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Register a new userTuning the properties of magnetic CdMnTe quantum dots
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Added by
Sebastian Mackowski
Publication date
2003
fields
Physics
and research's language is
English
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We show that CdMnTe self-assembled quantum dots can be formed by depositing a submonolayer of Mn ions over a ZnTe surface prior to deposition of the CdTe dot layer. Single dot emission lines and strongly polarized quantum dot photoluminescence in an applied magnetic field confirm the presence of Mn in individual quantum dots. The width of PL lines of the single CdMnTe dots is 3 meV due to magnetic moment fluctuations of the Mn ions. After rapid thermal annealing, the emission lines of individual magnetic quantum dots narrow significantly to 0.25 meV showing that effect of magnetic fluctuations is strongly reduced most probably due to an increase in the average quantum dot size. These results suggest a way to tune the spin properties of magnetic quantum dots.
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We demonstrate that resonant excitation of CdMnTe self-assembled quantum dots creates an ensemble of spin-polarized magnetic polarons at B=0 T. The strong spatial confinement characteristic of quantum dots significantly increases the stability of magnetic polarons so that the optically induced spin alignment is observed for temperatures > 120 K.
The magnetic and structural properties of highly ordered (S ~ 0.82) epitaxial Fe50-xMnxPt50 thin films were investigated. We report the change in the magnetic properties of Mn doped FePt epitaxial thin films. This study differs from the earlier experimental studies on Mn doped FePt based alloys. Ordered L10 Fe50-xMnxPt50 (x=0, 6, 9, 12 and 15) thin films with a constant thickness of 45 nm were prepared by co-sputtering Fe50Pt50 and Mn50Pt50 on to MgO (100) single crystal substrate. We find a significant increase in the coercivity for Fe-Mn-Pt thin films. We have shown that this increase in magnetic properties coincide with the tetragonal distortion, while the recent first principles study of Mn doped FePt showed the sub lattice ordering of ferromagnetically aligned Mn atoms would lead to increase in magnetic properties in the FeMnPt ternary alloy system with fixed Pt concentration. At x=12 the coercivity has increased by 46.4 % when compared to Fe50Pt50. The increase in magnetic properties in Fe50-xMnxPt50 is due to the tetragonal distortion as experimental c/a ratio is larger than the expected c/a ratio for ferromagnetically ordered Mn atoms in the sublattice at the concentration x=12. Thus we show that high temperature deposition and high temperature annealing is one of the methods to achieve large coercivity in Mn doped FePt as it leads to tetragonal distortion.
Using the tight-binding approximation we calculated the magnetic susceptibility of graphene quantum dots (GQD) of different geometrical shapes and sizes, smaller than the magnetic length, when the magnetic properties are governed by the electron edge states. Two types of edge states can be discerned: the zero-energy states (ZES) located exactly at the zero-energy Dirac point, and the dispersed edge states (DES) with the energy close, but not exactly equal to zero. DES are responsible for the temperature independent diamagnetic response, while ZES provide the temperature dependent spin Curie paramagnetism. The hexagonal, circular and randomly shaped GQDs contain mainly DES and, as a result, they are diamagnetic. The edge states of the triangular GQDs are ZES and these dots reveal the interplay between the spin paramagnetism, dominating for small dots and at low temperatures, and bulk orbital diamagnetism, dominating for large dots and at high temperatures.
We show that through the resonant optical excitation of spin-polarized excitons into CdMnTe magnetic quantum dots, we can induce a macroscopic magnetization of the Mn impurities. We observe very broad (4 meV linewidth) emission lines of single dots, which are consistent with the formation of strongly confined exciton magnetic polarons. Therefore we attribute the optically induced magnetization of the magnetic dots results to the formation of spin-polarized exciton magnetic polarons. We find that the photo-induced magnetization of magnetic polarons is weaker for larger dots which emit at lower energies within the QD distribution. We also show that the photo-induced magnetization is stronger for quantum dots with lower Mn concentration, which we ascribe to weaker Mn-Mn interaction between the nearest neighbors within the dots. Due to particular stability of the exciton magnetic polarons in QDs, where the localization of the electrons and holes is comparable to the magnetic exchange interaction, this optically induced spin alignment persists to temperatures as high as 160 K.
The magnetic and electronic properties of strontium titanate with different carbon dopant configurations are explored using first-principles calculations with a generalized gradient approximation (GGA) and the GGA+U approach. Our results show that the structural stability, electronic properties and magnetic properties of C-doped SrTiO3 strongly depend on the distance between carbon dopants. In both GGA and GGA+U calculations, the doping structure is mostly stable with a nonmagnetic feature when the carbon dopants are nearest neighbors, which can be ascribed to the formation of a C-C dimer pair accompanied by stronger C-C and weaker C-Ti hybridizations as the C-C distance becomes smaller. As the C-C distance increases, C-doped SrTiO3 changes from an n-type nonmagnetic metal to ferromagnetic/antiferromagnetic half-metal and to an antiferromagnetic/ferromagnetic semiconductor in GGA calculations, while it changes from a nonmagnetic semiconductor to ferromagnetic half-metal and to an antiferromagnetic semiconductor using the GGA+U method. Our work demonstrates the possibility of tailoring the magnetic and electronic properties of C-doped SrTiO3, which might provide some guidance to extend the applications of strontium titanate as a magnetic or optoelectronic material.
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