Semiconductor electronics has so far been based on the transport of charge carriers while storage of information has mainly relied upon the collective interactions of spins. A new discipline known as spintronics proposes to exploit the strong mutual influence of magnetic and electrical properties in magnetic semiconductors, which promise new types of devices and computer technologies. The mechanism for such phenomena involves the concept of magnetic polarons—microscopic clouds of magnetization composed of charge carriers and neighboring magnetic ions—which determine most of the electrical, magnetic, and optical properties of the material. In spite of the importance of this quasiparticle, its observation remains a formidable challenge. Here we report that, using the positive muon as both a donor center and a local magnetic probe, we have been able to generate and detect the magnetic polaron and determine its size and magnetic moment in the magnetic semiconductor EuS.

Zinc-doped InP(Zn) colloidal quantum dots (QDs) with narrow size distribution and low defect concentration were grown for the first time via a novel phosphine synthetic route and over a wide range of Zn doping. We report the influence of Zn on the optical properties of the obtained quantum dots. We propose a mechanism for the introduction of Zn in the QDs and show that the incorporation of Zn atoms into the InP lattice leads to the formation of Zn acceptor levels and a luminescence tail in the red region of the spectra. Using photochemical etching with HF, we confirmed that the Zn dopant atoms are situated inside the InP nanoparticles. Moreover, doping with Zn is accompanied with the coverage of the QDs by a zinc shell. During the synthesis Zn myristate covers the QD nucleus and inhibits the particle growth. At the same time the zinc shell leads to an increase of the luminescence quantum yield through the reduction of phosphorous dangling bonds. A scenario for the growth of the colloidal InP(Zn) QDs was proposed and discussed.

Temperature dependences of resistivity, magnetic susceptibility, and charge-carrier concentration and mobility in single-crystalline PbTe:V samples with a varied impurity content are investigated. It is shown that vanadium forms a donor level located ∼20 meV below the conduction-band bottom. The electron mobility is as high as 10⁵ cm² V⁻¹ s⁻¹ in the samples with N_V ≤ 0.21 at % and proves to be more than an order of magnitude higher in the samples with the highest vanadium content N_V = 0.26 at %. In the same samples, the real part of the conductivity is characterized by a pronounced frequency dependence. An increase in vanadium concentration is accompanied by a decrease in the effective magnetic moment of impurity atoms. The features of electron transport in PbTe:V may be caused by a variable vanadium valence and by the effect of interimpurity correlations.

We have studied a portion of the ternary system Pb-V-Te. Pseudobinary joins have been identified, the vanadium solubility along the V3Te4-PbTe join has been determined, and the lattice parameter of th