17 research outputs found
Polymer electrolyte membranes and process for the production thereof
The process for the production of a polymer electrolyte membrane, comprises the successive steps of: preparing a mixed solution of a Room Temperature Ionic Liquid (RTIL), at least one alkaline metal salt and a photosensitive hydrogen abstracting component at a temperature in the range 20 to 70 °C, wherein the RTIL is a compound consisting of at least one organic cation and at least one organic or inorganic anion; adding to the solution a polymeric material at a temperature in the range of 20-70 °C; blending the solution added with the polymeric material at a temperature in the range of 70-140 °C to get a uniform mixture; pressing the mixture between two sheets at a temperature in the range of 60 - 150 °C and a pressure in the range of 20 - 80 bar, so that a film is formed; and exposing the film to UV light, so that the polymeric material of the film is cross-linked and the polymer electrolyte membrane is obtained
Ionic Conduction Properties of PVDFâHFP Type Gel Polymer Electrolytes with Lithium Imide Salts
Ionic conduction mechanisms of polyvinylidenefluoride-hexafluoropropylene type polymer electrolytes with LiN(CF3SO2)(2)
External microbeam PIGE study of Li and F distribution in PVDF_HFP electrolyte gel/polymer for lithium battery application
Structure and transport properties of polymer gel electrolytes based on PVDF-HFP and LiN(CF3SO2)2
Conduction properties of PVDF-type polymer electrolytes with lithium salts LiN(CF3SO2)2 and LiN(C2F5SO2)2
Facile Synthesis of Highly Graphitized Carbon via Reaction of CaC2 with Sulfur and Its Application for Lithium/Sodium-Ion Batteries
Facile Synthesis of Highly Graphitized Carbon via Reaction of CaC2 with Sulfur and Its Application for Lithium/Sodium-Ion Batterie
Nitrogen-doped single walled carbon nanohorns enabling effective utilization of Ge nanocrystals for next generation lithium ion batteries
Nitrogen-doped single walled carbon nanohorns enabling effective utilization of Ge nanocrystals for next generation lithium ion batterie
Damage formation in Sn film anodes of Na-ion batteries
Sn anodes for Na-ion batteries exhibit a promising initial capacity of 847 mAh gâ1, which however, cannot be retained throughout continuous cycling due to the 420% volume changes that Sn experiences during sodiation. Previous experimental studies suggest that fracture does not occur in the submicron Sn particles during the formation of Na-Sn alloys; however, such colossal volume changes must result in microstructural damage. In the present work, the damage mechanisms during sodiation are isolated and accentuated by employing a Sn thick film of 0.5 mm as the anode. This simplified planar geometry allows to dispense with the influence of the binder and carbon additives that are required in porous electrodes. Post-mortem electron microscopy revealed new deformation mechanisms for anode materials, as multiple whiskers nucleated on the surface of the Sn, whereas pores formed within the Sn (over the Na-ion penetration distance) after electrochemical cycling. These mechanisms were in addition to the dry lake-bed fracture that was also observed. A comparative study on a Sn thin-film anode of 0.06 mm revealed the formation of fracture and pores after cycling, but no whiskers. The whiskers and pores observed in the thick Sn film anode may be more subtle at the nanoscale, and therefore have not been reported for submicron Sn particles in porous electrodes during sodiation