Solvothermal Synthesis of Bi2Se3 Hexagonal Nanosheet Crystals

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.

2010 ◽  
Vol 03 (02) ◽  
pp. 125-129 ◽  
Author(s):  
CAIQUAN ZHANG ◽  
YALI CUI ◽  
DIDI ◽  
KUNPING YAN ◽  
CHAO CHEN ◽  
...  

Facile procedures to synthesize large quantities of uniform and well dispersed magnetite particles in water were developed through a solvothermal method. Magnetite microspheres were obtained by using FeCl 3 · 6H 2 O , urea and polyethylene glycol as the starting materials in ethylene glycol at 200°C for 8 h. The samples were characterized by using X-ray diffraction, transmission electron microscopy, scanning electron microscopy and vibrating sample magnetometry. Experimental results revealed that the particles were well dispersed with uniform particle size and diameters in the range 260 to 280 nm. The saturation magnetization value was 71.5 emu/g with negligible remanence.


2016 ◽  
Vol 40 ◽  
pp. 72-78 ◽  
Author(s):  
Jia Wei Sheng ◽  
Li Ping Zhang ◽  
Jun Yan ◽  
Qing Sun ◽  
Jian Zhang

The mechanical destruction of the pyrophyllite structure and final ground products upon grinding with a laboratory planetary ball mill were investigated using high-resolution transmission electron microscope (HRTEM) coupled with selected area electron diffraction (SAED), field emission scanning electron microscope (SEM) and X-ray diffraction (XRD). Grinding produced a profound structural alteration, resulting in increasing amorphization. Increasing the intensity of grinding resulted in acceleration of the mechanically induced amorphization of the pyrophyllite structure. The pyrophyllite phase was transformed into its anhydride phase during the process of the prolonged grinding. Increasing the grinding intensity resulted in faster destruction of the pyrophyllite structure. The plate-like microcrystal exhibited the 2M-pyrophyllite crystal structure. The pyrophyllite anhydride phase was existed after grinding.


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...


2007 ◽  
Vol 7 (2) ◽  
pp. 525-529 ◽  
Author(s):  
Bo Zhou ◽  
Jun-Jie Zhu

A chemical co-reduction route in aqueous solution was developed to synthesize Bi100−xSbx alloys at room temperature. The hydrolyses of Bi(III) and Sb(III) were effectively avoided by selecting proper raw materials and coordinator. X-ray diffraction analysis indicated that the as-prepared Bi100−xSbx alloys were homogeneous and phase-pure, and the Bi/Sb ratios in the alloys were very close to those in the aqueous solutions. The transmission electron microscope observation showed that the as-prepared Bi100−xSbx (x = 0∼100) alloys were particles with a size of tens of nanometers. The selected area electron diffraction patterns confirmed the high crystallinity, the homogeneousness, and the composition controllability of as-prepared alloys. All these characters and the nanometer-scaled size of the alloys are believed to be beneficial to the thermoelectric property of the Bi100−xSbx alloys.


2014 ◽  
Vol 936 ◽  
pp. 986-991
Author(s):  
Chuan Hui Gao ◽  
Li Ding ◽  
Yu Min Wu ◽  
Chuan Xing Wang ◽  
Jun Xu

A low-cost raw material, bittern obtained from the production process of sea salt, was used to prepare magnesium oxysulfate hydrate (MgSO4·5Mg (OH)2·2H2O, abbreviated as 152MOS) whiskers via hydrothermal synthesis with ammonia and magnesium sulfate as the other starting raw materials. The bittern was firstly filtered and then used directly without de-coloring. X-ray powder diffraction (XRD), transmission electron microscope (TEM), selected area electron diffraction (SAED), energy dispersive X-ray spectroscopy (EDX) and scanning electron microscope (SEM) were employed to investigate the composition and morphology of the products. It was found that the 152MOS whiskers synthesized from bittern at 190°C for 3 hours exhibited fanlike morphology. The formation of the fanlike whiskers was inhibited and most of the whiskers presented as single fibers when ethanol was used as crystal control agent in the hydrothermal process. From the two-dimensional steps observed at tips of the whiskers, a possible growth mechanism was speculated that it was the extension of dislocations that made the growth of the whiskers.


2014 ◽  
Vol 881-883 ◽  
pp. 1101-1104 ◽  
Author(s):  
Min Jie Zhou ◽  
Peng Cui

In this work, flower-like ZnIn2S4 microspheres were synthesized using a solvothermal method. The as-synthesized samples were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), and ultraviolet-visible diffuse reflectance spectroscopy (DRS) techniques. The photocatalytic activity of the ZnIn2S4 microspheres was investigated. The ZnIn2S4 microspheres exhibit much higher photocatalytic activity than pure P25 TiO2.


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.


2011 ◽  
Vol 675-677 ◽  
pp. 835-838
Author(s):  
Jing Wang ◽  
Si Jing Fu ◽  
Hong Cheng

The present work reported the preparation of TiC/Fe-based composite by the synthesis reaction from Ti, C and Fe. The sintered composites were characterized by X-ray diffraction, scanning electron microscope and transmission electron microscope. TiC, Fe3C and α-Fe were detected by X-ray diffraction analysis. The scanning and transmission electron micrographs revealed the morphology and distribution of the reinforcements, the microstructure of Fe matrix, the interfacial structure of TiC particle-to-Fe matrix. Moreover, the formation reason of the voids in composite was also discussed.


2011 ◽  
Vol 233-235 ◽  
pp. 2289-2293
Author(s):  
Pin Jiang Li ◽  
Wen Jun Fa ◽  
Yan Ge Zhang ◽  
Bao Jun Huang ◽  
Yi Dong Zhang

Hairball-like bismuth trisulphide microcrystallines has been successfully prepared via one step solvothermal process and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and high-resolution transmission electron microscopy (HRTEM) techniques. The morphologies of the Bi2S3 microcrystallines were influenced by reaction time, temperature, the mole ratio of the reactants and concentration of starting materials, and the growth process has been proposed. The electrochemical behavior of Bi2S3 was investigated using the cyclic voltammetry.


2001 ◽  
Vol 15 (30) ◽  
pp. 1455-1458 ◽  
Author(s):  
H. CHEN ◽  
X. K. LU ◽  
S. Q. ZHOU ◽  
X. H. HAO ◽  
Z. X. WANG

Single phase AlN nanowires are fabricated by a sublimation method. They were characterized by means of X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), typical selected area electron diffraction (SAED) and high-resolution transmission electron microscopy (HRTEM). The SEM and TEM images show that most of the nanowires have diameters of about 10–60 nm. The crystal structure of AlN nanowires revealed by XRD, SAED and HRTEM shows the AlN nanowires have a wurtzite structure.


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