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GaAs-InGaAs-GaAs core-shell-shell nanowire (NW) structures were grown by gas source molecular beam epitaxy using the selective-area, self-assisted, vapor-liquid-solid method. The structural, morphological, and optical properties of the NWs were examined for different growth conditions of the InGaAs shell. With increasing In concentration of the InGaAs shell, the growth transitioned from preferential deposition at the NW base to the Stranski-Krastanov growth mode where InGaAs islands formed along the NW length. This trend is explained within a nucleation model where there is a critical In flux below which the conformal growth is suppressed and the shell forms only at the NW base. Low growth temperature produced a more uniform In distribution along the NW length but resulted in quenching of the photoluminescence (PL) emission. Alternatively, reducing the shell thickness and increasing the V/III flux ratio resulted in conformal InGaAs shell growth and quantum dot-like PL emission. Our results indicate a pathway toward the conditions for conformal InGaAs shell growth required for satisfactory optoelectronic performance.

Recent investigations of III-V semiconductor nanowires have revealed periodic zinc-blende twins, known as twinning superlattices, that are often induced by a high-impurity dopant concentration. In the present study, the relationship between the nanowire morphology, crystal structure, and impurity dopant concentration (Te and Be) of twinning superlattices has been studied in GaAs nanowires grown by molecular beam epitaxy using the self-assisted (with a Ga droplet) vapor-liquid-solid process. The contact angle between the Ga droplet and the nanowire top facet decreased linearly with the dopant concentration, whereas the period of the twinning superlattices increased with the doping concentration and was proportional to the nanowire radius. Our model, which is based entirely on surface energetics, is able to explain a unified formation mechanism of twinning superlattices in doped semiconductor nanowires.

GaAs nanowire (NW) arrays were grown on Si substrates by selective-area molecular beam epitaxy (MBE) using the self-assisted vapor-liquid-solid (VLS) method. In the self-assisted VLS method, the GaAs NW diameter is determined by the size of a Ga droplet at the top of the NW. Absorption of the solar spectrum for photovoltaic devices is optimum with a GaAs NW diameter of ∼170 nm, requiring a Ga droplet during the growth of a similar size. Control of the Ga droplet size, and therefore the NW diameter, is demonstrated by controlling the V/III flux ratio during the MBE growth. A V/III flux ratio near unity rapidly increased the Ga droplet volume during the NW growth, thereby creating an inverse-tapered (funnel-shaped) NW morphology. Numerical simulations indicated that the inverse-tapered NW showed strong broadband absorption of the solar spectrum due to the absorption of consecutively longer wavelengths toward the base of the NW.

International audience; We report on the selective area growth of InAs nanowires (NWs) by the catalyst-free vapor−solid method. Well-ordered InAs NWs were grown on GaAs(111)B and Si(111) substrates patterned with a dielectric mask using hydride vapor phase epitaxy (HVPE). Vertical and high aspect ratio InAs NWs with a hexagonal shape were grown on both GaAs and Si substrates. The impact of the growth conditions on the InAs morphology was investigated. The final shape of the InAs crystal was tuned from a NW to a nanoplatelet by controlling growth conditions such as growth temperature, vapor phase composition, and mask pattern. The influence of the aperture size on the nucleation density and then on the morphology of InAs is discussed. Small openings resulted in the formation of a single nucleus per hole, which was then converted to a NW. For larger apertures, the number of nuclei increased, leading to both three-dimensional crystals and NWs. The effect of growth temperature and the III/V ratio on the kinetics and thermodynamics of InAs growth is also discussed. The growth was first optimized on a GaAs(111)B substrate and then performed on Si, which is more suitable to develop devices. Finally, the absorbance and photoluminescence measurements were carried out on the InAs NW arrays, demonstrating the high potential of HVPE-grown InAs NWs for future multispectral photo-detection devices.

International audience; We report for the first time on the hydride vapor phase epitaxy (HVPE) growth of long (26 μm) InAs nanowires on Si(111) substrate grown at a standard rate of 50 μm h−1. The nanowires grow vertically along the (111)B direction and exhibit a well faceted hexagonal shape with a constant diameter. The effect of the experimental parameters, growth temperature and III/V ratio, is investigated. The thermodynamic and kinetic mechanisms involved during the growth of such long nanowires are identified. It is demonstrated that growth occurs through direct condensation of InCl and As4/As2 gaseous species. Dechlorination of adsorbed InCl molecules is the limiting step at low temperature. Structural analysis through high resolution transmission electron microscopy (HRTEM) and high-angle annular dark-field (HAADF) imaging was performed. The high As4 partial pressure of the HVPE environment induces the presence of both wurtzite and zinc-blende phases. The results emphasize the potential of the low cost HVPE technique for the monolithic integration of arrays of long InAs nanowires on silicon.

International audience; Au droplets are used as a catalyst for the growth of nanowires on Si(111) substrate via the vapor-liquid-solid (VLS) mechanism. The dewetting of a Au thin film is the most common method to obtain these droplets. The control of this step is crucial to adjust the density and the diameter of the nanowires during VLS growth. When the Si(111) substrate is covered with a silicon dioxide layer, the kinetics of Au droplet formation is strongly modified. The dependence of the diameter and spatial distribution of the droplets on the surface have been studied by scanning electron microscopy with respect to the thickness of the silicon dioxide layer, the thickness of the Au film and the temperature of the substrate during deposition and post-deposition annealing. In-situ low energy electron microscopy and low energy electron diffraction revealed the dynamics of the Au droplet formation after annealing. The Au droplets are shown to catalyze the decomposition of silicon dioxide at high temperature (> 650-700 °C) and form a wetting layer of Au-(33)-Si(111). Consequently, the droplets absorb silicon atoms from the substrate, migrate perpendicular to the atomic steps and grow by the Smoluchowski ripening process.

Here, a new promising perovskite structure of KMnF3 has been fabricated and characterized, which yields bandgap of 1.6 eV with fascinating moisture-resistance and phase stability. Investigation of structural, optical, stability and transport properties have done by XRD, SEM, UV–vis–NIR spectroscopy, photoluminescence and electrical conductivity test. Such examination indicated the high carrier mobility (18 cm2/V s) and density (1014/cm3) even after a long interval between each excitation. These transport properties are comparable to that of the organic perovskite, indicating the importance of KMnF3 for solar device applications.

The commonly employed methyl-ammonium containing perovskites are unstable at high temperature or under moisture attack, thus limiting their commercial applications. To overcome this barrier, a new perovskite possessing both thermal stability and water resistance has been constructed, involving pyrrolidinium rings (CH2)4NH2PbI3 (PyPbI3), through a simple solution-processing method. It presents not only prolonged moisture resistance and a favorable bandgap of 1.80 eV, as determined by P-XRD and UV absorption, but also excellent thermal stability, as verified via the in situ XRD technique. The new structure may be applicable to perovskite solar cells with improved thermal stability and water resistance.

The incorporation of Si into vapor-liquid-solid GaAs nanowires often leads to p-type doping, whereas it is routinely used as an n-dopant of planar layers. This property limits the applications of GaAs nanowires in electronic and optoelectronic devices. The strong amphoteric behavior of Si in nanowires is not yet fully understood. Here, we present the first attempt to quantify this behavior as a function of the droplet composition and temperature. It is shown that the doping type critically depends on the As/Ga ratio in the droplet. In sharp contrast to vapor-solid growth, the droplet contains very few As atoms, which enhance their reverse transfer from solid to liquid. As a result, Si atoms preferentially replace As in GaAs, leading to p-type doping in nanowires. Hydride vapor phase epitaxy provides the highest As concentrations in the catalyst droplets during their vapor-liquid-solid growth, resulting in n-type dopant behavior of Si. We present experimental data on n-doped Si-doped GaAs nanowires grown by this method and explain the doping within our model. These results give a clear route for obtaining n-type or p-type Si doping in GaAs nanowires and may be extended to other III-V nanowires.

Formation of twin boundaries during the growth of semiconductor nanowires is very common. However, the effects of such planar defects on the electronic and optical properties of nanowires are not very well understood. Here, we use a combination of ab initio simulation and experimental techniques to study these effects. Twin boundaries in GaP are shown to act as an atomically-narrow plane of wurtzite phase with a type-I homostructure band alignment. Twin boundaries and stacking faults (wider regions of the wurtzite phase) lead to the introduction of shallow trap states observed in photoluminescence studies. These effects should have a profound impact on the efficiency of nanowire-based devices., 24 pages, 11 figures, 1 table

InSb nanowire (NW) arrays fabricated by a top-down etching process were investigated for multispectral infrared photodetection. A 2.5 ?m thick film of InSb was grown on Si (100) by molecular beam epitaxy using an AlSb buffer layer to alleviate defects associated with lattice mismatch strain, as confirmed by scanning electron microscopy and x-ray diffraction. Using a Ti mask patterned by electron beam lithography, InSb NW arrays with diameters ranging from 300 to 1300 nm (100 nm steps) and pitches ranging from 1000 nm to 3500 (500 nm steps) were reactive ion etched from the thin film. For each 100 nm increase in NW diameter, the peak absorptance wavelength, as measured by Fourier transform infrared spectroscopy, increased by 0.53???0.2 ?m. The ability of InSb nanowires to produce highly tunable absorptance from 1.61 to 6.86 ?m was demonstrated.

Semiconductor nanowires (NWs) represent a new class of materials and a shift from conventional two-dimensional bulk thin films to three-dimensional devices. Unlike thin film technology, lattice mismatch strain in NWs can be relaxed elastically at the NW free surface without dislocations. This capability can be used to grow unique heterostructures and to grow III-V NWs directly on inexpensive substrates, such as Si, rather than lattice-matched but more expensive III-V substrates. This capability, along with other unique properties (quantum confinement and light trapping), makes NWs of great interest for next generation optoelectronic devices with improved performance, new functionalities, and reduced cost. One of the many applications of NWs includes energy conversion. This review will outline applications of NWs in photovoltaics, thermoelectrics, and betavoltaics (direct conversion of solar, thermal, and nuclear energy, respectively, into electrical energy) with an emphasis on III-V materials. By transitioning away from bulk semiconductor thin films or wafers, high efficiency photovoltaic cells comprised of III-V NWs grown on Si would improve performance and take advantage of cheaper materials, larger wafer sizes, and improved economies of scale associated with the mature Si industry. The thermoelectric effect enables a conversion of heat into electrical power via the Seebeck effect. NWs present an opportunity to increase the figure of merit (ZT) of thermoelectric devices by decreasing the thermal conductivity (κ) due to surface phonon backscattering from the NW surface boundaries. Quantum confinement in sufficiently thin NWs can also increase the Seebeck coefficient by modification of the electronic density of states. Prospects for III-V NWs in thermoelectric devices, including solar thermoelectric generators, are discussed. Finally, betavoltaics refers to the direct generation of electrical power in a semiconductor from a radioactive source. This betavoltaic process is similar to photovoltaics in which photon energy is converted to electrical energy. In betavoltaics, however, energetic electrons (beta particles) are used instead of photons to create electron-hole pairs in the semiconductor by impact ionization. NWs offer the opportunity for improved beta capture efficiency by almost completely surrounding the radioisotope with semiconductor material. Improving the efficiency is important in betavoltaic design because of the high cost of materials and manufacturing, regulatory restrictions on the amount of radioactive material used, and the enabling of new applications with higher power requirements.

In an effort to control aggregation and sintering of phosphor nanoparticles at elevated annealing temperatures, glycothermally synthesized cerium-doped yttrium aluminum garnet (Ce:YAG) nanoparticles were annealed in a matrix of aluminum oxide between 1000 °C and 1200 °C. Scanning electron microscopy images showed that glycothermal synthesis yields ~100 nm particles, and that the alumina matrix was able to control grain growth of Ce:YAG at annealing temperatures up to 1200 °C. Analysis by x-ray diffraction and Fourier transform infrared spectroscopy showed an increase in the degree of crystallinity at increasing temperatures as well as the evolution of alumina phases. Photoluminescence of the composite product showed the expected broad Ce:YAG spectrum, with characteristic chromium R lines present due to the formation of corundum at 1200 °C with trace chromium content. The same procedure was performed to synthesize a Ce:YAG/Cr:Al2O3 nanocomposite, yielding photoluminescence of both the expected Ce:YAG and Cr:Al2O3 peaks as well as clear evidence of energy transfer between Ce and Cr centers in YAG. The luminescence of these composites was used to determine their CIE colour co-ordinates. It was found that the colour profile of the resulting emission may be tuned by adjusting the Cr content and annealing conditions of the composite materials.