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1.
Sn掺杂ZnO半导体纳米带的制备、结构和性能 总被引:7,自引:0,他引:7
在无催化剂的条件下, 利用碳热还原反应气相沉积法制备出了高产率单晶Sn掺杂ZnO纳米带. XRD和TEM研究表明纳米带为结晶完好的纤锌矿结构, 生长方向沿[0001], EDS分析表明纳米带中Sn元素含量约为1.9%. 室温光致发光谱(PL)显示掺锡氧化锌纳米带存在强的绿光发射峰和较弱的紫外发射峰, 谱峰峰位中心分别位于494.8 nm和398.4 nm处, 并对发光机制进行了分析. 这种掺杂纳米带有望作为理想的结构单元应用于纳米尺度光电器件领域. 相似文献
2.
Saw-like nanostructures composed of single-crystalline ZnO nanobelts and single-crystalline ZnS nanowires have been successfully synthesized by a vapor-solid process. Several techniques, including scanning electron microscope, transmission electron microscopy, and photoluminescence spectroscopy, were used to investigate the structures, morphology, and photoluminescence properties of the products. Due to the similar crystal habits of wurtzite ZnO and ZnS with chemically active Zn-terminated (0001) and chemically inactive O-terminated (or S-terminated) (000) polar surfaces, hierarchical saw-like nanostructures were considered to be formed by the initiation of a chemically active Zn-terminated ZnO (0001) polar surface. Photoluminescence properties of the heterostructures, different from pure ZnO nanobelts or ZnS nanowires, were also studied at room temperature. 相似文献
3.
Synthesis and synchrotron light-induced luminescence of ZnO nanostructures: nanowires, nanoneedles, nanoflowers, and tubular whiskers 总被引:1,自引:0,他引:1
Sun XH Lam S Sham TK Heigl F Jürgensen A Wong NB 《The journal of physical chemistry. B》2005,109(8):3120-3125
ZnO nanostructures, including single-crystal nanowires, nanoneedles, nanoflowers, and tubular whiskers, have been fabricated at a modestly low temperature of 550 degrees C via the oxidation of metallic Zn powder without a metal catalyst. Specific ZnO nanostructures can be obtained at a specific temperature zone in the furnace depending on the temperature and the pressure of oxygen. Scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), and X-ray diffraction (XRD) studies show that ZnO nanostructures thus prepared are single crystals with a wurtzite structure. X-ray excited optical luminescence (XEOL) from the ZnO nanostructures show noticeable morphology-dependent luminescence. Specifically, ZnO nanowires of around 15 nm in diameter emit the strongest green light. The morphology of these nanostructures, their XEOL, and the implication of the results will be discussed. 相似文献
4.
MoO(3) nanostructures with different morphologies, such as helical nanosheets, crosslike nanoflowers, and nanobelts, have been synthesized on a large scale by an environmentally friendly chemical route. The evolution process from helical nanosheets to crosslike nanoflowers to nanobelts is observed for the first time. The influences of reaction time and the molar ratio of molybdenum and H(2)O(2) on the morphologies of MoO(3) nanostructures have been investigated. The synthetic process is environmentally friendly and may be extended to synthesize nanostructures of other metal (W, Ti, and Cr) oxides. 相似文献
5.
Tong Y Liu Y Dong L Zhao D Zhang J Lu Y Shen D Fan X 《The journal of physical chemistry. B》2006,110(41):20263-20267
ZnO nanostructures, including nanotowers, nanovolcanoes, nanorods, nanotubes, and nanoflowers, have been grown by using the hydrothermal technique. Most of the ZnO nanostructures show the perfect hexagonal cross section and well-faceted top and side surfaces. The basic chemistry and growth mechanism are discussed. By increasing the reaction time, the volcano-like and tube-like ZnO structures were formed due to the Ostwald ripening process and the selective adsorption of the complexes. By using the seed layer, the dense-arrayed, regular oriented ZnO nanorods were obtained due to the decreased nucleation barrier and the abundant interfaces as well as the increasing surface roughness. 相似文献
6.
Well‐Defined Flowerlike NdOCl Nanostructures: Nonaqueous Sol–Gel Synthesis,Nanoscale Characterization and Their Magnetic and Photoluminescence Properties 下载免费PDF全文
Dr. Xinghua Li Dr. Xia Deng Dr. Hao Zhu Juan Feng Prof. Yong Peng Prof. Jintao Bai Dr. Xinliang Zheng Dr. Haibo Fan Mingzi Wang Dr. Haowei Chen 《化学:亚洲杂志》2014,9(2):584-589
A facile nonaqueous solution route for the fabrication of NdOCl nanostructures based on a ligand‐exchange protocol and further thermal decomposition in organic medium, using only chloride salt as the neodymium source, is reported and the formation mechanism is proposed. The morphology, crystal structure, and chemical compositions of the sample were characterized at the nanoscale. XRD results and selected‐area electron diffraction patterns show that the sample is purely tetragonal NdOCl without any other impurity phases. TEM results show that the NdOCl nanostructures have a well‐defined flowerlike shape, which looks like a chrysanthemum just about to bloom. Magnetization measurements reveal that the NdOCl nanoflowers show room‐temperature ferromagnetism. The photoluminescence properties were also studied. These results are significant for fundamental research and promising applications of rare‐earth‐based nanostructures. 相似文献
7.
Dr. Yao Ma Dr. Xiao Sun Dr. Nianjun Yang Dr. Junhai Xia Dr. Lei Zhang Prof. Dr. Xin Jiang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(35):12370-12375
Carbon nanostructures with precisely controlled shapes are difficult materials to synthesize. A facet‐selective‐catalytic process was thus proposed to synthesize polymer‐linked carbon nanostructures with different shapes, covering straight carbon nanofiber, carbon nano Y‐junction, carbon nano‐hexapus, and carbon nano‐octopus. A thermal chemical vapor deposition process was applied to grow these multi‐branched carbon nanostructures at temperatures lower than 350 °C. Cu nanoparticles were utilized as the catalyst and acetylene as the reaction gas. The growth of those multi‐branched nanostructures was realized through the selective growth of polymer‐like sheets on certain indexed facets of Cu catalyst. The vapor–facet–solid (VFS) mechanism, a new growth mode, has been proposed to interpret such a growth in the steps of formation, diffusion, and coupling of carbon‐containing oligomers, as well as their final precipitation to form nanostructures on the selective Cu facets. 相似文献
8.
Bin-ping Zhuang Fa-chun Lai Li-mei Lin Ming-bao Lin Yan Qu Zhi-gao Huang 《化学物理学报(中文版)》2010,23(1):79-83
ZnO nanobelts, hollow microspheres, and urchins have been prepared on copper foil via a simply low temperature evaporation route. The microstructure, morphologies, and photolu-minescence of the ZnO nanostructures were studied with X-ray diffraction, Raman spectra, scanning electron microscopy and photoluminescence spectra. The width of the nanobelts was about 500 nm and the length was longer than 10μm. The diameter of the hollow microspheres was between 5 and 10μm. A possible growth mechanism of the nanobelts, microspheres and urchins was proposed. The photoluminescence spectrum exhibited strong deep level energy emissions and a weak near band edge emission. These ZnO nanostructures on a copper substrate have the advantages of naturally good adhesion and electrical connection between the ZnO nanostructures and the conductive substrate. 相似文献
9.
Xiaojun Yi Prof. Gang Yu Fangfang Chang Zhi Hui Xie Tan Nhat Tran Prof. Bo Nian Hu Prof. Chuan‐Jian Zhong 《化学:亚洲杂志》2014,9(9):2612-2620
The ability to control the morphology and phase structure of alloy nanowires is essential for the exploitation of their unique functional properties. This report describes the findings of an investigation of the growth mechanism in the electrochemically controlled growth of Au? Pt alloy nanostructures. By using a template‐free alternating‐current deposition method with different combinations of waveform, voltage, and frequency, controllability over the alloy morphology, composition, and phase structure has been clearly demonstrated for the growth of the nanostructures across the gap of two microelectrodes. The growth is proposed to involve an initial facet‐selective nucleation–growth process followed by two competing nucleation–growth pathways that are highly tunable by the applied frequency and voltage. The findings provided new insights into the mechanism that underlies the controlled fabrication of alloy nanowires and nanodendrites with structurally tailorable functional properties. 相似文献
10.
R. J. H. Morris M. G. Dowsett S. H. Dalal D. L. Baptista K. B. K. Teo W. I. Milne 《Surface and interface analysis : SIA》2007,39(11):898-901
In this paper we demonstrate how secondary ion mass spectrometry (SIMS) can be applied to ZnO nanowire structures for gold catalyst residue determination. Gold plays a significant role in determining the structural properties of such nanowires, with the location of the gold after growth being a strong indicator of the growth mechanism. For the material investigated here, we find that the gold remains at the substrate–nanowire interface. This was not anticipated as the usual growth mechanism associated with catalyst growth is of a vapour–liquid–solid (VLS) type. The results presented here favour a vapour–solid (VS) growth mechanism instead. Copyright © 2007 John Wiley & Sons, Ltd. 相似文献
11.
Catalyst-nanostructure interfacial lattice mismatch in determining the shape of VLS grown nanowires and nanobelts: a case of Sn/ZnO 总被引:3,自引:0,他引:3
Vapor-liquid-solid (VLS) is a well-established process in catalyst-guided growth of nanowires. The catalyst particle is generally believed to be in liquid state during growth, and it is the site for adsorbing incoming molecules; the crystalline structure of the catalyst may not have any influence on the structure of the grown one-dimensional nanostructures. In this paper, using tin particle guided growth of ZnO nanostructures as a model system, we show that the interfacial region of the tin particle with the ZnO nanowire/nanobelt could be ordered (or partially crystalline) during the VLS growth, although the local growth temperature is much higher than the melting point of tin, and the crystallographic lattice structure at the interface is important in defining the structural characteristics of the grown nanowires and nanobelts. The interface prefers to take the least lattice mismatch; thus, the crystalline orientation of the tin particle may determine the growth direction and the side surfaces of the nanowires and nanobelts. This result may have important impact on the understanding of the physical chemical process in the VLS growth. 相似文献
12.
13.
PLD-assisted VLS growth of aligned ferrite nanorods, nanowires, and nanobelts-synthesis, and properties 总被引:4,自引:0,他引:4
Morber JR Ding Y Haluska MS Li Y Liu JP Wang ZL Snyder RL 《The journal of physical chemistry. B》2006,110(43):21672-21679
We report here a systematic synthesis and characterization of aligned alpha-Fe2O3 (hematite), epsilon-Fe2O3, and Fe3O4 (magnetite) nanorods, nanobelts, and nanowires on alumina substrates using a pulsed laser deposition (PLD) method. The presence of spherical gold catalyst particles at the tips of the nanostructures indicates selective growth via the vapor-liquid-solid (VLS) mechanism. Through a series of experiments, we have produced a primitive "phase diagram" for growing these structures based on several designed pressure and temperature parameters. Transmission electron microscopy (TEM) analysis has shown that the rods, wires, and belts are single-crystalline and grow along <111>m or <110>h directions. X-ray diffraction (XRD) measurements confirm phase and structural analysis. Superconducting quantum interference device (SQUID) measurements show that the iron oxide structures exhibit interesting magnetic behavior, particularly at room temperature. This work is the first known report of magnetite 1D nanostructure growth via the vapor-liquid-solid (VLS) mechanism without using a template, as well as the first known synthesis of long epsilon-Fe2O3 nanobelts and nanowires. 相似文献
14.
To investigate the effect of sulfur-sulfur and metal-ligand coordination on the molecular structure and morphology of self-assembled nanostructures, metal-free 2,3,9,10,16,17,23,24-octakis(isopropylthio)phthalocyanine H(2)Pc(β-SC(3)H(7))(8) (1) and its copper and lead congeners CuPc(β-SC(3)H(7))(8) (2) and PbPc(β-SC(3)H(7))(8) (3) are synthesized and fabricated into organic nanostructures by a phase-transfer method. The self-assembly properties are investigated by electronic absorption and Fourier transform infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). Experimental results reveal different molecular packing modes in these aggregates, which in turn result in self-assembled nanostructures with different morphologies ranging from nanobelts for 1 through nanoribbons for 2 to cluster nanoflowers for 3. Intermolecular π-π and sulfur-sulfur interactions between metal-free phthalocyanine 1 lead to the formation of nanobelts. The additional Cu-S coordination bond between the central copper ion of 2 and the sulfur atom of the adjacent molecule of 2 in cooperation with the intermolecular π-π stacking interaction increases the intermolecular interaction, and results in the formation of long nanoribbons for 2. In contrast to compounds 1 and 2, the special molecular structure of complex 3, together with the intermolecular π-π stacking interaction and additional Pb-S coordination bond, induces the formation of Pb-connected pseudo-double-deckers during the self-assembly process, which in turn further self-assemble into cluster nanoflowers. In addition, good semiconducting properties of the nanostructures fabricated from phthalocyanine derivatives 1-3 were also revealed by I-V measurements. 相似文献
15.
Synthesis of porous and nonporous ZnO nanobelt, multipod, and hierarchical nanostructure from Zn-HDS
Zn based hydroxide double salts (Zn-HDS) with an interlayer spacing of 20 Å was produced by dissolving dumbbell-like ZnO crystal. The resulting Zn-HDS with a ribbon-like shape has a suitable morphology to explore the remarkably mild procedure for synthesis of ZnO nanobelts. We found that the intercalated water molecules into the Zn-HDS could play a key role in the ZnO nanobelts porosity. The nonporous ZnO nanobelts were successfully synthesized from the Zn-HDS by soft-solution process at 95 °C through mild dehydration agent as Na2CO3. As-synthesized ZnO nanobelts were grown along not only the [0 1 −1 0], but also the [2 −1 −1 0]. On the other hand, the porous ZnO nanobelts were obtained from the Zn-HDS by calcinations at 200 and 400 °C. In addition, flower-like ZnO multipod and hierarchical nanostructures were produced from the Zn-HDS by using of strong dehydration agent (NaOH) through hydrothermal reaction at 150 and 230 °C. 相似文献
16.
Dr. Peng Li Dr. Dingsheng Wang Zhe Wei Dr. Qing Peng Prof. Dr. Yadong Li 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(11):3735-3740
In this study, we report a simple solution‐phase method to prepare ZnO nanostructures with controllable morphologies. By using oleylamine (OAm) and dodecanol (DDL) as solvents, zinc oxide nanocrystals with tunable sizes and diverse shapes (hexagonal pyramids, bulletlike, and pencil‐like shapes) have been obtained under mild conditions. At the same time, the introduction of presynthesized gold nanocrystals can also lead to the hybrid nanostructures of gold–zinc oxide hexagonal nanopyramids. In addition, the possible formation mechanism of the as‐prepared ZnO nanostructures has been investigated. Notably, the unique optical properties of the ZnO nanostructures with different sizes and shapes have also been discussed. We hope that this strategy will be a general and effective method for fabricating other metal oxide nanocrystals. 相似文献
17.
Behnaz Hatamluyi Fatemeh Modarres Zahed Zarrin Es'haghi Majid Darroudi 《Electroanalysis》2020,32(8):1818-1827
A novel platform based incorporation of carbon quantum dots (CQDs) and zinc oxide nanoflowers (ZnO‐NFs) decorated with poly cetyltrimethylammonium bromide (CTAB) was developed as electrochemical sensor for the sensitive and selective simultaneous detection of Paracetamol (PAR) and Ciprofloxacin (CIP) in biological samples. For this, CQDs and ZnO‐NFs were first deposited on a glassy carbon electrode (GCE) and subsequently a Poly (CTAB) layer was grown onto their surfaces through electro‐polymerization. The synthesized nanostructures and the corresponding fabricated sensor were characterized by the techniques of TEM, XRD, FE‐SEM, and EDX analysis. Moreover electrochemical characterization by CV and DPV were performed to elucidate the construction process and electron transfer abilities of the CQDs/ZnO‐NFs/Poly(CTAB)/GCE. Increased sensitivity and efficiency of this sensing system was obtained due to the synergistic effects of CQDs, ZnO‐NFs and Poly (CTAB) with multi‐signal amplification. Under the optimum conditions, the DPV response of proposed sensor to PAR and CIP was linear at 0.05–30.0 μM and 0.01–30.0 μM, with the detection limit of 2.47 nM and 1.97 nM respectively. The sensor possessed high stability, reproducibility, sensitivity, and selectivity toward PAR and CIP detection, over potential interferents and presented high recovery percentage in the real sample matrices. 相似文献
18.
Borchers C Müller S Stichtenoth D Schwen D Ronning C 《The journal of physical chemistry. B》2006,110(4):1656-1660
Vapor-liquid-solid is a well-established process in catalyst guided growth of 1-D nanostructures, i.e., nanobelts and nanowires. The catalyst particle is generally believed to be in the liquid state during growth, and is the site for impinging molecules. The crystalline structure of the catalyst may not have any influence on the structure of the grown nanostructures. In this work, using Au guided growth of ZnO, we show that the interfaces between the catalyst droplet and the nanostructure grow in well-defined mutual crystallographic relationships. The nanostructure defines the crystallographic orientation of the solidifying Au droplet. Possible alloy, intermetallic, or eutectic phase formation during catalysis are elucidated with the help of a proposed ternary Au-Zn-O phase diagram. 相似文献
19.
Saji Thomas Kochuveedu Ji Hye Oh Prof. Young Rag Do Prof. Dong Ha Kim 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(24):7467-7472
A simple strategy was used to enhance band emission through the transfer of defect emission from ZnO to Au by using the energy match between the defect emission of ZnO and the surface plasmon absorbance of Au NPs through decorating the surface of ZnO nanoflowers with Au nanoparticles (Au NPs). The ZnO nanostructure, which was comprised of six nanorods that were attached on one side in a flower‐like fashion, was synthesized by using a hydrothermal method. The temperature‐dependent morphology and detailed growth mechanism were studied. The influence of the density of the Au NPs that were deposited onto the surface of ZnO on photoluminescence was investigated to optimize the configuration of the ZnO/Au system in terms of the maximum band emission. The sequential transfer of defect energy from ZnO to Au and electron transfer from excited Au to ZnO was proposed as a possible mechanism for the enhanced band emission. 相似文献
20.
Uniform ZnO nanorods arrays are grown directly from and on Zn foils in pure water under hydrothermal conditions at a relatively
low temperature. The nanorods are 80–200 nm in diameter and ∼ 1 μm in length, which grow on the Zn foil along the [001] direction.
By changing the pure water to a urea solution, a Zn compound ([Zn5(OH)6(CO3)2], a precursor of ZnO nanoflowers film, is created by self-assembly. The ZnO nanoflowers film can be easily obtained by heating
the [Zn5(OH)6(CO3)2] compound in N2 at 350∘C for 5–6 hours. Possible growth processes of the ZnO nanorods arrays and the [Zn5(OH)6(CO3)2] nanoflowers are discussed. Photoluminescence properties of the as-prepared ZnO nanostructures have been measured. The ZnO
nanorods array synthesized using our method has minimal defects so that only band-gap emission is observed. However, the ZnO
nanoflowers film, obtained by heating the [Zn5(OH)6(CO3)2] nanoflower precursor in N2, is polycrystalline and displays strong defect-related emission. 相似文献