Jančar, Boštjan

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Author's Bibliography

Exchange-Bias and Grain-Surface Relaxations in Nanostructured NiO/Ni Induced by a Particle Size Reduction

Kremenović, Aleksandar; Jančar, Boštjan; Ristić, Mira; Vucinić-Vasić, Milica; Rogan, Jelena; Pacevski, Aleksandar; Antić, Bratislav

(Amer Chemical Soc, Washington, 2012)

TY  - JOUR
AU  - Kremenović, Aleksandar
AU  - Jančar, Boštjan
AU  - Ristić, Mira
AU  - Vucinić-Vasić, Milica
AU  - Rogan, Jelena
AU  - Pacevski, Aleksandar
AU  - Antić, Bratislav
PY  - 2012
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2223
AB  - Transition-metal-oxide/transition-metal nanocomposites, such as NiO/Ni, FeO/Fe, and CoO/Co, have been the subject of much recent investigation (i) because of their potential applications and (ii) because they are good model systems for studies of some effects on the nanoscale. They are used, for example, as catalysts, fuel-cell electrodes, magnetic memories, etc. When a nanocomposite is composed of both ferromagnetic (FM) and antiferromagnetic (AFM) nanoparticles, interesting physical properties can occur, such as the phenomenon of exchange bias (EB). A Ni/NiO nanocomposite obtained by the thermal decomposition of nickel(II) acetate tetrahydrate, Ni(CH3COO)(2)center dot 4H(2)O, at 300 degrees C, is composed of NiO (62%) and Ni (38%) with crystallite sizes of 11 and 278 nm, respectively. We observed an increase in the crystallite size for NiO and decrease of crystallite size for Ni, a decrease in the microstrain for both and an increase in the NiO phase content with thermal annealing in air, while high-energy ball milling leads to a decrease of the crystallite size, an increase in the size of the agglomerates, and microstrain as well as reduction, NiO - gt  Ni. The lattice parameters of the nanosized NiO and Ni show a deviation from the value for the bulk counterparts as a consequence of crystallite size reduction and the grain-surface relaxation effect. The exchange bias found in a milled sample with particles of 10 nm (NiO) and 11 nm (Ni) disappears for larger particles as a consequence of a coupling-area decrease between the antiferromagnetic and ferromagnetic particles. Due to reduction/oxidation (NiO  lt - gt  Ni) and size as well as surface-relaxation effects the saturation magnetization value increases/decreases with milling/annealing, respectively. Having in mind the effect of size on the exchange bias, coercivity, and magnetization values, it is possible, by annealing/milling, to tailor the composition and particle size and then control the exchange bias and improve the other magnetic properties of the Ni/NiO.
PB  - Amer Chemical Soc, Washington
T2  - Journal of Physical Chemistry C
T1  - Exchange-Bias and Grain-Surface Relaxations in Nanostructured NiO/Ni Induced by a Particle Size Reduction
EP  - 4364
IS  - 7
SP  - 4356
VL  - 116
DO  - 10.1021/jp206658v
ER  - 
@article{
author = "Kremenović, Aleksandar and Jančar, Boštjan and Ristić, Mira and Vucinić-Vasić, Milica and Rogan, Jelena and Pacevski, Aleksandar and Antić, Bratislav",
year = "2012",
abstract = "Transition-metal-oxide/transition-metal nanocomposites, such as NiO/Ni, FeO/Fe, and CoO/Co, have been the subject of much recent investigation (i) because of their potential applications and (ii) because they are good model systems for studies of some effects on the nanoscale. They are used, for example, as catalysts, fuel-cell electrodes, magnetic memories, etc. When a nanocomposite is composed of both ferromagnetic (FM) and antiferromagnetic (AFM) nanoparticles, interesting physical properties can occur, such as the phenomenon of exchange bias (EB). A Ni/NiO nanocomposite obtained by the thermal decomposition of nickel(II) acetate tetrahydrate, Ni(CH3COO)(2)center dot 4H(2)O, at 300 degrees C, is composed of NiO (62%) and Ni (38%) with crystallite sizes of 11 and 278 nm, respectively. We observed an increase in the crystallite size for NiO and decrease of crystallite size for Ni, a decrease in the microstrain for both and an increase in the NiO phase content with thermal annealing in air, while high-energy ball milling leads to a decrease of the crystallite size, an increase in the size of the agglomerates, and microstrain as well as reduction, NiO - gt  Ni. The lattice parameters of the nanosized NiO and Ni show a deviation from the value for the bulk counterparts as a consequence of crystallite size reduction and the grain-surface relaxation effect. The exchange bias found in a milled sample with particles of 10 nm (NiO) and 11 nm (Ni) disappears for larger particles as a consequence of a coupling-area decrease between the antiferromagnetic and ferromagnetic particles. Due to reduction/oxidation (NiO  lt - gt  Ni) and size as well as surface-relaxation effects the saturation magnetization value increases/decreases with milling/annealing, respectively. Having in mind the effect of size on the exchange bias, coercivity, and magnetization values, it is possible, by annealing/milling, to tailor the composition and particle size and then control the exchange bias and improve the other magnetic properties of the Ni/NiO.",
publisher = "Amer Chemical Soc, Washington",
journal = "Journal of Physical Chemistry C",
title = "Exchange-Bias and Grain-Surface Relaxations in Nanostructured NiO/Ni Induced by a Particle Size Reduction",
pages = "4364-4356",
number = "7",
volume = "116",
doi = "10.1021/jp206658v"
}
Kremenović, A., Jančar, B., Ristić, M., Vucinić-Vasić, M., Rogan, J., Pacevski, A.,& Antić, B.. (2012). Exchange-Bias and Grain-Surface Relaxations in Nanostructured NiO/Ni Induced by a Particle Size Reduction. in Journal of Physical Chemistry C
Amer Chemical Soc, Washington., 116(7), 4356-4364.
https://doi.org/10.1021/jp206658v
Kremenović A, Jančar B, Ristić M, Vucinić-Vasić M, Rogan J, Pacevski A, Antić B. Exchange-Bias and Grain-Surface Relaxations in Nanostructured NiO/Ni Induced by a Particle Size Reduction. in Journal of Physical Chemistry C. 2012;116(7):4356-4364.
doi:10.1021/jp206658v .
Kremenović, Aleksandar, Jančar, Boštjan, Ristić, Mira, Vucinić-Vasić, Milica, Rogan, Jelena, Pacevski, Aleksandar, Antić, Bratislav, "Exchange-Bias and Grain-Surface Relaxations in Nanostructured NiO/Ni Induced by a Particle Size Reduction" in Journal of Physical Chemistry C, 116, no. 7 (2012):4356-4364,
https://doi.org/10.1021/jp206658v . .
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Poly(D,L-lactide-co-glycolide)/hydroxyapatite core-shell nanospheres. Part 1: A multifunctional system for controlled drug delivery

Vukomanović, Marija; Škapin, Srečo Davor; Jančar, Boštjan; Maksin, Tatjana; Ignjatović, Nenad; Uskoković, Vuk; Uskoković, Dragan

(2011)

TY  - JOUR
AU  - Vukomanović, Marija
AU  - Škapin, Srečo Davor
AU  - Jančar, Boštjan
AU  - Maksin, Tatjana
AU  - Ignjatović, Nenad
AU  - Uskoković, Vuk
AU  - Uskoković, Dragan
PY  - 2011
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5650
AB  - Biodegradable poly(D,L-lactide-co-glycolide) (PLGA) and bioactive hydroxyapatite (HAP) are selected for the formation of a multifunctional system with the specific core-shell structure to be applied as a carrier of a drug. As a result, both components of PLGA/HAp core-shells are able to capture one part of the drug. Polymeric shells consisting of small nanospheres up to 20 nm in size act as a matrix in which one part of the drug is dispersed. In the same time, ceramic cores are formed of rod-like hydroxyapatite particles at the surface of which another part of the drug is adsorbed onto the interface between the polymer and the ceramics. The content of the loaded drug, as well as the selected solvent/non-solvent system, have a crucial influence on the resulting PLGA/HAp morphology and, finally, unimodal distribution of core-shells is obtained. The redistribution of the drug between the organic and inorganic parts of the material is expected to provide an interesting contribution to the kinetics of the drug release resulting in non-typical two-step drug release. (C) 2010 Elsevier B.V. All rights reserved.
T2  - Colloids and Surfaces B: Biointerfaces
T1  - Poly(D,L-lactide-co-glycolide)/hydroxyapatite core-shell nanospheres. Part 1: A multifunctional system for controlled drug delivery
EP  - 413
IS  - 2
SP  - 404
VL  - 82
DO  - 10.1016/j.colsurfb.2010.09.011
UR  - https://hdl.handle.net/21.15107/rcub_dais_2749
ER  - 
@article{
author = "Vukomanović, Marija and Škapin, Srečo Davor and Jančar, Boštjan and Maksin, Tatjana and Ignjatović, Nenad and Uskoković, Vuk and Uskoković, Dragan",
year = "2011",
abstract = "Biodegradable poly(D,L-lactide-co-glycolide) (PLGA) and bioactive hydroxyapatite (HAP) are selected for the formation of a multifunctional system with the specific core-shell structure to be applied as a carrier of a drug. As a result, both components of PLGA/HAp core-shells are able to capture one part of the drug. Polymeric shells consisting of small nanospheres up to 20 nm in size act as a matrix in which one part of the drug is dispersed. In the same time, ceramic cores are formed of rod-like hydroxyapatite particles at the surface of which another part of the drug is adsorbed onto the interface between the polymer and the ceramics. The content of the loaded drug, as well as the selected solvent/non-solvent system, have a crucial influence on the resulting PLGA/HAp morphology and, finally, unimodal distribution of core-shells is obtained. The redistribution of the drug between the organic and inorganic parts of the material is expected to provide an interesting contribution to the kinetics of the drug release resulting in non-typical two-step drug release. (C) 2010 Elsevier B.V. All rights reserved.",
journal = "Colloids and Surfaces B: Biointerfaces",
title = "Poly(D,L-lactide-co-glycolide)/hydroxyapatite core-shell nanospheres. Part 1: A multifunctional system for controlled drug delivery",
pages = "413-404",
number = "2",
volume = "82",
doi = "10.1016/j.colsurfb.2010.09.011",
url = "https://hdl.handle.net/21.15107/rcub_dais_2749"
}
Vukomanović, M., Škapin, S. D., Jančar, B., Maksin, T., Ignjatović, N., Uskoković, V.,& Uskoković, D.. (2011). Poly(D,L-lactide-co-glycolide)/hydroxyapatite core-shell nanospheres. Part 1: A multifunctional system for controlled drug delivery. in Colloids and Surfaces B: Biointerfaces, 82(2), 404-413.
https://doi.org/10.1016/j.colsurfb.2010.09.011
https://hdl.handle.net/21.15107/rcub_dais_2749
Vukomanović M, Škapin SD, Jančar B, Maksin T, Ignjatović N, Uskoković V, Uskoković D. Poly(D,L-lactide-co-glycolide)/hydroxyapatite core-shell nanospheres. Part 1: A multifunctional system for controlled drug delivery. in Colloids and Surfaces B: Biointerfaces. 2011;82(2):404-413.
doi:10.1016/j.colsurfb.2010.09.011
https://hdl.handle.net/21.15107/rcub_dais_2749 .
Vukomanović, Marija, Škapin, Srečo Davor, Jančar, Boštjan, Maksin, Tatjana, Ignjatović, Nenad, Uskoković, Vuk, Uskoković, Dragan, "Poly(D,L-lactide-co-glycolide)/hydroxyapatite core-shell nanospheres. Part 1: A multifunctional system for controlled drug delivery" in Colloids and Surfaces B: Biointerfaces, 82, no. 2 (2011):404-413,
https://doi.org/10.1016/j.colsurfb.2010.09.011 .,
https://hdl.handle.net/21.15107/rcub_dais_2749 .
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Local environment of Co2+ ions intercalated in VOx/hexadecylamine nanotubes

Kremenović, Aleksandar; Antić, Bratislav; Vucinić-Vasić, Milica; Ristić, Mira; Jančar, Boštjan; Rogan, Jelena

(Int Union Crystallography, Chester, 2011)

TY  - JOUR
AU  - Kremenović, Aleksandar
AU  - Antić, Bratislav
AU  - Vucinić-Vasić, Milica
AU  - Ristić, Mira
AU  - Jančar, Boštjan
AU  - Rogan, Jelena
PY  - 2011
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1771
PB  - Int Union Crystallography, Chester
T2  - Acta Crystallographica A-Foundation and Advances
T1  - Local environment of Co2+ ions intercalated in VOx/hexadecylamine nanotubes
EP  - C324
SP  - C324
VL  - 67
UR  - https://hdl.handle.net/21.15107/rcub_technorep_1771
ER  - 
@article{
author = "Kremenović, Aleksandar and Antić, Bratislav and Vucinić-Vasić, Milica and Ristić, Mira and Jančar, Boštjan and Rogan, Jelena",
year = "2011",
publisher = "Int Union Crystallography, Chester",
journal = "Acta Crystallographica A-Foundation and Advances",
title = "Local environment of Co2+ ions intercalated in VOx/hexadecylamine nanotubes",
pages = "C324-C324",
volume = "67",
url = "https://hdl.handle.net/21.15107/rcub_technorep_1771"
}
Kremenović, A., Antić, B., Vucinić-Vasić, M., Ristić, M., Jančar, B.,& Rogan, J.. (2011). Local environment of Co2+ ions intercalated in VOx/hexadecylamine nanotubes. in Acta Crystallographica A-Foundation and Advances
Int Union Crystallography, Chester., 67, C324-C324.
https://hdl.handle.net/21.15107/rcub_technorep_1771
Kremenović A, Antić B, Vucinić-Vasić M, Ristić M, Jančar B, Rogan J. Local environment of Co2+ ions intercalated in VOx/hexadecylamine nanotubes. in Acta Crystallographica A-Foundation and Advances. 2011;67:C324-C324.
https://hdl.handle.net/21.15107/rcub_technorep_1771 .
Kremenović, Aleksandar, Antić, Bratislav, Vucinić-Vasić, Milica, Ristić, Mira, Jančar, Boštjan, Rogan, Jelena, "Local environment of Co2+ ions intercalated in VOx/hexadecylamine nanotubes" in Acta Crystallographica A-Foundation and Advances, 67 (2011):C324-C324,
https://hdl.handle.net/21.15107/rcub_technorep_1771 .