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Online since: January 2007
Authors: Duck Kyeom Kim, William Carty, Ungsoo Kim, Eui Seok Choi, Jae Hwan Pee
Instead, network structure is
clearly shown in a drop
As the phase separation starts, the particles covered with PAA or PMAA tend to form an interconnected structure to reduce the free energy of the system.
The process for forming an interconnected structure is facilitated by the shrinking of sprayed droplets.
This results in a network structure between SS and PVA, leading to homogeneous distribution of PVA
Iler, The Chemistry of Silica; John Wiley & Sons, New York, 1979.
As the phase separation starts, the particles covered with PAA or PMAA tend to form an interconnected structure to reduce the free energy of the system.
The process for forming an interconnected structure is facilitated by the shrinking of sprayed droplets.
This results in a network structure between SS and PVA, leading to homogeneous distribution of PVA
Iler, The Chemistry of Silica; John Wiley & Sons, New York, 1979.
Online since: May 2005
Authors: E.Ö. Sveinbjörnsson, T. Rödle, H.Ö. Ólafsson, G. Gudjónsson, Fredrik Allerstam, R. Jos
Transmission line method (TLM) structures
were included to study the contact properties.
The oxide thickness is extracted from capacitance-voltage (CV) measurements on MOS structures close to the measured transistors and is 1960Å and 550Å for sample AAlOx and BN2O, respectively.
Measurements on the TLM structures in sample AAlOx gave a specific contact resistance ρc=9.1x10-3 Ωcm2 and a specific sheet resistance ρs=7.3x103 Ω/□.
Oxidising in alumina environment introduces impurities into the oxide, which affect the oxidation chemistry.
In 6H-SiC MOS structures we have found a large density of traps near the conduction band edge [5] and we speculate that these traps are similar to the NITs found at the 4H-SiC/SiO2 interface.
The oxide thickness is extracted from capacitance-voltage (CV) measurements on MOS structures close to the measured transistors and is 1960Å and 550Å for sample AAlOx and BN2O, respectively.
Measurements on the TLM structures in sample AAlOx gave a specific contact resistance ρc=9.1x10-3 Ωcm2 and a specific sheet resistance ρs=7.3x103 Ω/□.
Oxidising in alumina environment introduces impurities into the oxide, which affect the oxidation chemistry.
In 6H-SiC MOS structures we have found a large density of traps near the conduction band edge [5] and we speculate that these traps are similar to the NITs found at the 4H-SiC/SiO2 interface.
Online since: October 2013
Authors: Wen Hai Gai, Yuan Yuan Liu, Ran Guo
The analysis of events once again confirms that the material characteristic depends largely on the atomic structure of the material and its microstructure.
The materials exists differences in the structure of the different scales.
In 2006, Du [14] made use of molecular dynamics method to study the polymerization of the molecular structure of the ceramic material silicon - oxygen, and focused on the study from the point defects to the development of line defects and surface defects.
Annual Review of Physical Chemistry, 1981, 34(1): 103-127 [11]M.
Physical Review Letters, 1986, 56(14): 1505-1512 [14]Du J, Corrales L R.First sharp diffraction peak in silicate glasses: Structure and scattering length dependence.Phys.Rev.B, 2005, 72:092201 [15] Qingsheng Yang, Daihua Zheng.
The materials exists differences in the structure of the different scales.
In 2006, Du [14] made use of molecular dynamics method to study the polymerization of the molecular structure of the ceramic material silicon - oxygen, and focused on the study from the point defects to the development of line defects and surface defects.
Annual Review of Physical Chemistry, 1981, 34(1): 103-127 [11]M.
Physical Review Letters, 1986, 56(14): 1505-1512 [14]Du J, Corrales L R.First sharp diffraction peak in silicate glasses: Structure and scattering length dependence.Phys.Rev.B, 2005, 72:092201 [15] Qingsheng Yang, Daihua Zheng.
Online since: September 2007
Authors: Elena V. Bogdanova, Alla S. Tregubova, M.P. Scheglov, Mikael Syväjärvi, Rositza Yakimova, V.V. Zelenin, Pavel L. Abramov, Sergey P. Lebedev, D.K. Nel'son, Boris S. Razbirin, Alexander A. Lebedev
Petersburg 194021,
Russian Federation
2
Department of Physics, Chemistry and Biology, Linkoping University, SE-58183,
Linkoping, Sweden
a
shura.lebe@ioffe.mail.ru; broy@ifm.liu.se.
An analysis of the topographs demonstrated that the epitaxial layer has a structure of 3C-SiC and at these thicknesses is mostly constituted of twinning regions of various sizes, which are oriented at an angle of 60 o with respect to one other and are manifested in the topographs as dark or light areas.
This region is in the reflecting position in the topograph (light area) and shows a finer defect structure, mainly characterized by presence of dislocations with a density of ~10 5 cm-2.
The large thickness of the layers obtained, low twin density, and uniformity of their electrical parameters show that the structures studied can be used as substrates for fabrication of device structures based on 3C-SiC.
An analysis of the topographs demonstrated that the epitaxial layer has a structure of 3C-SiC and at these thicknesses is mostly constituted of twinning regions of various sizes, which are oriented at an angle of 60 o with respect to one other and are manifested in the topographs as dark or light areas.
This region is in the reflecting position in the topograph (light area) and shows a finer defect structure, mainly characterized by presence of dislocations with a density of ~10 5 cm-2.
The large thickness of the layers obtained, low twin density, and uniformity of their electrical parameters show that the structures studied can be used as substrates for fabrication of device structures based on 3C-SiC.
Online since: March 2007
Authors: Yu Zhen Lv, Lin Guo, Chun Ping Li, X.B. Xu, X.C. Ai, J.P. Zhang
Zhang
2
1
School of Materials Science and Engineering,
Beijing University of Aeronautics and Astronautics, Beijing, 100083, China
2
Institute of Chemistry, Chinese Academy of Science, Beijing, 100080, China
a
Chunping@buaa.edu.cn, bGuolin@buaa.edu.cn
Keywords: synthesis; temperature-dependent photoluminescence; ZnO nanorods
Abstract.
The ZnO luminescent properties are strongly influenced by the preparation method and their electronic and crystalline structures.
However, to establish an applicable process for the integrated photonic devices, one may have to develop a relatively low temperature and simple growth method for growing desired structures.
XRD and SEM measurements were carried out for structure and morphological characterization, respectively.
XRD spectrum, as shown in Fig. 2, indicates that the ZnO nanorods have hexagonal wurtzite structure, and no defects or other elements were detected. 30 40 50 60 70 80 0 200 400 600 800 1000 1200 1400 1600 202 201112 200103 110 102 101 002 100 intensity (a.u.) 2 θ (degree) Fig. 1.
The ZnO luminescent properties are strongly influenced by the preparation method and their electronic and crystalline structures.
However, to establish an applicable process for the integrated photonic devices, one may have to develop a relatively low temperature and simple growth method for growing desired structures.
XRD and SEM measurements were carried out for structure and morphological characterization, respectively.
XRD spectrum, as shown in Fig. 2, indicates that the ZnO nanorods have hexagonal wurtzite structure, and no defects or other elements were detected. 30 40 50 60 70 80 0 200 400 600 800 1000 1200 1400 1600 202 201112 200103 110 102 101 002 100 intensity (a.u.) 2 θ (degree) Fig. 1.
Online since: May 2011
Authors: Qi Gang Deng, Zhe Li, Xiao Ming Huang, Yong Jie Zheng, Jing Zhi Tian, Tao Jing
Cage-Shape Macroporous/Mesoporous 3DOM SiO2 Immobilized Papain
Jingzhi Tian a, Tao Jing b, Xiaoming Huang, Yongjie Zheng,
Qigang Deng and Zhe Li
School of Chemistry & Chemical Engineering,Qiqihar University, Qiqihar 161006, China;
atjz6666@163.com, bjtkr@163.com
Key Words: macroporous material; SiO2; immobilization; papain; relative activity
Abstract.
The results indicate that the PS is regularly range, surface heart cubic structure by variation of the conditions of synthesis and assembly.
In order to further study of the 3DOM SiO2 pore structure, N2 is determined as adsorbate adsorption-desorption.
Combined with SEM and TEM results, we can draw a conclusion that the prepared catalysts are macroporous/mesoporous structure.
The experiment indicated that the SiO2 materials obtained has a structure of macroporous and ordered cage-shape, evenly distributed, an average particle size is about 150 nm.
The results indicate that the PS is regularly range, surface heart cubic structure by variation of the conditions of synthesis and assembly.
In order to further study of the 3DOM SiO2 pore structure, N2 is determined as adsorbate adsorption-desorption.
Combined with SEM and TEM results, we can draw a conclusion that the prepared catalysts are macroporous/mesoporous structure.
The experiment indicated that the SiO2 materials obtained has a structure of macroporous and ordered cage-shape, evenly distributed, an average particle size is about 150 nm.
Online since: September 2011
Authors: Hong Jin Qi, Wen Qin Du, Jian Feng Di, Xiao Xia He
There have been many models and approaches for complex shaped pores confined by yarns and/or fiber in different region of fabric, but they have not yet satisfied the requirement of characterization of fabric pore structure and size distribution due to the complexity and easy deformation of weave pore [5-7].
Based on the above, the study was carried out according to surface chemistry and hydromechanics at temperature 20 ˚C ± 1 ˚C and 65% ± 2% RH.
Owing to warp-weft structure, these mutually perpendicular pores distribution along the fabric plane leads to a complex configuration, and hence liquid transport in capillary along any yarn axis is always influenced by the pore channel perpendicular to it and hence by liquid behavior in the pore.
Thanks to above, this definition of pore size can be used to quantitatively evaluate different pore sizes and pore structures, especially the partially ordered flexible pore system with certain structure such as fabric, non-woven as well as soft leather.
Based on the above, the study was carried out according to surface chemistry and hydromechanics at temperature 20 ˚C ± 1 ˚C and 65% ± 2% RH.
Owing to warp-weft structure, these mutually perpendicular pores distribution along the fabric plane leads to a complex configuration, and hence liquid transport in capillary along any yarn axis is always influenced by the pore channel perpendicular to it and hence by liquid behavior in the pore.
Thanks to above, this definition of pore size can be used to quantitatively evaluate different pore sizes and pore structures, especially the partially ordered flexible pore system with certain structure such as fabric, non-woven as well as soft leather.
Online since: January 2011
Authors: Gui Yang Liu, Bao Sen Wang, Jun Ming Guo, Ying He
Flameless solution combustion synthesis of Al3+ doped LiMn2O4
Guiyang Liu1, a, Junming Guo2, Bao-sen Wang1, Ying He1
1College of Science, Honghe University, Mengzi Yunnan, China 661100
2School of Chemistry and Biotechnology, Yunnan University of Nationalities, Kunming Yunnan, China 650031
aliuguiyang@tsinghua.org.cn
Keywords: flameless solution combustion synthesis, lithium ion batteries, spinel LiMn2O4, doping
Abstract: Single phase Al3+ doped LiMn2O4 has been prepared by flameless solution combustion synthesis method at 600oC for 1h.
The main peaks of all the products correspond to the spinel LiMn2O4 with cubic structure (JCPDS 35-0782, a=0.8248nm).
The reason may be attributed to the stability of the lattice structure.
The lattice structure became more stable when Mn3+/Mn4+ were replaced by Al3+ partly, because the Al-O bond is more stable than Mn-O bond.
The more stable lattice structure can avoid the collapsing when insertion/desertion of the Li+ ions when charge and discharge [10].
The main peaks of all the products correspond to the spinel LiMn2O4 with cubic structure (JCPDS 35-0782, a=0.8248nm).
The reason may be attributed to the stability of the lattice structure.
The lattice structure became more stable when Mn3+/Mn4+ were replaced by Al3+ partly, because the Al-O bond is more stable than Mn-O bond.
The more stable lattice structure can avoid the collapsing when insertion/desertion of the Li+ ions when charge and discharge [10].
Online since: September 2006
Authors: Seiichiro Koda, Fuyuki Kano, Hiroshi Uchida, Kazuko Sugimoto
Synthesis of Oxide Thin Films on Silicon Substrate
using Supercritical Carbon Dioxide Fluid
Fuyuki Kano, Hiroshi Uchida, Kazuko Sugimoto and Seiichiro Koda
Department of Chemistry, Faculty of Science and Technology, Sophia University
7-1 Kioi-cho, Chiyoda-ku, Tokyo 102-8554, Japan
Keywords: supercritical fluid, carbon dioxide, titanium oxide, silicon wafer
ABSTRACT
Thin films of titanium oxide (TiO2) were synthesized from Titanium diisopropoxide
bis(dipivaloylmethanate) [Ti(O-i-Pr)2(dpm)2] as a source material using supercritical carbon dioxide
(CO2) fluid.
For achieving advanced integration of memory devices, the techniques for oxide film deposition have to satisfy some requests like (1) conformal deposition on the substrate with complicated structure such as nano-trench and hole units, (2) selective control of chemical composition for multicomponent films, and (3) crystallization at lower temperatures to avoid the oxidation of Si surface, etc.
However, the conventional film-deposition techniques have hardly satisfied these demands simultaneously; for instance, chemical vapor deposition (CVD) process enables to deposit uniform films of organized complicated structure whereas it still has difficulty in controlling the individual amount of source supply which determines the chemical composition of the resultant multicomponent films.
The present authors consider that the material characteristics, such as microstructure and crystal structure, of the products using SCFD process would be influenced significantly by the temperature and/or pressure of the supercritical fluid, because the physical properties of the fluid vary greatly according to these parameters.
In this study, therefore, the influence of the various parameters for the supercritical CO2 fluid on the structure of the resulting oxide films by SCFD process was investigated.
For achieving advanced integration of memory devices, the techniques for oxide film deposition have to satisfy some requests like (1) conformal deposition on the substrate with complicated structure such as nano-trench and hole units, (2) selective control of chemical composition for multicomponent films, and (3) crystallization at lower temperatures to avoid the oxidation of Si surface, etc.
However, the conventional film-deposition techniques have hardly satisfied these demands simultaneously; for instance, chemical vapor deposition (CVD) process enables to deposit uniform films of organized complicated structure whereas it still has difficulty in controlling the individual amount of source supply which determines the chemical composition of the resultant multicomponent films.
The present authors consider that the material characteristics, such as microstructure and crystal structure, of the products using SCFD process would be influenced significantly by the temperature and/or pressure of the supercritical fluid, because the physical properties of the fluid vary greatly according to these parameters.
In this study, therefore, the influence of the various parameters for the supercritical CO2 fluid on the structure of the resulting oxide films by SCFD process was investigated.
Online since: March 2015
Authors: Shen Zhou Lu, Shan Shan Zhang, Tian Zhu, Fang Zhang, Jiao Jiao Li, Rui Jiang
Excellent Cell Compatibility in Time Controlled Silk Fibroin Hydrogels
Fang Zhanga, Jiaojiao Lib, Rui Jiangc, Shanshan Zhangd, Tian Zhue
and Shenzhou Lu*f
College of Textile and Clothing Engineering, Soochow University, Suzhou 215123, People’s Republic of China
National Engineering Laboratory for Modern Silk, Soochow University, Suzhou 215123, People’s Republic of China
afang.zhang0807@foxmail.com, blijiaojiaobest@126.com, cshibadongsushe@163.com, dzhangshanshanfzx@126.com, e906634298@qq.com, flushenzhou@suda.edu.cn
Key words: Silk fibroin, Hydrogel, Structure, Cell compatibility.
Introduction Hydrogels, a sort of three dimensional network structure macromolecular materials, hold large amounts of water stably but do not dissolve in these solutions. [1] Eminent mechanical properties and good biocompatibility furnish hydrogels extensive application in the field of clinical medicine, such as drug delivery carriers [2], tissue engineering scaffolds [3].
Wu, N-Lauroyl sarcosine sodium salt mediated formation of hydroxyapatite microspheres via a hydrothermal route, Materials Chemistry and Physics. 135 (2012) 32-37
Introduction Hydrogels, a sort of three dimensional network structure macromolecular materials, hold large amounts of water stably but do not dissolve in these solutions. [1] Eminent mechanical properties and good biocompatibility furnish hydrogels extensive application in the field of clinical medicine, such as drug delivery carriers [2], tissue engineering scaffolds [3].
Wu, N-Lauroyl sarcosine sodium salt mediated formation of hydroxyapatite microspheres via a hydrothermal route, Materials Chemistry and Physics. 135 (2012) 32-37