Highly efficient avalanche multiphoton luminescence from coupled Au nanowires in the visible region

We report highly efficient avalanche multiphoton luminescence(MPL)from ordered-arrayed gold nanowires(NWs).The time-average excitation intensity I_(exc) is as low as 5.0-9.1 kW/cm~2.The intensity of avalanche MPL I_(MPL) is about 10~4 times larger than that of three-photon luminescence,the slope ■logI_(MPL)/■logI_(exc) of avalanche MPL reaches as high as 18.3 and the corresponding polarization dependence of I_(MPL) has a form of cos~(50)■_p.The emission dynamics of avalanche MPL and three-photon luminesc...     

Highly efficient multiphoton-absorption-induced luminescence from gold nanoparticles

We demonstrate that highly efficient photoluminescence is generated from gold nanoparticles as small as a few nanometers in diameter upon irradiation with sub-100-fs pulses of 790-nm light. Strong emission is observed at excitation intensities comparable to or less than those typically used for multiphoton imaging of fluorescently labeled biological samples. The particles have polarized emission, can radiate more efficiently than single molecules, do not exhibit significant blinking, and are photostable under hours of continuous excitation. These observations suggest that metal nanoparticles are a viable alternative to fluorophores or semiconductor nanoparticles for biological labeling and imaging.     

Time-resolved investigation of bright visible wavelength luminescence from sulfur-doped ZnO nanowires and micropowders

Sulfur-doped zinc oxide (ZnO) nanowires grown on gold-coated silicon substrates inside a horizontal tube furnace exhibit remarkably strong visible wavelength emission with a quantum efficiency of 30%, an integrated intensity 1600 times stronger than band edge ultraviolet emission, and a spectral distribution that closely matches the dark-adapted human eye response. By comparatively studying sulfur-doped and undoped ZnO micropowders, we clarify how sulfur doping and nanostructuring affect the visible luminescence and the underlying energy transfer mechanisms.     

Highly efficient luminescence from a hybrid state found in strongly quantum confined PbS nanocrystals

We report that high quality PbS nanocrystals, synthesized in the strong quantum confinement regime, have quantum yields as high as 70% at room temperature. We use a combination of modelling and photoluminescence up-conversion to show that we obtain a nearly monodisperse size distribution. Nevertheless, the emission displays a large nonresonant Stokes shift. The magnitude of the Stokes shift is found to be directly proportional to the degree of quantum confinement, from which we establish that the emission results from the recombination of one quantum confined charge carrier with one localized or surface-trapped charge carrier. Furthermore, the surface state energy is found to lie outside the bulk bandgap so that surface-related emission only commences for strongly quantum confined nanocrystals, thus highlighting a regime where improved surface passivation becomes necessary.     

On the origin of the visible luminescence from porous silicon

A correlation between the photoluminescence, chemical bonds and structure of c-Si subjected to electrochemical and laser induced chemical etching has been obtained by X-ray photoelectron spectroscopy, IR spectroscopy and Raman scattering. Photoluminescence is very strongly related to the chemical bonding and depends on the Si, O and C content and the presence of different oxidized states of Si which are different for porous silicon prepared on Si substrates of different electrical resistivity. Porous silicon having Si oxidized states typical for Si suboxides exhibits very intensive photoluminescence. The influence of the doping level of c-Si on the process of electrochemical etching as well as the influence of the laser power on the process of stain etching are discussed.     

Highly efficient luminescence from hybrid structures of ZnO/multi-walled carbon nanotubes for high performance display applications

We report an interesting observation on strong enhancement in green luminescence from hybrid ZnO/multi-walled carbon nanotubes (MWCNTs). The hybrid structures were synthesized via a high temperature sintering method. The strong green emission at 510 nm has been attributed to surface defects of ZnO, originating from interactions between ZnO and the MWCNT surface, which has been confirmed by high resolution transmission electron microscopy and x-ray photoelectron spectroscopy. Furthermore, the two-dimensional (2D) layer of this hybrid material shows a high degree of homogeneity and 82% transparency. Time resolved emission spectroscopy measurement shows a photoluminescence decay time in microseconds, which is suitable for making optoelectronic devices.     

Highly efficient visible light photocatalysis of novel CuS/ZnO heterostructure nanowire arrays

Here, a facile approach for the fabrication of CuS nanoparticle (NP)/ZnO nanowire (NW) heterostructures on a mesh substrate through a simple two-step solution method is demonstrated. Successive ionic layer adsorption and reaction (SILAR) was employed to uniformly deposit CuS NPs on the hydrothermally grown ZnO NW array. The synthesized CuS/ZnO heterostructure NWs exhibited superior photocatalytic activity under visible light compared to bare ZnO NWs. This strong photocatalytic activity under visible light is due to the interfacial charge transfer (IFCT) from the valence band of the ZnO NW to the CuS NP, which reduces CuS to Cu(2)S. After repeated cycles of photodecolorization of Acid Orange 7 (AO7), the photocatalytic behavior of CuS/ZnO heterostructure NWs exhibited no significant loss of activity. Furthermore, our CuS/ZnO NWs/mesh photocatalyst floats in solution via partial superhydrophobic modification of the NWs.     

Exciton and biexciton luminescence from single GaN/AlN quantum dots in nanowires

We present a microphotoluminescence study of single GaN/AlN quantum dots embedded in single nanowires. At low excitation power, single exciton lines with full width at half-maximum as narrow as 1 meV are observed. The study of the excitation power dependence of the emission allows us to identify the biexciton transitions with binding energies ranging from 20 to 40 meV.     

Red luminescence from hydrothermally synthesized Eu-doped ZnO nanoparticles under visible excitation

Eu-doped ZnO nanoparticles were synthesized by hydrothermal method. The Eu-dopant concentration has been varied by varying the amount of Eu-dopant concentration. These nanoparticles were structurally characterized by X-ray diffraction, transmission electron microscopy and selected area electron diffraction and it confirms the formation of nanoparticles having standard wurtzite structure. Photoluminescence studies show that these nanoparticles exhibit a sharp red luminescence due to the intra-4f transitions of Eu³⁺ ions at an excitation of 397 nm and 466 nm. Luminescence quenching is observed in the nanoparticles as the Eu-dopant concentration increases. Incorporation of Eu in the nanoparticles was confirmed by the energy dispersive X-ray studies.     

Tailoring the photoluminescence of ZnO nanowires using Au nanoparticles

Rational design of hybrid nanostructures through attaching nanowires with nanoparticles is an effective route to enhance the existing functionalities or to explore new ones. We carry out a systematic investigation on the photoluminescence of ZnO nanowire-Au nanoparticle hybrid nanostructures synthesized by attaching Au nanoparticles onto ZnO nanowires. Citrate-stabilized 40?nm Au nanoparticles effectively quench the green emission and enhance the UV emission of the ZnO nanowires, which is consistent with the wavelength-dependent generation of surface plasmon. The UV/green emission intensity ratio could be reversibly and reproducibly tailored by attaching/detaching Au nanoparticles. This enhancement of UV emission diminishes if the Au nanoparticles are coated with a polymer layer. We also find that the orange-red emission of the ZnO nanowires is related to the excess oxygen on the ZnO surface, and it is also tunable via annealing and surface modifications.     

High-resolution detection of Au catalyst atoms in Si nanowires

The potential for the metal nanocatalyst to contaminate vapour-liquid-solid grown semiconductor nanowires has been a long-standing concern, because the most common catalyst material, Au, is highly detrimental to the performance of minority carrier electronic devices. We have detected single Au atoms in Si nanowires grown using Au nanocatalyst particles in a vapour-liquid-solid process. Using high-angle annular dark-field scanning transmission electron microscopy, Au atoms were observed in higher numbers than expected from a simple extrapolation of the bulk solubility to the low growth temperature. Direct measurements of the minority carrier diffusion length versus nanowire diameter, however, demonstrate that surface recombination controls minority carrier transport in as-grown n-type nanowires; the influence of Au is negligible. These results advance the quantitative correlation of atomic-scale structure with the properties of nanomaterials and can provide essential guidance to the development of nanowire-based device technologies.     

TiO2光催化活性向可见光区拓展的研究进展

TiO2光催化剂可用于光分解有机污染物,组装太阳能电池,光分解水制氢气或氧气等领域。本文对可见光响应的TiO2光催化剂国内外研究进行了综述,概述了采用敏化,掺杂等方法可使二氧化钛光催化活性从紫外光区拓展到可见光区,并对未来的研究方向进行了展望。     

Highly efficient coupling of photons from nanoemitters into single-mode optical fibers

Highly efficient coupling of photons from nanoemitters into single-mode optical fibers is demonstrated using tapered fibers. A percentage (7.4 ± 1.2%) of the total emitted photons from single CdSe/ZnS nanocrystals were coupled into a 300 nm diameter tapered fiber. The dependence of the coupling efficiency on the taper diameter was investigated and the coupling efficiency was found to increase exponentially with decreasing diameter. This method is very promising for nanoparticle sensing and single-photon sources.     

Color-selective photocurrent enhancement in coupled J-aggregate/nanowires formed in solution

J-aggregates are ordered clusters of coherently coupled molecular dyes, (1) and they have been used as light sensitizers in film photography due to their intense absorptions. Hybrid structures containing J-aggregates may also have applications in devices that require spectral specificity, such as color imaging or optical signaling. (2) However the use of J-aggregates in optoelectronic devices has posed a long-standing challenge (3, 4) due to the difficulty of controlling aggregate formation and the low charge carrier mobility of many J-aggregates in solid state. In this paper, we demonstrate a modular method to assemble three different cyanine J-aggregates onto CdSe nanowires, resulting in a photodetector that is color-sensitized in three specific, narrow absorption bands. Both the J-aggregate and nanowire device components are fabricated from solution and the sensitizing wavelength is switched from blue to red to green, using only solution-phase exchange of the J-aggregates on the same underlying device.     

Periodic magnetoresistance oscillations induced by superconducting vortices in single crystal Au nanowires

We show in this paper that it is possible to induce superconducting vortices in a gold nanowire connected to superconducting electrodes. The gold nanowire acquires superconductivity by the proximity effect. The differential magnetoresistance of the nanowire beyond a critical magnetic field shows uniform oscillations with increasing field with a period of Φ(0)/(2πr(2)) (Φ(0) = h/2e is the superconducting flux quantum, r = 35 nm is the radius of the nanowire). Our analysis indicates that these periodic oscillations are the signatures of the sequential generation and moving of vortices across the gold nanowire.