Przemysław Niemiec

Dr. Przemysław Niemiec

orcid

Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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22 August 2023 in Ceramics International
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Journal Article
Closed access
PNPrzemysław Niemiec
Przemysław Niemiec
DBDariusz Bochenek
Dariusz Bochenek
DBDagmara Brzezińska
Dagmara Brzezińska

1 May 2015 in Materials Chemistry and Physics
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Journal Article
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DBDariusz Bochenek
Dariusz Bochenek
PNPrzemysław Niemiec
Przemysław Niemiec
RSRyszard Skulski
Ryszard Skulski
ACArtur Chrobak
Artur Chrobak
Paweł WawrzałaPaweł Wawrzała
Paweł Wawrzała

16 November 2018 in Applied Physics A
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Journal Article
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JBJoanna A. Bartkowska
Joanna A. Bartkowska
DBDariusz Bochenek
Dariusz Bochenek
PNPrzemysław Niemiec
Przemysław Niemiec
Aurivillius-type ceramics Bi6Fe2−xMnxTi3O18 x = 0, 0.3, 0.9, 1.5 were obtained by a solid-state reaction method using high-purity TiO2, Bi2O3, Fe2O3 and Mn2O3 powders. The milled powder was calcined at 1113 K for 4 h. After calcination, the powder was milled again than pressed into pellets and sintered at 1213 K for 4 h. It was detected that the addition of manganese ions to the multiferroic five-layer Aurivillius-type structure affects the size of the grains. It was found that, the certain amount of manganese ions causes that the polarization of the material doped by them, have the direction opposite to the direction of the applied electric field. The doped material behaves like dia-electric material. The presented research complements the research concerning the Aurivillius ceramics doped with manganese. An attempt was made to explain the reasons for the negative values of dielectric constant and dielectric loss, that occur in manganese-doped five-layer Aurivillius type ceramics and which have not been described in the literature so far.

19 April 2024 in Materials
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Journal Article
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DBDariusz Bochenek
Dariusz Bochenek
PNPrzemysław Niemiec
Przemysław Niemiec
DBDagmara Brzezińska
Dagmara Brzezińska
Grzegorz DerczGrzegorz Dercz
Grzegorz Dercz
GZGrzegorz Ziółkowski
Grzegorz Ziółkowski
JSJan Suchanicz
Jan Suchanicz
The purpose of the present study was to learn the morphological, structural, ferroelectric, dielectric, electromechanical, magnetoelectric, and magnetic properties, and DC conductivity of BaTiO3-Ni0.64Zn0.36Fe2O4 (BT-F) multiferroic composites compacted via the free sintering method. The influence of the ferrite content in ceramic composite materials on the functional properties is investigated and discussed. X-ray diffraction studies confirmed the presence of two main phases of the composite, with strong reflections originating from BaTiO3 and weak peaks originating from nickel-zinc ferrite. BT-F ceramic composites have been shown to exhibit multiferroism at room temperature. All studied compositions have high permittivity values and low dielectric loss, while the ferroelectric properties of the BT component are maintained at a high level. On the other hand, magnetic properties depend on the amount of the ferrite phase and are the strongest for the composition with 15 wt.% of F (magnetization at RT is 4.12 emu/g). The magnetoelectric coupling between BT and F phases confirmed by the lock-in technique is the largest for 15 wt.% ferrite. In the present work, the process conditions of the free sintering method for obtaining BT-F multiferroic composite with good electrical and magnetic properties (in one material) were optimized. An improved set of multifunctional properties allows the expansion of the possibilities of using multiferroic composites in microelectronics.

1 January 2014 in Materials Characterization
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Journal Article
Closed access
DBDariusz Bochenek
Dariusz Bochenek
PNPrzemysław Niemiec
Przemysław Niemiec
ACArtur Chrobak
Artur Chrobak
GZGrzegorz Ziółkowski
Grzegorz Ziółkowski
ABArtur Błachowski
Artur Błachowski

1 July 2017 in Materials Chemistry and Physics
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Journal Article
Closed access
DBDariusz Bochenek
Dariusz Bochenek
PNPrzemysław Niemiec
Przemysław Niemiec
PGPiotr Guzdek
Piotr Guzdek
MWM. Wzorek
M. Wzorek