Artur Wilson Carbonari

Prof. Artur Wilson Carbonari

Instituto de Pesquisas Energéticas e Nucleares, São Paulo, Brazil
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orcid

Research Focus & Metrics

Academic Career Length

34Years (1993-Present)

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

Representative Publications

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1 November 1996 in Journal of Magnetism and Magnetic Materials
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Journal Article
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Artur Wilson CarbonariArtur Wilson Carbonari
Artur Wilson Carbonari
RSR N Saxena
R N Saxena
WPW. Pendl
W. Pendl
JFJ. Mestnik Filho
J. Mestnik Filho
RAR N Attili
R N Attili
SSS.D. de Souza
S.D. de Souza

11 December 2019 in ACS Applied Nano Materials
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Journal Article
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ACAlex da Cunha Campos
Alex da Cunha Campos
SPSuane de Castro Paes
Suane de Castro Paes
BCBruno Santos Correa
Bruno Santos Correa
GPGabriel Adolfo Cabrera Pasca
Gabriel Adolfo Cabrera Pasca
MCMessias de Souza Costa
Messias de Souza Costa
Artur Wilson CarbonariArtur Wilson Carbonari
Artur Wilson Carbonari

25 October 2021 in Scientific Reports
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Journal Article
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RSRenata V. Santos
Renata V. Santos
GCGabriel A. Cabrera-Pasca
Gabriel A. Cabrera-Pasca
CCCleidilane S. Costa
Cleidilane S. Costa
BBBrianna Bosch-Santos
Brianna Bosch-Santos
LOLarissa Otubo
Larissa Otubo
Artur Wilson CarbonariArtur Wilson Carbonari
Artur Wilson Carbonari
We herein report a comprehensive investigation on the magnetic, structural, and electric properties of CoO nanoparticles with different sizes by local inspection through hyperfine interactions measured in a wide range of temperatures (10–670 K) by using radioactive $$^{111}$$ 111 In( $$^{111}$$ 111 Cd) tracers with the perturbed angular correlations technique. Small cobalt oxide nanoparticles with the characteristic size of 6.5 nm have been prepared by the wet chemical route that turned out to be essential to incorporate radioactivity tracers during nucleation and growth of the particles. Nanocrystalline samples with 22.1 nm size were obtained by thermal treatments under low pressure of helium at 670 K. The hyperfine data were correlated with X-ray diffraction, ZFC–FC magnetic measurements, and transmission electron microscopy to describe the structure, magnetic properties, size, and shape of samples. An analysis of the temperature evolution of hyperfine parameters revealed that the structural distortion and the magnetic disorder in the core and on the surface layer play an important role in the magnetic behavior of CoO nanoparticles.

26 April 2004 in Physical Review B
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Artur Wilson CarbonariArtur Wilson Carbonari
Artur Wilson Carbonari
JMJ. Mestnik-Filho
J. Mestnik-Filho
RSR. N. Saxena
R. N. Saxena
MLM. V. Lalić
M. V. Lalić
Time differential perturbed γ−γ angular correlation technique has been used to measure the magnetic hyperfine field at both Mn and Ce atom sites in CeMn2Ge2 and CeMn2Si2 intermetallic compounds. The probe nucleus 111In→111Cd was used to investigate the hyperfine interaction at Mn sites, while the 140La→140Ce was used to measure the magnetic hyperfine field at Ce. Present measurements cover the temperature range from 10 to 460 K in both compounds. Measurements with 111Cd probe show pure electric quadrupole interactions above 420 K in both compounds and a combined magnetic dipole and electric quadrupole interaction below respective magnetic transition temperatures. While the temperature dependence of the hyperfine field at 111Cd on Mn site in the CeMn2Si2 showed a standard behavior for an antiferromagnetic compound below TN≈408K, the temperature dependence of magnetic hyperline field (MHF) in CeMn2Ge2 showed a transition from ferromagnetic to antiferromagnetic phase at around 320 K and from antiferromagnetic to paramagnetic phase at 420 K. No hyperfine field was observed at 140Ce in CeMn2Si2 in the temperature range from 10 K to 400 K. A unique and well-defined magnetic interaction is observed at Ce sites in CeMn2Ge2 below 320 K, corresponding to a ferromagnetic ordering of Mn moments. The temperature dependence of MHF, however, shows a sharp deviation from an expected Brillouin-like behavior for temperatures below 120 K. The additional magnetic interaction is believed to result from the polarization of Ce spin moments induced by the magnetic field from Mn moments.

1 August 2015 in Journal of Magnetism and Magnetic Materials
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Journal Article
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CCCleidilane Sena Costa
Cleidilane Sena Costa
MCM.S. Costa
M.S. Costa
EME.L. Muñoz
E.L. Muñoz
GPGabriel Adolfo Cabrera Pasca
Gabriel Adolfo Cabrera Pasca
LPL.F.D. Pereira
L.F.D. Pereira
JCJosé A. H. Coaquira
José A. H. Coaquira

4 March 2016 in AIP Advances
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Journal Article
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ECE. L. Correa
E. L. Correa
BBB. Bosch-Santos
B. Bosch-Santos
FCF. H. M. Cavalcante
F. H. M. Cavalcante
BCB. S. Correa
B. S. Correa
RFRafael S Freitas
Rafael S Freitas
MPM. P. A. Potiens
M. P. A. Potiens
The magnetic behavior of Gd2O3 nanoparticles, produced by thermal decomposition method and subsequently annealed at different temperatures, was investigated by magnetization measurements and, at an atomic level, by perturbed γ − γ angular correlation (PAC) spectroscopy measuring hyperfine interactions at 111In(111Cd) probe nuclei. Nanoparticle structure, size and shape were characterized by X-ray diffraction (XRD) and Transmission Electron Microscopy (TEM). Magnetization measurements were carried out to characterize the paramagnetic behavior of the samples. XRD results show that all samples crystallize in the cubic-C form of the bixbyite structure with space group Ia3. TEM images showed that particles annealed at 873 K present particles with highly homogeneous sizes in the range from 5 nm to 10 nm and those annealed at 1273 K show particles with quite different sizes from 5 nm to 100 nm, with a wide size distribution. PAC and magnetization results show that samples annealed at 873 and 1273 K are paramagnetic. Magnetization measurements show no indication of blocking temperatures for all samples down to 2 K and the presence of antiferromagnetic correlations.