2004
DOI: 10.1016/j.jmmm.2003.12.377
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Magnetic study on Co3O4 nanoparticles

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Cited by 95 publications
(50 citation statements)
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“…The inset in this figure shows the temperature dependence of the reciprocal magnetization 1/M, as measured in the FC process with the field of 0.01 T. As temperature is lowered from room temperature, a very sharp cusp at about 29 K is observed in the M ZFC curve with a dc magnetic field of 0.01 T, while a gradual increase of M FC appears, especially, below 50 K. Namely, an increasingly strong irreversibility is observed between M ZFC and M FC, with the onset of about 300 K. For M FC with the magnetic field of 1 T, it exhibits a behavior similar to that of M FC with the dc magnetic field of 0.01 T. As is well known, the blocking temperature T B (the temperature above which one particle has enough time, within the observation time, to reverse its moments to the applied field [21]) is the temperature correspondent to the maximum of M ZFC , or around 29 K. While bulk Cr is an antiferrromagnet with a Néel temperature T N of 311 K [22], Cr nanoparticles exhibit mainly antiferromagnetic (AFM) properties, in addition to a weak ferromagnetic (WFM) component [16]. According to Néel [23], WFM behaviors from very fine antiferromagnetic particles can be attributed to the uncompensated spins on the surfaces of the fine particles, which was also verified for a lot of AFM nanoparticles such as MnO [24], Co 3 O 4 [25] and Cr 2 O 3 [16] ones, etc. Moreover, ␤-Cr 2 N shows Pauli paramagnetic down to 1.8 K [26].…”
Section: Resultsmentioning
confidence: 89%
“…The inset in this figure shows the temperature dependence of the reciprocal magnetization 1/M, as measured in the FC process with the field of 0.01 T. As temperature is lowered from room temperature, a very sharp cusp at about 29 K is observed in the M ZFC curve with a dc magnetic field of 0.01 T, while a gradual increase of M FC appears, especially, below 50 K. Namely, an increasingly strong irreversibility is observed between M ZFC and M FC, with the onset of about 300 K. For M FC with the magnetic field of 1 T, it exhibits a behavior similar to that of M FC with the dc magnetic field of 0.01 T. As is well known, the blocking temperature T B (the temperature above which one particle has enough time, within the observation time, to reverse its moments to the applied field [21]) is the temperature correspondent to the maximum of M ZFC , or around 29 K. While bulk Cr is an antiferrromagnet with a Néel temperature T N of 311 K [22], Cr nanoparticles exhibit mainly antiferromagnetic (AFM) properties, in addition to a weak ferromagnetic (WFM) component [16]. According to Néel [23], WFM behaviors from very fine antiferromagnetic particles can be attributed to the uncompensated spins on the surfaces of the fine particles, which was also verified for a lot of AFM nanoparticles such as MnO [24], Co 3 O 4 [25] and Cr 2 O 3 [16] ones, etc. Moreover, ␤-Cr 2 N shows Pauli paramagnetic down to 1.8 K [26].…”
Section: Resultsmentioning
confidence: 89%
“…Co 3 O 4 is an antiferromagnetic material and in the bulk form, its Néel temperature has been reported to lie between 30 K and 40 K. 24 There have been some reports on hysteresis, time dependence of magnetization, exchange bias and finite size effects in bare, coated and dispersed Co 3 O 4 nanoparticles and various claims have been made in support of spin glass like and superparamagnetic behavior in these particles. [24][25][26][27][28][29][30][31][32][33] It will be, therefore, worthwhile to investigate their magnetic behavior carefully. In the present work, we present a de-tailed study on non-equilibrium features such as temperature, time and field dependence of magnetization, aging and memory effects.…”
Section: 19-21mentioning
confidence: 99%
“…C obalt oxide (Co 3 O 4 ) is a technologically important material with a variety of applications such as lithium ion batteries (Wang et al, 2002;Yuan et al, 2003), gas sensors (Li and Xu, 2005), magnetic materials (Ichiyanagi et al, 2004), and catalysts (Tang et al, 2006). Various techniques have been developed for the preparation of Co 3 O 4 powders, which include thermal decomposition method (Ardizzone et al, 1995;Liao and Liang, 2004;Wang and Zhu, 2005), sol-gel process (Cao et al, 2003), hydrothermal method (Cote et al, 2002;Meskin et al, 2003), and solvothermal (He et al, 2004;Nethravathi et al, 2005).…”
Section: Introductionmentioning
confidence: 99%