scholarly journals Fast Preparation of Porous MnO/C Microspheres as Anode Materials for Lithium-Ion Batteries

2017 ◽  
Author(s):  
Jing Su ◽  
Hao Liang ◽  
Xian-Nian Gong ◽  
Xiao-Yan Lv ◽  
Yun-Fei Long ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Large Scale ◽  
Electrochemical Impedance ◽  
Lithium Ion ◽  
Precipitation Method ◽  
Electrochemical Performances ◽  
Cyclic Voltammograms

Porous MnO/C microspheres have been successfully fabricated by a fast co-precipitation method in a T-shaped microchannel reactor. The structures, compositions and electrochemical performances of the obtained MnO/C microspheres are characterized by X-ray diffraction, emission scanning electron microscopy, transmission electron microscopy (HRTEM), Brunauer–Emmett–Teller analysis, charge-discharge testing, cyclic voltammograms, and electrochemical impedance spectra. Experimental results reveal that the as-prepared MnO/C, with a specific surface area of 96.66 m2·g–1 and average pore size of 24.37 nm, exhibits excellent electrochemical performance, with a discharge capacity of 655.4 mAh·g–1 after cycling 50 times at 1 C and capacities of 808.3, 743.7, 642.6, 450.1, and 803.1 mAh·g–1 at 0.2, 0.5, 1, 2, and 0.2 C, respectively. Moreover, the controlled method of using a micro-channel reactor, which can produce larger specific surface area porous MnO/C with improved cycling performance by shortening lithium-ion diffusion distances, can be easily applied in real production on a large-scale.

CVD Synthesis of Multi-Walled Carbon Nanotubes onto Different Catalysts at Low Temperature

NANO ◽  
2018 ◽  
Vol 13 (04) ◽  
pp. 1850036 ◽  
Author(s):  
Guiqiang Diao ◽  
Hao Li ◽  
Hao Liang ◽  
Iryna Ivanenko ◽  
Tetiana Dontsova ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Carbon Nanotubes ◽  
Low Temperature ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Sol Gel ◽  
Lithium Ion ◽  
Multi Walled Carbon Nanotubes ◽  
Walled Carbon Nanotubes

Multi-walled carbon nanotubes (MWCNTs) were synthesized onto a series of individual and bimetallic catalysts by the chemical vapor deposition (CVD) of acetylene at low temperature (600[Formula: see text]C). The catalysts were prepared by two methods, i.e., precipitation and sol–gel, with two different carriers – MgO and Al2O3. The catalysts were characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermal gravimetric (TG) analysis, low-temperature adsorption of nitrogen. The yield of the MWCNTs was calculated in two ways, while the highest yield of 800% was achieved onto the two-component NiO/Co2O3/MgO catalyst, SEM and transmission electron microscopy (TEM) results confirm that uniform tube-like structure MWCNTs with the yield of 410% were obtained onto Co2O3/Al2O3 catalyst. These MWCNTs are smooth and pointing in the same direction. Their tube diameter is about 20[Formula: see text]nm, which is the smallest around all observed MWCNTs. Moreover, nonuniform curved bamboo-like MWCNTs with nozzles in the yield of 760% were obtained onto NiO/V2O3/MgO catalyst. Their diameter ranges from 25[Formula: see text]nm to 50[Formula: see text]nm. Results show that single-component catalyst promotes the growth of uniform and smaller nanotubes. Among the as-grown nanotubes, their specific surface area increases and average pores diameter reduces after the treatment with concentrated nitric acid at reflux and washing condition. The largest specific surface area (305[Formula: see text]m2/g) and average pores diameter (26[Formula: see text]m2/g) are processed to MWCNTs grown onto the NiO/Co2O3/MgO catalyst. MWCNTs with such large structural adsorption characteristics and purity of more than 99% obtained with yield 800% show potential use for preparation of nanocomposites as anode materials in lithium ion batteries.

Carbon Nanotube Anodes for Lithium Ion Batteries

2001 ◽  
Vol 706 ◽  
Author(s):  
Ryne P. Raffaelle ◽  
Thomas Gennett ◽  
Jeff Maranchi ◽  
Prashant Kumta ◽  
Aloysius F. Hepp ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Carbon Nanotubes ◽  
Specific Surface ◽  
Lithium Ion Batteries ◽  
Surface Area ◽  
Specific Surface Area ◽  
Anode Materials ◽  
Lithium Ion ◽  
Carbonaceous Materials ◽  
Walled Carbon Nanotubes

AbstractHighly purified single-wall carbon nanotubes (SWCNT) were investigated for use as an anode material for thin film lithium ion batteries. The high purity nanotubes were obtained through chemical refinement of soot generated by pulsed laser ablation. The purity of the nanotubes was determined via thermogravimetric analysis, scanning electron microscopy, and transmission electron microscopy. The specific surface area and lithium capacity of the SWCNT's was compared to that of other conventional anode materials (i.e., carbon black, graphite, and multi-walled carbon nanotubes). The Brunauer, Emmett, and Teller (BET) technique based on nitrogen adsorption was used to measure the specific surface area of the various anode materials. The SWCNT's exhibited a specific surface area on the order of 915 m2/g, much higher than the other carbonaceous materials. Cyclic voltammetric behavior and the lithium-ion capacity of the materials were measured using a standard 3-electrode electrochemical cell. The cyclic voltammetry showed evidence of “staging” that was similar to other carbonaceous materials. The electrochemical discharge capacity of the purified single walled carbon nanotubes was in excess of 1300 mAh/g after 30 charge/discharge cycles when tested using a current density of 20μA/cm2.

Mesoporous CuO–ZnO p–n heterojunction based nanocomposites with high specific surface area for enhanced photocatalysis and electrochemical sensing

2016 ◽  
Vol 6 (9) ◽  
pp. 3238-3252 ◽  
Author(s):  
Sumit Chabri ◽  
Arnab Dhara ◽  
Bibhutibhushan Show ◽  
Deepanjana Adak ◽  
Arijit Sinha ◽  
...  
Keyword(s):  
Solid State ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
High Specific Surface Area ◽  
Electrochemical Sensing ◽  
Solid State Reactions ◽  
Core Shell ◽  
Electrochemical Performances ◽  
Microstructural Refinement

Mesoporous and core–shell like (p)CuO–(n)ZnO nanocomposites were prepared using microstructural refinement and solid state reactions, which showed enhanced photochemical and electrochemical performances.

Synthesis of Novel Core-Shell Structured Hydroxyapatite/Meso-Silica for Removal of Methylene Blue from Aqueous Solutions

2012 ◽  
Vol 463-464 ◽  
pp. 543-547 ◽  
Author(s):  
Cheng Feng Li ◽  
Xiao Lu Ge ◽  
Shu Guang Liu ◽  
Fei Yu Liu
Keyword(s):  
Methylene Blue ◽  
Aqueous Solutions ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Low Cost ◽  
Nitrogen Adsorption ◽  
Precipitation Method ◽  
Core Shell ◽  
Adsorption Desorption

Core-shell structured hydroxyapatite (HA)/meso-silica was prepared and used as absorbance of methylene blue (MB). HA/meso-silica was synthesized in three steps: preparation of nano-sized HA by wet precipitation method, coating of dense silica and deposition of meso-silica shell on HA. As-received samples were characterized by Fourier transformed infare spectra, small angle X-ray diffraction, nitrogen adsorption-desorption isotherm and transmission electron microscopy. A wormhole framework mesostructure was found for HA/meso-silica. The specific surface area and pore volume were 128 m2•g-1 and 0.36 cm3•g-1, respectively. From the adsorption isotherm, HA/meso-silica with the great specific surface area exhibited a prominent adsorption capacity of MB (134.0 mg/g) in comparison with bare HA (0 mg/g). This study might shed light on surface modification of conventional low-cost adsorbents for removal of organic pollutants from aqueous solutions.

Study on Nano-Hydroxyapatite Assisted Preparing by Ionic Liquids

2014 ◽  
Vol 1015 ◽  
pp. 501-504 ◽  
Author(s):  
Yong Guang Bi ◽  
Xu Si Xu
Keyword(s):  
Grain Size ◽  
Ionic Liquids ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Large Scale ◽  
Preparation Method ◽  
Raw Material ◽  
Large Scale Preparation ◽  
Scale Preparation

Papers with Ca (NO3)2• 4H2O and (NH4)2HPO4as raw material, prepared by ionic liquids assisted nanoHAP, resulting hexagonal nanoHAP are crystal grain size are 10-20nm level, are smaller nanometer range ; specific surface area, the findings show that ionic liquids have the technology to promote the significance of the preparation method can provide a reference for large-scale preparation of biomedical nanomaterials.

Synthesis and Thermal Stability of HfO2 Nanoparticles

2010 ◽  
Vol 1256 ◽  
Author(s):  
Girija Shankar Chaubey ◽  
Yuan Yao ◽  
Julien Pierre Amelie Makongo Mangan ◽  
Pranati Sahoo ◽  
Pierre F. P. Poudeu ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Large Scale ◽  
Average Diameter ◽  
Scale Production ◽  
Simple Method ◽  
Good Thermal Stability ◽  
Large Scale Production

AbstractA simple method is reported for the synthesis of monodispersed HfO2 nanoparticles by the ammonia catalyzed hydrolysis and condensation of hafnium (IV) tert-butoxide in the presence of surfactants at room temperature. Transmission electron microscopy shows faceted nanoparticles with an average diameter of 3-4 nm. As-synthesized nanoparticles are amorphous in nature and crystallize upon moderate heat treatment. The HfO2 nanoparticles have a narrow size distribution, large specific surface area and good thermal stability. Specific surface area was about 239 m2/g on as-prepared nanoparticle samples while those annealed at 500 °C have specific surface area of 221 m2/g indicating that there was no significant increase in particle size. This result was further confirmed by TEM images of nanoparticles annealed at 300 °C and 500 °C. X-ray diffraction studies of the crystallized nanoparticles revealed that HfO2 nanoparticles were monoclinic in structure. The synthetic procedure used in this work can be readily modified for large scale production of monodispersed HfO2 nanoparticles.

Synthesis and Characterization of Porous Mo-W Oxide Nanostructures

2008 ◽  
Vol 8 (12) ◽  
pp. 6445-6450
Author(s):  
F. Paraguay-Delgado ◽  
Y. Verde ◽  
E. Cizniega ◽  
J. A. Lumbreras ◽  
G. Alonso-Nuñez
Keyword(s):  
Electron Microscopy ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Synthesis Method ◽  
Atomic Ratio ◽  
High Specific Surface Area ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Before And After

The present study reports the synthesis method, microstructure characterization, and thermal stability of nanostructured porous mixed oxide (MoO3-WO3) at 550 and 900 °C of annealing. The material was synthesized using a hydrothermal method. The precursor was prepared by aqueous solution using ammonium heptamolibdate and ammonium metatungstate, with an atomic ratio of Mo/W = 1. The pH was adjusted to 5, and then the solution was transferred to a teflon-lined stainless steel autoclave and heated at 200 °C for 48 h. The resultant material was washed using deionized water. The specific surface area, morphology, composition, and microstructure before and after annealing were studied by N2 physisorption, scanning electron microscopy (SEM), analytical transmission electron microscopy (TEM), and X-Ray diffraction (XRD). The initial synthesized materials showed low crystallinity and high specific surface area around (141 m2/g). After thermal annealing the material showed higher crystallinity and diminished its specific surface area drastically.

Synthesis and Photocatalytic Property of BiVO4/FeVO4 Composite Novel Photocatalyst

2010 ◽  
Vol 129-131 ◽  
pp. 784-788 ◽  
Author(s):  
Min Wang ◽  
Qiong Liu ◽  
Dong Zhang
Keyword(s):  
Photocatalytic Activity ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Photocatalytic Property ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
Experimental Conditions ◽  
Triclinic Phase ◽  
Xrd Patterns

BiVO4/FeVO4 composite photocatalyst samples were prepared by calcining the mixture of FeVO4 and BiVO4 precusor which were prepared through liquid phase precipitation method for further increasing the photocatalytic efficiency of FeVO4. The catalysts were characterized by X-ray diffraction (XRD), scanning electron microsoope（SEM）and specific surface area (BET). The photocatalytic activity was evaluated by photocatalytic degradation of methyl orange (MO) solution under visible light. The XRD patterns indicate that BiVO4/FeVO4 composite photocatalysts consist of triclinic phase and the lattice was not distorted beacause of doping Bi. But the morphology change greatly and the specific surface area has little change. In the experimental conditions used, the optimal photocatalytic activity for all the prepared samples was reached when BiVO4 doping was 22 at%. The degradation rate of MO was increased by 20％ or so than that of pure FeVO4.

Graphene modified Li-rich cathode material Li[Li0.26Ni0.07Co0.07Mn0.56]O2 for lithium ion battery

2014 ◽  
Vol 07 (06) ◽  
pp. 1440013 ◽  
Author(s):  
Xiangjun Li ◽  
Hongxing Xin ◽  
Xiaoying Qin ◽  
Xueqin Yuan ◽  
Di Li ◽  
...  
Keyword(s):  
Electrochemical Impedance ◽  
Rate Capability ◽  
Lithium Ion ◽  
Cycling Performance ◽  
Precipitation Method ◽  
Electrochemical Performances ◽  
Charge Transfer Reaction ◽  
Ion Diffusion ◽  
Co Precipitation ◽  
Kinetics Of

Lithium and Mn rich solid solution materials Li [ Li 0.26 Ni 0.07 Co 0.07 Mn 0.56] O 2 were synthesized by a carbonate co-precipitation method and modified with a layer of graphene. The graphene-modified cathodes exhibit improved rate capability and cycling performance as compared to the bare cathodes. Electrochemical impedance spectroscopy (EIS) analyses reveal that the improved electrochemical performances are due to acceleration kinetics of lithium-ion diffusion and the charge transfer reaction of the graphene-modified cathodes.

The Influence of Sinterng Temperature on the Phase, Microstructure and Textual Properties of Hollow Hydroxyapatite Microspheres

2011 ◽  
Vol 239-242 ◽  
pp. 2274-2279 ◽  
Author(s):  
Ying Chun Wang ◽  
Wen Hai Huang ◽  
Ai Hua Yao ◽  
De Ping Wang
Keyword(s):  
Specific Surface ◽  
Pore Size ◽  
Surface Area ◽  
Specific Surface Area ◽  
Pore Volume ◽  
Sintering Temperature ◽  
Total Pore Volume ◽  
Precipitation Method ◽  
Simple Method ◽  
Air Atmosphere

A simple method to prepare hollow hydroxyapatite (HAP) microspheres with mespores on the surfaces is performed using a precipitation method assisted with Li2O-CaO-B2O3(LCB) glass fabrication process. This research is concerned with the effect of sintering temperature on the microstructure evolution, phase purity, surface morphology, specific surface area, and porosity after sintering process. The microspheres were sintered in air atmosphere at temperatures ranging from 500 to 900 °C. The starting hollow HAP microspheres and the sintered specimens were characterized by scanning electron microscope, X-ray diffractometer, specific surface area analyzer, and Hg porosimetry, respectively. The as-prepared microspheres consisted of calcium deficient hydroxyapatite. The results showed that the as-prepared hollow HAP microspheres had the highest specific surface areas, and the biggest total pore volume. The pore size distribution of the as-prepared hollow HAP microspheres were mainly the mesopores in the range of 2～40 nm. The specific surface area and total pore volume of hollow HAP microspheres decreased with increasing sintering temperature. Whereas the mean pore size increased with increasing sintering temperature. It showed that at 700°C, Ca-dHAP decomposes into a biphasic mixture of HAP and β-calcium phosphate(TCP).

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