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1.
Zn_(1-x)Cu_x O(x=0.00, 0.01, 0.03, and 0.05) nanoparticles are synthesized via the sol-gel technique using gelatin and nitrate precursors. The impact of copper concentration on the structural, optical, and antibacterial properties of these nanoparticles is demonstrated. Powder x-ray diffraction investigations have illustrated the organized Cu doping into ZnO nanoparticles up to Cu concentration of 5%(x = 0.05). However, the peak corresponding to CuO for x= 0.01 is not distinguishable. The images of field emission scanning electron microscopy demonstrate the existence of a nearly spherical shape with a size in the range of 30–52 nm. Doping Cu creates the Cu–O–Zn on the surface and results in a decrease in the crystallite size. Photoluminescence and absorption spectra display that doping Cu causes an increment in the energy band gap. The antibacterial activities of the nanoparticles are examined against Escherichia coli(Gram negative bacteria)cultures using optical density at 600 nm and a comparison of the size of inhibition zone diameter. It is found that both pure and doped ZnO nanoparticles indicate appropriate antibacterial activity which rises with Cu doping.  相似文献   

2.
利用火焰喷雾法成功制备了纳米级的ZnO和MgxZn1-xO颗粒. 通过对样品的X射线衍射谱和场发射扫描电子显微镜照片分析,发现制备的颗粒大小较为均匀,直径在20nm左右;镁元素的掺入引起晶格常数变小. 通过透射光谱和光致发光谱的测量,发现MgxZn1-xO颗粒的禁带宽度远大于ZnO颗粒的禁带宽度,同时对两组样品的紫外发光和可见发光的强度变化和发光机理进行了探讨. 关键词: 火焰喷雾 ZnO 禁带宽度 纳米颗粒  相似文献   

3.
In the present work, we report the synthesis and optical properties of ZnS nanoparticles produced by the mechano-chemical route. We used zinc acetate and sodium sulphide as source materials in a high energy planetary ball mill at rotation speed of 300 rpm and vial rotation speed of 600 rpm with ball to powder (BPR or charge ratio CR) 5:1 for 30 and 90 min. The milled powders were washed with methanol to remove impurity and dried at 300 °C for 1 h. The prepared nanoparticles have been characterized using X-ray diffraction (XRD), Field emission scanning electron microscope (FESEM), UV–vis–NIR spectrophotometer and Fluorescence spectroscopy. The crystallite size of the synthesized ZnS nanoparticles is found to be in the range 7–8 nm which was calculated using Debye–Scherer's formula. The value of optical band gap has been found to be in the range 3.80–4.15 eV. Room temperature photoluminescence (PL) spectrum of ZnS samples exhibit a blue emission peaked at 466 nm under UV excitation.  相似文献   

4.
方合  王顺利  李立群  李培刚  刘爱萍  唐为华 《物理学报》2011,60(9):96102-096102
利用532 nm脉冲激光对沉浸在去离子水及十二烷基硫酸钠(SDS)水溶液中的金属锌靶进行液相激光烧蚀,合成了ZnO纳米颗粒和Zn/ZnO核壳结构的纳米粒子. 应用X射线衍射仪,透射电子显微镜,紫外可见光分光光度计和荧光光度计表征产物的微观结构和光学性能,并探讨其形成机理. 结果表明:在去离子水中分别烧蚀2 h和4 h生成的ZnO纳米粒子的平均粒径分别为43 nm和19 nm. 激光的长时间作用可以使纳米粒子粒径减小. 在0.005 mol/L的SDS水溶液中合成了Zn/ZnO核壳结构的纳米粒子,这是由于S 关键词: 脉冲激光烧蚀 ZnO纳米粒子 核壳结构 光致发光  相似文献   

5.
ZnS:Mn nanoparticles of size variation 11–17 nm were synthesized by a simple and inexpensive chemical method and confirmed by transmission electron microscopy (TEM). Presuming electronic energy loss (S e>S n, S n being nuclear energy loss) to be the dominant phenomenon, they were irradiated by 80-MeV energetic oxygen ions with fluence of 1011 to 1013 ions/cm2. Photoluminescence (PL) spectra revealed three major emission bands ~445 nm, ~582 nm and ~706 nm; which are ascribed to D–A pair transition, Mn emission and surface state led fluorescence activation. The recovery of Mn emission and tunable surface state emission have been observed with ion fluence variation. Infra-red (IR) spectra of irradiated samples show great extent of oscillation with respect to amplitude due to ion fluence variation however, phonon energy (~98 MeV) remains unchanged. The possible applications of these modified properties in nanophotonics are also highlighted.  相似文献   

6.
利用简单的氨还原方法制备了GaN:Tb纳米颗粒. X射线衍射结果显示纳米颗粒为六方结构, 根据Scherrer公式, 计算得到了GaN:Tb纳米颗粒的平均晶粒大小为21.2 nm; 透射电子显微镜结果显示为GaN:Tb纳米颗粒尺寸均匀, 尺寸大小约为20 nm; 除正常的GaN Raman振动模式外, 还观察到了251和414 cm-1 2个额外的Raman散射峰, 前者是表面无序或尺寸限制效应造成的, 而后者则是八面体Ga-N6振动模式; 最后, 测量了GaN:Tb纳米颗粒的室温光致发光谱, 获得了Tb3+离子在可见光区(位于493.9, 551.2, 594.4和630.1 nm)的本征发光.  相似文献   

7.
We present in this paper a study of the structural and photoluminescence (PL) properties of terbium (Tb) doped zinc oxide (ZnO) nanoparticles synthesized by a simple low temperature chemical precipitation method, using zinc acetate and terbium nitrate in an isopropanol medium with diethanolamine (DEA) as the capping agent at 60 ℃. The as-prepared samples were heat treated and the PL of the annealed samples were studied. The prepared nanoparticles were characterized with X-ray diffraction (XRD). The XRD patterns show the pattern of typical ZnO nanoparticles and correspond with the standard XRD pattern given by JCPDS card No. 36-1451, showing the hexagonal phase structure. The PL intensity was enhanced due to Tb^3+ doping, and it decreased at higher concentrations of Tb^3+ doping after reaching a certain optimum concentration. The PL spectra of Tb^3+ doped samples exhibited blue, bluish green, and green emissions at 460 nm (5^D3 - 7^F3), 484 nm (5^D4 - 7^F6), and 530 nm (5^D4 - 7^F5), respectively, which were more intense than the emissions for the undoped ZnO sample. Based on the results, an energy level schematic diagram was proposed to explain the possible electron transition processes.  相似文献   

8.
Luminescence induced by elastic deformation of ZnS:Mn nanoparticles   总被引:1,自引:0,他引:1  
When the thin film of ZnS:Mn nanoparticles deposited on a glass substrate is elastically deformed by applying a load, then initially the mechanoluminescence (ML) intensity increases with time, attains a peak value Im at a particular time tm, and later on it decreases with time. The rise and decay characteristics of the ML produced during release of the load are also similar to those produced during the application of load. Similar rise, occurrence of peak and then decrease in ML intensity are also found, when the film is deformed impulsively by dropping a steel ball of small mass from a low height; however, in this case, the time durations for the occurrence of ML and decay time of ML are very short. In the cases of loading and impulsive deformation ,after tm, initially the ML intensity decreases at a fast rate and then at a slow rate, in which the decay time of fast decrease is equal to the time-constant for rise of pressure and the decay time for slow decrease is equal to the relaxation time of the surface charges. In the case of loading, the peak intensity Im and the total intensity IT of ML increase quadratically with the magnitude of applied pressure; however, in the case of impulsive deformation, both the Im and IT increase linearly with the height through which the ball is dropped on to the sample. In the case of deformation of the samples at a fixed strain rate, Im should increase linearly with the applied pressure. The elastico ML in ZnS:Mn nanoparticles can be understood on the basis of the piezoelectrically-induced electron detrapping model, in which the local piezoelectric field near the Mn2+ centres reduces the trap-depth, and therefore, the detrapping of filled electron traps takes place, and subsequently the energy released non-radiatively during the electron-hole recombination excites the Mn2+ centres and de-excitation gives rise to the ML. The equal number of photons emitted during the application of pressure, release of pressure, and during the successive applications of pressure, indicates that the detrapped electron-traps get filled during the relaxation of the surface charges induced by the application and release of pressure because the charge carriers move to reduce the surface charges. On the basis of the piezoelectrically-induced electron detrapping model, expressions are derived for different characteristics of the ML of ZnS:Mn nanoparticles and a good agreement is found between the theoretical and experimental results. The expressions explored for the dependence of ML intensity on several parameters may be useful in tailoring the suitable nanomaterials capable of exhibiting ML during their elastic deformation. The values of the relaxation time of surface charges, time-constant for the rise of pressure, and the threshold pressure can be determined from the measurement of the time-dependence of ML. It seems that the trapping and detrapping of charge carriers in materials can be studied using ML.  相似文献   

9.
A boehmite whisker powder with the aspect ratio and mean diameter of 10-40 and 2-6 nm was prepared by the sol-gel process using aluminum alkoxide as precursor. The main absorption bands located at 234 (5.31 eV), and 254.5 (4.88 eV) nm are presented in the excitation spectrum of sample. It is observed that all the spectra show two main broad bands emission whose maximum shows a large shift, which depends on the excitation wavelength. It is suggested that the ultraviolet photoluminescence emission in boehmite whisker prepared by the sol-gel process may be associated with anionic vacancies (F and F+ centers, or grouping of these two types of defects), and the non-bridging oxygen hole center (NBOHC)=Al-O.  相似文献   

10.
Monodispersive ZnO nanoparticles each with a hexagonal wurtzite structure are facilely prepared by the hightemperature organic phase method.The UV-visible absorption peak of ZnO nanoparticles presents an obvious blue-shift from 385 nm of bulk ZnO to 369 nm.Both the real part and the image part of the complex permittivity of ZnO nanoparticles from 0.1 GHz to 10 GHz linearly decrease without obvious resonance peak appearing.The real parts of intrinsic permittivity of ZnO nanoparticles are about 5.7 and 5.0 at 0.1 GHz and 10 GHz respectively,and show an obvious size-dependent behavior.The dielectric loss angle tangent(tan 5) of ZnO nanoparticles with a different weight ratio shows a different decreasing law with the increase of frequency.  相似文献   

11.
The influence of PVP on the magnetic properties of NiSn nanoparticles prepared by polyol method has been studied. NiSn nanoparticles exhibit superparamagnetic behavior although there is a ferromagnetic contribution due to particles agglomerated below the blocking temperature. The particle size is controlled by the addiction of PVP in varying amounts. The addition of PVP also favours the particles isolation, narrow the particle size distribution and decrease the interparticle interaction strength increasing the superparamagnetic contribution.  相似文献   

12.
尤娜  刘海林  李美亚  熊锐 《物理实验》2011,31(2):11-14,19
采用热分解法制备了单相的锰铁氧纳米颗粒,X射线衍射以及透射电镜测量显示其颗粒大小约为20 nm.磁滞回线测量显示室温超顺磁性.零场和非零场磁测量显示制备的MnFe2O4纳米粒子平均截止温度为84.3 K,样品中最大颗粒的截止温度为230 K,且平均截止温度与外场H2/3存在线性关系.  相似文献   

13.
Cu掺杂氧化锌薄膜的发光特性研究   总被引:15,自引:0,他引:15       下载免费PDF全文
通过射频反应溅射法在Si(111)衬底上制备了不同Cu掺杂量的ZnO薄膜.室温下测量了样品的光致发光(PL)谱,所有样品的PL谱中均观察到435?nm左右的蓝光发光带,该发光带的强度与Cu掺杂量和溅射功率有关.当溅射功率为150?W,Cu掺杂量为2.5%时,ZnO薄膜的PL谱中出现了较强的蓝光双峰,而溅射功率为100?W,Cu掺杂量为1.5%时,出现了位于437nm(2.84eV)处较强的蓝光峰,后者的取向性较好.还研究了掺杂量和溅射功率对发光特性的影响,并对样品的蓝光发光机制进行了探讨. 关键词: ZnO薄膜 Cu掺杂 光致发光谱 射频反应共溅射  相似文献   

14.
徐磊华  强颖怀  江利 《发光学报》2011,32(3):227-231
以正硅酸乙酯(TEOS)为SiO2的前驱物,硝酸镉为镉源,硫脲为硫源,用溶胶-凝胶法制备了CdS量子点掺杂的SiO2干凝胶,利用XRD、紫外-可见吸收光谱、光致发光谱对其性质进行研究.样品的测试结果表明在SiO2干凝胶的网状结构中形成了CdS量子点,平均粒径为5.1 nm.SiO2凝胶中CdS吸收峰位置明显蓝移.在一定...  相似文献   

15.
《Composite Interfaces》2013,20(7):425-432
Abstract

ZnS nanoparticles and Mn2+-doped ZnS nanoparticles were prepared by a reverse micelle reaction system. In addition, ZnS and Mn2+-doped ZnS nanoparticles were modified with poly(vinyl alcohol) (PVA) and 1-dodecanethiol (C12H25SH). The average particle size of the ZnS sample is determined around 2.3 nm by using the well-known Scherrer equation, which is in accordance with the results obtained from UV–vis and TEM analysis. Fluorescence intensity of the Mn2+-doped ZnS nanoparticles increases with increasing Mn2+ content compared with undoped ZnS nanoparticles, and coating PVA can also make fluorescence intensity increase. Different Zn2+/S2- or C12H25SH/Zn2+ can affect intensity of PL emission peak and its position, which is discussed in this paper.  相似文献   

16.
This paper is focusing on the synthesis of Zn1−xFexS nano-particles with x = 0, 0.1 and 0.2 by chemical co-precipitation method, the prepared of which are characterized by XRD, EDS, TEM, PL, magnetization versus field behavior and M-T curve. In the XRD patterns, Zn1−xFexS nano-particles are shown of cubic zinc blende structure, and the broadening diffraction peaks consistent with the small-size characteristic of nano-materials. The diameter of nano-particles is between 3.3 and 5.5 nm according to the HR-TEM images. The EDS data confirm the existence of Fe ions in Fe-doped ZnS nanoparticles. There we found that Fe-doping did not import new energy bands or defect states, but reduced the intensity of PL peaks. The magnetization versus field behaviors were illustrated by the M-H curves at both 5 K and 300 K, respectively, where no remanence or coercive force was observed. This phenomenon indicates that the Zn1−xFexS (x = 0.1) nano-particles are superparamagnetic. The zero-field-cooled (ZFC) and field-cooled (FC) magnetization curves further reveal that the blocking temperature (TB) of the superparamagnetic behavior might be below 5 K.  相似文献   

17.
Mn–Zn ferrite nanoparticles (Mn1−xZnxFe2O4) are synthesized by a hydrothermal precipitation approach using metal sulfate solution and aqueous ammonia. The analysis methods of XRPD, TEM, TGA, and VSM are used to characterize the magnetic nanoparticles. Through the characterization of the precipitated nanoparticles, the effects of the reacting component proportions and preparation techniques on the Curie temperature, the magnetization, and the size distribution of Mn–Zn ferrite nanoparticles are discussed. Furthermore, the Mn–Zn ferrite nanoparticles are used to prepare ferrofluid. Variation of the magnetic properties of the ferrite nanoparticles with the composition content x of Zn and the magnetic moment of the nanoparticles are discussed.  相似文献   

18.
We applied the microwave-assisted heating method to prepare the pyridine dialkyldithiophosphate-encapsulated Ni (Ni-DDP) nanoparticles. The surface-encapsulated Ni particles were characterized by Fourier transform infrared spectrometer, thermogravimetric analysis, X-ray diffraction, and transmission electron microscopy. Their tribological behavior in lubricate base oil was investigated on four-ball machines. The results show that uniform Ni-DDP nanoparticles about 12 nm can be obtained using microwave heating device and also they exhibit good tribological behaviors dispersed in liquid paraffin.  相似文献   

19.
We synthesized zinc sulfide (ZnS) nanopowders with size ranging from 2 to 100 nm by a simple, low-cost, and mass production chemical method. The nanoparticles (NPs) were characterized by X-ray powder diffraction (XRD), atomic force microscopy (AFM), transmission electron microscopy (TEM), and UV-vis absorption spectroscopy. Our study concerns also the change in the refractive index of deionized water in presence of ZnS nanospheres. We present experimental results on effective index variation of water dispersed ZnS NPs at different wavelengths in visible spectrum.  相似文献   

20.
ZnS nanoparticles were prepared by a simple chemical method and using PVP (poly vinylpyrrolidone) as capping agent. The sample was characterized by UV-vis spectrophotometer, X-ray diffraction (XRD) and Z-scan technique. XRD pattern showed that the ZnS nanoparticles had zinc blende structure with an average size of about 2.18 nm. The value of band gap of these nanoparticles was measured to be 4.20 eV. The nonlinear optical properties of ZnS nanoparticles in aqueous solution were studied by Z-scan technique using CW He-Ne laser at 632.8 nm. The nonlinear absorption coefficient (β) was estimated to be as high as 3.2×10−3 cm/W and the nonlinear refractive index (n2) was in order of 10−8 cm2/W. The sign of the nonlinear refractive index obtained negative that indicated this material exhibits self-defocusing optical nonlinearity.  相似文献   

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