Observation of memory behaviour in cadmium sulphide nanorods doped ferroelectric liquid crystal mixture

In this study, cadmium sulphide (CdS) nanorods doped ferroelectric liquid crystal (FLC) sample cells have been prepared and studied. A memory effect has been observed in CdS nanorods (≤0.3?wt%) doped FLC mixture and confirmed by textures, dielectric and optical studies. The addition of nanorods increases the memory behaviour and efficiency. The occurrence of memory behaviour has been explained due to charge transfer from liquid crystal molecules to CdS nanorods and exists there for 5–15?min in 0.1–0.3?wt% CdS nanorods doped samples. An improvement in polarization, switching time, threshold voltage and rise time parameters has also been noticed in CdS nanorods doped FLC samples.     

ZnO nanoparticles favours heterogeneous nucleation in PET–ZnO nanocomposites

The structural and chemical properties with non-isothermal crystallization kinetics of PET–ZnO nanocomposites have been reported in this article. ZnO nanoparticles have been synthesized via chemical route with average diameter 19 nm which made confirm by transmission electron microscopy and X-ray diffractometer (XRD) techniques. PET–ZnO nanocomposites have been prepared by solution casting method. The structural and chemical changes occurred in poly (ethylene terephthalate) after inclusion of ZnO nanoparticles have been studied with the help of XRD and Fourier transform infrared spectroscopy, respectively. It was observed from differential scanning calorimeter that ZnO nanoparticles work as nucleating agent for heterogeneous nucleation in PET matrix under non-isothermal crystallization process. The combined Avrami and Ozawa models have been proved adequate to explain non-isothermal crystallization kinetics of PET–ZnO nanocomposites, and also, ZnO nanoparticles have been caused to reduce crystallization activation energy in pristine PET as per the applied Kissinger model.     

Synthesis and characterization of ZnO-Ag core-shell nanocomposites with uniform thin silver layers

This paper presents an investigation on the synthesis and characterization of ZnO-Ag core-shell nanocomposites. ZnO nanorods were employed as core material for Ag seeds, and subsequent nucleation and growth of reduced Ag by formaldehyde formed the ZnO-Ag core-shell nanocomposites. The ZnO-Ag nanocomposites were annealed at different temperature to improve the crystallinity and binding strength of Ag nanoparticles. The morphology, microstructure and optical properties of the ZnO-Ag core-shell nanocomposites were characterized by X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy, ultraviolet-visible (UV-vis) absorption and photoluminescence measurement. It was demonstrated that very small face-center-cubic Ag nanoparticles were coated on the surface of ZnO nanorods. The ultraviolet absorption and surface plasmon absorption band of ZnO-Ag core-shell nanocomposites exhibited some redshifts relative to pure ZnO nanorods and monometallic Ag nanoparticles. The coating of Ag nanocrystals onto the ZnO nanorods completely quenched the photoluminescence. These observations reflected the strong interfacial interaction between ZnO nanorods and Ag nanoparticles. The effect of Ag coating thickness on the morphology and optical properties of ZnO-Ag core-shell nanocomposites was also investigated. Moreover, the growth mechanism of ZnO-Ag core-shell nanocomposites was also proposed and discussed in detail.     

SWCNT doped ferroelectric liquid crystal: The electro-optical properties with enhanced dipolar contribution

Effect of single wall carbon nanotubes (SWCNTs) on electro-optical performance of a ferroelectric liquid crystal (FLC) has been studied. Voltage dependent spontaneous polarization and response time measurement has been made for the pure and SWCNT doped FLC system. Dielectric measurement has also been performed to understand the existing interaction between SWCNTs and FLC molecules. The results have shown increase in the value of spontaneous polarization and relative permittivity with slight slower response for the doped system. The observed properties of doped system revealed that the SWCNTs can perform well with FLC at low applied electric field to enhance the performance of LC devices.     

Synthesis and characterisation: Zinc oxide–sulfide nanocomposites

A novel synthesis method is presented for the preparation of nanosized-semiconductor zinc oxide–sulphide (ZnO/ZnS) core–shell nanocomposites, both formed sequentially from a single-source solid precursor. ZnO nanocrystals were synthesized by a simple co-precipitation method and ZnO/ZnS core–shell nanocomposites were successfully fabricated by sulfidation of ZnO nanocrystals via a facile chemical synthesis at room temperature. The as-obtained samples were characterized by X-ray diffraction and transmission electron microscopy. The results showed that the pure ZnO nanocrystals were hexagonal wurtzite crystal structures and the ZnS nanoparticles were sphalerite structure with the size of about 10 nm grown on the surface of the ZnO nanocrystals. Optical properties measured reveal that ZnO/ZnS core–shell nanocomposites have integrated the photoluminescent effect of ZnO and ZnS. Based on the results of the experiments, a possible formation mechanism of ZnO/ZnS core–shell nanocomposites was also suggested. This treatment is suggested to improve various properties of optoelectronically valuable ZnO/ZnS nanocomposites. These nanosized semiconductor nanocomposites can form a new class of luminescent materials for various applications.     

Different strategies for the synthesis of graphene/ZnO composite and its photocatalytic properties

Owing to its unique physical and chemical properties, graphene has attracted tremendous attention in the preparation of graphene-based composites for various applications. In this study, two different strategies have been developed to load zinc oxide (ZnO) nanorods onto reduced graphene oxide (RGO) sheets, i.e., in situ growth and a self-assembly approach. The microstructure and morphology of the synthesized RGO/ZnO nanocomposites was investigated by X-ray diffraction (XRD), Raman spectroscopy, field emission scanning electron microscopy (FESEM) and Brunauer–Emmett–Teller (BET) measurements. Fluorescence emission spectra (PL) of RGO/ZnO composites were performed to attribute quality of combination between RGO and ZnO. Significantly enhanced photocatalytic activity of RGO/ZnO nanocomposites in comparison to bare ZnO nanoparticles was revealed by the degradation of methylene blue under irradiation, which can be attributed to the inhibition of electron–hole pair recombination and enhanced adsorption due to the presence of RGO sheets.     

Fabrication of Prussian blue nanocubes through reducing a single-source precursor with graphene oxide and their electrocatalytic activity for H2O2

Nanostructured ZnO has been synthesized by wet chemical route. Poly(vinylpyrrolidone) is used for stabilization and surface passivation of synthesized nanoparticles, thus tailoring the growth of ZnO at nanoscale. Structural characterization using X-ray diffraction, scanning electron microscopy, high-resolution transmission electron micoroscopy and Fourier transformed infrared spectroscopy of the synthesized nanoparticles confirm the evolution of nanocrystalline ZnO prevailing in hexagonal wurtzite phase. UV–Vis and photoluminescence spectroscopy studies show blue shift phenomenon in the synthesized nanoparticle in contrast to the bulk ZnO furnishing evidence in support of quantum size effect. The nanocomposites of ZnO and poly [9,9-dioctylfluorenyl-2,7-diyl] are prepared and characterized to investigate its luminescent and spectral emission effects. The nanocomposites are then incorporated in light-emitting diodes, and influence of ZnO on the device performance has been explored via electroluminescence, current density evaluation, and corresponding CIE coordinates calculation.     

Carbon quantum dots supported ZnO sphere based photocatalyst for dye degradation application

A Carbon quantum dots supported ZnO hollow Sphere (ZnO/C-dots) were synthesized through a solvothermal method using polyethylene glycol 400 (PEG 400) as a solvent. The phase and crystal structure of as-prepared ZnO/C-dots photocatalyst were characterized by powder X-ray diffraction (XRD). The surface morphology and size of the composite were analyzed using field emission scanning microscopy (FE-SEM). The optical properties of the as-prepared nanocomposites were examined using UV–visible (UV–Vis) spectrometer. The photocatalytic activity of pure ZnO and ZnO/C-dots nanocomposites were evaluated by the degradation of methylene blue (MB) under UV–Visible light irradiation. The ZnO/C-dots nanocomposites exhibited maximum photocatalytic MB dye degradation efficiency of 96% which is much higher that the pure ZnO (63%). The enhanced photocatalytic activity of ZnO/C-dots is due to the extended light absorption in the visible region and suppressed photoexcited electron-hole pair recombination rate. Moreover, the activity of photocatalyst after five cycles exhibits high stability, which is vital for the sustainable photocatalytic procedures. It is concluded that the prepared ZnO/C-dots composite have low cost, good stability and has a great potential application for Photocatalytic dye degradation.     

The Effect of Zinc Oxide and Calcium Carbonate Nanoparticles on the Thermal Conductivity of Polypropylene

The thermal conductivity (TC) of compression-moulded polypropylene (PP) and PP filled with 5–15% zinc oxide (ZnO) or calcium carbonate (CaCO₃) nanoparticles, prepared by extrusion, was studied using a thermal conductivity analyzer (TCA). The effect of nanoparticle content and crystallinity on the thermal conductivity was investigated using conventional methods, including SEM, XRD, and DSC. The incorporation of nanoparticles improved the crystallinity and thermal conductivity simultaneously. The experimental TC values of the PP nanocomposites with different level of nanoparticles concentration showed a linear increase with an increase in crystallinity. The TC improvement in PP/ZnO nanocomposite was greater than that of PP/calcium carbonate nanocomposites. This fact can be attributed to the intrinsic, better thermal conductivity of the ZnO nanoparticles. Several models were used for prediction of the TC in the nanocomposites. In the PP/ZnO nanocomposites the TC values correlated well with the values predicted by the Series, Maxwell, Lewis and Nielson, Bruggeman, and De Loor models up to 10 wt%.     

Charge transport studies on chemically grown manganite based heterostructures

In this communication, we have successfully fabricated mixed valent La_0.7Ca_0.3MnO₃ (LCMO) manganite based (i) ZnO/LCMO/LAO and (ii) LMO/LCMO/LAO (LMO: LaMnO_3–d thin layer; LAO: LaAlO₃ substrate) thin film heterostructures using chemical solution deposition (CSD) method. 100 nm LCMO layer was initially grown on single crystalline (100) LAO substrate followed by the growth of 50 nm ZnO and LMO layers separately on the two different heterostructures. In the present study, upper layers of ZnO and LMO were intentionally prepared at 700 °C for 12 h under air environment, thereby some naturally created oxygen vacancies are expected to be present in their lattices. Presence of oxygen vacancies makes ZnO and LMO layers as n–type oxides in the heterostructures. Temperature dependent current–voltage (I–V) characteristics and interface resistivity (under different applied electric fields across interface only) were carried out to understand their charge transport behavior. A strong effect of electric field on the resistivity behavior has been observed due to a reasonable electrically polarizable (active) nature of ZnO and LMO thin layers. Zener double exchange (ZDE) polynomial law has been employed to understand various scattering processes as source of resistivity across, both, ZnO/LCMO and LMO/LCMO interfaces. Transport properties and charge conduction mechanisms have been discussed and compared for both the interfaces in the context of interface state and barrier between electrically active layer and LCMO film. Also, power consumption criteria have been discussed in detail for the presently studied heterostructures for their practical device applications such as field effect devices, memory devices, read–write head devices or any other spintronic devices.     

Effects of nanoparticle doping on the phase transitional behaviour of ferroelectric liquid crystal Langmuir–Blodgett composite films

Langmuir–Blodgett films of ferroelectric liquid crystals (FLCs) doped with a low concentration of functionalized Al: ZnO (AZO) nanoparticles were prepared and characterized. Pressure–area isotherms show that the nanoparticles as well as FLC composite systems have the capability to form stable monolayers at the air–water interface. The molecular interaction between nanoparticles and FLC molecules increased during barrier compression, which resulted in increased surface pressure. We observed various phases in isotherms with increasing concentration of nanoparticles in the FLC matrix. An X-ray diffraction profile at a low angle confirmed that FLCs retain their layer structure at a low concentration doping of AZO nanoparticles in the FLC matrix. Atomic force microscopy images indicate that low wt% composites are uniformly deposited without disturbing the translation behaviour of SmC* liquid crystals.     

ZnO/ZnS核-壳量子点的双光子吸收效应

利用飞秒激光Z-扫描与泵浦-探测技术,研究了室温下ZnO/ZnS与ZnO/ZnS/Ag核-壳胶体量子点的双光子吸收效应.研究发现:ZnO基核-壳量子点的本征双光子吸收系数比ZnO体材料增大了3个数量级;测量得到的660 nm处的ZnO/ZnS核-壳量子点双光子吸收截面约为4.3×10^-44 cm⁴·s·photon^-1,比相应的ZnS、ZnSe及 CdS量子点大2个数量级;当ZnO/ZnS核-壳量子点镶嵌了银纳米点时,非线性吸收有所增强.ZnO基复合纳米结构的双光子吸收增强可归因于量子限域与局域场效应.     

PREPARATION OF STRIPE-SHAPED DOMAIN STRUCTURE IN FERROELECTRIC LIQUID CRYSTAL AND THE FABRICATION OF SPATIAL LIGHT MODULATOR

The stripe-shaped domain (SSD) structure was prepared in the initial ferroelectric liquid crystal (FLC) alignment without the application of an external electric field, which was realized by the aligning layer modification through the doping of tin tetra-2, 4-dimethyl phenoxy phthalocyanine (SnPc) into the rubbed polyimide films. Atomic force microscopy was used to investigate the alignment films and the corresponding aligning ability was evaluated through the pre-tilt angle measurement. The memory capability and the contrast ratio of thus aligned SSFLC cells have been enhanced and improved with the appearance of the SSD structure. The electrically controlled 64×64 FLC spatial light modulator was fabricated using the improved ligning method, which proves valuable for the practical device fabrication.     

ZnO/Ag纳米复合物的制备及光学性质

采用ZnO纳米晶表面还原Ag+的方法合成了ZnO/Ag纳米复合物,并研究了其光学性质.透射电镜和XRD谱表征了ZnO/Ag纳米复合物的晶体形貌和结构,吸收光谱和荧光光谱证明ZnO和Ag之间存在电子传递.在325 nm激光激发下观察到了ZnO/Ag纳米复合物的表面增强共振拉曼散射.     

In situ deposition of flower-like ZnO on silk fibroin fibers

In this paper, a convenient biomineralization technique has been developed to form and assemble flower-like zinc oxide (ZnO) on silk fibroin fiber (SFF). Therein, SFF functions as supporting substrate and reactive sites for the in situ generation of ZnO particles. The photoluminescence (PL) of the resulting nanocomposite ZnO/SFF is investigated extensively. The PL peaks are mainly in the visible region (red), which is different from the usual ZnO region (green and violet). As-prepared ZnO/SFF nanocomposites could be useful in the medical field, photoelectron transfer devices, biomolecular detection, and antibacterial agents.     

紫外发光增强的石墨烯-氧化锌纳米复合物

采用溶剂热法在相同条件下分别制备了纯ZnO和石墨烯-氧化锌纳米复合物,通过SEM、TEM、拉曼和红外光谱等手段,对纳米复合物样品进行了形貌和结构表征。实验结果显示ZnO纳米颗粒成功地分散在少层石墨烯上。通过对比纯ZnO与复合物的形貌和光致发光谱,发现在没有石墨烯时,ZnO能够择优取向生长成六方棱柱,紫外发光峰弱且宽;在有石墨烯时,ZnO聚集成表面不规则的球形颗粒,紫外发光峰强且窄。上述结果表明ZnO形貌的变化和石墨烯的等离子体效应共同影响了ZnO的紫外发光,但石墨烯的表面等离子体效应起主导作用。     

Low-field transport properties of (1−x)La0.7Ca0.2 Sr0.1MnO3+x(ZnO) composites

Composite samples (1−x)La_0.7Ca_0.2Sr_0.1MnO₃(LCSMO)+x(ZnO) with different ZnO doping levels x have been investigated systematically. The structure and morphology of the composites have been studied by the X-ray diffraction (XRD) and scanning electronic microscopy (SEM). The XRD and SEM results indicate that no reaction occurs between LCSMO and ZnO grains, and that ZnO segregates mostly at the grain boundaries of LCSMO. The magnetic properties reveal that the ferromagnetic order of LCSMO is weakened by addition of ZnO. The results also show that ZnO has a direct effect on the resistance of LCSMO/ZnO composites, especially on the low-temperature resistance. With increase of the ZnO doping level, T_P shifts to a lower temperature and the resistance increases. It is interesting to note that an enhanced magnetoresisitance (MR) effect for the composites is found over a wide temperature range from low temperature to room temperature in an applied magnetic field of 3 kOe. The maximum MR appears at x=0.1. The low field magnetoresistance (LFMR) results from spin-polarized tunneling. However, around room temperature, the enhanced MR of the composites is caused by magnetic disorder.     

New phenomenon in the channels of mesoporous silicate CMI-1: quantum size effect and two-photon absorption of ZnO nanoparticles

Quantum size effect (QSE) and very efficient laser action were observed in ZnO-mesoporous CMI-1 silica nanocomposites prepared through the incorporation of ZnO nanoparticles inside the channels of a silica mesoporous material CMI-1. The incorporation was made by direct impregnation of the mesoporous material in a zinc nitrate aqueous solution followed by calcination. The PL spectrum of the nanocomposites presents a significant blue-shift corresponding to the enhancement of the semiconductor band gap. Being excited by incident photons with energy of 1.82 eV, the ZnO nanoparticles exhibit spontaneous emission due to the excitonic recombination. In our samples, spontaneous emission turns to stimulated emission when the pumping intensity reaches a threshold value. This effect implies a two-photon excitation which was never observed with ZnO nanoparticles. This paper deals with results about the characteristics of the matrix and the nanocomposites and the lasing effect. A two-photon excitation phenomenon has been observed. PACS 81.05.Zx; 78.45.+h; 78.55.-m; 78.30.Fs; 72.80.Tm; 61.43.Gt; 61.46.+w; 61.66.Fn     

Synthesis,Characterization and Fluorescence Properties of Novel Porous Fe/ZnO Nano-Hybrid Assemblies by Using Berberis thunbergii Extract

Journal of Fluorescence - In this work, novel Fe/ZnO nanocomposites (NCs) and Fe nanoparticles loaded onto porous ZnO nanostructures have been synthesized via a simple biotechnological route by...     

Ag-ZnO纳米复合热电材料的制备及其性能研究

ZnO是一类具有潜力的热电材料, 但其较大声子热导率影响了热电性能的进一步提高. 纳米复合是降低热导率的有效途径. 本文以醋酸盐为前驱体, 溶胶-凝胶法制备了Ag-ZnO纳米复合热电材料. 扫描电镜照片显示ZnO颗粒呈现多孔结构, Ag纳米颗粒分布于ZnO的晶粒之间. Ag-ZnO纳米复合材料的电导率比未复合ZnO材料高出100倍以上, 而热导率是未复合ZnO材料的1/2. 同时, 随着Ag添加量的增加, 赛贝克系数的绝对值逐渐减小. 综合以上原因, 添加7.5%mol Ag的Ag-ZnO纳米复合材料在700 K时的热电优值达到0.062, 是未复合ZnO材料的约25倍. 在ZnO基体中添加导电金属颗粒有利于产生导电逾渗通道, 提高材料体系的电导率, 但同时导致赛贝克系数的绝对值减小. 总热导率的差异来源于声子热导率的差异. 位于ZnO晶界的纳米Ag颗粒, 有利于降低声子热导率. 关键词： 热电材料 ZnO 纳米复合 热导率