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Bingsuo Zou

Publications and source records attributed to Bingsuo Zou.

10 recordsLinked to original sources
PubMed2006

High-quality alloyed CdSxSe1-x whiskers as waveguides with tunable stimulated emission.

High-quality ultra-long alloyed CdS(x)Se(1)(-)(x) (0 < or = x < or = 1) whiskers were obtained by a simple thermal evaporation route. The near band-edge emission in these whiskers can be effectively guided at the sub-millimeter scale under continuous-wave laser excitation. As good optical waveguide cavities, the whiskers exhibit stimulated emissions under pulsed light excitation at room temperature for all compositions 0 < or = x < or = 1. The spectral positions of the sharp emission lines of the whiskers were tuned by their compositions, covering the spectral range from green to red.

Journal Article↗
PubMed2006

A simple solution route to single-crystalline Sb2O3 nanowires with rectangular cross sections.

We report a simple solution route to large-scale synthesis of uniform, single-crystalline, and well-faceted orthorhombic antimony trioxide (Sb(2)O(3)) nanowires with rectangular cross sections by direct air oxidation of bulk metal antimony (Sb) in a mixed solution made of ethylenediamine (EDA) and deionized water (DIW). The as-synthesized products were analyzed by range of methods, such as XRD, SEM, EDX, TEM, SAED, HRTEM, FTIR, Raman, UV-vis absorption, and photoluminescence (PL) spectra. The as-synthesized Sb(2)O(3) nanowires with rectangular cross sections are usually hundreds of micrometers in length, typically 80-100 nm in width, and 60-80 nm in thickness. The novel room temperature photoluminescence properties of Sb(2)O(3) nanowires with rectangular cross sections displayed a significant UV luminescence with a strong emission band at 374 nm, which was reported for the first time, indicating the as-synthesized products with an optical band gap E(g) = 3.3 eV. It is expected that as-synthesized Sb(2)O(3) nanowires would be a new member of functional materials and used in the manufacture of advanced nanodevices.

Antimony↗
PubMed2006

Lasing mechanism of ZnO nanowires/nanobelts at room temperature.

ZnO has become the focus of photonics and optoelectronic research. We prepared pure Mn(II) doped ZnO nanowires with a controlled reduction reaction by carbon in an asymmetrical tube. Careful time-resolved photoluminescence experimental study indicates three types of lasing mechanisms: exciton-exciton interaction, bipolaronic exciton condensation, and plasma; these exist in different ZnO nanowires, which can be changed by doping Mn in ZnO nanowire. The transformation between varied mechanisms is discussed in detail with their spectral behaviors. These results are important in the design of future violet-blue luminescence and display devices.

Journal Article↗
PubMed2005

Stimulated emissions in aligned CdS nanowires at room temperature.

Aligned CdS nanowires (NWs) were obtained through a simple thermal evaporation process with highly active CdS nanoparticles as the evaporation source. These NWs show prominent optical waveguides behavior under a continuous-wave (CW) laser excitation. Excitation intensity-dependent photoluminescence (PL) measurements show that these NWs exhibited both broad and supernarrow stimulated emission (lasing) under intense pulse optical excitation at room temperature. Raman scattering and time-resolved PL measurements were used to investigate the optical properties. The results indicated that the stimulated emission in these NWs involves the electron-hole plasma (EHP) and Farby-Perot (F-P) optical resonant processes at room temperature.

Journal Article↗
PubMed2005

Color-tunable photoluminescence of alloyed CdS(x)Se(1-x) nanobelts.

High-quality CdSxSe1-x nanobelts of variable composition (0 </= x </= 1) were fabricated by a simple one-step thermal evaporation route. Photoluminescence measurements showed that all the CdSxSe1-x nanobelts have a single near-bandedge emission band, and their spectral maximum positions can be tuned from approximately 508 nm (for pure CdS) to approximately 705 nm (for pure CdSe). These kinds of nanobelts may have potential applications in adjustable nano/micro photoelectric devices in the visible region.

Journal Article↗
PubMed2005

A new route to zinc-blende CdSe nanocrystals: mechanism and synthesis.

We report the possible mechanism of forming of CdSe nanocrystals in the high boiling point solvents with long alkane chains and a novel Non-TOP-Based route to zinc-blende CdSe nanocrystals. A new mechanism shows that there exits a redox reaction in the long alkane chain solvents: Se is reduced to H2Se gas; at the same time, the long alkane chains are oxidated to alkene chains; then, the Cd complex reacts with H2Se to form CdSe nanocrystals. Possible chemical reaction equations involved in the process of forming the CdSe nanocrystals have been discussed. The alkene chain and H2Se were detected respectively by a series of experiments to support the new mechanism. Under the guidance of this mechanism, we have developed a much cheaper and greener Non-TOP-Based route for the synthesis of a size series of high-quality zinc-blende (cubic) CdSe nanocrystals. Low-cost, green, and environmentally friendlier reagents are used, without use of expensive solvents such as trioctylphosphine (TOP) or tributylphosphine (TBP). The new route enables us to achieve high-quality CdSe nanocrystals with sharp ultraviolet and visible (UV-vis) absorption peaks, controllable size (2.0-5.0 nm), bright photoluminescence (PL), narrow PL full width of half-maximum (fwhm) (29-48 nm), and high PL quantum yield (up to 60%) without any size sorting.

Cadmium↗
PubMed2005

Exciton interactions in CdS nanocrystal aggregates in reverse micelle.

Here we report the formation and spectroscopic properties of cadmium sulfide (CdS) nanocrystal systems: individual nanocrystal and CdS aggregates. The optical absorption and luminescence spectra of the aggregated CdS nanocrystals and individual nanocrystal show exciton aggregate and individual exciton characteristics. Although it is not Bose-Einstein condensation, such aggregated quantum dots (QDs) seem to supply us opportunity to study the interactions and condensation of excitons in multi-QDs system, not in the separated QDs system.

Journal Article↗
PubMed2004

Time-resolved spectroscopic behavior of Fe2O3 and ZnFe2O4 nanocrystals.

Using nanosecond (ns) and femtosecond (fs) time-resolved absorption spectroscopies (pump-probe technique), the carrier dynamics in transition metal oxide nanocrystals of alpha-Fe2O3 and ZnFe2O4 was studied during the photolysis process. For Fe2O3 and ZnFe2O4 nanocrystals, the fs measurements detect similar profiles of a positive nonlinear absorption in their capped nanocrystals, whereas much weak signals in the naked particles. In the nanosecond measurements Fe2O3 and ZnFe2O4 nanocrystals show obvious excitation-power dependent absorption properties and at the low pump power they show weak photobleaching, but at high pump power they produce positive nonlinear absorptions. For Fe2O3 nanocrystals, the threshold power of negative absorption (bleach) to positive absorption increases with reducing size, whereas for the ZnFe2O4 samples, the threshold powers reach minimum at a critical size of 11 nm, grow for both the bigger and the smaller nanocrystals. These results reflect the influences of their microscopic magnetic couplings and carrier correlation on biexciton absorption in Fe2O3 and ZnFe2O4 nanocrystals. All the results indicate that the time resolved photoabsorption techniques are useful to study the microscopic spin interactions and carrier correlations in transition metal oxide nanocrystals.

Journal Article↗