scholarly journals Synthesis of Monodisperse Walnut-Like SnO2Spheres and Their Photocatalytic Performances

2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Jing Wang ◽  
Hui-qing Fan ◽  
Hua-wa Yu

Novel walnut-like SnO2spheres have been synthesized using a one-step hydrothermal reaction with SnCl2·2H2O and KOH as raw materials. The morphology, microstructure, and optical properties of the products were characterized by X-ray powder diffraction (XRD), Raman spectrum, scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED), and ultraviolet-visible (UV-Vis) absorption spectroscopy. The detailed studies revealed that these synthesized spheres are highly monodisperse and have a uniform size of approximately 250 nm. Photocatalytic activity of the prepared SnO2spheres was evaluated by the degradation of methylene orange. The synthesized SnO2spheres exhibited excellent photocatalytic degradation. In addition, a possible formation mechanism of the walnut-like nanostructures was proposed based on reaction time-dependent experiments.

2018 ◽  
Vol 53 ◽  
pp. 7-12
Author(s):  
Mao Hua Li ◽  
Xiao Fei Li ◽  
Wen Sheng Ran ◽  
Bo Yang

The worm-like morphology of silver sulfide (Ag2S) was successfully prepared via hydrothermal reaction at 150°C by using silver nitrate (AgNO3) and thioacetamide(CH3CSNH2) as both the sliver sources and sulfur sources, β-cyclodextrin as the template agent, and water as the solvent. The worm-like of Ag2S are characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), x-ray diffraction (XRD), x-ray photoelectronspectroscopy (XPS), energy dispersivex-ray (EDX), high-resolution transmission electron microscopy (HRTEM) and selected area electron diffraction (SEAD). Ultraviolet-visible spectra (UV-vis) and photoluminescencespectroscopy (PL) were used in an optical study of the products. The results showed that the existence of β-cyclodextrin is crucial to the formation of worm-like Ag2S, and the optoelectronics test results showed that the sample have a broad absorption in ultraviolet and visible light 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.


2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Anukorn Phuruangrat ◽  
Nuengruethai Ekthammathat ◽  
Budsabong Kuntalue ◽  
Phattranit Dumrongrojthanath ◽  
Somchai Thongtem ◽  
...  

Undoped and Ce doped Bi2MoO6samples were synthesized by hydrothermal reaction at 180°C for 20 h. Phase, morphology, atomic vibration, and optical properties were characterized by X-ray powder diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman spectrophotometry, Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED), and UV-visible spectroscopy. In this research, the products were orthorhombic Bi2MoO6nanoplates with the growth direction along the [0b0], including the asymmetric and symmetric stretching and bending modes of Bi–O and Mo–O. Undoped and Ce doped Bi2MoO6samples show a strong absorption in the UV region.


2014 ◽  
Vol 496-500 ◽  
pp. 297-300 ◽  
Author(s):  
Bi Tao Liu ◽  
Liang Liang Tian ◽  
Ling Ling Peng

A series of composites of the high photoactivity of {001} facets exposed BiOCl and grapheme sheets (GS) were synthesized via a one-step hydrothermal reaction. The obtained BiOCl/GS photocatalysts were characterized by X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy, transmission electron microscopy (TEM), Ultraviolet-visible (UV-Vis) diffuse reflectance spectroscopy. The as-prepared BiOCl/GS photocatalyst showed enhanced photocatalytic activity for the degradation of methyl orange (MO) under UV and visible light (λ > 400 nm). The enhanced photocatalytic activity could be attributed to oxygen vacancies of the {001} facets of BiOCl/GS and the high migration efficiency of photo-induced electrons, which could suppress the charge recombination effectively.


2011 ◽  
Vol 399-401 ◽  
pp. 693-697 ◽  
Author(s):  
Shuang Jie Song ◽  
Xue Ying Nai ◽  
Wu Li ◽  
Cheng Cai Zhu ◽  
Qing Fen Meng

A type of calcium borate whiskers with highly thermal stability was synthesized by hydrothermal method at 180 °C for 2 h, using borax, calcium chloride and sodium hydroxide as raw reactants. The X-ray powder diffraction (XRD) indicated that as-prepared products were composed of monoclinic Ca2B2O5·H2O phase. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) images showed calcium borate whiskers with a length of 50~100 μm and diameter 1.0 ~3.0 μm. Selected-area electron diffraction (SAED) pattern showed that the calcium borate whiskers were single crystalline structure. The adjustment of temperature of hydrothermal reaction, can lead to obvious morphology changes of products, and the possible chemical reaction and growth mechanism were proposed. Furthermore, the analysis of thermogravimetry (TG) showed the calcium borate whiskers released crystal water at 370~425 °C.


2019 ◽  
Vol 2019 ◽  
pp. 1-10 ◽  
Author(s):  
Suziete B. S. Gusmão ◽  
Anupama Ghosh ◽  
Thalles M. F. Marques ◽  
Odair P. Ferreira ◽  
Anderson O. Lobo ◽  
...  

A nanoheterostructure of titanate nanotubes decorated with anatase nanoparticles (TiNT@AnNP) was synthesized for the first time by a microwave-assisted hydrothermal one-pot reaction. Characterization by X-ray diffraction, Raman spectroscopy, scanning electron microscopy, energy-dispersive X-ray spectroscopy, high-resolution transmission electron microscopy, selected-area electron diffraction, and X-ray photoelectron spectroscopy showed highly crystalline and nanometer-sized TiNT@AnNP. The synthesized TiNT@AnNP degraded an anionic dye (Remazol blue) more efficiently under UV-visible light (380–780 nm) than a commercial anatase-TiO2 precursor. We correlated this increased efficiency of photodegradation to the large surface area and the efficient separation of photoinduced electron-hole pairs. Finally, we propose a mechanism to highlight the influence of a microwave-assisted hydrothermal synthesis in the production of TiNT@AnNP for environmental applications.


2014 ◽  
Vol 931-932 ◽  
pp. 231-234 ◽  
Author(s):  
Anukorn Phuruangrat ◽  
Nuengruethai Ekthammathat ◽  
Budsabong Kuntalue ◽  
Phattharanit Dumrongrojthanath ◽  
Somchai Thongtem ◽  
...  

0–3 % Ho doped Bi2MoO6 samples were synthesized by hydrothermal reaction at 180 °C for 20 h. Their phase, morphologies, atomic vibration and optical properties were characterized by X-ray powder diffraction (XRD), Raman spectrophotometry, Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED) and UV-visible spectroscopy. In this research, the products were orthorhombic Bi2MoO6 nanoplates with asymmetric and symmetric stretching and bending modes of MoO6 octahedrons, and their strong absorption in the UV visible region.


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.


1984 ◽  
Vol 222 (1229) ◽  
pp. 427-438 ◽  

Silicified macrohairs from mature and immature lemmas of the grass Phalaris canariensis L. have been studied by scanning (s.e.m.) and transmission electron microscopy (t.e.m.) and energy dispersive X-ray analysis (e.d.X.a.) at various times after emergence of the inflorescence. Within the macrohairs a variety of morphologies of silica particles was observed. E.d.X.a. revealed the time-dependent concentrations in the macrohairs of the elements K, Cl, P, and S, in addition to Si. Much lower levels of these elements were found in highly silicified mature macrohairs than in the immature macrohairs. It is proposed that the hairs are silicified under strict cellular control.


2011 ◽  
Vol 189-193 ◽  
pp. 1275-1279
Author(s):  
Ying Wang ◽  
Gao Yang Zhao ◽  
Li Yuan

The crystalline phase and morphology of the products formed during the synthesis of yttrium oxide via the hydrothermal treatment yttrium nitrate were characterized by X-ray diffraction, transmission electron microscopy and scanning electron microscopy. Products with high OH/NO3ratios are formed with the increasing of hydrothermal treatment. The crystalline phases are evolved from Y2(OH)5.14(NO3)0.86•H2O toY4O(OH)9(NO3) and finally Y(OH)3. The hydrothermal reaction conditions play an important role in the synthesis of the microstructures. Results show the particle size and final morphology of samples could be controlled by reaction temperature, reaction time, and OH-concentration. Sheets, hexagonal and needle-like Y2O3powders are obtained with the hydrothermal treatment of yittrium nitrate at 180 oC to 200oC for 2-8 hours at pH 9-13.


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