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تسجيل مستخدم جديدMagnetization Enhancement in Magnetite Nanoparticles Capped with Alginic Acid
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We report on the effect of organic acid capping on the behavior of magnetite nanoparticles. The nanoparticles of magnetite were obtained using microwave activated process, and the magnetic properties as well as the electron magnetic resonance behavior were studied for the Fe3O4 nanoparticles capped with alginic acid. The capped nanoparticles exhibit improved crystalline structure of the surface which leads to an enhanced magnetization. The saturation magnetization Ms increases to ~75% of the bulk magnetization. The improved structure also facilitates quantization of spin-wave spectrum in the finite size nanoparticles and this in turn is responsible for unconventional behavior at low temperatures. In magnetic resonance these anomalies are manifested as an unusual increase in the resonant field Hr(T) and also as a maximum of the spectroscopic splitting geff parameter at low temperatures. The unconventional behavior of the nanoparticles also leads to pronounced upturn of magnetization at low temperatures and a deviation from the Bloch law M(T) T^3/2.
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Morphology, structure and magnetic properties of nanocomposites of magnetite (Fe3O4) nanoparticles and alginic acid (AA) are studied. Magnetite Fe3O4 nanoparticles and the nanoparticles capped with alginic acid exhibit very distinct properties. The c
hemical bonding between alginic acid and surface of magnetite nanoparticles results in recovery of surface magnetization. On the other hand, it also leads to enhanced surface spin disorder and unconventional behavior of magnetization observed in Fe3O4-AA nanocomposites at low temperatures.
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Magnetite (Fe$_{3}$O$_{4}$), an archetypal transition metal oxide, has been used for thousands of years, from lodestones in primitive compasses[1] to a candidate material for magnetoelectronic devices.[2] In 1939 Verwey[3] found that bulk magnetite u
ndergoes a transition at T$_{V}$ $approx$ 120 K from a high temperature bad metal conducting phase to a low-temperature insulating phase. He suggested[4] that high temperature conduction is via the fluctuating and correlated valences of the octahedral iron atoms, and that the transition is the onset of charge ordering upon cooling. The Verwey transition mechanism and the question of charge ordering remain highly controversial.[5-11] Here we show that magnetite nanocrystals and single-crystal thin films exhibit an electrically driven phase transition below the Verwey temperature. The signature of this transition is the onset of sharp conductance switching in high electric fields, hysteretic in voltage. We demonstrate that this transition is not due to local heating, but instead is due to the breakdown of the correlated insulating state when driven out of equilibrium by electrical bias. We anticipate that further studies of this newly observed transition and its low-temperature conducting phase will shed light on how charge ordering and vibrational degrees of freedom determine the ground state of this important compound.
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