Structure and electrochemical performance of nanosized Li1.1(Ni0.35Co0.35Mn0.30)O2 powders for lithium-ion battery

2014 ◽  
Vol 07 (05) ◽  
pp. 1450061 ◽  
Author(s):  
Jianqiu Deng ◽  
Hao Liu ◽  
Jin Pan ◽  
C. Y. Chung ◽  
Qingrong Yao ◽  
...  
Keyword(s):  
Average Particle Size ◽  
Rate Capability ◽  
Lithium Ion ◽  
Cycling Performance ◽  
Precipitation Method ◽  
Average Particle ◽  
Nanosized Powders ◽  
Co Precipitation ◽  
Good Cycling Stability ◽  
Charge Discharge

Pure Li 1.1 Ni 0.35 Co 0.35 Mn 0.30 O 2 nanosized powders have been successfully synthesized by improved hydroxide co-precipitation method, and characterized with X-ray powder diffraction and scanning electron microscopy (SEM). The electrochemical properties of cathodes and Li 1.1 Ni 0.35 Co 0.35 Mn 0.30 O 2/ Li 4 Ti 5 O 12 full cells have been studied by charge–discharge tests and cyclic voltammetry. The Li 1.1 Ni 0.35 Co 0.35 Mn 0.30 O 2 powders have a typical layered hexagonal crystal structure with an average particle size of about 780 nm. The cathodes exhibit high capacities and good cycling performance. The initial discharge capacity of the cathodes is 154.8 mAhg-1 at 0.5 C between 2.5 V and 4.3 V, and the capacity retention keeps 80.6% after 50 charge–discharge cycles. The Li 1.1 Ni 0.35 Co 0.35 Mn 0.30 O 2/ Li 4 Ti 5 O 12 cells also deliver high specific capacities, good cycling stability and rate capability. This work demonstrates that Li 1.1 Ni 0.35 Co 0.35 Mn 0.30 O 2 is a promising cathode material for lithium-ion batteries.

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.

Morphology-Controlled CaCO3 Nanostructures by Modified Co-Precipitation in Pulsed Mode

2015 ◽  
Vol 752-753 ◽  
pp. 148-153
Author(s):  
M.M. Nassar ◽  
Taha Ebrahiem Farrag ◽  
M.S. Mahmoud ◽  
Sayed Abdelmonem
Keyword(s):  
Particle Size ◽  
Calcium Carbonate ◽  
Rotation Speed ◽  
Average Particle Size ◽  
Calcium Nitrate ◽  
Precipitation Method ◽  
Average Particle ◽  
X Ray ◽  
Co Precipitation ◽  
Pulsed Mixing

Calcium carbonate nanoparticles and nanorods were synthesized by precipitation from saturated sodium carbonate and calcium nitrate aqueous solutions through co precipitation method. A new rout of synthesis was done by both using pulsed mixing method and controlling the addition of calcium nitrate. The effect of the agitation speed, and the temperature on particle size and morphology were investigated. Particles were characterized using X-ray Microanalysis, X-ray analysis (XRD) and scanning electron microscopy (SEM). The results indicated that increasing the mixer rotation speed from 3425 to 15900 (rpm) decreases the average particle size to 64±7 nm. A rapid nucleation then aggregation induced by excessive shear force phenomena could explain this observation. Moreover, by increasing the reaction temperature, the products were converted from nanoparticle to nanorods. The maximum attainable aspect ratio was 6.23 at temperature of 75°C and rotation speed of 3425. Generally, temperature raise promoted a significant homoepitaxial growth in one direction toward the formation of calcite nanorods. Overall, this study can open new avenues to control the morphology of the calcium carbonate nanostructures.

LiFe1-xMnxPO4/C COMPOSITE AS CATHODE MATERIAL FOR LITHIUM ION BATTERY

2011 ◽  
Vol 04 (04) ◽  
pp. 319-322 ◽  
Author(s):  
AI FANG LIU ◽  
ZU BIAO WEN ◽  
YA FEI LIU ◽  
ZHONG HUA HU
Keyword(s):  
Electron Microscope ◽  
Electrochemical Performance ◽  
Cathode Material ◽  
Lithium Ion Battery ◽  
Average Particle Size ◽  
High Capacity ◽  
Lithium Ion ◽  
Carbon Layer ◽  
Average Particle ◽  
Charge Discharge

LiFe 1-x Mn x PO 4/ C composites were prepared as cathode material for lithium ion battery via solid-state reaction and using glucose as reducing agent and carbon source. The crystal structure and morphology were investigated by X-ray diffraction (XRD), scanning electron microscope (SEM) and transmission electron microscope (TEM). The resultant samples were pure olivine compounds with an orthorhombic structure. Their electrochemical performance was studied by galvanostatic charge–discharge test and cyclic voltammetry. The results showed that the sample LiFe0.8Mn0.2PO4/C with an average particle size of 400 nm exhibited the largest discharge capacity of 150 mAh g-1, excellent reversibility of charge–discharge and high capacity retention of 97% after a 50-cycle CV scanning. The improved electrical conductivity corresponding to the fine carbon layer around the LiFe0.8Mn0.2PO4 individual particle can be responsible for all these excellent electrochemical performance.

Effect of Surfactant on the Preparation of Nano-powder for Yb Doping Laser Transparent YAG Ceramic

2013 ◽  
Vol 32 (5) ◽  
pp. 511-515 ◽  
Author(s):  
Xiao Guo Cao ◽  
Jia Wang ◽  
Qi Bai Wu ◽  
Hai Yan Zhang
Keyword(s):  
Particle Size ◽  
Polyethylene Glycol ◽  
Average Particle Size ◽  
Ammonium Bicarbonate ◽  
Spherical Particles ◽  
Precipitation Method ◽  
Average Particle ◽  
X Ray Diffraction ◽  
Nano Powder ◽  
Co Precipitation

AbstractYb:YAG transparent ceramic nano-powder was prepared by chemical co-precipitation method, with ammonium bicarbonate as the precipitant and polyethylene glycol as surfactant. The addition of polyethylene glycol can reduce the agglomeration and particle size of the prepared Yb:YAG powder. The morphology, thermal stability and phase structure of Yb:YAG nano-powder were charactered by scanning electron microscopy (SEM), thermogravimetry and differential thermal analysis (TG-DTA), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy. The results show that well-crystallized nano-powder was obtained by calcining the precursors at 900 °C for 3 h. The average particle size of Yb:YAG powder is about 100–200 nm. When the volume amount of polyethylene glycol is 2.0%, well-dispersed Yb:YAG powder with spherical particles of 100 nm diameter was obtained.

scholarly journals Fabrication and Magnetic Properties of Mn1 - xZnxFe2O4 (0 ≤ x ≤ 0.8) Nanoparticles

2009 ◽  
Vol 19 (1) ◽  
pp. 19-25
Author(s):  
Pham Hoai Linh ◽  
Tran Dang Thanh ◽  
Do Hung Manh ◽  
Nguyen Chi Thuan ◽  
Le Van Hong ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Biomedical Applications ◽  
Spinel Ferrite ◽  
Average Particle Size ◽  
Precipitation Method ◽  
Average Particle ◽  
Promising Candidate ◽  
Zn Concentration ◽  
Co Precipitation ◽  
Curie Temperature Tc

In this paper, we report results on the fabrication and magnetic properties of spinel ferrite Mn1-xZnxFe2O4 (0 ≤ x ≤ 0.8) nanoparticles. The nanoparticles were synthesized by a co-precipitation method. The effects of substituting Zn for Mn on the magnetic properties and particles size were focused. It was found that the phase-formation temperature is 90OC and the average particle size decreases from 40 nm to 10 nm when increased Zn concentration from zero to 0.8. The Curie temperature TC strongly decreases from 585 K (x = 0) to 320 K (x = 0.8) concomitantly with a decrease of the saturation magnetization MS. With a TC of 320 K and MS of 17 emu/g, the x=0.8 sample could be a promising candidate for some biomedical applications.

scholarly journals Study Microstructure of Fe3O4 Modification Using PEG 4000 form Iron Sand at Wari Ino Beach As A Biosensor Application

2021 ◽  
Vol 8 (3) ◽  
pp. 168-171
Author(s):  
Kurnia Kurnia ◽  
Meidy Kaseside ◽  
Steven Iwamony
Keyword(s):  
Average Particle Size ◽  
Precipitation Method ◽  
High Dispersion ◽  
Average Particle ◽  
X Ray Diffraction ◽  
Xrd Pattern ◽  
Peg 4000 ◽  
Biosensor Application ◽  
Scherrer Formula ◽  
Co Precipitation

Fe3O4 encapsulated PEG form iron sand at wari ino beach has been successfully synthesized by co-precipitation method. The average particle size  of the nanoparticle 11,3 nm was determined by scherrer formula. Fe3O4 modification PEG 4000 was successfully encapsulated the samples  by the presence C-O-C and CH bonding that were characterized using Fourier Transform Infra Red (FTIR), X-Ray Diffraction (XRD) pattern  shows that all samples  are formed by single  phase cubic spinel magnetite  , and Scanning Electron Microscopy (SEM) shows the  high dispersion capability while encapsulated process using  PEG. The results of the characterization show that the Fe3O4 successfully encapsulated by PEG 4000.

Exploring the interaction of l-cysteine capped CuS nanoparticles with bovine serum albumin (BSA): a spectroscopic study

RSC Advances ◽  
2016 ◽  
Vol 6 (63) ◽  
pp. 58288-58295 ◽  
Author(s):  
S. Prasanth ◽  
D. Rithesh Raj ◽  
T. V. Vineeshkumar ◽  
Riju K. Thomas ◽  
C. Sudarsanakumar
Keyword(s):  
Particle Size ◽  
Bovine Serum Albumin ◽  
Serum Albumin ◽  
Bovine Serum ◽  
Copper Sulfide ◽  
Average Particle Size ◽  
Precipitation Method ◽  
Average Particle ◽  
Spectroscopic Techniques ◽  
Co Precipitation

l-Cysteine capped copper sulfide nanoparticles with an average particle size of 6 nm were synthesized using a chemical co-precipitation method and their interactions with bovine serum albumin were explored using various spectroscopic techniques.

Preparation of Nanostructured Metal Ferrite Particles by Sonochemistry

2005 ◽  
Vol 277-279 ◽  
pp. 1044-1048 ◽  
Author(s):  
Eun Hee Kim ◽  
Hyo Sook Lee ◽  
Hui Ping Shao
Keyword(s):  
Magnetic Field ◽  
Particle Size ◽  
Cobalt Ferrite ◽  
Average Particle Size ◽  
Iron Chloride ◽  
Precipitation Method ◽  
Average Particle ◽  
Sonochemical Method ◽  
Iron Ferrite ◽  
Co Precipitation

Nanostructured iron and cobalt ferrite particles were prepared from iron chloride and cobalt chloride, respectively, using the sonochemical method. The particles were compared with those synthesized using the co-precipitation method. The properties of the particles were characterized using various techniques, such as XRD, TEM, VSM and a SQUID magnetometer. The iron ferrite particles had an average particle size of about 15 nm and a magnetization value of 83 emu/g at a magnetic field of 50 kOe, while the particle size of cobalt ferrite was about 5 nm and its magnetization value was 33 emu/g at the same magnetic field.

Effect of pH on Zinc Oxide Powder Prepared by a Chemical Co-Precipitation Method

2010 ◽  
Vol 93-94 ◽  
pp. 691-694 ◽  
Author(s):  
Pusit Pookmanee ◽  
Issara Attaveerapat ◽  
Jiraporn Kittikul ◽  
Sukon Phanichphant
Keyword(s):  
Zinc Oxide ◽  
Average Particle Size ◽  
Ammonium Hydroxide ◽  
Zinc Nitrate ◽  
Oxide Powder ◽  
Precipitation Method ◽  
Average Particle ◽  
X Ray ◽  
Zinc Oxide Powder ◽  
Co Precipitation

Zinc oxide powder was prepared by a chemical co-precipitation method. Zinc nitrate and ammonium hydroxide were used as the starting precursors. The white precipitated powder was formed after adding ammonium hydroxide until the pH of final solution was 7-9. The powder was filtered and dried at 100 °C for 24h. The phase of zinc oxide powder was studied by X-ray diffractometer (XRD). Hexagonal single phase of zinc oxide was obtained without calcination step. The morphology of zinc oxide powder was investigated by scanning electron microscope (SEM). The particle was irregular in shape and highly agglomerated with an average particle size of 0.1 µm. The chemical composition of zinc oxide powder was determined by energy dispersive X-ray spectrometer (EDXS). The elemental composition of zinc oxide showed the characteristic X-ray energy value as follows: zinc of Lα = 1.012 keV, Kα = 8.630 keV and Kβ = 9.570 keV and oxygen of Kα = 0.525 keV, respectively.

Fabrication and Characterization of YAG Nanopowders by Co-Precipitation under Ultrasonic Radiation

2011 ◽  
Vol 284-286 ◽  
pp. 839-843 ◽  
Author(s):  
Li Li Wang ◽  
Jin Chen ◽  
Guang Cheng Yang ◽  
Fu De Nie
Keyword(s):  
Average Particle Size ◽  
Precipitation Method ◽  
Average Particle ◽  
Synthetic Process ◽  
Ultrasonic Radiation ◽  
Ft Ir ◽  
Fabrication And Characterization ◽  
Co Precipitation ◽  
Carbonate Precursor

A carbonate precursor with high sintering activity was prepared by co-precipitation method under ultrasonic radiation. This precursor precipitant completely transformed to pure YAG phase after being calcined at 900 °C for 4 h. The properties of YAG nanopowders obtained under different synthetic process were studied by XRD, TG-DSC, FT-IR and SEM. The results show that the ultrasonic radiation can fine the precursor and reduce its agglomeration. YAG nanopowders with an average particle size of about 60 nm were obtained and particles were sphere-shaped with good dispersity.

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