT:PSS is a conductive polymer (Poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate)). The data sug-gest that we have an interface layer for electrodes, made of aluminum. An interface reaction occurs in both cases: for aluminum as top and as bottom electrode. In contrast, the organic PE-DOT:PSS electrode shows no chemical interaction with the P(VDF-TrFE) polymer. The much lower reactivity of organic electrodes, compared to aluminum, gives a direct hint to im-proved functional properties of thin organic ferroelectric films.
- 1 January 2007
- Published by Springer Nature in MRS Proceedings
- Vol. 997
No Interfacial Layer for PEDOT Electrodes on PVDF: Characterization of Reactions at the Interface P(VDF/TrFE)/Al and P(VDF/TrFE)/PEDOT:PSS
With photoelectron spectroscopy, we study the interface chemistry of the copolymer poly(vinylidene fluoride trifluoroethylene) (P(VDF-TrFE)) and different electrode materials. We compare the interfaces aluminum/P(VDF-TrFE) and PEDOT:PSS/P(VDF-TrFE). PEDOT:PSS is a conductive polymer (Poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate)). The data sug-gest that we have an interface layer for electrodes, made of aluminum. An interface reaction occurs in both cases: for aluminum as top and as bottom electrode. In contrast, the organic PE-DOT:PSS electrode shows no chemical interaction with the P(VDF-TrFE) polymer. The much lower reactivity of organic electrodes, compared to aluminum, gives a direct hint to im-proved functional properties of thin organic ferroelectric films.
- 1 January 2007
- Published by Springer Nature in MRS Proceedings
- Vol. 996
Al-Oxynitride Buffer Layer Facilities for PrOX/SiC Interfaces
We investigate the dielectric properties of Praseodymium based oxides and silicates by preparing MIS structures consisting of a metal layer (M), PrOX (praseodymium oxide) as a high-k insulating layer (I), and silicon (Si) or silicon carbide (SiC) as semiconductor substrates (S).The use of a buffer layer between PrOX and SiC is necessary as we found destructive interactions like silicate and graphite formation between these materials. Based on a higher permittivity value than SiO2 and a good lattice matching in conjunction with nearly the same thermal expansion coefficient to SiC, we focus on aluminum oxynitride (AlON) as a suitable buffer layer for this high-k/wide-bandgap system. We report on results achieved by Synchrotron Radiation Photoemission Spectroscopy (SRPES) and by electrical measurements.In our spectroscopic investigations we found a stable AlON/3C-SiC interface as well as no elemental carbon and silicate contributions in the core levels after thin PrOX deposition and annealing up to 900°C.In electrical characterizations of PrOX/AlON stacks on silicon we already found a strong improvement in the leakage current down to values of 10-7 A/cm2 at an CET of 4nm. We observed an interface state density in the range of 5x1011-1x1012/eVcm2 and 1-5x1012/eVcm2 on Si and SiC, respectively.
- 1 January 2007
- Published by Springer Nature in MRS Proceedings
- Vol. 996
Al-Oxynitride Buffer Layer Facilities for PrOX/SiC Interfaces
We investigate the dielectric properties of Praseodymium based oxides and silicates by preparing MIS structures consisting of a metal layer (M), PrOX (praseodymium oxide) as a high-k insulating layer (I), and silicon (Si) or silicon carbide (SiC) as semiconductor substrates (S).The use of a buffer layer between PrOX and SiC is necessary as we found destructive interactions like silicate and graphite formation between these materials. Based on a higher permittivity value than SiO2 and a good lattice matching in conjunction with nearly the same thermal expansion coefficient to SiC, we focus on aluminum oxynitride (AlON) as a suitable buffer layer for this high-k/wide-bandgap system. We report on results achieved by Synchrotron Radiation Photoemission Spectroscopy (SRPES) and by electrical measurements.In our spectroscopic investigations we found a stable AlON/3C-SiC interface as well as no elemental carbon and silicate contributions in the core levels after thin PrOX deposition and annealing up to 900°C.In electrical characterizations of PrOX/AlON stacks on silicon we already found a strong improvement in the leakage current down to values of 10-7 A/cm2 at an CET of 4nm. We observed an interface state density in the range of 5x1011-1x1012/eVcm2 and 1-5x1012/eVcm2 on Si and SiC, respectively.
- 31 July 2006
- Published by Elsevier in Materials Science and Engineering: C
- Vol. 26 (5-7) , 1122-1126
Silicate formation at the interface of Pr-oxide as a high-K dielectric and Si(001) surfaces
- 31 July 2006
- Published by Elsevier in Materials Science and Engineering: C
- Vol. 26 (5-7) , 1122-1126
Silicate formation at the interface of Pr-oxide as a high-K dielectric and Si(001) surfaces
- 1 January 2006
- Published by Springer Nature in MRS Proceedings
- Vol. 914
Characterization of Chemical Bonding in Low-K Dielectric Materials for Interconnect Isolation: A XAS and EELS Study
The use of low dielectric constant materials in the on-chip interconnect process reduces interconnect delay, power dissipation and crosstalk noise. To achieve the requirements of the ITRS for 2007-2009 minimal sidewall damage from etch, ash or cleans is required. In chemical vapor deposited (CVD) organo-silicate glass (OSG) which are used as intermetal dielectric (IMD) materials the substitution of oxygen in SiO2 by methyl groups (-CH3) reduces the permit-tivity significantly (from 4.0 in SiO2 to 2.6-3.3 in the OSG), since the electronic polarizability is lower for Si-C bonds than for Si-O bonds.However, plasma processing for resist stripping, trench etching and post-etch cleaning removes C and H containing molecular groups from the near-surface layer of OSG. Therefore, compositional analysis and chemical bonding characterization of structured IMD films with nanometer resolution is necessary for process optimization.OSG thin films as-deposited and after plasma treatment are studied using X-ray absorp-tion spectroscopy (XAS) and electron energy loss spectroscopy (EELS). In both techniques, the fine structure near the C1s absorption or energy loss edge, respectively, allows to identify C-H, C-C, and C-O bonds. This gives the opportunity to differentiate between individual low-k mate-rials and their modifications. The O1s signal is less selective to individual bonds. XAS spectra have been recorded for non-patterned films and EELS spectra for patterned structures. The chemical bonding is compared for as-deposited and plasma-treated low-k materials. The Fluo-rescence Yield (FY) and the Total Electron Yield (TEY) recorded while XAS measurement are compared. Examination of the C 1s near-edge structures reveal a modified bonding of the re-maining C atoms in the plasma-treated sample regions.
- 1 January 2006
- Published by Springer Nature in MRS Proceedings
- Vol. 914
Characterization of Chemical Bonding in Low-K Dielectric Materials for Interconnect Isolation: A XAS and EELS Study
The use of low dielectric constant materials in the on-chip interconnect process reduces interconnect delay, power dissipation and crosstalk noise. To achieve the requirements of the ITRS for 2007-2009 minimal sidewall damage from etch, ash or cleans is required. In chemical vapor deposited (CVD) organo-silicate glass (OSG) which are used as intermetal dielectric (IMD) materials the substitution of oxygen in SiO2 by methyl groups (-CH3) reduces the permit-tivity significantly (from 4.0 in SiO2 to 2.6-3.3 in the OSG), since the electronic polarizability is lower for Si-C bonds than for Si-O bonds.However, plasma processing for resist stripping, trench etching and post-etch cleaning removes C and H containing molecular groups from the near-surface layer of OSG. Therefore, compositional analysis and chemical bonding characterization of structured IMD films with nanometer resolution is necessary for process optimization.OSG thin films as-deposited and after plasma treatment are studied using X-ray absorp-tion spectroscopy (XAS) and electron energy loss spectroscopy (EELS). In both techniques, the fine structure near the C1s absorption or energy loss edge, respectively, allows to identify C-H, C-C, and C-O bonds. This gives the opportunity to differentiate between individual low-k mate-rials and their modifications. The O1s signal is less selective to individual bonds. XAS spectra have been recorded for non-patterned films and EELS spectra for patterned structures. The chemical bonding is compared for as-deposited and plasma-treated low-k materials. The Fluo-rescence Yield (FY) and the Total Electron Yield (TEY) recorded while XAS measurement are compared. Examination of the C 1s near-edge structures reveal a modified bonding of the re-maining C atoms in the plasma-treated sample regions.
- 1 January 2006
- Published by Springer Nature in MRS Proceedings
- Vol. 917
Silicate Formation at the Interface of high-k dielectrics and Si(001) Surfaces
- 1 January 2006
- Published by Springer Nature in MRS Proceedings
- Vol. 917
Silicate Formation at the Interface of high-k dielectrics and Si(001) Surfaces
- 15 September 2003
- Published by Elsevier in Materials Science and Engineering: B
- Vol. 102 (1-3) , 284-288
Photoelectron spectra of Al dopants in 4H–SiC
- 15 September 2003
- Published by Elsevier in Materials Science and Engineering: B
- Vol. 102 (1-3) , 284-288
Photoelectron spectra of Al dopants in 4H–SiC
- 1 June 2003
- Published by Elsevier in Synthetic Metals
- Vol. 138 (1-2) , 135-140
Valence states of poly(3-hexyl-thiophene) as probed by photoelectron spectra at resonant excitation
- 1 June 2003
- Published by Elsevier in Synthetic Metals
- Vol. 138 (1-2) , 135-140
Valence states of poly(3-hexyl-thiophene) as probed by photoelectron spectra at resonant excitation