Crystal structure and compositional analysis of epitaxial (K0.56Na0.44)NbO3films prepared by hydrothermal method

2016 ◽  
Vol 31 (6) ◽  
pp. 693-701 ◽  
Author(s):  
Takahisa Shiraishi ◽  
Hiro Einishi ◽  
Takao Shimizu ◽  
Hiroshi Funakubo ◽  
Minoru Kurosawa ◽  
...  

Abstract

Author(s):  
A. Olsen ◽  
J.C.H. Spence ◽  
P. Petroff

Since the point resolution of the JEOL 200CX electron microscope is up = 2.6Å it is not possible to obtain a true structure image of any of the III-V or elemental semiconductors with this machine. Since the information resolution limit set by electronic instability (1) u0 = (2/πλΔ)½ = 1.4Å for Δ = 50Å, it is however possible to obtain, by choice of focus and thickness, clear lattice images both resembling (see figure 2(b)), and not resembling, the true crystal structure (see (2) for an example of a Fourier image which is structurally incorrect). The crucial difficulty in using the information between Up and u0 is the fractional accuracy with which Af and Cs must be determined, and these accuracies Δff/4Δf = (2λu2Δf)-1 and ΔCS/CS = (λ3u4Cs)-1 (for a π/4 phase change, Δff the Fourier image period) are strongly dependent on spatial frequency u. Note that ΔCs(up)/Cs ≈ 10%, independent of CS and λ. Note also that the number n of identical high contrast spurious Fourier images within the depth of field Δz = (αu)-1 (α beam divergence) decreases with increasing high voltage, since n = 2Δz/Δff = θ/α = λu/α (θ the scattering angle). Thus image matching becomes easier in semiconductors at higher voltage because there are fewer high contrast identical images in any focal series.


2012 ◽  
Vol 476-478 ◽  
pp. 1138-1141
Author(s):  
Zhi Qiang Wei ◽  
Qiang Wei ◽  
Li Gang Liu ◽  
Hua Yang ◽  
Xiao Juan Wu

Ag nanoparticles were successfully synthesized by hydrothermal method under the polyol system combined with traces of sodium chloride, Silver nitrate(AgNO3) and polyvinylpyrrolidone (PVP) acted as the silver source and dispersant respectively. The samples by this process were characterized via X-ray powder diffraction (XRD), Brunauer–Emmett–Teller (BET) adsorption equation, transmission electron microscopy (TEM) and the corresponding selected area electron diffraction (SAED) to determine the chemical composition, particle size, crystal structure and morphology. The experiment results indicate that the crystal structure of the samples is face centered cubic (FCC) structure as same as the bulk materials, The specific surface area is 24 m2/g, the particle size distribution ranging from10 to 50 nm, with an average particle size about 26 nm obtained by TEM and confirmed by XRD and BET results.


2014 ◽  
Vol 30 (2) ◽  
pp. 286-294 ◽  
Author(s):  
Jianxin Zhu ◽  
Kevin Yoo ◽  
Akhila Denduluri ◽  
Wenting Hou ◽  
Juchen Guo ◽  
...  

Abstract


2013 ◽  
Vol 631-632 ◽  
pp. 176-180 ◽  
Author(s):  
Ying Hao Xie ◽  
Zhan Chang Pan ◽  
Zhi Gang Wei ◽  
Wei Lin Feng ◽  
Jun Hui Zuo ◽  
...  

In this paper, nano TiO2 loaded on activated carbon fiber(ACF) was prepared by hydrothermal method as TiO2/ACF photocatalytic.The material crystal structure, the superficial appearance of catalyst, were analyzed and measured by XRD and SEM images.Moreover, it used for photocatalytic oxidation As(Ⅲ).The effect of pH on the oxidation of As(Ⅲ) was studied. The oxidation of As(Ⅲ) efficiency increasing markedly with pH, and the catalytic efficiency is much higher in the alkaline environment than in the acidic environment.


Minerals ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 659
Author(s):  
Evgeny Nazarchuk ◽  
Dmitri Charkin ◽  
Oleg Siidra ◽  
Stepan Kalmykov

A new organically templated uranyl molybdate [C3H9NH+]4[(UO2)3(MoO4)5] was prepared by a hydrothermal method at 220 °C. The compound is monoclinic, Сс, a = 16.768(6), b = 20.553(8), c = 11.897(4) Å, β = 108.195(7), V = 3895(2) Å3, R1 = 0.05. The crystal structure is based upon [(UO2)3(MoO4)5]4− uranyl molybdate layers. The isopropylammonium cations are located in the interlayer. The layers in the structure of [C3H9NH+]4[(UO2)3(MoO4)5] are considered as modular architectures. Topological analysis of layers with UO2:TO4 ratio of 3:5 (TVI = S, Cr, Se, Mo) was performed. Modular description is employed to elucidate the relationships between different structural topologies of [(UO2)3(TO4)5]4− layers and inorganic uranyl-based nanotubules. The possible existence of uranyl molybdate nanotubules is discussed.


2019 ◽  
Vol 9 (3) ◽  
pp. 226-231 ◽  
Author(s):  
Solange Ivette Rivera Manrique ◽  
Felipe de Jesús Carrillo Romo ◽  
Antonieta García Murillo ◽  
Carlos Eduardo Rodríguez García ◽  
Jorge Roberto Oliva Uc

Introduction: Rare earth-doped Upconverting Nanoparticles (UCN's) can convert near-infrared photons into visible photons via multiphoton processes, which makes it a good material for generating white light. The production of luminescent materials for technology applications focuses on controlling powder characteristics such as chemical homogeneity and low impurity levels. Objective: In this research study, we synthesized Er3+ (1%) Tm3+ (1%) Yb3+ (at different percentages) by co-doping Y2O3 NPs, using the Controlled-Pressure Hydrothermal Method (CPHM), with nitrogen. The ratio used was chosen to conduct a detailed photolumniscence analysis. Methods: Samples of Y2O3: Er3+ (1%) Tm3+ (1%) Yb3+ (at 1.5%, 2%, and 2.5%) were prepared using the controlled-pressure hydrothermal method (CPHM). Each solution was transferred into a mini-clave drive Büchiglasuster with an inner Teflon vessel. In this case, the mini-clave was heated at 190°C for 3 h, and nitrogen was used to control the pressure. The initial pressure was 20 bars; it was increased during the process to 42 bars. The powders obtained were washed with distilled water using centrifugation at 4000 rpm for 15 min. The washed product was dried to 120°C, followed by subsequent heat treatment at 1000°C for 5 h. Results: The representative XRD patterns for the Y2O3: Er3+ (1%) Tm3+ (1%) and Yb3+ (at 1.5%, 2%, 2.5%) doped samples confirms the presence of a cubic Y2O3 crystal structure. Scanning Electron Microscope (SEM) images show that the morphology of these particles is spherical. Upconversion photoluminescence spectra of Y2O3:Er3+ (1% mol) Tm3+ (1% mol) Yb3+ (1.5% mol), Yb3+ (2.0% mol), and Yb3+ (2.5% mol), after 908-nm excitation. Blue, green, and red bands are centred at 440 nm, 469 nm, 618 nm, and 678 nm, respectively. Conclusion: The controlled-pressure hydrothermal method is a productive method for synthesizing rare earth-doped and codoped Y2O3; when Er3+, Yb3+, and Tm3+ ions are introduced into the host matrix, they do not cause any changes in the cubic structure nor influence the crystal structure. This method can used to synthesize any type of nanoparticle, because it involves low pressure (10-20 bars), low temperatures, and short time reactions.


2015 ◽  
Vol 30 (17) ◽  
pp. 2611-2617 ◽  
Author(s):  
Yuzuru Miyazaki ◽  
Takaki Nakajo ◽  
Yuta Kikuchi ◽  
Kei Hayashi

Abstract


1994 ◽  
Vol 113 (2) ◽  
pp. 373-378 ◽  
Author(s):  
Masanori Kikuchi ◽  
Atsushi Yamazaki ◽  
Ryohei Otsuka ◽  
Masaru Akao ◽  
Hideki Aoki

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