Experimental Measurements of Electron Stopping Power at Low Energies

The electron stopping power has been measured for twelve elements and fifteen compounds, over the energy range from 1 eV to 10 keV, by the analysis of electron energy loss spectra, optical data, and photon mass absorption data. Values of the effective mean ionization potential Jeff and the effective number of participating electrons Neff have also been determined in each case. The results obtained have been compared with other experimental data, with first-principles theoretical calculations, and with a number of proposed analytical models

Olivine-Based Blended Compounds as Positive Electrodes for Lithium Batteries

Blended cathode materials made by mixing LiFePO4 (LFP) with LiMnPO4 (LMP) or LiNi1/3Mn1/3Co1/3O2 (NMC) that exhibit either high specific energy and high rate capability were investigated. The layered blend LMP–LFP and the physically mixed blend NMC–LFP are evaluated in terms of particle morphology and electrochemical performance. Results indicate that the LMP–LFP (66:33) blend has a better discharge rate than the LiMn1−yFeyPO4 with the same composition (y = 0.33), and NMC–LFP (70:30) delivers a remarkable stable capacity over 125 cycles. Finally, in situ voltage measurement methods were applied for the evaluation of the phase evolution of blended cathodes and gradual changes in cell behavior upon cycling. We also discuss through these examples the promising development of blends as future electrodes for new generations of Li-ion batteries

Schiff Base as Additive for Preventing Gas Evolution in Li₄Ti₅O₁₂-Based Lithium-Ion Battery

Lithium titanium oxide (Li₄Ti₅O₁₂)-based electrodes are very promising for long-life cycle batteries. However, the surface reactivity of Li₄Ti₅O₁₂ in organic electrolytes leading to gas evolution is still a problem that may cause expansion of pouch cells. In this study, we report the use of Schiff base (1,8-diazabicyclo[5.4.0]­undec-7-ene) as an additive that prevents gas evolution during cell aging by a new mechanism involving the solid electrolyte interface on the anode surface. The in situ ring opening polymerization of cyclic carbonates occurs during the first cycles to decrease gas evolution by 9.7 vol % without increasing the internal resistance of the battery