Search for: All records

Abstract The preparation of 0.58 Li₂S + 0.315 SiS₂+ 0.105 LiPO₃glass, and the impacts of polysulfide and P^1Pdefect structure impurities on the glass transition temperature (T_g), crystallization temperature (T_c), working range (ΔT≡ T_c‐ T_g), fragility index, and the Raman spectra were evaluated using statistical analysis. In this study, 33 samples of this glass composition were synthesized through melt‐quenching. Thermal analysis was conducted to determine the glass transition temperature, crystallization temperature, working range, and fragility index through differential scanning calorimetry. The quantity of the impurities described above was determined through Raman spectroscopy peak analysis. Elemental sulfur was doped into a glass to quantify the wt% sulfur content in the glasses. Linear regression analysis was conducted to determine the impact of polysulfide impurities and P^1Pdefect impurities on the thermal properties. Polysulfide impurities were found to decrease theT_gat rate of nearly 12°C per 1 wt% increase in sulfur concentration. The sulfur concentration does not have a statistically significant impact on the other properties (α = 0.05). The P^1Pdefect structure appears to decrease the resistance to crystallization of the glass by measurably decreasing the working range of the glasses, but further study is necessary to fully quantify and determine this. 

Na4P2S7-6xO4.62xN0.92x (NaPSON) glassy solid electrolytes (GSEs) were prepared and tested for their electrochemical properties and processability into thin films. The x = 0.2 composition (NaPSON-2) was found to be highly conducting, non-crystallizable, largely stable against Na-metal and supports symmetric cell cycling up to >100 µA cm-2 without shorting and for these reasons was processed into thin films drawn to 50 m and tested in symmetric and asymmetric cells. Measurements of the sodium ion conductivity using symmetric cells demonstrated that the conductivity of NaPSON-2 was unchanged by film forming. Galvanostatic cycling at 5 A cm-2 of 1.3 mm NaPSON-2 showed stability over 450 hours, while cycling a 50 m thin film showed a very slow growth in the resistance. Cyclic voltammetry and x-ray photoelectron spectroscopy of the NaPSON-2 thin film GSE revealed that it did not react with Na-metal at its surface, but rather in the bulk of the film, showing S, Na2S, and Na3P reaction products. The source of the surface stability was determined to be the preferential segregation of trigonally coordinated nitrogen. These low-cost and easily processed NaPSON GSEs provide a system of materials which could provide for significantly lower cost higher energy density grid-scale batteries. 

Glassy solid-state electrolytes present several advantages over other classes of solid-state electrolytes, but some material and design challenges must be overcome prior to commercialization. 

In this work we demonstrate that cell pressure controls the morphology and stability of electroplated sodium metal deposits on carbon black nucleation layers in ether-based electrolytes. At pressures below 500 kPa we observe the presence of three-dimensional Na nuclei accompanied by low Coulombic efficiencies (CEs less than 98%). Conversely, at pressures between 500 and 1272 kPa we observe smooth, planar Na deposits, high CEs up to 99.9%, and stable electrochemical cycling. Through a series of tests conducted at elevated current densities and with or without rest stages, our findings elucidate the balance of important competing time scales for creep and morphology evolution under pressure and the rate of charge transfer that determines Na morphology and stability. This highlights how chemo-mechanical effects at pressure ranges relevant for battery packaging in coin and pouch cells are key factors in the design and operation of Na metal batteries. 

Abstract While much of the current research on glassy solid electrolytes (GSEs) has focused on the binary Li₂S+P₂S₅system, compositions with Si are of interest because Si promotes stronger glass formation and allows low‐cost melt‐quenching (MQ) synthesis under ambient pressure. Another advantage is that they can be formed in homogeneous and continuous glass forms, as a result they are free of grain boundaries. In this work, we have examined the structures and electrochemical properties of bulk glass pieces of sulfide and oxy‐sulfide GSE compositions and have also expanded the study by using LiPON glass as a dopant to produce an entirely new class of nitrogen doped mixed oxy‐sulfide nitride (MOSN) GSEs. Upon doping with oxygen and nitrogen, the solid electrolyte interface (SEI) is stabilized and the doped MOSN GSE exhibits a critical current density (CCD) of 1.8 mA cm⁻²at 100 °C. We also report on improving the glass quality, the SEI engineering and its limitations, and future plans of improving the electrochemical performance of these homogeneous MQ MOSN GSEs. These fundamental results can help to understand the structures and doping effects of the bulk GSEs, and as such can provide a guide to design improved homogeneous grain‐boundary‐free GSEs.