Solvothermal synthesis of hexagonal ZnO nanorods and their photoluminescence properties

Pure hexagonal ZnO nanorods were synthesized by low-temperature (90 °C) solvothermal treatment of zinc acetate in 40-80 wt.% hydrazine hydrate aqueous solutions. The products were characterized by means of powder X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electronic microscopy (TEM), selected area electron diffraction (SAED), and room temperature photoluminescence (RTPL) spectra. They show a strong UV emission at around 380 nm upon excitation at 360 nm using a Xe lamp at room temperature. The influence on the quality of the nanorods was investigated while the content of the solvent changed. The as-synthesized ZnO nanorods are promising materials for nanoscale optoelectronic devices due to their excellent UV emission properties.     

ZnO纳米棒Al掺杂和A1,N共掺杂的制备技术与光致发光性能

采用水热法首先合成了Al掺杂ZnO(AZO)纳米棒,在此基础上通过550℃的氨气氛中退火制备了Al,N共掺杂ZnO(ANZ())纳米棒.运用X射线衍射(XRD),场发射扫描电镜(FESEM),透射电子显微镜(TEM),X射线能谱(EDS)和光致发光(PL)对样品进行了表征与分析.结果表明,制备的AZO和ANZ()纳米棒...     

ZnO单晶堆垒纳米棒的制备与表征

在Au点阵模板上磁控溅射ZnO薄膜,然后在O2气氛下1000℃退火制备了ZnO单晶堆垒纳米棒。采用扫描电子显微镜(SEM)、高分辨透射电子显微镜(HRTEM)、X射线衍射(XRD)和傅立叶变换红外(FTIR)光谱对样品进行分析。结果表明,ZnO纳米棒是由诸多单晶堆垒而成,每个单晶均为六方纤锌矿结构,纳米棒直径在100nm左右。初步探讨了ZnO单晶堆垒纳米棒可能的生长机理。     

Effect of reaction conditions on the morphology and optical properties of ZnO nanocrystals

We report a simple hydrothermal method at low temperature for synthesis of zinc oxide (ZnO) nanorods followed by ultrasonication. The samples were characterized by powder X-ray diffraction (XRD), Fourier transform infrared spectroscopy, transmission electron microscopy (TEM), UV–Vis absorption spectrophotometer and photoluminescence (PL) spectroscopy. The XRD results shows the prepared ZnO nanocrystals are in wurtzite structure. TEM results indicate the growth of ZnO nanorods with increasing reaction stirring time and morphology also get affected after ultrasonication. PL studies also reveal the presence of defects considered as the main reason for the green emission in PL with increasing reaction time and blue shift in UV emission corresponds to reduction of tensile strain.     

Hydrothermal synthesis of nanostructured zinc oxide and study of their optical properties

Nanostructured ZnO (nanorods, nanoshuttles) have been synthesized by hydrothermal approach using ZnCl₂ or Zn(NO₃)₂·6H₂O as zinc sources and cetyltrimethylammonium bromide as structure-directing agent. Techniques X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV–visible absorption, Fourier transform infrared spectroscopy (FTIR) and Raman spectroscopy have been used to characterize the structure, morphology and composition of the nanostructured zinc oxide. The optical properties of the as-obtained materials were also studied and showing that it is possible to apply the ZnO nanoshuttles and nanorods on the UV filter, photocatalysis, and special optical devices.     

Effect of morphology in the photocatalytic degradation of methyl violet dye using ZnO nanorods

In the present work, high purity ZnO nanorods were synthesized by solid state reaction method at different annealing temperatures (250–400 °C). The structural, morphological and optical characteristic of the ZnO nanorods were studied. X-ray diffraction results confirmed that the ZnO nanorods have Wurtzite structure with high crystal quality. The grain size has increased from 23 to 27 nm with increasing temperature. The scanning electron microscopy and high resolution-transmission electron microscopy photographs showed the formation of ZnO nanorods. The bonding natures of the synthesized nanorods were analyzed by Fourier transform infra-red spectroscopy. The blue shift in the absorption edge was observed from the UV–Vis spectrum. The photoluminescence spectra showed two emission peaks corresponding to blue and red emissions. The photocatalytic performance of these nanorods was evaluated using methyl violet dye. The result showed that photocatalytic performance is highly depends on the morphology of the nanorods.     

海胆形氧化锌纳米结构的制备与光催化性能

以Zn(AC)2.2H2O为原料,NH3.H2O为络合剂,在NaBH4辅助下140℃水热反应2 h制备出ZnO纳米棒自组装的海胆形结构。采用X射线衍射仪、扫描电镜和透射电镜对产物进行表征。结果表明,海胆形ZnO结构的直径约为3～17μm,它是由直径约为100 nm,长度约为500 nm～3μm范围的ZnO纳米棒自组装而成。提出了ZnO纳米棒自组装海胆形结构的可能生长机理。NaBH4与溶液中的少量H+结合生成H2气泡,ZnO纳米晶吸附在H2的气液界面形成了纳米颗粒自组装的微球,随着反应时间的延长,组装成微球的ZnO纳米颗粒沿[0001]方向取向生长成ZnO纳米棒,最终形成ZnO纳米棒自组装的海胆形颗粒。室温下以海胆形ZnO纳米结构和ZnO纳米棒为光催化剂,以偶氮染料甲基橙作为光催化研究对象,紫外光照70 min,对甲基橙的降解率分别为97%和67%。     

Preparation and characterization of ZnO/ZnS core/shell nanocomposites through a simple chemical method

In this paper, we reported the preparation of ZnO/ZnS core/shell nanocomposites by sulfidation of ZnO nanostructures via a simple hydrothermal method. The precursors of bare ZnO nanoparticles and ZnO nanorods were synthesized by a surfactant-assisted hydrothermal growth. The structural, morphological, and element compositional analysis of bare ZnO nanostructures and ZnO/ZnS core/shell nanocomposites were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy, energy-dispersive X-ray spectroscopy, and transmission electron microscopy techniques. The XRD results indicated that the phase of bare ZnO nanoparticles and ZnO nanorods was wurtzite structure, and the phase of coated ZnS nanoparticles on the surface of bare ZnO nanostructures was sphalerite structure with the size of about 8 nm. Photoluminescence measurement was carried out, and the PL spectra of ZnO/ZnS core/shell nanocomposites revealed an enhanced UV emission and a passivated orange emission compared to that of bare ZnO nanostructures. In addition, the growth mechanism of ZnO/ZnS core/shell nanostructures through hydrothermal method was preliminarily discussed.     

Synthesis,microstructure and photoluminescence of well-aligned ZnO nanorods on Si substrate

Well-aligned zinc oxide (ZnO) nanorods were densely grown on Si substrate using ZnO thin-film seed layer without any catalysts and/ or additives by a simple solid–vapour phase thermal sublimation technique. The growth mechanism can be interpreted as self-catalyst of zinc particles based on vapour–solid (VS) mechanism. High-resolution transmission electron microscopy (HRTEM) image and selected area electron diffraction (SAED) pattern confirmed that the single-crystalline growth of the nanorods were preferentially along c-axis of hexagonal crystal system. High-crystal quality ZnO nanorods with strong near band edge emission centred at 380 nm can be achieved on Si substrate by the introduction of sufficient oxygen during the nanorod growth processing.     

Growth of aligned hexagonal ZnO nanorods on FTO substrate for dye-sensitized solar cells (DSSCs) application

This article reports a facile growth of well-crystalline aligned hexagonal ZnO nanorods on fluorine-doped tin-oxide (FTO) substrate via non-catalytic thermal evaporation process. The morphological investigations done by field-emission scanning electron microscope (FESEM) and transmission electron microscopy (TEM) reveal that the grown products are aligned hexagonal ZnO nanorods which are grown in a very high density over the whole substrate surface. The detailed structural properties observed by high-resolution TEM equipped with selected area electron diffraction (SAED) and X-ray diffraction (XRD) pattern confirmed that the synthesized nanorods are well-crystalline possessing wurtzite hexagonal phase and preferentially grown along the c-axis direction. A sharp and strong UV emission at 381 nm in room-temperature photoluminescence (PL) spectrum showed that the as-grown ZnO nanorods possess excellent optical properties. The as-grown nanorods were used as photo-anode for the fabrication of dye-sensitized solar cells (DSSCs) which exhibits an overall light-to-electricity conversion efficiency (ECE) of 0.7% with V(oc) of 0.571 V, J(sc) of 2.02 mA/cm2 and FF of 0.58.     

Facile preparation of Ag/ZnO nanoparticles via photoreduction

Ag/ZnO nanoparticles can be obtained via photocatalytic reduction of silver nitrate at ZnO nanorods when a solution of AgNO₃ and nanorods ZnO suspended in ethyleneglycol is exposed to daylight. The mean size of the deposited sphere like Ag particles is about 5 nm. However, some of the particles can be as large as 20 nm. The ZnO nanorods were pre-prepared by basic precipitation from zinc acetate di-hydrate in the ionic liquid 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide. They are about 50–300 nm in length and 10–50 nm in width. Transmission electron microscopy (TEM), energy-dispersive X-ray analysis (EDS), X-ray powder diffraction (XRD), UV–Vis spectroscopy, X-ray photoelectron spectroscopy (XPS), and photoluminescence (PL) were used to characterize the resulting Ag/ZnO nanocomposites.     

Fast UV detection and hydrogen sensing by ZnO nanorod arrays grown on a flexible Kapton tape

ZnO nanorod arrays were grown on a flexible Kapton tape using microwave-assisted chemical bath deposition. High crystalline properties of the produced nanorods were proven by X-ray diffraction patterns and field emission scanning electron microscopy. Additionally, the photoluminescence spectrum showed higher UV peaks compared with visible peaks, which indicates that the ZnO nanorods had high quality and low number of defects. The metal-semiconductor-metal (MSM) configuration was used to fabricate UV and hydrogen gas detectors based on the ZnO nanorods grown on a flexible Kapton tape. Upon exposure to 395 nm UV light, the UV device exhibited fast response and decay times of 37 ms and 44 ms, respectively, at a bias voltage of 30 V. The relative sensitivities of the gas sensor made of the ZnO nanorod arrays, at hydrogen concentration of 2 %, at room temperature, 150 °C and 200 °C, are 0.42, 1.4 and 1.75 respectively.     

RGO/ZnO纳米棒复合材料的合成及光催化性能

采用水热合成法制备ZnO纳米棒及RGO/ZnO纳米棒复合材料。研究不同含量的RGO对RGO/ZnO纳米棒复合材料光催化活性的影响。采用X射线衍射仪(XRD)、场发射电子显微镜(FESEM)、光电子能谱仪(XPS)及漫反射紫外-可见吸收光谱(UV-Vis)检测手段对RGO/ZnO进行表征。结果显示:RGO与ZnO纳米棒成功复合。加入GO的含量不同,获得的RGO/ZnO样品在可见光区域的吸光度值不同。以甲基橙作为模拟污染物的光催化结果表明,RGO/ZnO复合材料具有高的紫外-可见光光降解效率,加入GO与ZnO的质量比为3%时,样品紫外-可见光光催化性能最佳,120min内甲基橙基本可以完全降解;且在波长大于400nm可见光照射下,RGO/ZnO具有一定的可见光活性,180min内其降解甲基橙效率最大可达26.2%。同时,RGO/ZnO具有较好的光稳定性。     

室温固相法合成ZnO纳米棒及其光学特性

在氯化钠存在下,以硫酸锌和氢氧化钠为原料,采用一步室温固相法制备了纳米氧化锌.XRD、TEM分析结果表明:所得纳米氧化锌为棒状,直径约10nm左右,长度约100～160nm.利用紫外-可见分光光度计测试了光吸收性能,发现ZnO纳米棒对200～380nm波长范围的光有很强吸收性,在可见光范围内,也有较强的吸收.ZnO纳米棒在550nm左右具有较弱的荧光发光峰且ZnO纳米棒较普通氧化锌发光峰波长发生了明显的红移.     

Structural analysis of vertically-aligned single crystalline ZnO nanorods grown on different seed layers with chemical solution deposition

We report the structural properties of the vertically-oriented ZnO nanorods fabricated on various ZnO seed layers with chemical solution deposition (CSD) technique. The ZnO nanorods were prepared using an aqueous solution with Zinc nitrate (Zn(NO3)2 x 6H2O, Aldrich) and hexamethylenetetramine (HMT, Aldrich) in a convection oven. A-plane sapphire substrates with a deposited ZnO thin film were placed upside down in a quartz holder to avoid any micro-crystalline contamination. Especially, our hydro-thermal syntheses are automatically processed on precision pump drive systems (Masterflex) to accurately control the pH of the aqueous solution. The [002] crystal orientation of the ZnO seed layer was observed by the X-ray diffraction pattern. Structural features of ZnO nanorods were systematically analyzed by scanning electron microscopy and tunneling electron microscopy, together with selective area electron diffraction patterns. Experimental observations clearly demonstrated the dependence of the growth direction of the ZnO nanorods on the crystal structures of the ZnO seed layers.     

原位生成法制备单分散的纳米氧化锌分散液

用ZnCl2作原料,PVP作分散剂,在160℃下采用原位生成法制得单分散、具有良好晶体结构和规则外形的ZnO纳米单晶分散液,用透射电子显微镜、X射线衍射、紫外/可见分光光度计等测试手段对其进行了表征.讨论了工艺条件对纳米ZnO尺寸和形貌的影响,并对其生长机理做了初步探讨.     

Fabrication of vertically aligned ultrafine ZnO nanorods using metal-organic vapor phase epitaxy with a two-temperature growth method

We report the fabrication of vertically aligned ultrafine ZnO nanorods using metal-organic vapor phase epitaxy and applying a two-temperature growth method. First, thick nanorods were grown vertically on the substrate at a lower temperature. Then, ultrafine ZnO nanorods with an average diameter of 17.7?nm were grown from the tips of the thick nanorods at a higher temperature. The direction of the ultrafine ZnO nanorods followed that of the preformed vertically aligned thick nanorods. Electron microscopy revealed that the ultrafine nanorods were single crystals and the growth direction was along the c axis. Excellent photoluminescence characteristics of the nanorods were confirmed.     

Growth of well-aligned ZnO nanorods using auge catalyst by vapor phase transportation

Well-aligned ZnO nanorods have been achieved using new alloy (AuGe) catalyst. Zn powder was used as a source material and it was transported in a horizontal tube furnace onto an AuGe deposited Si substrates. The structural and optical properties of ZnO nanorods were characterized by scanning electron microscopy, high resolution X-ray diffraction, and photoluminescence. ZnO nanorods grown at 650 degrees C on 53 nm thick AuGe layer show uniform shape with the length of 8 +/- 0.5 microm and the diameter of 150 +/- 5 nm. Also, the tilting angle of ZnO nanorods (+/- 5.5 degrees) is confirmed by HRXRD. High structural quality of the nanorods is conformed by the photoluminescence measurement. All samples show strong UV emission without considerable deep level emission. However, weak deep level emission appears at high (700 degrees C) temperature due to the increase of oxygen desertion.     

Synthesis, microstructure and photoluminescence of well-aligned ZnO nanorods on Si substrate

Well-aligned zinc oxide (ZnO) nanorods were densely grown on Si substrate using ZnO thin-film seed layer without any catalysts and/or additives by a simple solid–vapour phase thermal sublimation technique. The growth mechanism can be interpreted as self-catalyst of zinc particles based on vapour–solid (VS) mechanism. High-resolution transmission electron microscopy (HRTEM) image and selected area electron diffraction (SAED) pattern confirmed that the single-crystalline growth of the nanorods were preferentially along c-axis of hexagonal crystal system. High-crystal quality ZnO nanorods with strong near band edge emission centred at 380 nm can be achieved on Si substrate by the introduction of sufficient oxygen during the nanorod growth processing.     

Rapid growth of nanotubes and nanorods of würtzite ZnO through microwave-irradiation of a metalorganic complex of zinc and a surfactant in solution

Large quantities of single-crystalline ZnO nanorods and nanotubes have been prepared by the microwave irradiation of a metalorganic complex of zinc, in the presence of a surfactant. The method is simple, fast, and inexpensive (as it uses a domestic microwave oven), and yields pure nanostructures of the hexagonal würtzite phase of ZnO in min, and requires no conventional templating. The ZnO nanotubes formed have a hollow core with inner diameter varying from 140–160 nm and a wall of thickness, 40–50 nm. The length of nanorods and nanotubes varies in the narrow range of 500–600 nm. These nanostructures have been characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and selected area electron diffraction (SAED). The ZnO nanorods and nanotubes are found by SAED to be single-crystalline. The growth process of ZnO nanorods and nanotubes has been investigated by varying the surfactant concentration and microwave irradiation time. Based on the various results obtained, a tentative and plausible mechanism for the formation of ZnO nanostructures is proposed.