Facile Synthesis and Growth Mechanism of SiO2 Nanotubes with ZnS Nanowires as Intermediates

2016 ◽  
Vol 16 (4) ◽  
pp. 3890-3894 ◽  
Author(s):  
Hui Xin Chuo ◽  
Li Li Wu

SiO2 nanotubes with good chemical purity and well defined morphology were synthesized successfully in a one-step gas phase condensation process using gold catalyst. The as-synthesized products were characterized by transmission electron microscopy and nanoprobe X-ray energy dispersive. In the observations, a growth mechanism of the nanotubes is suggested. The new synthetic route to prepare SiO2 nanotubes is favorable to satisfy the special needs in commercial and industrial application and can be easily applied to other semiconductor materials.

2013 ◽  
Vol 4 ◽  
pp. 699-704 ◽  
Author(s):  
Raju Prakash ◽  
Katharina Fanselau ◽  
Shuhua Ren ◽  
Tapan Kumar Mandal ◽  
Christian Kübel ◽  
...  

A carbon-encapsulated Fe3O4 nanocomposite was prepared by a simple one-step pyrolysis of iron pentacarbonyl without using any templates, solvents or surfactants. The structure and morphology of the nanocomposite was investigated by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, Brunauer–Emmett–Teller analysis and Raman spectroscopy. Fe3O4 nanoparticles are dispersed intimately in a carbon framework. The nanocomposite exhibits well constructed core–shell and nanotube structures, with Fe3O4 cores and graphitic shells/tubes. The as-synthesized material could be used directly as anode in a lithium-ion cell and demonstrated a stable capacity, and good cyclic and rate performances.


Nanomaterials ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1537
Author(s):  
David L. Burnett ◽  
Christopher D. Vincent ◽  
Jasmine A. Clayton ◽  
Reza J. Kashtiban ◽  
Richard I. Walton

Iridium-containing NaTaO3 is produced using a one-step hydrothermal crystallisation from Ta2O5 and IrCl3 in an aqueous solution of 10 M NaOH in 40 vol% H2O2 heated at 240 °C. Although a nominal replacement of 50% of Ta by Ir was attempted, the amount of Ir included in the perovskite oxide was only up to 15 mol%. The materials are formed as crystalline powders comprising cube-shaped crystallites around 100 nm in edge length, as seen by scanning transmission electron microscopy. Energy dispersive X-ray mapping shows an even dispersion of Ir through the crystallites. Profile fitting of powder X-ray diffraction (XRD) shows expanded unit cell volumes (orthorhombic space group Pbnm) compared to the parent NaTaO3, while XANES spectroscopy at the Ir LIII-edge reveals that the highest Ir-content materials contain Ir4+. The inclusion of Ir4+ into the perovskite by replacement of Ta5+ implies the presence of charge-balancing defects and upon heat treatment the iridium is extruded from the perovskite at around 600 C in air, with the presence of metallic iridium seen by in situ powder XRD. The highest Ir-content material was loaded with Pt and examined for photocatalytic evolution of H2 from aqueous methanol. Compared to the parent NaTaO3, the Ir-substituted material shows a more than ten-fold enhancement of hydrogen yield with a significant proportion ascribed to visible light absorption.


2012 ◽  
Vol 600 ◽  
pp. 174-177 ◽  
Author(s):  
Jian Fei Xia ◽  
Zong Hua Wang ◽  
Yan Zhi Xia ◽  
Fei Fei Zhang ◽  
Fu Qiang Zhu ◽  
...  

Zirconia-graphene composite (ZrO2-G) has been successfully synthesized via decomposition of ZrOCl2•6H2O in a water-isopropanol system with dispersed graphene oxide (GO) utilizing Na2S as a precursor could enable the occurrence of the deposition of Zr4+ and the deoxygenation of GO at the same time. Transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD) techniques were used to characterize the samples. It was found that graphene were fully coated with ZrO2, and the ZrO2 existing in tetragonal phase, which resulted in the formation of two-dimensional composite.


2020 ◽  
Vol 14 (2) ◽  
pp. 113-118
Author(s):  
Daniel Ursu ◽  
Anamaria Dabici ◽  
Marinela Miclau ◽  
Nicolae Miclau

We report for the first time the fabrication of hierarchical ordered superstructure CuB2O4 with flower-like morphology via a one-step, low temperature hydrothermal method. The tetragonal structure of CuB2O4 was determined by X-ray diffraction and high-resolution transmission electron microscopy. Optical measurements attested of the quality of the fabricated CuB2O4 and high temperature X-ray diffraction confirmed its thermal stability up to 600 ?C. The oriented attachment growth and the hierarchical self-assembly of micrometer-sized platelets producing hierarchical superstructures with flower-like morphology are designed by pH of the hydrothermal solution. The excellent band gap, high thermal stability and hierarchical structure of the CuB2O4 are promising for the photovoltaic and photocatalytic applications.


Nanomaterials ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 1298 ◽  
Author(s):  
Muhammad Arif Khan ◽  
Nafarizal Nayan ◽  
Shadiullah Shadiullah ◽  
Mohd Khairul Ahmad ◽  
Chin Fhong Soon

In the present work, a facile one-step hydrothermal synthesis of well-defined stabilized CuO nanopetals and its surface study by advanced nanocharacterization techniques for enhanced optical and catalytic properties has been investigated. Characterization by Transmission electron microscopy (TEM) analysis confirmed existence of high crystalline CuO nanopetals with average length and diameter of 1611.96 nm and 650.50 nm, respectively. The nanopetals are monodispersed with a large surface area, controlled morphology, and demonstrate the nanocrystalline nature with a monoclinic structure. The phase purity of the as-synthesized sample was confirmed by Raman spectroscopy and X-ray diffraction (XRD) patterns. A significantly wide absorption up to 800 nm and increased band gap were observed in CuO nanopetals. The valance band (VB) and conduction band (CB) positions at CuO surface are measured to be of +0.7 and −1.03 eV, respectively, using X-ray photoelectron spectroscopy (XPS), which would be very promising for efficient catalytic properties. Furthermore, the obtained CuO nanopetals in the presence of hydrogen peroxide ( H 2 O 2 ) achieved excellent catalytic activities for degradation of methylene blue (MB) under dark, with degradation rate > 99% after 90 min, which is significantly higher than reported in the literature. The enhanced catalytic activity was referred to the controlled morphology of monodispersed CuO nanopetals, co-operative role of H 2 O 2 and energy band structure. This work contributes to a new approach for extensive application opportunities in environmental improvement.


2019 ◽  
Vol 43 (3-4) ◽  
pp. 135-139
Author(s):  
Pegah Farokhian ◽  
Manouchehr Mamaghani ◽  
Nosrat Ollah Mahmoodi ◽  
Khalil Tabatabaeian ◽  
Abdollah Fallah Shojaie

An efficient protocol for the facile synthesis of a series of pyrido[2,3- d]pyrimidine derivatives has been developed applying Fe3O4–ZnO–NH2–PW12O40 nanocatalyst in water. This novel method has the benefits of operational simplicity, green aspects by avoiding toxic solvents and high to excellent yields of products. Fe3O4–ZnO–NH2–PW12O40 was synthesized and characterized by Fourier transform infrared, X-ray diffraction, vibrating sample magnetometer, scanning electron microscopy, energy-dispersive X-ray spectroscopy, and transmission electron microscopy analyses. The nanocatalyst is readily isolated and recovered from the reaction mixture by an external magnet.


2016 ◽  
Vol 09 (03) ◽  
pp. 1650045 ◽  
Author(s):  
Pei-Ying Li ◽  
Kai-Yu Cheng ◽  
Xiu-Cheng Zheng ◽  
Pu Liu ◽  
Xiu-Juan Xu

Chitosan-ionic liquid conjugation (CILC), which was prepared through the reaction of 1-(4-bromobutyl)-3-methylimidazolium bromide (BBMIB) with chitosan, was firstly used to prepare functionalized graphene composite via the chemical reduction of graphene oxide (GO). The obtained water soluble graphene-based composite was characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), ultraviolet-visible (UV–Vis) spectroscopy and so on. CILC-RGO showed excellent dispersion stability in water at the concentration of 2.0 mg/mL, which was stable for several months without any precipitate. This may be ascribed to the electrostatic attraction and [Formula: see text]–[Formula: see text] interaction between CILC and graphene.


2020 ◽  
Vol 98 (12) ◽  
pp. 771-778
Author(s):  
Xin Chang ◽  
Xiangyang Xu ◽  
Zhifeng Gao ◽  
Yingrui Tao ◽  
Yixuan Yin ◽  
...  

A nanocomposite, reduced graphene oxide (RGO) modified ZnCo2O4 (ZnCo2O4–RGO) was synthesized via one-step solvothermal method for activating persulfate (PS) to degrade bisphenol A (BPA). The morphology and structure of the nanocomposite were identified by X-ray diffraction, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, and transmission electron microscopy. RGO provides nucleation sites for ZnCo2O4 to grow and inhibits the agglomeration of the nanoparticles. The influence of different reaction conditions on the oxidation of BPA catalyzed by ZnCo2O4–RGO was investigated, including the content of RGO, the dosage of catalyst, the concentration of humic acid (HA), anions in the environment, the reaction temperature, and pH. BPA can be totally degraded within 20 min under optimized reaction conditions. The presence of HA, Cl−, and NO3− only has a slight effect on the oxidation of BPA, whereas the presence of either H2PO4− or HCO3− can greatly inhibit the reaction. ZnCo2O4–RGO shows good cycling stability and practical application potential. A reaction mechanism of the degradation of BPA was also explored.


2019 ◽  
Vol 2019 ◽  
pp. 1-9 ◽  
Author(s):  
Chunyan Wang ◽  
Lianwei Shan ◽  
Dongyuan Song ◽  
Yanwei Xiao ◽  
Jagadeesh Suriyaprakash

In this letter, we investigated the photocatalytic activity of the newly formed rGO/PbTiO3 composites, which are synthesized by a one-step hydrothermal route. By adjusting the amount of reduced graphene oxide (rGO) (0, 0.15, 0.30, 0.60, and 1.20 wt%) with the PbTiO3, we constructed various photocatalysts for this investigation. The crystal structure and morphology of the various composites were studied by powder X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM). Photoelectron spectroscopic study revealed that the band structure of the newly formed composites and efficient charge separation can be obtained by the interfaces of various rGO content. In addition, the photocatalytic performance of the synthesized composites was explored by H2 evolution and rhodamine blue (RhB) degradation. The obtained results indicated that the addition of the appropriate amount of rGO could improve the activity of pure PbTiO3, significantly.


2020 ◽  
Vol 13 (02) ◽  
pp. 2051005 ◽  
Author(s):  
Godlaveeti Sreenivasa Kumar ◽  
Somala Adinarayana Reddy ◽  
Hussen Maseed ◽  
Nagireddy Ramamanohar Reddy

In this work, we present the synthesis of a ternary CeO2–SnO2/rGO nanocomposite by using a facile one-step hydrothermal method. The as-synthesized composite was structural, chemical, morphological, elemental information studied by using different characterization techniques X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy and field emission scanning electron microscope (FESEM), energy dispersive X-ray spectroscopy (EDAX) and transmission electron microscope (TEM). The CeO2–SnO2/rGO exhibited an excellent specific capacitance of 156[Formula: see text]F[Formula: see text][Formula: see text] at 0.5[Formula: see text]A/g in the presence of 3 M KOH solution. The synergic effect of CeO2, SnO2 and graphene composite coated on Ni foam endowed a high specific capacitance than their individual compounds. This work suggests that the novel ternary composite is a promising candidate for the high performance electrochemical energy storage and conversion systems.


Sign in / Sign up

Export Citation Format

Share Document