Enhancement of electrochemical performance of LiFePO4 nanoparticles by direct nanocoating with conductive carbon layers

2016 ◽  
Vol 09 (04) ◽  
pp. 1641007 ◽  
Author(s):  
Joanna Świder ◽  
Marcin Molenda ◽  
Andrzej Kulka ◽  
Janina Molenda

The results of simple and environmental-friendly method of the carbon nanocoatings on low-conductive cathode material have been shown in this work. The carbon nanocoatings were prepared during wet impregnation process of precursor derived from hydrophilic polymer based on poly([Formula: see text]-vinylformamide) modified by pyromellitic acid. The crystal structures and morphology of all composites were characterized by X-ray powder diffraction (XRD), low temperature nitrogen adsorption/desorption measurements (N2-BET) and transmission electronic microscopy (TEM). The electrical properties of the obtained composites were examined by EC studies. The electrochemical performance was carried out in galvanostatic mode with stable charge–discharge current and performed in Li/Li[Formula: see text]/(CCL/LiFePO[Formula: see text] type cells. The process of formation CCL/LiFePO4 nanocomposite significantly enhances the electrical conductivity of the material and improves its capacity retention and electrochemical performance.

Nanomaterials ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1519
Author(s):  
Jong Gyeong Kim ◽  
Sunghoon Han ◽  
Chanho Pak

The price and scarcity of platinum has driven up the demand for non-precious metal catalysts such as Fe-N-C. In this study, the effects of phosphoric acid (PA) activation and phosphorus doping were investigated using Fe-N-C catalysts prepared using SBA-15 as a sacrificial template. The physical and structural changes caused by the addition of PA were analyzed by nitrogen adsorption/desorption and X-ray diffraction. Analysis of the electronic states of Fe, N, and P were conducted by X-ray photoelectron spectroscopy. The amount and size of micropores varied depending on the PA content, with changes in pore structure observed using 0.066 g of PA. The electronic states of Fe and N did not change significantly after treatment with PA, and P was mainly found in states bonded to oxygen or carbon. When 0.135 g of PA was introduced per 1 g of silica, a catalytic activity which was increased slightly by 10 mV at −3 mA/cm2 was observed. A change in Fe-N-C stability was also observed through the introduction of PA.


MRS Advances ◽  
2018 ◽  
Vol 3 (61) ◽  
pp. 3543-3549
Author(s):  
Pablo González ◽  
Andrea C. De Los Santos ◽  
Jorge R. Castiglioni ◽  
María A. De León

ABSTRACTA raw clay from Uruguay was modified with aluminium to obtain an aluminium pillared clay (Al-PILC). The solids were characterized by scanning electron microscopy, X-ray diffraction and nitrogen adsorption-desorption isotherms. The Al-PILC retained the typical laminar structure of montmorillonite. The specific surface area and the microporous volume of the Al-PILC, 235 m2 g-1 and 0.096 cm3 g-1, respectively, were much higher than those of the clay. The phosphate adsorption capacity of the Al-PILC was higher than those of the clay. The phosphate adsorption kinetic followed the pseudo-first-order model for both, the clay and the Al-PILC, and the phosphate adsorption isotherm for the Al-PILC fit the Freundlich model.


2016 ◽  
Vol 2016 ◽  
pp. 1-13 ◽  
Author(s):  
Manuel Sánchez-Cantú ◽  
Clara Barcelos-Santiago ◽  
Claudia M. Gomez ◽  
Esthela Ramos-Ramírez ◽  
Ma. de Lourdes Ruiz Peralta ◽  
...  

Three hydrocalumite-like compounds in a Ca/Al ratio of 2 containing nitrate and acetate anions in the interlaminar region were prepared by a simple, economic, and environmentally friendly method. The solids were characterized by X-ray powder diffraction (XRD), thermogravimetric (TG) analysis, nitrogen adsorption-desorption at −196°C, scanning electron microscopy (SEM), infrared spectroscopy (FTIR), and UV-Vis Diffuse Reflectance Spectroscopy (DRS). The catalytic activity of the calcined solids at 700°C was tested in the photodegradation of 2,4-dichlorophenoxyacetic acid (2,4-D) where 57% degradation of 2,4-D (40 ppm) and a mineralization percentage of 60% were accomplished within 150 minutes. The photocatalytic properties were attributed to mayenite hydration, since the oxide ions in the cages are capable of reacting with water to form hydroxide anions capable of breaking down the 2,4-D molecules.


1991 ◽  
Vol 69 (10) ◽  
pp. 1511-1515 ◽  
Author(s):  
Awad I. Ahmed ◽  
S. E. Samra ◽  
S. A. El-Hakam

CuO–Al2O3 catalysts containing various amounts of copper oxide have been prepared by precipitation. The phase changes were studied by X-ray diffraction. The results obtained revealed that the thermal treatment of solid CuO–Al2O3 at 700 °C produced only crystalline CuO. Heating to 900 °C led to the formation of copper alumina spinel together with unreacted CuO and γ-Al2O3. The spinel content was found to increase with increasing copper content. Nitrogen adsorption–desorption isotherms on the calcined samples have been measured. Surface areas have been calculated and the pore structure analysed. The textural properties of the system were found to depend on both the copper content and the calcination temperature. Key words: CuO, Al2O3 catalysts, structure, surface area, pore structure.


2021 ◽  
Vol 1162 ◽  
pp. 65-73
Author(s):  
Rakhmawati Farma ◽  
Ona Lestari ◽  
Erman Taer ◽  
Apriwandi ◽  
Minarni ◽  
...  

Heavy metal such as Cu, Fe, and Zn are the most serious contributers to environmental problems. The removal of heavy metal from the environment is the research interest nowdays. The adsorption of Cu, Fe and Zn from wastewater was investigated with various activated carbons as adsorbents. The activated carbons were produced from oil palm leaves by using multi-activation methods. The H3PO4, NaOH, ZnCl2 and KOH were chosen as chemical activating agents. Batch adsorption experiment was used to test the ability of activated carbon to remove Cu, Fe, and Zn from wastewater. The surface characteristics of activated carbon were evaluated using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray (EDX), Fourier transform infrared spectroscopy (FTIR), and nitrogen adsorption-desorption isotherms. The Activated carbons were able to purify wastewater with a maximum turbidity level of 2.83 NTU. The AC-H3PO4 activated carbon showed the highest absorbability of Cu metal as 91.540%, while the highest absorbabilities of Zn and Fe metals were indicated by AC-KOH activated carbon of 22.853% and 82.244% absorption respectively. Therefore, these results enable the oil palm leaves to become a high potential for activated carbon as removal the heavy metals.


Materials ◽  
2019 ◽  
Vol 12 (11) ◽  
pp. 1771 ◽  
Author(s):  
Stefan Neatu ◽  
Mihaela M. Trandafir ◽  
Adelina Stănoiu ◽  
Ovidiu G. Florea ◽  
Cristian E. Simion ◽  
...  

This study presents the synthesis and characterization of lanthanum-modified alumina supported cerium–manganese mixed oxides, which were prepared by three different methods (coprecipitation, impregnation and citrate-based sol-gel method) followed by calcination at 500 °C. The physicochemical properties of the synthesized materials were investigated by various characterization techniques, namely: nitrogen adsorption-desorption isotherms, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and H2–temperature programmed reduction (TPR). This experimental study demonstrated that the role of the catalytic surface is much more important than the bulk one. Indeed, the incipient impregnation of CeO2–MnOx catalyst, supported on an optimized amount of 4 wt.% La2O3–Al2O3, provided the best results of the catalytic combustion of methane on our catalytic micro-convertors. This is mainly due to: (i) the highest pore size dimensions according to the Brunauer-Emmett-Teller (BET) investigations, (ii) the highest amount of Mn4+ or/and Ce4+ on the surface as revealed by XPS, (iii) the presence of a mixed phase (Ce2MnO6) as shown by X-ray diffraction; and (iv) a higher reducibility of Mn4+ or/and Ce4+ species as displayed by H2–TPR and therefore more reactive oxygen species.


2019 ◽  
Vol 942 ◽  
pp. 40-49
Author(s):  
Yulia Murashkina ◽  
Olga B. Nazarenko

Natural zeolite of Shivirtui deposit (Russia) was modified with nanofibers of aluminum oxyhydroxide AlOOH. Aluminum oxyhydroxide nanofibers were produced at the heating and oxidation of aluminum powder with water. The properties of modified zeolite were investigated by means of X-ray diffraction, transmission electronic microscopy, scanning electronic microscopy, low-temperature nitrogen adsorption, thermal analysis, and Fourier transform infrared spectroscopy. It was found that water content in the modified sample of zeolite was about 15 %. Based on the study of the physical and chemical properties, shivirtui zeolite modified with nanofibers of aluminum oxyhydroxide can be proposed for use as a flame-retardant additive to polymers.


2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Bahaa Abu-Zied ◽  
Abdullah M. Asiri

Nanocrystalline Ni-La-Fe-O catalysts having the general formula NiLaxFe2−xO4(0.00≤x≤2.00) were synthesized by the combustion route employing urea as a combustion fuel. The calcination process was affected at 500°C. The structural properties of the obtained catalysts were systematically investigated by X-ray powder diffraction (XRD), scanning electronic microscopy (SEM), energy-dispersive X-ray spectra (EDX), and nitrogen adsorption at −196°C. Crystalline NiFe2O4and La2NiO4phases were detected for the catalysts havingx=0.00and 2.00, respectively, as a result of solid-solid interaction between mixtures precursors. The activity of the obtained catalysts was checked for hydrogen peroxide decomposition at 35–55°C. A synergic effect was observed for the catalysts havingx-value of 1.00 and 1.50. Such effect was attributed to the increase in the number of the active constituents involved in the catalytic decomposition of H2O2.


2017 ◽  
Vol 2017 ◽  
pp. 1-11 ◽  
Author(s):  
Olga V. Alekseeva ◽  
Anna N. Rodionova ◽  
Nadezhda A. Bagrovskaya ◽  
Alexander V. Agafonov ◽  
Andrew V. Noskov

Organobentonite powder was synthesized and characterized using laser diffraction, X-ray diffraction, low-temperature nitrogen adsorption-desorption technique, and dynamic light scattering. Obtained powder was found as material with mesopores. The organobentonite particles were larger than pure bentonite one. Hydroxyethyl cellulose (HEC) was filled with organobentonite particles by mechanical dispersion, and produced composite films were researched by the number of methods. New data relating to structure, tensile properties, and antimicrobial activity of HEC/organobentonite composites were obtained. Using results of X-ray diffraction, the reflections assigned to crystal filler in polymer material were proved. Concentration effect of the filling agent on tensile properties of composite film was revealed. Data of infrared (IR) spectrometry indicated a decrease in the density of hydrogen-bond net in HEC/organobentonite composite as compared with pristine HEC. Using microbiological tests, it was found that the HEC/organobentonite films exhibited bacteriostatic action against S. aureus and fungistatic action against molds.


2017 ◽  
Vol 373 ◽  
pp. 299-302
Author(s):  
Bo Zhou ◽  
Chong Yang Li ◽  
Ning Qi ◽  
Zhi Quan Chen

Porous ZnO were synthesized with soft template method using zinc acetate Zn (CH3COO)2·2H2O as precursor and block copolymer F127 as the surfactant. Nitrogen adsorption-desorption measurements indicate that the ZnO sample contains large pores with mean diameter of about 30 nm. However, both small-angle X-ray diffraction and transmission electron microscope measurements indicate that the pore ordering is missing. Positron lifetime measurements reveal two long lifetime components in the porous ZnO. The longest lifetime τ4 (75 ns) corresponds to ortho-positronium (o-Ps) annihilation in large pores. The pore size estimated from τ4 is about 10.6 nm. This is much smaller than that estimated from Nitrogen adsorption-desorption measurements. In addition, the intensity I4 is only about 2.2%. This is probably due to the chemical quenching and/or inhibition of positronium formation induced by ZnO, which reduces o-Ps lifetime and intensity, and leads to under estimation of the pore size.


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