scholarly journals Assembly of MXene/PP Separator and Its Enhancement for Ni-Rich LiNi0.8Co0.1Mn0.1O2 Electrochemical Performance

Polymers ◽  
2020 ◽  
Vol 12 (10) ◽  
pp. 2192
Author(s):  
Qiu-Shi Rao ◽  
Song-Yi Liao ◽  
Xing-Wen Huang ◽  
Yue-Zhu Li ◽  
Yi-Dong Liu ◽  
...  
Keyword(s):  
Electrochemical Performance ◽  
High Performance ◽  
Large Scale ◽  
Lithium Ion ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir ◽  
Near Future ◽  
Spraying Method

In this work, a few-layer MXene is prepared and sprinkled on a commercial polypropylene (PP) separator by a facile spraying method to enhance the electrochemistry of the Ni-rich LiNi0.8Co0.1Mn0.1O2 (NCM811) cathode. Scanning electron microscope (SEM) and X-ray diffraction (XRD) are used to characterize the morphology and structure of MXene. Fourier transform infrared spectroscopy (FT-IR) and a contact angle tester are used to measure the bond structure and surface wettability PP and MXene/PP separator. The effect of the MXene/PP separator on the electrochemical performance of ternary NCM811 material is tested by an electrochemical workstation. The results show that the two-dimensional MXene material could improve the wettability of the separator to the electrolyte and greatly enhance the electrochemical properties of the NCM811 cathode. During 0.5 C current density cycling, the Li/NCM811 cell with MXene/PP separator remains at 166.2 mAh/g after the 100 cycles with ~90.7% retention. The Rct of MXene/PP cell is measured to be ~28.0 Ω. Combining all analyses results related to MXene/PP separator, the strategy by spraying the MXene on commercial PP is considered as a simple, convenient, and effective way to improve the electrochemical performance of the Ni-rich NCM811 cathode and it is expected to achieve large-scale in high-performance lithium-ion batteries in the near future.

scholarly journals Enhancement of Chloroprene/Natural/Butadiene Rubber Nanocomposite Properties Using Organoclays and Their Combination with Carbon Black as Fillers

Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1085
Author(s):  
Patricia Castaño-Rivera ◽  
Isabel Calle-Holguín ◽  
Johanna Castaño ◽  
Gustavo Cabrera-Barjas ◽  
Karen Galvez-Garrido ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Carbon Black ◽  
High Performance ◽  
Rubber Matrix ◽  
Butadiene Rubber ◽  
X Ray Diffraction ◽  
X Ray ◽  
Rubber Blends ◽  
Ft Ir ◽  
Chloroprene Rubber

Organoclay nanoparticles (Cloisite® C10A, Cloisite® C15) and their combination with carbon black (N330) were studied as fillers in chloroprene/natural/butadiene rubber blends to prepare nanocomposites. The effect of filler type and load on the physical mechanical properties of nanocomposites was determined and correlated with its structure, compatibility and cure properties using Fourier Transformed Infrared (FT-IR), X-ray Diffraction (XRD), Thermogravimetric Analysis (TGA) and rheometric analysis. Physical mechanical properties were improved by organoclays at 5–7 phr. Nanocomposites with organoclays exhibited a remarkable increase up to 46% in abrasion resistance. The improvement in properties was attributed to good organoclay dispersion in the rubber matrix and to the compatibility between them and the chloroprene rubber. Carbon black at a 40 phr load was not the optimal concentration to interact with organoclays. The present study confirmed that organoclays can be a reinforcing filler for high performance applications in rubber nanocomposites.

One Step Synthesis and Characterization of Zirconia-Graphene Composites

2012 ◽  
Vol 600 ◽  
pp. 174-177 ◽  
Author(s):  
Jian Fei Xia ◽  
Zong Hua Wang ◽  
Yan Zhi Xia ◽  
Fei Fei Zhang ◽  
Fu Qiang Zhu ◽  
...  
Keyword(s):  
Synthesis And Characterization ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Graphene Composite ◽  
Transmission Electron ◽  
One Step ◽  
Ft Ir ◽  
Xrd Techniques

Zirconia-graphene composite (ZrO2-G) has been successfully synthesized via decomposition of ZrOCl2•6H2O in a water-isopropanol system with dispersed graphene oxide (GO) utilizing Na2S as a precursor could enable the occurrence of the deposition of Zr4+ and the deoxygenation of GO at the same time. Transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD) techniques were used to characterize the samples. It was found that graphene were fully coated with ZrO2, and the ZrO2 existing in tetragonal phase, which resulted in the formation of two-dimensional composite.

Hydrothermal synthesis, crystal structure and properties of a two-dimensional uranyl coordination polymer based on a flexible zwitterionic ligand

2018 ◽  
Vol 74 (3) ◽  
pp. 366-371 ◽  
Author(s):  
Wen Cui ◽  
Ruyu Wang ◽  
Xi Shu ◽  
Yu Fan ◽  
Yang Liu ◽  
...  
Keyword(s):  
Coordination Polymer ◽  
Hydrothermal Reaction ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
Uranyl Compounds ◽  
X Ray ◽  
Potential Applications ◽  
Ft Ir ◽  
Fuel Reprocessing ◽  
Ft Ir Spectroscopy

The interaction between the uranyl cation, (UO2)2+, and organic species is of interest due to the potential applications of the resulting compounds with regard to nuclear waste disposal and nuclear fuel reprocessing. The hydrothermal reaction of various uranyl compounds with flexible zwitterionic 1,1′-[1,4-phenylenebis(methylene)]bis(pyridin-1-ium-4-carboxylate) dihydrochloride (Bpmb·2HCl) in deionized water containing drops of H2SO4resulted in the formation of a novel two-dimensional uranyl coordination polymer, namely poly[tetraoxido{μ2-1,1′-[1,4-phenylenebis(methylene)]bis(pyridin-1-ium-4-carboxylate)}di-μ3-sulfato-diuranium(VI)], [(UO2)2(SO4)2(C20H16N2O4)]n, (1). Single-crystal X-ray diffraction reveals that this coordination polymer exhibits a layered arrangement and the (UO2)2+centre is coordinated by five equatorial O atoms. The structure was further characterized by FT–IR spectroscopy, powder X-ray diffraction (PXRD) and thermogravimetric analysis (TGA). The polymer shows high thermal stability up to 696 K. Furthermore, the photoluminescence properties of (1) has also been studied, showing it to exhibit a typical uranyl fluorescence.

scholarly journals Fabrication of MoS2 Nanoflakes Supported on Carbon Nanotubes for High Performance Anode in Lithium-Ion Batteries (LIBs)

2019 ◽  
Vol 2019 ◽  
pp. 1-7
Author(s):  
T. Minh Nguyet Nguyen ◽  
Vinh-Dat Vuong ◽  
Mai Thanh Phong ◽  
Thang Van Le
Keyword(s):  
Carbon Nanotubes ◽  
Lithium Ion Batteries ◽  
High Performance ◽  
Lithium Ion ◽  
Interlayer Spacing ◽  
X Ray Diffraction ◽  
Multiwalled Carbon ◽  
X Ray ◽  
Functionalized Multiwalled Carbon Nanotubes ◽  
20 Nm

Molybdenum disulfide (MoS2), an inorganic-layered material similar to structure of graphite, was randomly dispersed onto the surface of functionalized multiwalled carbon nanotubes to synthesized nanocomposite MoS2/CNT. The as-obtained product was characterized via SEM, TEM, TGA, X-ray diffraction, and Raman spectroscopies. It was confirmed from XRD that MoS2 layers with interlayer spacing of 0.614 nm were successfully produced. TEM images and Raman spectra indicated a random distribution of 20 nm sized nanoflake MoS2 on the surface of MWNTs. The electrochemical performance of materials are expected to pave the way for the utilized anode material for lithium-ion batteries.

Electrochemical Performance Cr Doped Spinel LiMn2O4 Cathode for Lithium Ion Batteries

2014 ◽  
Vol 636 ◽  
pp. 49-53
Author(s):  
Si Qi Wen ◽  
Liang Chao Gao ◽  
Jia Li Wang ◽  
Lei Zhang ◽  
Zhi Cheng Yang ◽  
...  
Keyword(s):  
Electrochemical Performance ◽  
Lithium Ion Batteries ◽  
Electrochemical Impedance ◽  
Sol Gel ◽  
Lithium Ion ◽  
Cycling Performance ◽  
Cycle Performance ◽  
X Ray Diffraction ◽  
X Ray ◽  
Discharge Test

To improve the cycle performance of spinel LiMn2O4as the cathode of 4 V class lithium ion batteries, spinel were successfully prepared using the sol-gel method. The dependence of the physicochemical properties of the spinel LiCrxMn2-xO4(x=0,0.05,0.1,0.2,0.3,0.4) powders powder has been extensively investigated by using X-ray diffraction (XRD), scanning electron microscope (SEM), charge-discharge test and electrochemical impedance spectroscopy (EIS). The results show that as Mn is replaced by Cr, the initial capacity decreases, but the cycling performance improves due to stabilization of spinel structure. Of all, the LiCr0.2Mn1.8O4has best electrochemical performance, 107.6 mAhg-1discharge capacity, 96.1% of the retention after 50 cycles.

One- and two-dimensional PbII compounds resulting from reaction of PbBr2 and Pb(SCN)2 with pyrimidine-2-thione

2021 ◽  
Vol 77 (7) ◽  
Author(s):  
Vânia Denise Schwade ◽  
Bárbara Tirloni
Keyword(s):  
Structural Characterization ◽  
Diffuse Reflectance ◽  
Tautomeric Form ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
One Dimensional ◽  
X Ray ◽  
Ft Ir ◽  
Compound Ii

Pyrimidine-2-thione (HSpym) reacts with lead(II) thiocyanate and lead(II) bromide in N,N-dimethylformamide (DMF) to form poly[(μ-isothiocyanato-κ2 N:S)(μ4-pyrimidine-2-thiolato-κ6 N 1,S:S:S:S,N 3)lead(II)], [Pb(C4H3N2S)(NCS)] n or [Pb(Spym)(NCS)] n , (I), and the polymeric one-dimensional (1D) compound catena-poly[[μ4-bromido-di-μ-bromido-(μ-pyrimidine-2-thiolato-κ3 N 1,S:S)(μ-pyrimidine-2-thione-κ3 N 1,S:S)dilead(II)] N,N-dimethylformamide monosolvate], {[Pb2Br3(C4H3N2S)(C4H4N2S)]·C3H7NO} n or {[Pb2Br3(Spym)(HSpym)]·DMF} n , (IIa), respectively. Poly[μ4-bromido-di-μ3-bromido-(μ-pyrimidine-2-thiolato-κ3 N 1,S:S)(μ-pyrimidine-2-thione-κ3 N 1,S:S)dilead(II)], [Pb2Br3(C4H3N2S)(C4H4N2S)] n or [Pb2Br3(Spym)(HSpym)] n , (IIb), could be obtained as a mixture with (IIa) when using a lesser amount of solvent. In the crystal structures of the pseudohalide/halide PbII stable compounds, coordination of anionic and neutral HSpym has been observed. Both Spym− (in the thiolate tautomeric form) and NCS− ligands were responsible for the two-dimensional (2D) arrangement in (I). The Br− ligands establish the 1D polymeric arrangement in (IIa). Eight-coordinated metal centres have been observed in both compounds, when considering the Pb...S and Pb...Br interactions. Both compounds were characterized by FT–IR and diffuse reflectance spectroscopies, as well as by powder X-ray diffraction. Compound (IIa) and its desolvated version (IIb) represent the first structurally characterized PbII compounds containing neutral HSpym and anionic Spym− ligands. After a prolonged time in solution, (IIa) is converted to another compound due to complete deprotonation of HSpym. The structural characterization of (I) and (II) suggests HSpym as a good candidate for the removal of PbII ions from solutions containing thiocyanate or bromide ions.

Facile Synthesis of Electrospun LiNi0.5Co0.2Mn0.3O2 Nanofiber as High-Performance Cathode for Lithium-Ion Batteries

2017 ◽  
Vol 727 ◽  
pp. 663-669
Author(s):  
Zhi Yuan Cao ◽  
Yu Feng Song ◽  
Xia Shen ◽  
Jian Hui Fang
Keyword(s):  
High Performance ◽  
Lithium Ion ◽  
Electrospun Nanofibers ◽  
Precipitation Method ◽  
Diffraction Field ◽  
X Ray Diffraction ◽  
Ft Ir ◽  
Co Precipitation ◽  
Ion Intercalation ◽  
Ft Ir Spectroscopy

Ni-rich layer LiNi0.5Co0.2Mn0.3O2 cathode materials have been synthesized by Electrospinning and co-precipitation method. The physical, chemical, and electrochemical properties of the LiNi0.5Co0.2Mn0.3O2 nanofibers were investigated by X-ray diffraction, field emission−scanning electron microscopy (FESEM), Fourier transform infrared (FT-IR) spectroscopy,Brunauer, Emmett, and Teller (BET) measurements, and galvanostatic tests. The electrospun nanofibers with small particle size and hollow tubes provided fast lithium ion intercalation and de-intercalation properties, leading to an enhanced electrochemical capability for LiNi0.5Co0.2Mn0.3O2 nanofibers.

scholarly journals Effect of Si Addition on Mechanical and Electrochemical Properties of Al-Fe-Cu-La Alloy for Current Collector of Lithium Battery

Metals ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 1072 ◽  
Author(s):  
Xu ◽  
Ding ◽  
Yang ◽  
Zhang ◽  
Gao ◽  
...  
Keyword(s):  
Electrochemical Performance ◽  
High Performance ◽  
Lithium Ion ◽  
Temperature Stability ◽  
Current Collector ◽  
High Temperature Stability ◽  
X Ray Diffraction ◽  
Tafel Polarization ◽  
Increasing Demand ◽  
Si Addition

The increasing demand for high-performance current collectors of lithium ion secondary batteries requires that the employed aluminum alloys have better mechanical properties and superior electrochemical performance. The effect of Si addition on the microstructure, tensile and electrochemical performance of Al-Fe-Cu-La alloy was investigated by optical microscopy, X-ray diffraction, scanning electron microscopy, a tensile test, conductivity test and Tafel polarization curve test. Experimental results indicated that Si addition to the Al-Fe-Cu-La alloy helped to refine the longitudinal grain size of the alloy. The Si-containing phase (AlFeSi) nucleated and grew along the surface of the AlFeLa phase. The Si addition to the Al-Fe-Cu-La alloy could greatly increase the tensile strength in the temperature range of −20 °C to 50 °C and improve high temperature stability of the alloy. Also, the addition of Si promoted the formation of the AlFeSi ternary phase, which helped to improve the corrosion resistance of the alloy.

From Layered Ni(OH)2 Thin Films to Ni(so4)0.3(OH)1.4 Nanobelts through so42- Inserting in Colloid-Based Route

2011 ◽  
Vol 295-297 ◽  
pp. 1548-1553
Author(s):  
Zhi Yong Jia
Keyword(s):  
Electron Microscopy ◽  
Thin Films ◽  
Large Scale ◽  
Ph Value ◽  
Shape Evolution ◽  
X Ray Diffraction ◽  
Weak Base ◽  
X Ray ◽  
Ft Ir ◽  
Scanning Electron

The single-crystalline nanobelts of monoclinic Ni(SO4)0.3(OH)1.4have been synthesized on a large scale through a convenient, low-temperature hydrothermal method. The influences of reaction time, pH value, concentration of ammonia on the phase and shape evolution of nanobelts were systematically investigated. It was found that the initial layered Ni(OH)2 thin films as intermediates could be split and converted into the monoclinic Ni(SO4)0.3(OH)1.4nanobelts through SO42-ions inserting process. The formation mechanism of nanobelts involved in the inserting process and the corresponding drive force have been investigated in detail by means of X-ray diffraction (XRD), and scanning electron microscopy (SEM), FT-IR spectra and pH value analyses. In addition to, we have also found that the ammonia molecules acted as both weak base and ligand agent was crucial to the controlling nucleation and inserting process in the formation process of nanobelts.

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