ABSTRACT
Lithium (Li) metal has garnered significant attention as the preferred anode for high-energy lithium metal batteries. However, safety concerns arising from the growth of Li dendrites have hindered the advancement of Li metal batteries. In this study, we first elucidate the impact of external pressure and internal stress on dendrite growth and dissolution behavior of Li metal batteries during continuous charging-discharging cycles, employing a developed electrochemomechanical phase-field model. A typical parameter is defined to calculate the amount of dead Li that affects the electrochemical performance of Li metal batteries during multiple cycles. The underlying mechanisms of dendrites observed from in situ experiments are explained through the developed phase-field model. After charging/discharging, dendrites with a treelike structure yield a greater amount of dead Li compared to those with a needlelike configuration. Increasing the pressure appropriately can effectively reduce the growth points of dendrites and suppress the Li dendrite growth. Excessive pressure not only induces dendritic fractures that lead to the formation of dead Li but also undermines the battery performance. The accumulated internal stress might threaten the structural stability of the Li metal, thereby influencing the evolution of the Li dendrite morphology. A reasonable strategy is proposed to strike a balance between external pressure and the growth and dissolution of Li dendrites. These findings offer valuable insights into the judicious application of pressure to mitigate the advancement of electroplating reactions.
ABSTRACT
Li metal has attracted considerable attention as the preferred anode material for high-energy batteries. However, Li dendrites have limited the development of Li-metal batteries. Herein, the effects of tuning the porous separator microstructure (SM) for guiding Li dendrite growth and reviving dead Li are revealed using a mechano-electrochemical phase-field model. A strategy of guiding, instead of suppression, was applied to avoid disordered Li dendrite growth. By analyzing the effects of the number of layers, thickness, degree of staggered overlap in the separator, interlayer spacing, and porosity of SM on Li dendrite behavior, we discovered that applying a rationally designed SM can finely guide the Li nucleation and growth direction toward dense deposition. The revival of dead Li was also observed via an in situ experiment on Li dendrites. The reactivation of dead Li after it recontacts Li metal was verified. These findings not only provide fundamental information for the tuning of the SM but can also help better understand the dendrite growth of other alkali metal-ion batteries.
ABSTRACT
Surface Enhanced Raman Scattering (SERS) combined with Thin Layer Chromatography (TLC) has been used for studying characteristic spectrum of molecules in situ in micrograms samples. There are very few report for applying the SERS-TCL method in the study of the effective ingredients of Chinese traditional herbs. Coptis Chinensis France is an often-used clinic Chinese traditional medicine. Its main effective components include berberine and so on, which have antibiotic very wide and also have curative effect on improving the functions of heart vascular cycles. Therefore the concentrations of berberine are very important for the quality control of the medicine. In this work, the ethanol extract of Coptis Chinensis France was first separated by TLC, the SERS was then measure directly after dropping silver gel on the separated spots. The method can be used for the finger print analysis of the berberine. 3 microL of alcohol extract of Coptis Chinensis France with total alkaloids concentration of 1.0 mg.mL was placed on silicon GF254 TLC plate. The sample was separated by developing solvent of n bulanol-Acitic acid-H2O (7:2:1 V/V). The positions of berberine in the sample were confirmed by the standard alkaloid solutions. The Rf values for berberine are 0.29. The silver gel was used as surface enhanced substrate and placed on the separated berberine spots. FT-SERS was measured directly by a Nicolet FT-Raman 910 spectrometer. Berberine belong to isoquinoline alkaloids. His structure can be found in reference. The date of spectrum of berberine can be seen that the band at 1,396 cm-1 due to Ar-OCH3 deformation vibrations was greatly enhanced, indicating that the molecule was absorbed on silver gel strongly through lone-pair electron in Ar-OCH3. The ring stretching mode occurring around 1,548 cm-1 represents isoquinoline ring in the molecule. The band at 727 cm-1 due to CH (ring) deformation vibrations was also enhanced.
