Fast synthesize ZnO quantum dots via ultrasonic method

Green emission ZnO quantum dots were synthesized by an ultrasonic sol–gel method. The ZnO quantum dots were synthesized in various ultrasonic temperature and time. Photoluminescence properties of these ZnO quantum dots were measured. Time-resolved photoluminescence decay spectra were also taken to discover the change of defects amount during the reaction. Both ultrasonic temperature and time could affect the type and amount of defects in ZnO quantum dots. Total defects of ZnO quantum dots decreased with the increasing of ultrasonic temperature and time. The dangling bonds defects disappeared faster than the optical defects. Types of optical defects first changed from oxygen interstitial defects to oxygen vacancy and zinc interstitial defects. Then transformed back to oxygen interstitial defects again. The sizes of ZnO quantum dots would be controlled by both ultrasonic temperature and time as well. That is, with the increasing of ultrasonic temperature and time, the sizes of ZnO quantum dots first decreased then increased. Moreover, concentrated raw materials solution brought larger sizes and more optical defects of ZnO quantum dots.     

A sol-gel method for preparing ZnO quantum dots with strong blue emission

ZnO quantum dots (QDs) with strong blue emission have been successfully synthesized by sol-gel method, and their crystal structures, sizes, and photoluminescence properties were characterized by X-ray diffractometer, scanning electron microscope, and ultraviolet-visible spectroscopy. It has been found that ZnO QDs had a hexagonal wurtzite crystal structure, and their average diameter was about 16.0-32.2 nm. Both the reaction time and temperature were found to have a strong influence on the average size and photoluminescence properties of ZnO QDs. Longer reaction time and higher reaction temperature resulted in larger average size for ZnO QDs. It has been shown that at reaction temperature 60 °C the emission intensity for ZnO QDs increased first with reaction time before 7 h and then decreased after 7 h. For the same reaction time 7 h, ZnO QDs synthesized at 60 °C showed the strongest emission intensity. It was found that annealing in nitrogen, vacuum, and air all resulted in an increase of the size of ZnO QDs and a reduction in their photoluminescence. The dependence of the size and properties of ZnO QDs on the reaction parameters as well as the annealing conditions has been discussed.     

Density controllable growth of ZnO quantum dots by MOCVD

High quality self-assemble ZnO quantum dots (QDs) have been successfully grown on the Si(111) substrates by metalorganic chemical vapor deposition (MOCVD). The diameter of ZnO QDs is about 10 nm in average, and the densities and the sizes of ZnO QDs can be well controlled by adjusting the growth temperature, which were evident in the SEM images. The properties and stress involved in ZnO QDs are studied by X-ray diffraction. In addition, room temperature photoluminescence spectra reveal that the ZnO QDs exhibit a band gap blue shift because of the quantum confinement effects.     

巯基丙酸分子对CdSe核壳量子点和 ZnO纳米粒子薄膜之间电荷转移的影响

通过稳态光谱和时间分辨荧光光谱研究了巯基丙酸(MPA)分子对由量子点到ZnO纳米粒子薄膜的电荷转移过程的影响。研究发现,相对于CdSe纳米粒子薄膜样品,没有MPA分子参与作用的CdSe/ZnO薄膜样品和有MPA分子连接的CdSe/MPA/ZnO薄膜样品中都存在从CdSe量子点到ZnO纳米粒子薄膜的有效电荷分离过程,但是相对于CdSe/ZnO样品, CdSe/MPA/ZnO样品中电荷转移速率明显变小。这表明MPA分子本身它并不能促进CdSe到ZnO电荷分离过程,因此可以认为用金属氧化物薄膜直接吸附量子点吸收材料,将能获得高功率转换效率的量子点敏化太阳能电池。     

超声法制备碳量子点发光性能的影响因素分析

超声法制备碳量子点过程简单,成本低廉,不易产生二次污染,应用前景广泛。为优化超声法制备碳量子点的各工艺参数,制备了关键工艺参数不同的碳量子点样品,测试其发射与激发光谱,分析了量子点浓度,溶剂种类,辅助剂种类、浓度,超声功率、时间等参数对碳量子点发光性能影响。结果表明超声法制备的碳量子点具有激发光波长依赖性,发射峰位置随激发波长的变化而发生明显改变;碳量子点浓度增加,发光强度由于非辐射能量传递和团聚作用,先增大后减小;由于溶剂效应,碳量子点在乙醇中比在水中发光强度更强,波长更短,且浓度越大时波峰移动越明显;相比盐酸,以NaOH为辅助剂制备的碳量子点表面钝化程度高,发光强度强;增加辅助剂NaOH浓度可提高量子点表面钝化程度,增大发光强度;同等时间下增加超声功率或同等功率下适量增加超声时间,可制备更多的碳量子点样品,但超声时间过长,碳量子点容易发生团聚猝灭现象。以上影响因素分析为超声法制备碳量子点的工艺参数优化提供了理论基础,有利于碳量子点大规模低成本的生产应用。     

Influence of annealing temperature on the photoluminescence properties of ZnO quantum dots

The properties of ZnO quantum dots (QDs) synthesized by the sol-gel process are reported. The primary focus is on investigating the origin of the visible emission from ZnO QDs by the annealing process. The X-ray diffraction results show that ZnO QDs have hexagonal wurtzite structure and the QD diameter estimated from Debye-Scherrer formula is 8.9 nm, which has a good agreement with the results from transmission electron microscopy images and the theoretical calculation based on the Potential Morphing Method. The room-temperature photoluminescence spectra reveal that the ultraviolet excitation band has a red shift. Meanwhile, the main band of the visible emission shifts to the green luminescence band from the yellow luminescence one with the increase of the annealing temperature. A lot of oxygen atoms enter into Zn vacancies and form oxygen antisites with increasing temperature. That is probably the reason for the change of the visible emission band.     

Characterization of cavitation in a flow-through exposure chamber by means of a resonant bubble detector

Ultrasonic cavitation at frequencies of 0.514, 0.866, 1.03 and 1.61 MHz in water flowing through tubes was observed by counting bubbles downstream with a resonant bubble detector (RBD) operated at 0.89 or 1.7 MHz. In a 21 mm diameter, thin-walled tube, cavitation thresholds in tap water flowing at 5.3 cm s^?1 ranged from 2.0 – 2.5 bar at 0.514 MHz to 3 – 4 bar at 1.61 MHz. When high speed injections were employed to trigger the ultrasonic cavitation with hydrodynamically-generated bubbles, the thresholds were reduced to about 2 bar and bubble production was enhanced for 1.03 and 1.61 MHz exposures. Ultrasonic radiation forces on the bubbles and bubble coalescence appeared to cause, under some conditions, a reduction in bubble counts during subthreshold exposures when bubbles were injected into the flow. The RBD method is a useful tool for detecting and semi-quantitatively observing cavitation in a flow-through exposure system.     

Well-crystallized zinc oxide quantum dots with narrow size distribution

In this study, pulsed laser ablation, online annealing, and following size classification using a differential mobility analyzer (DMA) were employed to fabricate quantum dots (QDs) of zinc oxide (ZnO). The irregularly shaped ZnO particles were obtained at annealing temperature less than 873 K, which gradually transformed into spherical QDs with increasing the annealing temperature. Finally, ZnO QDs with narrow size distribution having spherical shapes were successfully obtained at temperatures above 1173 K under the DMA classification at a nominal size of 10 nm. TEM observation demonstrated that the ZnO QDs obtained by this process were well-crystallized single crystallites with a wurtzite structure. Further, ZnO QDs with average sizes in the range of 4.8–8.1 nm were successfully fabricated by reducing the specified sizes of DMA. These features of the fabricated ZnO QDs are favorable for investigation of intrinsic quantum size effect in ZnO.     

Photoluminescence study of ZnCdSe/ZnSe quantum dot systems

The optical properties of the populated ZnCdSe/ZnSe quantum dots have been studied by photoluminescence spectra measured with different laser excitation apertures at temperatures from 22 to 300 K. The differences of spectral features between small and large excitation spot suggest the existence of quantum dot size fluctuation in the system. The temperature evolution of photoluminescence spectral features revealed that two types of quantum dots with different densities and sizes coexist in ZnCdSe/ZnSe system. The energy spacings of the two kinds of quantum dot emissions are about 50 meV at various temperatures. The thermally activated lateral transfer processes of carriers populated in the two sorts of quantum dots are investigated by temperature dependences of spectral intensities.     

Controlling the energy transfer between near-field optically coupled ZnO quantum dots

We performed time-resolved spectroscopy of ZnO quantum dots (QD), and observed exciton energy transfer and dissipation between QD via an optical near-field interaction. Two different sizes of ZnO QD with resonant energy levels were mixed to test the energy transfer and dissipation using time-resolved photoluminescence spectroscopy. The estimated energy transfer time was 144 ps. Furthermore, we demonstrated that the ratio of energy transfer between the resonant energy states could be controlled.     

Emulsification mechanism in an ultrasonic microreactor: Influence of surface roughness and ultrasound frequency

An ultrasonic microreactor with rough microchannels is presented in this study for oil-in-water (O/W) emulsion generation. Previous accounts have shown that surface pits or imperfections localize and enhance cavitation activity. In this study cavitation bubbles are localized on the rough microchannels of a borosilicate glass microreactor. The cavitation bubbles in the microchannel are primarily responsible for emulsification in the ultrasonic microreactor. We investigate the emulsification mechanism in the rough microchannels employing high-speed imaging to reveal the different emulsification modes influenced by the size and oscillation intensity of the cavitation bubbles. The effect of emulsification modes on the O/W emulsion droplet size distribution for different surface roughness and frequency is demonstrated. The positive effect of the frequency on minimizing the droplet size utilizing a reactor with large pits is presented. We also demonstrate microreactor systems for a successful generation of miniemulsions with high dispersed phase volume fractions up to 20%. The observed emulsification mechanism in the rough microchannel offers new insights into the utility and scale-up of ultrasonic microreactors for emulsification.     

Synthesis of stable dispersion of ZnO quantum dots in aqueous medium showing visible emission from bluish green to yellow

Aqueous dispersion of 4-8 nm size stable ZnO quantum dots (QDs) exhibiting luminescence in the visible region have been synthesized by a simple solution growth technique at room temperature. Silica has been used as capping agent to control the particle size as well as to achieve uniform dispersion of QDs in aqueous medium. X-ray diffractometer (XRD) analysis reveals formation phase pure ZnO particles having wurzite (hexagonal) structure. Atomic force microscope (AFM) images show that the particles are spherical in shape, having average crystalline sizes ∼4, 5.5 and 8 nm for samples prepared at pH values of 10, 12 and 14, respectively. From the optical absorption studies, the band gap energy of QDs is found to be blue shifted as compared to bulk ZnO (3.36 eV) due to the quantum confinement effect and is consistent with the band gap calculated by using effective-mass approximation model. The photoluminescence (PL) observed in these QDs has been attributed to the presence of defect centers.     

Fixed-distance coupling and encapsulation of heterogeneous quantum dots using phonon-assisted photo-curing

We propose a novel method of coupling heterogeneous quantum dots at fixed distances and capsulating the coupled quantum dots by utilizing nanometric local curing of a photo-curable polymer caused by multistep electronic transitions based on a phonon-assisted optical near-field process between quantum dots. Because the coupling and the capsulating processes are triggered only when heterogeneous quantum dots floating in a solution closely approach each other to induce optical near-field interactions between them, the distances between the coupled quantum dots are physically guaranteed to be equal to the scale of the optical near fields. To experimentally verify our idea, we fabricated coupled quantum dots, consisting of CdSe and ZnO quantum dots and a UV-curable polymer. We also measured the photoluminescence properties due to the quantum-dot coupling and showed that the individual photoluminescences from the CdSe and ZnO quantum dots exhibited a trade-off relationship.     

Effect of ultrasonic wave on the syntheses of Au and ZnO nanoparticles by laser ablation in water

We synthesized Au and ZnO nanoparticles by laser ablation in distilled water with the superposition of an ultrasonic wave. The effect of the ultrasonic wave was examined on the optical absorbance of colloidal solution and the crystallinity of synthesized nanoparticles. The absorbance of colloidal solution was enhanced by the ultrasonic wave, indicating more efficient production rate of nanoparticles. In addition, the ultrasonic wave enhanced the crystallinity of synthesized nanoparticles. These enhancements are attributed to the fact that the ultrasonic wave drives the repetitive formations and collapses of cavitation bubbles.     

Synthesis of ZnO quantum dots and their agglomeration mechanisms along with emission spectra based on ageing time and temperature

The ZnO quantum dots (QDs) were synthesized with improved chemical solution method. The size of the ZnO QDs is exceedingly uniform with a diameter of approximately 4.8 nm, which are homogeneously dispersed in ethanol. The optical absorption edge shifts from 370 nm of bulk material to 359 nm of QD materials due to the quantum size effect, while the photoluminescence peak shifts from 375 nm to 387 nm with the increase of the density of ZnO QDs. The stability of ZnO QDs was studied with different dispersion degrees at 0 ℃ and at room temperature of 25 ℃. The agglomeration mechanisms and their relationship with the emission spectra were uncovered for the first time. With the ageing of ZnO QDs, the agglomeration is aggravated and the surface defects increase, which leads to the defect emission.     

Effect of annealing temperature on density of ZnO quantum dots

ZnO quantum dots (QDs) were fabricated on Si (001) substrates by pulsed laser deposition (PLD) and subsequent thermal annealing. X-ray diffraction and transmission electron microscopy analyses revealed that the ZnO QDs had polycrystalline hexagonal wurtzite structure. The size and density of ZnO QDs were investigated by atomic force microscopy. It has been found that the density decreased while the size increased with increasing annealing temperature. The analysis of size distribution of the dots shows an obvious bimodal mode according to scaling theory. The Raman spectrum shows a typical resonant multi-phonon form for the ZnO QDs. The collapse from the top of the dots was observed firstly after the samples were exposed in air for 30 days.     

Electron dynamics in modulation p-doped InGaAs/GaAs quantum dots

We investigate the electron dynamics of p-type modulation doped and undoped InGaAs/GaAs quantum dots using up-conversion photoluminescence at low temperature and room temperature. The rise time of the p-doped sample is significantly shorter than that of the undoped at low temperature. With increasing to room temperature the undoped sample exhibits a decreased rise time whilst that of the doped sample does not change. A relaxation mechanism of electron-hole scattering is proposed in which the doped quantum dots exhibit an enhanced and temperature independent relaxation due to excess built-in holes in the valence band of the quantum dots. In contrast, the rise time of the undoped quantum dots decreases significantly at room temperature due to the large availability of holes in the ground state of the valence band. Furthermore, modulation p-doping results in a shorter lifetime due to the presence of excess defects.     

Control of spin state in CdSe quantum dots by coupling with magnetic semiconductor quantum dots

We studied spin states of CdSe quantum dots (QDs) coupled with CdMnSe QDs by probing circular polarization of photoluminescence spectrum under external magnetic fields. The bandgap energies of CdSe and CdMnSe QDs are close to each other and photoluminescence mainly originates from CdSe QDs due to relatively low radiation efficiency of CdMnSe QDs. The photoluminescence lifetime as well as its intensity was decreased with increasing magnetic field, which was ascribed to the increase in the ground state wavefunctions in CdMnSe QDs. The decrease was more pronounced for spin down electrons, which was explained by the difference in spin up and down wave functions under magnetic fields. Our results show that the spin state of CdSe QDs can be manipulated by coupling with CdMnSe QDs.     

Optical study of single InAs on In0.12Ga0.88As self-assembled quantum dots: biexciton binding energy dependence on the dots size

Single self-assembled InAs quantum dots embedded in a In_0.12Ga_0.88As quantum well and emitting in the near infrared have been optically investigated. The dependence on the excitation power of the single quantum dot photoluminescence has been used to identify the emission of the biexciton complex. The biexciton binding energy, which has been measured for a dozen dots, increases with increasing exciton transition energy for the dot sizes investigated in the present work, as a consequence of stronger confinement in a smaller quantum dot. The obtained data is compared with experimental results available in the literature for InAs quantum dots. PACS 78.67.Hc; 73.21.La; 78.55.Cr     

Observation of long-lived excitons in InAs quantum dots under thermal redistribution temperature

We study the temperature-dependent time-resolved photoluminescence (TRPL) of self-assembled InAs quantum dots (QDs). Under low excitation power, a surprisingly long PL decay time is observed at about 60 K, under the thermal redistribution temperature. The long decay time decreases with increasing excitation power but is nearly independent of the detection energy of TRPL measurements. A model considering the spin relaxation through the excited excitonic state is proposed to quantitatively explain the unusual phenomena. The rate equation analysis indicates that the observation of long-lived excitons is caused by the shortened spin-flip time.