Synthesis and Cathodoluminescence of CdS Nanowires

2011 ◽  
Vol 688 ◽  
pp. 301-306 ◽  
Author(s):  
Xiao Dan Hu ◽  
Hai Qian Zhang

CdS nanowires were synthesized with tetramethyl thiuram disulfide (TMTD) as a new sulphur source by a solvothermal method in ethylenediamine at 180°C for 24 h. The crystallinity, morphology and probable formation mechanism of CdS nanocrystals were investigated by X-ray diffraction (XRD), transmission electron microscopy (TEM) and selected area electron diffraction (SAED). The optical properties were investigated by ultraviolet-visible spectroscopy (UV-vis) and cathodoluminescence (CL). The results indicated that CdS nanocrystals were hexagonal and had a wire-like morphology with a diameter of 20 to 50 nm. There were blue shifts at the onset of absorption of the CdS nanowire, compared with the absorption of the bulk CdS. The cathodoluminescence (CL) implied that CdS nanowires possessed potential optical property in the visible region.

2011 ◽  
Vol 236-238 ◽  
pp. 1712-1716 ◽  
Author(s):  
Hai Tao Liu ◽  
Jun Dai ◽  
Jia Jia Zhang ◽  
Wei Dong Xiang

Bismuth selenide (Bi2Se3) hexagonal nanosheet crystals with uniform size were successfully prepared via a solvothermal method at 160°C for 22 h using bismuth trichloride(BiCl3) and selenium powder(Se) as raw materials, sodium bisulfite(NaHSO3) as a reducing agent, diethylene glycol(DEG) as solvent, and ammonia as pH regulator. Various techniques such as X-ray diffraction (XRD), field-emission scanning electron microscope (FESEM), high-resolution transmission electron microscope (HRTEM), and selected area electron diffraction (SAED) were used to characterize the obtained products. Results show that the as-synthesized samples are pure Bi2Se3 hexagonal nanosheet crystals. A possible growth mechanism for Bi2Se3 hexagonal nanosheet crystals is also discussed based on the experiment.


2011 ◽  
Vol 233-235 ◽  
pp. 1954-1957
Author(s):  
Xiao Yan Yan ◽  
Zhi Qiang Wei ◽  
Li Gang Liu ◽  
Xiao Juan Wu ◽  
Ge Zhang

Helical structure ZnS were successfully prepared via solvothermal method by the reaction of zinc acetate and sodium sulphide. The composition, morphology, and microstructure of the sample were characterized by X-ray diffraction (XRD), high resolution transmission electron microscopy (HRTEM), the corresponding selected area electron diffraction (SAED) and X-ray energy spectrum (EDS). The experiment results show that the sample is 1-D hexagonal crystal ZnS and grows along the [002] direction, and is helical structure, with lengths in the range of 100-200 nm, the diameter about 5-15 nm, and pitch about 20nm.


2006 ◽  
Vol 510-511 ◽  
pp. 658-661
Author(s):  
Hyoun Woo Kim ◽  
S.H. Shim ◽  
Ju Hyun Myung

One-dimensional structures of tin oxide (SnO2) on TiN-coated substrates were obtained by simple heating of Sn powders. X-ray diffraction, high-resolution transmission electron microscopy, and the selected area electron diffraction showed that 1D structures are composed of SnO2 with rutile structure. The photoluminescence of the structures in the visible region suggests possible applications in nanoscaled optoelectronic devices.


2014 ◽  
Vol 887-888 ◽  
pp. 174-180
Author(s):  
Fan Yang ◽  
Shan Cheng Yan ◽  
Bo Jun Wang ◽  
Zhen Hua Shuai ◽  
Ming Xia Zhang

In the present study, the heterostructures of ZnO Nanoparticle (NP)/CdS nanowire (NW), SnO2NP/CdS NW, NiS NP/CdS NW, FeS NP/CdS NW, Ag2S NP/CdS NW, and Au NP/CdS NW have been successfully fabricated via the two-stage solvothermal process. Field-emission scan electron microscopy (FESEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) were adopted to characterize the as-prepared products. The optical properties of the as-obtained heterostructures were separately investigated. New insights into understanding and controlling the synthesis of different NW heterostructures are demonstrated in the reliable solvothermal route. We demonstrate that CdS NWs synthesized for 2h are the bifunctional mediator acting as catalyst or active spot for the growth of NW heterostructures Furthermore, understanding and controlling this phenomenon is a great asset for the realization of the formation mechanism of the NW heterostructures and opens up new ways toward for construction of other semiconductor heterostructures with novel properties.


2009 ◽  
Vol 59 (12) ◽  
Author(s):  
Claudia Maria Simonescu ◽  
Valentin Serban Teodorescu ◽  
Camelia Capatina

This paper presents the obtaining of copper sulfide CuS (covelite) from Cu(CH3COO)2.H2O and thioacetamide (TAA) system. The reaction was conducted in presence or absence of sodium-bis(2-ethylhexyl) sulfosuccinate (Na-AOT). The effects of various reaction parameters on the size and on the shape of nanoparticles have been examined. CuS obtained was characterized by X ray diffraction, IR spectroscopy, TEM � transmission electron microscopy and SAED selected area electron diffraction. The influence of surfactant to the shape and size of CuS (covellite) nanocrystals was established. The size of the nanocrystals varied from 10-60 nm depending on the reaction conditions such as quantity of surfactant.


2021 ◽  
Author(s):  
Yan Chen ◽  
Yuemei Lan ◽  
Dong Wang ◽  
Guoxing Zhang ◽  
Wenlong Peng ◽  
...  

A series of Gd2-xMoO6:xEu3+(x=0.18-0.38) nanophosphors were synthesized by the solvothermal method. The properties of this nanophosphor were characterized by x-ray diffraction (XRD), transmission electron microscope (TEM), fluorescence spectra and diffuse...


2012 ◽  
Vol 512-515 ◽  
pp. 1511-1515
Author(s):  
Chun Lin Zhao ◽  
Li Xing ◽  
Xiao Hong Liang ◽  
Jun Hui Xiang ◽  
Fu Shi Zhang ◽  
...  

Cadmium sulfide (CdS) nanocrystals (NCs) were self-assembled and in-situ immobilized on the dithiocarbamate (DTCs)-functionalized polyethylene glycol terephthalate (PET) substrates between the organic (carbon disulfide diffused in n-hexane) –aqueous (ethylenediamine and Cd2+ dissolved in water) interface at room temperature. Powder X-ray diffraction measurement revealed the hexagonal structure of CdS nanocrystals. Morphological studies performed by scanning electron microscopy (SEM) and high-resolution transmission electron microscope (HRTEM) showed the island-like structure of CdS nanocrystals on PET substrates, as well as energy-dispersive X-ray spectroscopy (EDS) confirmed the stoichiometries of CdS nanocrystals. The optical properties of DTCs modified CdS nanocrystals were thoroughly investigated by ultraviolet-visible absorption spectroscopy (UV-vis) and fluorescence spectroscopy. The as-prepared DTCs present intrinsic hydrophobicity and strong affinity for CdS nanocrystals.


Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1712
Author(s):  
Appusamy Muthukrishnaraj ◽  
Salma Ahmed Al-Zahrani ◽  
Ahmed Al Otaibi ◽  
Semmedu Selvaraj Kalaivani ◽  
Ayyar Manikandan ◽  
...  

Towards the utilization of Cu2O nanomaterial for the degradation of industrial dye pollutants such as methylene blue and methyl orange, the graphene-incorporated Cu2O nanocomposites (GCC) were developed via a precipitation method. Using Hummers method, the grapheme oxide (GO) was initially synthesized. The varying weight percentages (1–4 wt %) of GO was incorporated along with the precipitation of Cu2O catalyst. Various characterization techniques such as Fourier-transform infra-red (FT-IR), X-ray diffraction (XRD), UV–visible diffused reflectance (UV-DRS), Raman spectroscopy, thermo gravimetric analysis (TGA), energy-dispersive X-ray analysis (EDX), and electro chemical impedance (EIS) were followed for characterization. The cabbage-like morphology of the developed Cu2O and its composites were ascertained from field-emission scanning electron microscopy (FESEM) and high-resolution transmission electron microscopy (HR-TEM). In addition, the growth mechanism was also proposed. The results infer that 2 wt % GO-incorporated Cu2O composites shows the highest value of degradation efficiency (97.9% and 96.1%) for MB and MO at 160 and 220 min, respectively. Further, its catalytic performance over visible region (red shift) was also enhanced to an appreciable extent, when compared with that of other samples.


2010 ◽  
Vol 97-101 ◽  
pp. 4213-4216
Author(s):  
Jian Xiong Liu ◽  
Zheng Yu Wu ◽  
Guo Wen Meng ◽  
Zhao Lin Zhan

Novel single-crystalline SnO2 zigzag nanoribbons have been successfully synthesized by chemical vapour deposition. Sn powder in a ceramic boat covered with Si plates was heated at 1100°C in a flowing argon atmosphere to get deposits on a Si wafers. The main part of deposits is SnO2 zigzag nanoribbons. They were characterized by means of X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM) and selected-area electron diffraction (SAED). SEM observations reveal that the SnO2 zigzag nanoribbons are almost uniform, with lengths near to several hundred micrometers and have a good periodically tuned microstructure as the same zigzag angle and growth directions. Possible growth mechanism of these zigzag nanoribbons was discussed. A room temperature PL spectrum of the zigzag nanoribbons shows three peaks at 373nm, 421nm and 477nm.The novel zigzag microstructures will provide a new candidate for potential application.


2013 ◽  
Vol 634-638 ◽  
pp. 2276-2279 ◽  
Author(s):  
Gang Xu ◽  
Min Zhang ◽  
Ping Ou ◽  
Yi Zhang ◽  
Gao Rong Han

Monodispersed Fe3O4 magnetite nanoparticles were successfully synthesized via a simple solvothermal method, in which Fe(NO3)3•9H2O was used as the starting materials, KOH as the mineralizer, and ethylene glycol (en) as the solvent. X-ray diffraction (XRD) and selected area electron diffraction (SAED) were employed to characterize the phase composition, transmission electron microscope (TEM) to observe the morphology and the particle size, and physical property measurement system (PPMS) to investigate the magnetic property of the synthesized powders, respectively. The synthesized Fe3O4 magnetite nanoparticles are of 50-100nm in size, and of notable ferromagnetic property. The saturation magnetization, remanent magnetization, and coercive field are 68.8emu•g-1, 12.9emu•g-1, 138.5Oe, respectively. Based on the experimental resuts, the formation mechanism and the well monodispersed reason of the solvothersized Fe3O4 nanoparticles are discussed.


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