No abstract

The possibility to grow in zincblende (ZB) and/or wurtzite (WZ) crystal phase widens the potential applications of semiconductor nanowires (NWs). This is particularly true in technologically relevant III-V compounds, such as GaAs, InAs, and InP, for which WZ is not available in bulk form. The WZ band structure of many III-V NWs has been widely studied. Yet, transport (that is, carrier effective mass) and spin (that is, carrier g-factor) properties are almost experimentally unknown. We address these issues in a well-characterized material: WZ indium phosphide. The value and anisotropy of the reduced mass (μ exc) and g-factor (g exc) of the band gap exciton are determined by photoluminescence measurements under intense magnetic fields (B, up to 28 T) applied along different crystallographic directions. μ exc is 14% greater in WZ NWs than in a ZB bulk reference and it is 6% greater in a plane containing the WZ ĉ axis than in a plane orthogonal to ĉ. The Zeeman splitting is markedly anisotropic with g exc = |ge| = 1.4 for B⊥ĉ (where ge is the electron g-factor) and g exc = |ge - gh,//| = 3.5 for B//ĉ (where gh,// is the hole g-factor). A noticeable B-induced circular dichroism of the emitted photons is found only for B//ĉ, as expected in WZ-phase materials.

Semiconductor nanowires (NWs) have the prospect of being employed as basic units for nanoscale devices and circuits. However, the impact of their one-dimensional geometry and peculiar crystal phase on transport and spin characteristics remains largely unknown. We determine the exciton reduced mass and gyromagnetic factor of (InGa)As NWs in the wurtzite phase by photoluminescence (PL) spectroscopy under very high magnetic fields. For B perpendicular to the NW ĉ axis, the exciton reduced mass is 10% greater than that expected for the zincblende phase and no field-induced circular polarization of PL is observed. For B parallel to ĉ, an exciton reduced mass 35% greater than that of the zincblende phase is derived. Moreover, a circular dichroism of 70% is found at 28 T. Finally, an analysis of the PL line shape points at two Zeeman split levels, whose separation corresponds to an exciton gyromagnetic factor |g(e) - g(h,∥)| = 5.8. These results provide a quantitative estimate of the basic electronic and spin properties of NWs and may guide a theoretical analysis of the band structure of these fascinating nanostructures.

We report on PbS colloidal nanocrystals that combine within one structure solubility in physiological solvents with near-infrared photoluminescence, and magnetic and optical properties tuneable by the controlled incorporation of magnetic impurities (Mn). We use high magnetic fields (B up to 30 T) to measure the magnetization of the nanocrystals in liquid and the strength of the sp-d exchange interaction between the exciton and the Mn-ions. With increasing Mn-content from 0.1% to 7%, the mass magnetic susceptibility increases at a rate of ∼ 10(-7) m(3) kg(-1) per Mn percentage; correspondingly, the exciton g-factor decreases from 0.47 to 0.10. The controlled modification of the paramagnetism, fluorescence and exciton g-factor of the nanocrystals is relevant to the implementation of these paramagnetic semiconductor nanocrystals in quantum technologies ranging from quantum information to magnetic resonance imaging.

The recent discovery of a polaron-associated zero phonon line in the band-edge photoluminescence of high optical quality EuTe crystals opens up the prospect of answering long-standing questions about the polaron internal structure, thermal stability, and generation efficiency. Here, a Schrödinger equation for the polaron was formulated and resolved by using both variational and self-consistent methods. The theory is in good agreement with measurements of the zero phonon line as a function of magnetic field and temperature, and it could be applied to other polaronic systems. It is deduced that, in EuTe, at 0 K, a polaron carries a magnetic moment of 610μ B , and its binding energy is 27 meV. However, this binding energy does not carry the usual meaning of thermal stability, because it decreases drastically when the sample is warmed up. For instance, at T = 100 K, the binding energy is already reduced to only 6 meV. The thermal destruction of a polaron is brought about by thermal fluctuations of the spin lattice that suppress the electron's self-energy. Photoluminescence excitation spectra of EuTe demonstrate that the photogeneration of polarons becomes increasingly inefficient when the energy of the pumping photon is increased above the band gap.