scholarly journals Particle Size Dependence of TiO2Electrodes in Rechargeable Lithium Battery

1996 ◽  
Vol 19 (3) ◽  
pp. 189-198 ◽  
Author(s):  
S. Y. Huang ◽  
G. Campet ◽  
N. Treuil ◽  
J. Porter ◽  
K. Chhor

Particle size effects in five anatase TiO2pellet electrodes with different particle sizes (4 ∼ 300nm) and surface areas (8 ∼ 380m2/g) were studied by XRD analysis, chronopotentiometry and chronoamperometry in Li/LiN(CF3SO2)2+ EC:DME/TiO2cells. Nanosized TiO2electrodes showed by 22% larger storage capacity, 50% lower overvoltage loss at the same current density, and 75% higher charge density for a given time than microsized ones; electric storage capacity enhances more rapidly with decreasing particle size and increasing surface area in a nanoscale region than in a microscale region. The particle size dependence may be explained by surface morphology of electrodes and existence of structural defects or distortion in the surface layer of TiO2nanosized particles.

CrystEngComm ◽  
2019 ◽  
Vol 21 (37) ◽  
pp. 5650-5657
Author(s):  
Hongxing Li ◽  
Xinru Song ◽  
Xing Yu ◽  
Jianhua Zhang ◽  
Zixiang Cui ◽  
...  

Spherical nano-selenium of different diameters was prepared and the particle size dependence of the melting thermodynamics of nano-selenium was explored.


2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Chunhua Liang ◽  
Hui Liu ◽  
Jianmin Zhou ◽  
Xiaochun Peng ◽  
Haizhou Zhang

Maghemite (γ-Fe2O3) nanopowders were synthesized under aeration (oxidizing) conditions by aqueous synthesis in this study. The microstructures of the prepared powders were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and BET-BJH. The XRD analysis and the chemical experiments showed that well-crystallized γ-Fe2O3 nanoparticles were successfully obtained with a mean particle size of approximately 17 nm. The prepared γ-Fe2O3 was spherical with a BET surface area of 14.357 m2/g and a total pore volume of 0.050 cm3/g. Varying the reaction conditions, such as pH, temperature, and reaction time, we obtained crystallized γ-Fe2O3 powders with different crystallization extent and different particle sizes. When the pH of the reaction suspension was increased, the reaction time was prolonged, and the reaction temperature was increased, the γ-Fe2O3 powders underwent superior crystallization and had larger particle sizes. All the obtained γ-Fe2O3 powders had significant photocatalytic activities under both UV and visible light irradiation for Orange I degradation, and the powders with better crystallization and larger particle size had relatively lower activities for Orange I photocatalytic degradation. The one-step aqueous synthesis method presented in this paper may provide an advantageous pathway to synthesize large quantities of this important iron oxide.


2016 ◽  
Vol 2016 ◽  
pp. 1-10 ◽  
Author(s):  
Shengli Li ◽  
Tingting Xu

The effect of NS particle size and content on the fresh properties of the grouting material based on the portland-sulphoaluminate composite system was analyzed. The experimental results indicated that air content increased and apparent density decreased, with increased NS content, but the NS particle sizes have minimal effect on the air content and apparent density. The setting time of mortar was significantly shortened, with increased NS content; however, NS particle sizes had little influence on the setting time. The effect of fluidity on the mortars adding NS with particle size of 30 nm is larger than NS with particle sizes of 15 and 50 nm and the fluidity decreased with increased NS content, but the fluidity of mortars with the particle sizes of 15 and 50 nm is almost not affected by the NS content. XRD analysis shows that the formation of ettringite was promoted and the process of hydration reaction of cement was accelerated with the addition of NS. At the microscopic level, the interfacial transition zone (ITZ) of the grouting material became denser and the formation of C-S-H gel was promoted after adding NS.


2012 ◽  
Vol 23 (08) ◽  
pp. 1240001 ◽  
Author(s):  
V. ALVIN SHUBERT ◽  
STEVEN P. LEWIS

Niobium carbide nanocrystals of ~1:1 stoichiometry have recently been observed for particle sizes ranging from Nb4C4 to Nb50C50 . Infrared (IR) spectroscopic measurements show that a new band of IR vibrational modes appears with increasing particle size at Nb9C9 . Using density-functional theory, we show that the vibrational modes in the new band involve structural features present only in nanocrystals with three or more atomic layers in every direction. The Nb9C9 nanocrystal is right at this structural threshold.


1999 ◽  
Vol 14 (9) ◽  
pp. 3599-3603 ◽  
Author(s):  
Li Shi ◽  
Ning-Bew Wong

Supported and unsupported γ-alumina membranes and alumina–titania composite membranes were prepared using the sol-gel method. In the course of preparation, effects of acid concentration, type of acid, alkoxide, and binder on the particle size of the sols and pore size of the membranes were investigated by thermogravimetry and differential thermal analysis, N2 physisorption, and light scattering. It was observed that the particle sizes of all the sols had only a small affect on the pore sizes of the membranes. Qualities of the membranes were improved by addition of polyvinyl alcohol as binder to the boehmite precursor. This resulted in less critical but more controllable drying and calcining procedures. Composite membranes with different pore sizes from 3.2 to 4.8 nm and surface areas retained above 100 m2/g could be regulated by different alumina-to-titania ratios.


2012 ◽  
Vol 11 (01) ◽  
pp. 1250010
Author(s):  
ARCHANA BHATT ◽  
MUNISH KUMAR

Simple theoretical method is developed to study the size dependence of equation of state of nanomaterials. The isothermal compression of Ni and ε- Fe has been computed for different particle sizes. A shift in compression curve is obtained by increasing the particle size. This demonstrates the softening of the material by increasing the particle size. For larger particle size (~100 nm) the compression curve resembles with that of the bulk. This demonstrates that the nanomaterial becomes bulk for larger particle size. The results have been compared with the available experimental data. A good agreement between theory and experiment demonstrates the validity of the method proposed in the present paper.


2018 ◽  
Vol 8 (1) ◽  
Author(s):  
Sudipta Goswami ◽  
Dipten Bhattacharya ◽  
Chandan K. Ghosh ◽  
Barnali Ghosh ◽  
S. D. Kaushik ◽  
...  

Energies ◽  
2021 ◽  
Vol 14 (24) ◽  
pp. 8435
Author(s):  
Jianguo Zhang ◽  
Xiyuan Li ◽  
Jihong Jiao ◽  
Jianbao Liu ◽  
Feng Chen ◽  
...  

In order to investigate the difference of pore structure characteristics between mudstone and coal under different particle size conditions, samples acquired from Henan province were smashed and screened into three different particle sizes (20–40, 80–100, and >200 mesh) to conduct the experiments, using the high-pressure mercury intrusion porosimetry (MIP) and low-temperature N2 adsorption (LT-N2A) techniques. The results demonstrated that the proportion of open pores or semi-enclosed pores increased, and the pores became preferable contacted each other for both mudstone and coal during the crushing process. These variations of pore structure characteristics in the coal were beneficial to methane storage and migration. The total specific surface areas and pore volumes all showed a tendency of increasing continually for both mudstone and coal, as the particle sizes decreased from the LT-N2A test. The mudstone and coal were non-rigid aggregates with micropores, plate-shaped pores, and slit-shaped pores developed inside. The effect of the crushing process on the pore shape for the mudstone and coal was inappreciable. Moreover, the influence of the particle sizes on the mesopore was the most significant, followed by the macropore; and on the micropore, the influence was negligible for both mudstone and coal. The crushing process only had a significant impact on the pore structure of mudstone with a particle size of less than 100 mesh, while it could still alter the pore structure of coal with a particle size of larger than 100 mesh. It is believed that this work has a significant meaning to explore the diffusion and migration rules of coal-bed methane in coal.


1971 ◽  
Vol 49 (21) ◽  
pp. 3411-3417 ◽  
Author(s):  
N. H. Sagert ◽  
R. M. L. Pouteau

Some rate data are reported for deuterium exchange between water and hydrogen using series of platinum–silica catalysts. Three different methods of preparing catalysts were used to give different series of metal particle sizes. Within each series, the particle size was increased by sintering batches in air, at temperatures up to 700 °C. These methods produced platinum particles ranging from 5 to 250 Å in diameter. Metal surface areas and particle sizes were measured by hydrogen chemisorption, X-ray diffraction, and electron microscopy.The specific rates, i.e., rates per unit surface area of platinum varied by a factor of three within each series, reaching a maximum for sintering temperatures of about 500 °C. These maximum rates, measured at 127 °C with a water-to-hydrogen ratio of 0.31, varied from 1.9 × 10−8 to 5 × 10−8 mol D2 cm−2 s−1. Thus no effect of particle size on rate was observed, and the differences noted are ascribed to other effects of the methods of preparing the catalysts.


Geofluids ◽  
2020 ◽  
Vol 2020 ◽  
pp. 1-13 ◽  
Author(s):  
Garri Gaus ◽  
Anton Kalmykov ◽  
Bernhard M. Krooss ◽  
Reinhard Fink

Crushing and grinding of carbonaceous shale samples is likely to enhance the accessibility of pores and embedded organic matter as compared to the intact rock. This may lead to an overestimation of the total (volume and sorptive) gas storage capacity. In order to investigate the importance of these effects we have measured unconfined apparent grain densities (helium pycnometry) and methane sorption capacities (high-pressure methane excess sorption) of four carbonaceous shales (Cambro-Ordovician Alum Shale, Jurassic Kimmeridge Clay, Jurassic/Cretaceous Bazhenov Shale, and Late Cretaceous Eagle Ford Shale) as a function of particle size. Measurements were first conducted on 38 mm diameter core plugs, which then were crushed and milled to successively smaller particle sizes (<10 mm, <2 mm, <64 μm, and <1 μm). Apparent grain densities of the smallest particle fractions of the Alum, Bazhenov and Kimmeridge samples were consistently higher by 0.5 to 1% than apparent grain densities of the original sample plugs. Methane excess sorption capacity increased significantly for particle sizes <64 μm for the Alum and <1 μm for the Bazhenov and Kimmeridge samples while no significant changes upon grinding were observed for the Eagle Ford Shale. For the Bazhenov Shale, the apparent grain density increased slightly from 2.446 g/cm3 to 2.450 g/cm3 upon particle size reduction from <64 μm to <1 μm while the maximum sorption capacity (“Langmuir volume”) increased substantially from 0.11 mmol/g to 0.19 mmol/g. Similarly, for the Kimmeridge Clay and Alum Shale, a slight increase of the apparent grain density from 1.546 g/cm3 to 1.552 g/cm3 and from 2.362 g/cm3 to 2.385 g/cm3, respectively, was accompanied by increases in sorption capacity from 0.37 mmol/g to 0.45 mmol/g and from 0.14 mmol/g to 0.185 mmol/g, respectively. The increase in sorption capacity indicates an opening of a considerable amount of micropores with large internal surface area upon physical disruption of the rock fabric and/or removal of included fluids. It may also be due to increased swelling abilities of clay minerals and organic matter upon destruction of the stabilizing rock fabric with decreasing particle size. Grain density and sorption isotherms measured on small particle sizes are likely to overestimate the gas storage capacities and the amounts of producible gas-in-place since under field conditions (largely undisrupted rock fabric), significant portions of this storage capacity are essentially inaccessible. Poor interconnectivity of the pore system and slow, diffusion-controlled transport will massively retard gas production. Based on these findings, particle sizes >64 μm should be used for porosity and sorption measurements because they are more likely to retain the properties of the rock fabric in terms of accessible pore volume and sorptive storage capacity.


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